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BRIGHTFOCUS FOUNDATION: Form 990, tax year 2023

View the entire original 990 at ProPublica ↗

Organization
BRIGHTFOCUS FOUNDATION (EIN 23-7337229)
Tax period
2023-04-01 to 2024-03-31
Filed
2024-12-05
IRS object ID
202413409349300636
Schema version
2023v5.1
Source
Download XML · Original 990 at ProPublica

Every field in the e-filed return. Faint text is the IRS element name, for citing.

Return header ReturnHeader

FieldValueIRS element (for citing)
Return2024-12-05T13:40:00-06:00ReturnTs
Tax Period End2024-03-31TaxPeriodEndDt

Preparer Firm PreparerFirmGrp

FieldValueIRS element (for citing)
Preparer Firm EIN881478669PreparerFirmEIN

Preparer Firm Name PreparerFirmName

FieldValueIRS element (for citing)
Business Name Line1CBIZ ADVISORS LLCBusinessNameLine1Txt

Preparer US Address PreparerUSAddress

FieldValueIRS element (for citing)
Address Line11899 L STREET NW 850AddressLine1Txt
CityWASHINGTONCityNm
State AbbreviationDCStateAbbreviationCd
ZIP20036ZIPCd
FieldValueIRS element (for citing)
Return Type990ReturnTypeCd
Tax Period Begin2023-04-01TaxPeriodBeginDt

Filer Filer

FieldValueIRS element (for citing)
EIN237337229EIN

Business Name BusinessName

FieldValueIRS element (for citing)
Business Name Line1BRIGHTFOCUS FOUNDATIONBusinessNameLine1Txt
FieldValueIRS element (for citing)
Business Name ControlBRIGBusinessNameControlTxt
Phone3019483244PhoneNum

US Address USAddress

FieldValueIRS element (for citing)
Address Line122512 GATEWAY CENTER DRIVEAddressLine1Txt
CityCLARKSBURGCityNm
State AbbreviationMDStateAbbreviationCd
ZIP20871ZIPCd

Business Officer BusinessOfficerGrp

FieldValueIRS element (for citing)
PersonSTACY PAGOS HALLERPersonNm
Person TitlePRESIDENT/CEOPersonTitleTxt
Phone3019483244PhoneNum
Signature2024-12-04SignatureDt
Discuss With Paid PreparerYes (1)DiscussWithPaidPreparerInd
FieldValueIRS element (for citing)
IRS Responsible Prty Info CurrYes (1)IRSResponsiblePrtyInfoCurrInd

Preparer Person PreparerPersonGrp

FieldValueIRS element (for citing)
Preparer PersonFRANK SMITHPreparerPersonNm
PTINP00639053PTIN
Phone2022274000PhoneNum
Preparation2024-12-04PreparationDt
FieldValueIRS element (for citing)
Tax2023TaxYr
Build TS2024-10-15 13:58:12ZBuildTS

Form 990 IRS990

FieldValueIRS element (for citing)
Principal OfficerSTACY PAGOS HALLERPrincipalOfficerNm

US Address USAddress

FieldValueIRS element (for citing)
Address Line122512 GATEWAY CENTER DRIVEAddressLine1Txt
CityCLARKSBURGCityNm
State AbbreviationMDStateAbbreviationCd
ZIP20871ZIPCd
FieldValueIRS element (for citing)
Gross Receipts$99,554,872GrossReceiptsAmt
Group Return For Affiliates0GroupReturnForAffiliatesInd
Organization501c3Yes (X)Organization501c3Ind
Website AddressWWW.BRIGHTFOCUS.ORGWebsiteAddressTxt
Type Of Organization CorpYes (X)TypeOfOrganizationCorpInd
Formation1973FormationYr
Legal Domicile StateDCLegalDomicileStateCd
Activity Or MissionBRIGHTFOCUS FOUNDATION (BRIGHTFOCUS) SEEKS A WORLD FREE FROM DISEASES OF MIND AND SIGHT.ActivityOrMissionDesc
Voting Members Governing Body11VotingMembersGoverningBodyCnt
Voting Members Independent11VotingMembersIndependentCnt
Total Employee69TotalEmployeeCnt
Total Volunteers70TotalVolunteersCnt
Total Gross UBI$0TotalGrossUBIAmt
Net Unrelated Bus Txbl Incm$0NetUnrelatedBusTxblIncmAmt
PY Contributions Grants$43,451,535PYContributionsGrantsAmt
CY Contributions Grants$43,373,203CYContributionsGrantsAmt
PY Program Service Revenue$0PYProgramServiceRevenueAmt
CY Program Service Revenue$0CYProgramServiceRevenueAmt
PY Investment Income-$268,284PYInvestmentIncomeAmt
CY Investment Income$4,702,264CYInvestmentIncomeAmt
PY Other Revenue$710,546PYOtherRevenueAmt
CY Other Revenue$587,403CYOtherRevenueAmt
PY Total Revenue$43,893,797PYTotalRevenueAmt
CY Total Revenue$48,662,870CYTotalRevenueAmt
PY Grants And Similar Paid$14,321,603PYGrantsAndSimilarPaidAmt
CY Grants And Similar Paid$10,704,093CYGrantsAndSimilarPaidAmt
PY Benefits Paid To Members$0PYBenefitsPaidToMembersAmt
CY Benefits Paid To Members$0CYBenefitsPaidToMembersAmt
PY Salaries Comp Emp Bnft Paid$6,392,782PYSalariesCompEmpBnftPaidAmt
CY Salaries Comp Emp Bnft Paid$6,876,671CYSalariesCompEmpBnftPaidAmt
PY Total Prof Fndrsng Expns$942,971PYTotalProfFndrsngExpnsAmt
CY Total Prof Fndrsng Expns$952,781CYTotalProfFndrsngExpnsAmt
CY Total Fundraising Expense$12,200,813CYTotalFundraisingExpenseAmt
PY Other Expenses$26,850,858PYOtherExpensesAmt
CY Other Expenses$27,683,861CYOtherExpensesAmt
PY Total Expenses$48,508,214PYTotalExpensesAmt
CY Total Expenses$46,217,406CYTotalExpensesAmt
PY Revenues Less Expenses-$4,614,417PYRevenuesLessExpensesAmt
CY Revenues Less Expenses$2,445,464CYRevenuesLessExpensesAmt
Total Assets BOY$58,626,477TotalAssetsBOYAmt
Total Assets EOY$63,464,652TotalAssetsEOYAmt
Total Liabilities BOY$35,064,709TotalLiabilitiesBOYAmt
Total Liabilities EOY$37,245,915TotalLiabilitiesEOYAmt
Net Assets Or Fund Balances BOY$23,561,768NetAssetsOrFundBalancesBOYAmt
Net Assets Or Fund Balances EOY$26,218,737NetAssetsOrFundBalancesEOYAmt
Info In Schedule O Part IIIYes (X)InfoInScheduleOPartIIIInd
MissionBRIGHTFOCUS FOUNDATION FUNDS EXCEPTIONAL RESEARCH WORLDWIDE TO DEFEAT ALZHEIMER'S DISEASE, MACULAR DEGENERATION, AND GLAUCOMA AND PROVIDES EXPERT INFORMATION ON THESE HEARTBREAKING DISEASES. PLEASE REFER TO SCHEDULE O FOR A COMPLETE OVERVIEW OF OUR MISSION.MissionDesc
Significant New Program Srvc0SignificantNewProgramSrvcInd
Significant Change0SignificantChangeInd
Expense$17,770,389ExpenseAmt
Grant$6,604,227GrantAmt
DescALZHEIMER'S DISEASE RESEARCH (ADR)PLEASE REFER TO SCHEDULE O FOR A COMPLETE DESCRIPTION OF THE ACCOMPLISHMENTS FOR ALZHEIMER'S DISEASE RESEARCH.Desc

Prog Srvc Accom Acty2 ProgSrvcAccomActy2Grp

FieldValueIRS element (for citing)
Expense$8,973,678ExpenseAmt
Grant$3,334,998GrantAmt
DescMACULAR DEGENERATION RESEARCH (MDR)PLEASE REFER TO SCHEDULE O FOR A COMPLETE DESCRIPTION OF THE ACCOMPLISHMENTS FOR MACULAR DEGENERATION RESEARCH.Desc

Prog Srvc Accom Acty3 ProgSrvcAccomActy3Grp

FieldValueIRS element (for citing)
Expense$2,058,076ExpenseAmt
Grant$764,868GrantAmt
DescNATIONAL GLAUCOMA RESEARCH (NGR) PLEASE REFER TO SCHEDULE O FOR A COMPLETE DESCRIPTION OF THE ACCOMPLISHMENTS FOR NATIONAL GLAUCOMA RESEARCH.Desc
FieldValueIRS element (for citing)
Total Program Service Expenses$28,802,143TotalProgramServiceExpensesAmt
Described In Section501c3Yes (1)DescribedInSection501c3Ind
Schedule B RequiredYes (1)ScheduleBRequiredInd
Political Campaign Acty0PoliticalCampaignActyInd
Lobbying ActivitiesYes (1)LobbyingActivitiesInd
Subject To Proxy Tax0SubjectToProxyTaxInd
Donor Advised Fund0DonorAdvisedFundInd
Conservation Easements0ConservationEasementsInd
Collections Of Art0CollectionsOfArtInd
Credit Counseling0CreditCounselingInd
Donor Rstr Or Quasi EndowmentsYes (1)DonorRstrOrQuasiEndowmentsInd
Report Land Building EquipmentYes (1)ReportLandBuildingEquipmentInd
Report Investments Other SecYes (1)ReportInvestmentsOtherSecInd
Report Program Related Invst0ReportProgramRelatedInvstInd
Report Other Assets0ReportOtherAssetsInd
Report Other LiabilitiesYes (1)ReportOtherLiabilitiesInd
Include FIN48 FootnoteYes (1)IncludeFIN48FootnoteInd
Independent Audit Fincl Stmt0IndependentAuditFinclStmtInd
Consolidated Audit Fincl StmtYes (1)ConsolidatedAuditFinclStmtInd
School Operating0SchoolOperatingInd
Foreign Office0ForeignOfficeInd
Foreign ActivitiesYes (1)ForeignActivitiesInd
More Than5000 K To OrgYes (1)MoreThan5000KToOrgInd
More Than5000 K To Individuals0MoreThan5000KToIndividualsInd
Professional FundraisingYes (1)ProfessionalFundraisingInd
Fundraising ActivitiesYes (1)FundraisingActivitiesInd
Gaming Activities0GamingActivitiesInd
Operate Hospital0OperateHospitalInd
Grants To OrganizationsYes (1)GrantsToOrganizationsInd
Grants To Individuals0GrantsToIndividualsInd
Schedule J RequiredYes (1)ScheduleJRequiredInd
Tax Exempt Bonds0TaxExemptBondsInd
Engaged In Excess Benefit Trans0EngagedInExcessBenefitTransInd
PY Excess Benefit Trans0PYExcessBenefitTransInd
Loan Outstanding0LoanOutstandingInd
Grant To Related Person0GrantToRelatedPersonInd
Business Rln With Org Mem0BusinessRlnWithOrgMemInd
Business Rln With Fam Mem0BusinessRlnWithFamMemInd
Business Rln With35 Ctrl Ent0BusinessRlnWith35CtrlEntInd
Deductible Non Cash ContriYes (1)DeductibleNonCashContriInd
Deductible Art Contribution0DeductibleArtContributionInd
Terminate Operations0TerminateOperationsInd
Partial Liquidation0PartialLiquidationInd
Disregarded EntityYes (1)DisregardedEntityInd
Related Entity0RelatedEntityInd
Related Organization Ctrl Ent0RelatedOrganizationCtrlEntInd
Trnsfr Exmpt Non Chrtbl Rltd Org0TrnsfrExmptNonChrtblRltdOrgInd
Activities Conducted Prtshp0ActivitiesConductedPrtshpInd
Schedule O RequiredYes (1)ScheduleORequiredInd
IRP Document96IRPDocumentCnt
IRP Document W2 G0IRPDocumentW2GCnt
Backup Wthld ComplianceYes (1)BackupWthldComplianceInd
Employee69EmployeeCnt
Employment Tax Returns FiledYes (1)EmploymentTaxReturnsFiledInd
Unrelated Bus Incm Over Limit0UnrelatedBusIncmOverLimitInd
Foreign Financial Account0ForeignFinancialAccountInd
Prohibited Tax Shelter Trans0ProhibitedTaxShelterTransInd
Taxable Party Notification0TaxablePartyNotificationInd
Nondeductible Contributions0NondeductibleContributionsInd
Quid Pro Quo ContributionsYes (1)QuidProQuoContributionsInd
Quid Pro Quo Contri DisclYes (1)QuidProQuoContriDisclInd
Form8282 Property Disposed Of0Form8282PropertyDisposedOfInd
Rcv Fnds To Pay Prsnl Bnft Cntrct0RcvFndsToPayPrsnlBnftCntrctInd
Pay Premiums Prsnl Bnft Cntrct0PayPremiumsPrsnlBnftCntrctInd
Indoor Tanning Services0IndoorTanningServicesInd
Subj To Tax Rmnrtn Ex Prcht Pymt0SubjToTaxRmnrtnExPrchtPymtInd
Subject To Excs Tax Net Invst Inc0SubjectToExcsTaxNetInvstIncInd
Info In Schedule O Part VIYes (X)InfoInScheduleOPartVIInd
Governing Body Voting Members11GoverningBodyVotingMembersCnt
Independent Voting Member11IndependentVotingMemberCnt
Family Or Business Rln0FamilyOrBusinessRlnInd
Delegation Of Mgmt Duties0DelegationOfMgmtDutiesInd
Change To Org Documents0ChangeToOrgDocumentsInd
Material Diversion Or Misuse0MaterialDiversionOrMisuseInd
Members Or Stockholders0MembersOrStockholdersInd
Election Of Board Members0ElectionOfBoardMembersInd
Decisions Subject To Approva0DecisionsSubjectToApprovaInd
Minutes Of Governing BodyYes (1)MinutesOfGoverningBodyInd
Minutes Of CommitteesYes (1)MinutesOfCommitteesInd
Officer Mailing Address0OfficerMailingAddressInd
Local Chapters0LocalChaptersInd
Form990 Provided To Gvrn BodyYes (1)Form990ProvidedToGvrnBodyInd
Conflict Of Interest PolicyYes (1)ConflictOfInterestPolicyInd
Annual Disclosure Covered PrsnYes (1)AnnualDisclosureCoveredPrsnInd
Regular Monitoring EnfrcYes (1)RegularMonitoringEnfrcInd
Whistleblower PolicyYes (1)WhistleblowerPolicyInd
Document Retention PolicyYes (1)DocumentRetentionPolicyInd
Compensation Process CEOYes (1)CompensationProcessCEOInd
Compensation Process OtherYes (1)CompensationProcessOtherInd
Investment In Joint Venture0InvestmentInJointVentureInd
States Where Copy Of Return Is FldAKStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldALStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldARStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldCAStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldCTStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldFLStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldGAStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldHIStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldILStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldKSStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldKYStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldMEStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldMDStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldMAStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldMIStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldMNStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldMOStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldMSStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldNCStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldNDStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldNHStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldNJStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldNMStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldNYStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldOHStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldOKStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldORStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldPAStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldRIStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldSCStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldTNStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldUTStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldVAStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldWAStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldWIStatesWhereCopyOfReturnIsFldCd
States Where Copy Of Return Is FldWVStatesWhereCopyOfReturnIsFldCd
Own WebsiteYes (X)OwnWebsiteInd
Other WebsiteYes (X)OtherWebsiteInd
Upon RequestYes (X)UponRequestInd

Books In Care Of Detail BooksInCareOfDetail

Business Name BusinessName

FieldValueIRS element (for citing)
Business Name Line1JONATHAN WALSHBusinessNameLine1Txt
FieldValueIRS element (for citing)
Phone3015569385PhoneNum

US Address USAddress

FieldValueIRS element (for citing)
Address Line122512 GATEWAY CENTER DRIVEAddressLine1Txt
CityCLARKSBURGCityNm
State AbbreviationMDStateAbbreviationCd
ZIP20871ZIPCd

Form990 Part VII Section A Form990PartVIISectionAGrp (23 entries)

TitleTitleTxtAverage Hours Per WeekAverageHoursPerWeekRtIndividual Trustee Or DirectorIndividualTrusteeOrDirectorIndOfficerOfficerIndReportable Comp From OrgReportableCompFromOrgAmtReportable Comp From Rltd OrgReportableCompFromRltdOrgAmtOther CompensationOtherCompensationAmtKey EmployeeKeyEmployeeIndHighest Compensated EmployeeHighestCompensatedEmployeeInd
PATRICIA M STEWART
CHAIR10.00Yes (X)Yes (X)$0$0$0
CECILIA ARRADAZA
VICE CHAIR6.00Yes (X)Yes (X)$0$0$0
SCOTT KAISER MD DIRECTOR
UNTIL 10/2023 THEN SECRETARY6.00Yes (X)Yes (X)$0$0$0
EDWARD FINLEY
TREASURER - UNTIL 12/20238.00Yes (X)Yes (X)$0$0$0
SHAWA GOTTLIEB
TREASURER - AS OF 12/20236.00Yes (X)Yes (X)$0$0$0
PAUL CAMPBELL
DIRECTOR5.00Yes (X)$0$0$0
HERBERT L DRAYTON III
DIRECTOR - AS OF 6/20235.00Yes (X)$0$0$0
DANA GRIFFIN
DIRECTOR5.00Yes (X)$0$0$0
TONYA MATTHEWS PHD
DIRECTOR5.00Yes (X)$0$0$0
ANN SECLOW
DIRECTOR5.00Yes (X)$0$0$0
JAN M STOUFFER PHD
DIRECTOR6.00Yes (X)$0$0$0
THOMAS F FREDDO OD PHD
DIRECTOR - AS OF 6/20235.00Yes (X)$0$0$0
STACY PAGOS HALLER
PRESIDENT/CEO45.00Yes (X)$410,407$0$57,485
NANCY LYNN
SR. VP STRATEGIC PARTNERSHIPS45.00$261,148$0$61,492Yes (X)
R BRIAN ELDERTON
SR. VP, DEVELOPMENT45.00$253,852$0$48,328Yes (X)
DAVID F MARKS CPA CMA
VP, FINANCE & ADMIN TILL 10/202345.00$156,941$0$54,684Yes (X)
DIANE BOVENKAMP PHD
VP, SCIENTIFIC AFFAIRS45.00$190,217$0$22,240Yes (X)
KACI BAEZ
VP, INTEGRATED MKTING & COMM.45.00$172,602$0$26,649Yes (X)
AYO ABRAHAM CPA CGMA
CONTROLLER UNTIL 8/202340.00$138,926$0$21,356Yes (X)
JEFFREY HONAKER
SR. MGR. OPS AND BUILDING40.00$112,157$0$44,404Yes (X)
LISA MORGAN
DIRECTOR OF ANNUAL GIVING40.00$128,316$0$33,647Yes (X)
PREETI SUBRAMANIAN PHD DIR
OF SCIENT. PROGRAMS, VISION SCIENCE40.00$135,115$0$15,657Yes (X)
SHARYN ROSSI PHD DIR OF
SCIENT. PROGRAMS, NEUROSCIENCE40.00$125,361$0$43,832Yes (X)
FieldValueIRS element (for citing)
Total Reportable Comp From Org$2,085,042TotalReportableCompFromOrgAmt
Tot Reportable Comp Rltd Org$0TotReportableCompRltdOrgAmt
Total Other Compensation$429,774TotalOtherCompensationAmt
Indiv Rcvd Greater Than100 K11IndivRcvdGreaterThan100KCnt
Former Ofcr Employees Listed0FormerOfcrEmployeesListedInd
Total Comp Greater Than150 KYes (1)TotalCompGreaterThan150KInd
Compensation From Other Srcs0CompensationFromOtherSrcsInd

Contractor Compensation ContractorCompensationGrp (5 entries)

Address Line1ContractorAddress/USAddress/AddressLine1TxtCityContractorAddress/USAddress/CityNmState AbbreviationContractorAddress/USAddress/StateAbbreviationCdZIPContractorAddress/USAddress/ZIPCdServicesServicesDescCompensationCompensationAmt
RKD GROUP
35 PARKWOOD DRIVE SUITE 160HOPKINTONMA01748PUBLIC AWARENESS CONSULTING & MATERIALS$9,668,749
ADSTRA LLC
750 COLLEGE ROAD EAST STE 201PRINCETONNJ08540MAIL LIST RENTAL$1,382,715
ALLEGIANCE GROUP
2300 CLARENDON BLVD SUITE 925ARLINGTONVA22201ONLINE PUBLIC AWARENESS CONSULTING$622,303
THREESIXTYEIGHT
212 S 14TH STREET SUITE BBATON ROUGELA70802ONLINE MARKETING CONSULTING$352,659
DATA MANAGEMENT INC
160 STONE STREETSTONEVILLENC27048DATABASE MANAGEMENT$273,722
FieldValueIRS element (for citing)
Cntrct Rcvd Greater Than100 K17CntrctRcvdGreaterThan100KCnt
Federated Campaigns$144,175FederatedCampaignsAmt
Fundraising$250,290FundraisingAmt
All Other Contributions$42,978,738AllOtherContributionsAmt
Noncash Contributions$87,848NoncashContributionsAmt
Total Contributions$43,373,203TotalContributionsAmt

Investment Income InvestmentIncomeGrp

FieldValueIRS element (for citing)
Total Revenue Column$798,230TotalRevenueColumnAmt
Exclusion$798,230ExclusionAmt

Royalties Revenue RoyaltiesRevenueGrp

FieldValueIRS element (for citing)
Total Revenue Column$453,517TotalRevenueColumnAmt
Exclusion$453,517ExclusionAmt

Gross Rents GrossRentsGrp

FieldValueIRS element (for citing)
Real$658,538RealAmt

Less Rental Expenses LessRentalExpensesGrp

FieldValueIRS element (for citing)
Real$190,252RealAmt

Rental Income Or Loss RentalIncomeOrLossGrp

FieldValueIRS element (for citing)
Real$468,286RealAmt

Net Rental Income Or Loss NetRentalIncomeOrLossGrp

FieldValueIRS element (for citing)
Total Revenue Column$468,286TotalRevenueColumnAmt
Exclusion$468,286ExclusionAmt

Gross Amount Sales Assets GrossAmountSalesAssetsGrp

FieldValueIRS element (for citing)
Securities$54,207,314SecuritiesAmt

Less Cost Oth Basis Sales Expnss LessCostOthBasisSalesExpnssGrp

FieldValueIRS element (for citing)
Securities$50,303,280SecuritiesAmt

Gain Or Loss GainOrLossGrp

FieldValueIRS element (for citing)
Securities$3,904,034SecuritiesAmt

Net Gain Or Loss Investments NetGainOrLossInvestmentsGrp

FieldValueIRS element (for citing)
Total Revenue Column$3,904,034TotalRevenueColumnAmt
Exclusion$3,904,034ExclusionAmt
FieldValueIRS element (for citing)
Fundraising Gross Income$64,000FundraisingGrossIncomeAmt
Contri Rpt Fundraising Event$250,290ContriRptFundraisingEventAmt
Fundraising Direct Expenses$398,470FundraisingDirectExpensesAmt

Net Incm From Fundraising Evt NetIncmFromFundraisingEvtGrp

FieldValueIRS element (for citing)
Total Revenue Column-$334,470TotalRevenueColumnAmt
Exclusion-$334,470ExclusionAmt

Other Revenue Misc OtherRevenueMiscGrp

FieldValueIRS element (for citing)
DescOTHER INCOMEDesc
Business900099BusinessCd
Total Revenue Column$70TotalRevenueColumnAmt
Exclusion$70ExclusionAmt
FieldValueIRS element (for citing)
Other Revenue Total$70OtherRevenueTotalAmt

Total Revenue TotalRevenueGrp

FieldValueIRS element (for citing)
Total Revenue Column$48,662,870TotalRevenueColumnAmt
Related Or Exempt Func Income$0RelatedOrExemptFuncIncomeAmt
Unrelated Business Revenue$0UnrelatedBusinessRevenueAmt
Exclusion$5,289,667ExclusionAmt

Grants To Domestic Orgs GrantsToDomesticOrgsGrp

FieldValueIRS element (for citing)
Total$7,478,202TotalAmt
Program Services$7,478,202ProgramServicesAmt

Foreign Grants ForeignGrantsGrp

FieldValueIRS element (for citing)
Total$3,225,891TotalAmt
Program Services$3,225,891ProgramServicesAmt

Comp Current Ofcr Directors CompCurrentOfcrDirectorsGrp

FieldValueIRS element (for citing)
Total$1,673,188TotalAmt
Program Services$1,075,672ProgramServicesAmt
Management And General$284,661ManagementAndGeneralAmt
Fundraising$312,855FundraisingAmt

Other Salaries And Wages OtherSalariesAndWagesGrp

FieldValueIRS element (for citing)
Total$3,983,008TotalAmt
Program Services$1,920,677ProgramServicesAmt
Management And General$1,463,124ManagementAndGeneralAmt
Fundraising$599,207FundraisingAmt

Pension Plan Contributions PensionPlanContributionsGrp

FieldValueIRS element (for citing)
Total$219,886TotalAmt
Program Services$105,789ProgramServicesAmt
Management And General$83,997ManagementAndGeneralAmt
Fundraising$30,100FundraisingAmt

Other Employee Benefits OtherEmployeeBenefitsGrp

FieldValueIRS element (for citing)
Total$663,765TotalAmt
Program Services$344,647ProgramServicesAmt
Management And General$218,083ManagementAndGeneralAmt
Fundraising$101,035FundraisingAmt

Payroll Taxes PayrollTaxesGrp

FieldValueIRS element (for citing)
Total$336,824TotalAmt
Program Services$177,521ProgramServicesAmt
Management And General$105,575ManagementAndGeneralAmt
Fundraising$53,728FundraisingAmt

Fees For Services Legal FeesForServicesLegalGrp

FieldValueIRS element (for citing)
Total$75,990TotalAmt
Program Services$38,302ProgramServicesAmt
Management And General$27,836ManagementAndGeneralAmt
Fundraising$9,852FundraisingAmt

Fees For Services Accounting FeesForServicesAccountingGrp

FieldValueIRS element (for citing)
Total$81,938TotalAmt
Program Services$41,300ProgramServicesAmt
Management And General$30,015ManagementAndGeneralAmt
Fundraising$10,623FundraisingAmt

Fees For Services Prof Fundraising FeesForServicesProfFundraising

FieldValueIRS element (for citing)
Total$952,781TotalAmt
Fundraising$952,781FundraisingAmt

Fees For Srvc Invst Mgmnt Fees FeesForSrvcInvstMgmntFeesGrp

FieldValueIRS element (for citing)
Total$273,750TotalAmt
Management And General$273,750ManagementAndGeneralAmt

Fees For Services Other FeesForServicesOtherGrp

FieldValueIRS element (for citing)
Total$1,594,728TotalAmt
Program Services$1,474,665ProgramServicesAmt
Management And General$120,063ManagementAndGeneralAmt

Advertising AdvertisingGrp

FieldValueIRS element (for citing)
Total$1,079,425TotalAmt
Program Services$596,196ProgramServicesAmt
Fundraising$483,229FundraisingAmt

Office Expenses OfficeExpensesGrp

FieldValueIRS element (for citing)
Total$970,677TotalAmt
Program Services$337,172ProgramServicesAmt
Management And General$453,550ManagementAndGeneralAmt
Fundraising$179,955FundraisingAmt

Information Technology InformationTechnologyGrp

FieldValueIRS element (for citing)
Total$831,368TotalAmt
Program Services$533,749ProgramServicesAmt
Management And General$195,594ManagementAndGeneralAmt
Fundraising$102,025FundraisingAmt

Occupancy OccupancyGrp

FieldValueIRS element (for citing)
Total$450,550TotalAmt
Program Services$263,051ProgramServicesAmt
Management And General$141,343ManagementAndGeneralAmt
Fundraising$46,156FundraisingAmt

Travel TravelGrp

FieldValueIRS element (for citing)
Total$333,566TotalAmt
Program Services$258,676ProgramServicesAmt
Management And General$36,837ManagementAndGeneralAmt
Fundraising$38,053FundraisingAmt

Conferences Meetings ConferencesMeetingsGrp

FieldValueIRS element (for citing)
Total$1,447,219TotalAmt
Program Services$1,387,712ProgramServicesAmt
Management And General$15,731ManagementAndGeneralAmt
Fundraising$43,776FundraisingAmt

Interest InterestGrp

FieldValueIRS element (for citing)
Total$335,181TotalAmt
Management And General$335,181ManagementAndGeneralAmt

Depreciation Depletion DepreciationDepletionGrp

FieldValueIRS element (for citing)
Total$611,056TotalAmt
Program Services$324,229ProgramServicesAmt
Management And General$207,081ManagementAndGeneralAmt
Fundraising$79,746FundraisingAmt

Insurance InsuranceGrp

FieldValueIRS element (for citing)
Total$89,387TotalAmt
Program Services$38,558ProgramServicesAmt
Management And General$29,158ManagementAndGeneralAmt
Fundraising$21,671FundraisingAmt

Other Expenses OtherExpensesGrp (4 entries)

DescDescTotalTotalAmtProgram ServicesProgramServicesAmtManagement And GeneralManagementAndGeneralAmtFundraisingFundraisingAmt
PUB. AWARENESS POSTAGE$8,449,837$4,024,943$525,953$3,898,941
PUB. AWARENESS PRINTING$7,323,026$3,404,221$456,105$3,462,700
PUB. AWARENESS COMP.$2,088,455$996,071$108,658$983,726
LIST RENTAL$1,647,708$754,899$102,155$790,654

Total Functional Expenses TotalFunctionalExpensesGrp

FieldValueIRS element (for citing)
Total$46,217,406TotalAmt
Program Services$28,802,143ProgramServicesAmt
Management And General$5,214,450ManagementAndGeneralAmt
Fundraising$12,200,813FundraisingAmt
FieldValueIRS element (for citing)
Joint CostsYes (X)JointCostsInd

Total Joint Costs TotalJointCostsGrp

FieldValueIRS element (for citing)
Total$18,479,592TotalAmt
Program Services$7,878,147ProgramServicesAmt
Management And General$1,129,037ManagementAndGeneralAmt
Fundraising$9,472,408FundraisingAmt

Cash Non Interest Bearing CashNonInterestBearingGrp

FieldValueIRS element (for citing)
BOY$205,653BOYAmt
EOY$829,628EOYAmt

Savings And Temp Cash Invst SavingsAndTempCashInvstGrp

FieldValueIRS element (for citing)
BOY$3,889,254BOYAmt
EOY$8,516,562EOYAmt

Pledges And Grants Receivable PledgesAndGrantsReceivableGrp

FieldValueIRS element (for citing)
BOY$6,522,988BOYAmt
EOY$6,199,054EOYAmt

Accounts Receivable AccountsReceivableGrp

FieldValueIRS element (for citing)
BOY$165,585BOYAmt
EOY$23,832EOYAmt

Inventories For Sale Or Use InventoriesForSaleOrUseGrp

FieldValueIRS element (for citing)
BOY$51,738BOYAmt
EOY$28,325EOYAmt

Prepaid Expenses Defrd Charges PrepaidExpensesDefrdChargesGrp

FieldValueIRS element (for citing)
BOY$50,244BOYAmt
EOY$998,282EOYAmt
FieldValueIRS element (for citing)
Land Bldg Equip Cost Or Other Bss$13,397,952LandBldgEquipCostOrOtherBssAmt
Land Bldg Equip Accum Deprec$5,550,668LandBldgEquipAccumDeprecAmt

Land Bldg Equip Basis Net LandBldgEquipBasisNetGrp

FieldValueIRS element (for citing)
BOY$8,128,279BOYAmt
EOY$7,847,284EOYAmt

Investments Pub Traded Sec InvestmentsPubTradedSecGrp

FieldValueIRS element (for citing)
BOY$39,542,541BOYAmt
EOY$31,237,150EOYAmt

Investments Other Securities InvestmentsOtherSecuritiesGrp

FieldValueIRS element (for citing)
EOY$7,784,535EOYAmt

Other Assets Total OtherAssetsTotalGrp

FieldValueIRS element (for citing)
BOY$70,195BOYAmt
EOY$0EOYAmt

Total Assets TotalAssetsGrp

FieldValueIRS element (for citing)
BOY$58,626,477BOYAmt
EOY$63,464,652EOYAmt

Accounts Payable Accr Expnss AccountsPayableAccrExpnssGrp

FieldValueIRS element (for citing)
BOY$1,112,727BOYAmt
EOY$2,580,327EOYAmt

Grants Payable GrantsPayableGrp

FieldValueIRS element (for citing)
BOY$33,119,925BOYAmt
EOY$24,991,458EOYAmt

Deferred Revenue DeferredRevenueGrp

FieldValueIRS element (for citing)
BOY$116,500BOYAmt
EOY$0EOYAmt

Mortg Notes Pybl Scrd Invst Prop MortgNotesPyblScrdInvstPropGrp

FieldValueIRS element (for citing)
BOY$0BOYAmt
EOY$9,000,000EOYAmt

Other Liabilities OtherLiabilitiesGrp

FieldValueIRS element (for citing)
BOY$715,557BOYAmt
EOY$674,130EOYAmt

Total Liabilities TotalLiabilitiesGrp

FieldValueIRS element (for citing)
BOY$35,064,709BOYAmt
EOY$37,245,915EOYAmt
FieldValueIRS element (for citing)
Organization Follows FASB117Yes (X)OrganizationFollowsFASB117Ind

No Donor Restriction Net Assets NoDonorRestrictionNetAssetsGrp

FieldValueIRS element (for citing)
BOY$10,360,299BOYAmt
EOY$12,270,789EOYAmt

Donor Restriction Net Assets DonorRestrictionNetAssetsGrp

FieldValueIRS element (for citing)
BOY$13,201,469BOYAmt
EOY$13,947,948EOYAmt

Total Net Assets Fund Balance TotalNetAssetsFundBalanceGrp

FieldValueIRS element (for citing)
BOY$23,561,768BOYAmt
EOY$26,218,737EOYAmt

Tot Liab Net Assets Fund Balance TotLiabNetAssetsFundBalanceGrp

FieldValueIRS element (for citing)
BOY$58,626,477BOYAmt
EOY$63,464,652EOYAmt
FieldValueIRS element (for citing)
Info In Schedule O Part XIYes (X)InfoInScheduleOPartXIInd
Reconcilation Revenue Expnss$2,445,464ReconcilationRevenueExpnssAmt
Net Unrlzd Gains Losses Invst-$94,500NetUnrlzdGainsLossesInvstAmt
Other Changes In Net Assets$306,005OtherChangesInNetAssetsAmt
Method Of Accounting AccrualYes (X)MethodOfAccountingAccrualInd
Accountant Compile Or Review0AccountantCompileOrReviewInd
FS AuditedYes (1)FSAuditedInd

FS Audited Basis FSAuditedBasisGrp

FieldValueIRS element (for citing)
Consolidated Basis Fincl StmtYes (X)ConsolidatedBasisFinclStmtInd
FieldValueIRS element (for citing)
Audit CommitteeYes (1)AuditCommitteeInd
Federal Grant Audit Required0FederalGrantAuditRequiredInd

Schedule A IRS990ScheduleA

FieldValueIRS element (for citing)
Public Organization170Yes (X)PublicOrganization170Ind

Gifts Grants Contri Rcvd170 GiftsGrantsContriRcvd170Grp

FieldValueIRS element (for citing)
Current Tax Year Minus4 Years$35,740,875CurrentTaxYearMinus4YearsAmt
Current Tax Year Minus3 Years$48,502,473CurrentTaxYearMinus3YearsAmt
Current Tax Year Minus2 Years$46,522,410CurrentTaxYearMinus2YearsAmt
Current Tax Year Minus1 Year$43,451,535CurrentTaxYearMinus1YearAmt
Current Tax Year$43,373,203CurrentTaxYearAmt
Total$217,590,496TotalAmt

Total Calendar Year170 TotalCalendarYear170Grp

FieldValueIRS element (for citing)
Current Tax Year Minus4 Years$35,740,875CurrentTaxYearMinus4YearsAmt
Current Tax Year Minus3 Years$48,502,473CurrentTaxYearMinus3YearsAmt
Current Tax Year Minus2 Years$46,522,410CurrentTaxYearMinus2YearsAmt
Current Tax Year Minus1 Year$43,451,535CurrentTaxYearMinus1YearAmt
Current Tax Year$43,373,203CurrentTaxYearAmt
Total$217,590,496TotalAmt
FieldValueIRS element (for citing)
Substantial Contributors Tot$431,008SubstantialContributorsTotAmt
Public Support Total170$217,159,488PublicSupportTotal170Amt

Gross Investment Income170 GrossInvestmentIncome170Grp

FieldValueIRS element (for citing)
Current Tax Year Minus4 Years$2,176,998CurrentTaxYearMinus4YearsAmt
Current Tax Year Minus3 Years$1,887,633CurrentTaxYearMinus3YearsAmt
Current Tax Year Minus2 Years$2,074,361CurrentTaxYearMinus2YearsAmt
Current Tax Year Minus1 Year$1,972,869CurrentTaxYearMinus1YearAmt
Current Tax Year$1,910,285CurrentTaxYearAmt
Total$10,022,146TotalAmt

Other Income170 OtherIncome170Grp

FieldValueIRS element (for citing)
Current Tax Year Minus2 Years$7,500CurrentTaxYearMinus2YearsAmt
Current Tax Year$70CurrentTaxYearAmt
Total$7,570TotalAmt
FieldValueIRS element (for citing)
Total Support$227,620,212TotalSupportAmt
Public Support CY1700.95400PublicSupportCY170Pct
Public Support PY1700.95300PublicSupportPY170Pct
Thirty Thr Pct Suprt Tests CY170Yes (X)ThirtyThrPctSuprtTestsCY170Ind

Form990 Schedule A Part VI Form990ScheduleAPartVIGrp

FieldValueIRS element (for citing)
Form And Line ReferenceSCHEDULE A, PART II, LINE 10, EXPLANATION OF OTHER INCOME:FormAndLineReferenceDesc
ExplanationSAVINGS BOND PAYOUT - 2021 AMOUNT: $ 7,500. MISCELLANEOUS - 2023 AMOUNT: $ 70.ExplanationTxt

Schedule B IRS990ScheduleB

Contributor Information ContributorInformationGrp

FieldValueIRS element (for citing)
ContributorRESTRICTEDContributorNum

Contributor Business Name ContributorBusinessName

FieldValueIRS element (for citing)
Business Name Line1RESTRICTEDBusinessNameLine1

Contributor US Address ContributorUSAddress

FieldValueIRS element (for citing)
Address Line1RESTRICTEDAddressLine1
Address Line2RESTRICTEDAddressLine2
CityRESTRICTEDCity
StateRESTRICTEDState
ZIP CodeRESTRICTEDZIPCode
FieldValueIRS element (for citing)
Total ContributionsRESTRICTEDTotalContributionsAmt

Schedule C IRS990ScheduleC

Total Grassroots Lobbying TotalGrassrootsLobbyingGrp

FieldValueIRS element (for citing)
Filing Organizations Total$0FilingOrganizationsTotalAmt

Total Direct Lobbying TotalDirectLobbyingGrp

FieldValueIRS element (for citing)
Filing Organizations Total$0FilingOrganizationsTotalAmt

Total Lobbying Expend TotalLobbyingExpendGrp

FieldValueIRS element (for citing)
Filing Organizations Total$0FilingOrganizationsTotalAmt

Other Exempt Purpose Expend OtherExemptPurposeExpendGrp

FieldValueIRS element (for citing)
Filing Organizations Total$45,579,597FilingOrganizationsTotalAmt

Total Exempt Purpose Expend TotalExemptPurposeExpendGrp

FieldValueIRS element (for citing)
Filing Organizations Total$45,579,597FilingOrganizationsTotalAmt

Lobbying Nontaxable Amount LobbyingNontaxableAmountGrp

FieldValueIRS element (for citing)
Filing Organizations Total$1,000,000FilingOrganizationsTotalAmt

Grassroots Nontaxable GrassrootsNontaxableGrp

FieldValueIRS element (for citing)
Filing Organizations Total$250,000FilingOrganizationsTotalAmt

Tot Lbbyng Grassroot Mns Non Tx TotLbbyngGrassrootMnsNonTxGrp

FieldValueIRS element (for citing)
Filing Organizations Total$0FilingOrganizationsTotalAmt

Tot Lbby Expend Mns Lbbyng Non Tx TotLbbyExpendMnsLbbyngNonTxGrp

FieldValueIRS element (for citing)
Filing Organizations Total$0FilingOrganizationsTotalAmt

Avg Lobbying Nontaxable Amount AvgLobbyingNontaxableAmountGrp

FieldValueIRS element (for citing)
Current Year Minus3$1,000,000CurrentYearMinus3Amt
Current Year Minus2$1,000,000CurrentYearMinus2Amt
Current Year Minus1$1,000,000CurrentYearMinus1Amt
Current Year$1,000,000CurrentYearAmt
Total$4,000,000TotalAmt
FieldValueIRS element (for citing)
Lobbying Ceiling$6,000,000LobbyingCeilingAmt

Avg Grassroots Nontaxable AvgGrassrootsNontaxableGrp

FieldValueIRS element (for citing)
Current Year Minus3$250,000CurrentYearMinus3Amt
Current Year Minus2$250,000CurrentYearMinus2Amt
Current Year Minus1$250,000CurrentYearMinus1Amt
Current Year$250,000CurrentYearAmt
Total$1,000,000TotalAmt
FieldValueIRS element (for citing)
Grassroots Ceiling$1,500,000GrassrootsCeilingAmt

Schedule D IRS990ScheduleD

CY Endwmt Fund CYEndwmtFundGrp

FieldValueIRS element (for citing)
Beginning Year Balance$310,022BeginningYearBalanceAmt
Contributions$23,199ContributionsAmt
Investment Earnings Or Losses-$23,199InvestmentEarningsOrLossesAmt
Other Expenditures$23,199OtherExpendituresAmt
End Year Balance$286,823EndYearBalanceAmt

CY Minus1 Yr Endwmt Fund CYMinus1YrEndwmtFundGrp

FieldValueIRS element (for citing)
Beginning Year Balance$325,000BeginningYearBalanceAmt
Contributions$14,978ContributionsAmt
Investment Earnings Or Losses-$14,978InvestmentEarningsOrLossesAmt
Other Expenditures$14,978OtherExpendituresAmt
End Year Balance$310,022EndYearBalanceAmt

CY Minus2 Yr Endwmt Fund CYMinus2YrEndwmtFundGrp

FieldValueIRS element (for citing)
Beginning Year Balance$302,000BeginningYearBalanceAmt
Contributions$13,634ContributionsAmt
Investment Earnings Or Losses$23,000InvestmentEarningsOrLossesAmt
Other Expenditures$13,634OtherExpendituresAmt
End Year Balance$325,000EndYearBalanceAmt

CY Minus3 Yr Endwmt Fund CYMinus3YrEndwmtFundGrp

FieldValueIRS element (for citing)
Beginning Year Balance$302,000BeginningYearBalanceAmt
Contributions$14,744ContributionsAmt
Other Expenditures$14,744OtherExpendituresAmt
End Year Balance$302,000EndYearBalanceAmt

CY Minus4 Yr Endwmt Fund CYMinus4YrEndwmtFundGrp

FieldValueIRS element (for citing)
Beginning Year Balance$302,000BeginningYearBalanceAmt
Contributions$14,778ContributionsAmt
Other Expenditures$14,778OtherExpendituresAmt
End Year Balance$302,000EndYearBalanceAmt
FieldValueIRS element (for citing)
Board Designated Balance EOY0.00000BoardDesignatedBalanceEOYPct
Prmnnt Endowment Balance EOY1.00000PrmnntEndowmentBalanceEOYPct
Term Endowment Balance EOY0.00000TermEndowmentBalanceEOYPct
Endowments Held Unrelated OrgYes (1)EndowmentsHeldUnrelatedOrgInd
Endowments Held Related Org0EndowmentsHeldRelatedOrgInd

Land LandGrp

FieldValueIRS element (for citing)
Investment Cost Or Other Basis$2,800,000InvestmentCostOrOtherBasisAmt
Other Cost Or Other Basis$1,147,363OtherCostOrOtherBasisAmt
Book Value$3,947,363BookValueAmt

Buildings BuildingsGrp

FieldValueIRS element (for citing)
Investment Cost Or Other Basis$1,629,400InvestmentCostOrOtherBasisAmt
Other Cost Or Other Basis$5,422,721OtherCostOrOtherBasisAmt
Depreciation$4,283,276DepreciationAmt
Book Value$2,768,845BookValueAmt

Equipment EquipmentGrp

FieldValueIRS element (for citing)
Other Cost Or Other Basis$2,181,715OtherCostOrOtherBasisAmt
Depreciation$1,068,672DepreciationAmt
Book Value$1,113,043BookValueAmt

Other Land Buildings OtherLandBuildingsGrp

FieldValueIRS element (for citing)
Other Cost Or Other Basis$216,753OtherCostOrOtherBasisAmt
Depreciation$198,720DepreciationAmt
Book Value$18,033BookValueAmt
FieldValueIRS element (for citing)
Total Book Value Land Buildings$7,847,284TotalBookValueLandBuildingsAmt

Other Securities OtherSecuritiesGrp (2 entries)

DescDescBook ValueBookValueAmtMethod ValuationMethodValuationCd
MAKENA PERPETUAL PRIVATE EQUITY FUND$3,717,628F
MAKENA PERPETUAL VENTURE CAPITAL FUND$4,066,907F
FieldValueIRS element (for citing)
Total Book Value Securities$7,784,535TotalBookValueSecuritiesAmt

Other Liabilities Org OtherLiabilitiesOrgGrp (3 entries)

DescDescAmtAmt
CHARITABLE GIFT ANNUITIES$536,350
CAPITAL LEASE OBLIGATIONS$112,780
RENTAL DEPOSITS$25,000
FieldValueIRS element (for citing)
Total Liability$674,130TotalLiabilityAmt
Footnote TextYes (X)FootnoteTextInd
Total Rev Etc Audited Fincl Stmt$73,443,828TotalRevEtcAuditedFinclStmtAmt
Net Unrealized Gains Invst-$94,500NetUnrealizedGainsInvstAmt
Donated Services And Use Fclts$24,713,985DonatedServicesAndUseFcltsAmt
Recoveries Prior Year Grants$435,223RecoveriesPriorYearGrantsAmt
Revenue Not Reported$25,054,708RevenueNotReportedAmt
Revenue Subtotal$48,389,120RevenueSubtotalAmt
Investment Expenses Not Incld$273,750InvestmentExpensesNotIncldAmt
Revenue Not Reported Fincl Stmt$273,750RevenueNotReportedFinclStmtAmt
Total Revenue Per Form990$48,662,870TotalRevenuePerForm990Amt
Tot Expns Etc Audited Fincl Stmt$70,786,859TotExpnsEtcAuditedFinclStmtAmt
Donated Services Use Fclts$24,713,985DonatedServicesUseFcltsAmt
Expenses Not Reported$24,713,985ExpensesNotReportedAmt
Expenses Subtotal$46,072,874ExpensesSubtotalAmt
Investment Expenses Not Incld2$273,750InvestmentExpensesNotIncld2Amt
Other Expenses Not Included-$129,218OtherExpensesNotIncludedAmt
Expenses Not Rpt Fincl Stmt$144,532ExpensesNotRptFinclStmtAmt
Total Expenses Per Form990$46,217,406TotalExpensesPerForm990Amt

Supplemental Information Detail SupplementalInformationDetail (3 entries)

Form And Line ReferenceFormAndLineReferenceDescExplanationExplanationTxt
PART V, LINE 4:THE EARNINGS ON THIS ENDOWMENT ARE AVAILABLE FOR THE ALZHEIMER'S DISEASE RESEARCH PROGRAM, ARE RECORDED AS TEMPORARILY RESTRICTED INVESTMENT INCOME, AND ARE RELEASED AS SPENT.
PART X, LINE 2:BRIGHTFOCUS PERFORMED AN EVALUATION OF UNCERTAINTY IN INCOME TAXES FOR THE YEAR ENDED MARCH 31, 2024, AND DETERMINED THAT THERE WERE NO MATTERS THAT WOULD REQUIRE RECOGNITION IN THE CONSOLIDATED FINANCIAL STATEMENTS OR THAT MAY HAVE ANY EFFECT ON ITS TAX-EXEMPT STATUS.
PART XII, LINE 4B - OTHER ADJUSTMENTS:CHANGE IN PRESENT VALUE OF GRANTS -129,218.

Schedule F IRS990ScheduleF

FieldValueIRS element (for citing)
Grant Records MaintainedYes (1)GrantRecordsMaintainedInd

Account Activities Outside US AccountActivitiesOutsideUSGrp (3 entries)

RegionRegionTxtOfficesOfficesCntEmployeeEmployeeCntType Of Activities ConductedTypeOfActivitiesConductedTxtRegion Total ExpendituresRegionTotalExpendituresAmt
EAST ASIA AND THE PACIFIC00GRANTMAKING$499,924
EUROPE00GRANTMAKING$2,067,294
NORTH AMERICA - CANADA AND MEXICO, BUT NOT THE UNITED STATES00GRANTMAKING$658,672
FieldValueIRS element (for citing)
Subtotal Offices0SubtotalOfficesCnt
Subtotal Employees0SubtotalEmployeesCnt
Continuation Total Office0ContinuationTotalOfficeCnt
Continuation Total Employee0ContinuationTotalEmployeeCnt
Total Office0TotalOfficeCnt
Total Employee0TotalEmployeeCnt
Subtotal Spent$3,225,890SubtotalSpentAmt
Continuation Spent$0ContinuationSpentAmt
Total Spent$3,225,890TotalSpentAmt

Grants To Org Outside US GrantsToOrgOutsideUSGrp (14 entries)

RegionRegionTxtPurpose Of GrantPurposeOfGrantTxtCash GrantCashGrantAmtManner Of Cash DisbursementMannerOfCashDisbursementTxtNon Cash AssistanceNonCashAssistanceAmt
NORTH AMERICAMACULAR DEGENERATION RESEARCH BY BRITTANY CARR, PHD, ENTITLED: (M2024011N)$450,000WIRE TRANSFER$0
EUROPE (INCLUDING ICELAND AND GREENLAND)MACULAR DEGENERATION RESEARCH BY MAXIMILIAN PFAU, PHD, ENTITLED: (M2024009N)$330,400WIRE TRANSFER$0
EUROPE (INCLUDING ICELAND AND GREENLAND)ALZHEIMER'S DISEASE RESEARCH BY MARIA LLORENS-MARTN, PHD, ENTITLED: (A2024021S)$300,000WIRE TRANSFER$0
EUROPE (INCLUDING ICELAND AND GREENLAND)ALZHEIMER'S DISEASE RESEARCH BY EMANUELA PASCIUTO, PHD, ENTITLED: (A2024020S)$300,000WIRE TRANSFER$0
EAST ASIA AND THE PACIFICALZHEIMER'S DISEASE RESEARCH BY GUOJUN BU, PHD, ENTITLED: (A2024019S)$300,000WIRE TRANSFER$0
EUROPE (INCLUDING ICELAND AND GREENLAND)ALZHEIMER'S DISEASE RESEARCH BY RAFFAELLA NATIVIO, PHD, ENTITLED: (A2024018S)$299,943WIRE TRANSFER$0
EUROPE (INCLUDING ICELAND AND GREENLAND)BIRAX RESEARCH FUNDING, ENTITLED: (CA2023002)$202,027WIRE TRANSFER$0
NORTH AMERICAALZHEIMER'S DISEASE RESEARCH BY JULIE OTTOY, PHD, ENTITLED: (A2024012F)$200,000WIRE TRANSFER$0
EUROPE (INCLUDING ICELAND AND GREENLAND)ALZHEIMER'S DISEASE RESEARCH BY GEMMA SALVAD, PHD, ENTITLED: (A2024007F)$200,000WIRE TRANSFER$0
EUROPE (INCLUDING ICELAND AND GREENLAND)ALZHEIMER'S DISEASE RESEARCH BY HELENA GELLERSEN, PHD, ENTITLED: (A2024013F)$199,967WIRE TRANSFER$0
EAST ASIA AND THE PACIFICNATIONAL GLAUCOMA RESEARCH BY JENNIFER FAN GASKIN, MBCHB, MD, FRANZCO, ENTITLED: (G2024011S)$199,924WIRE TRANSFER$0
EUROPE (INCLUDING ICELAND AND GREENLAND)ALZHEIMER'S DISEASE RESEARCH BY MARTIN J. DAHL, PHD, PHD, ENTITLED: (A2024006F)$199,130WIRE TRANSFER$0
EUROPE (INCLUDING ICELAND AND GREENLAND)NATIONAL GLAUCOMA RESEARCH BY DARRYL OVERBY, PHD, ENTITLED: (CG2020003)$35,828WIRE TRANSFER$0
NORTH AMERICAMIND AND SIGHT DISEASES RESEARCH FUNDING, ENTITLED: (CA2023003)$6,672WIRE TRANSFER$0
FieldValueIRS element (for citing)
Total501c3 Org14Total501c3OrgCnt
Total Other Org0TotalOtherOrgCnt
Transfer To Foreign Corp0TransferToForeignCorpInd
Interest In Foreign Trust0InterestInForeignTrustInd
Foreign Corp Ownership0ForeignCorpOwnershipInd
Passive Foreign Investmest Co0PassiveForeignInvestmestCoInd
Foreign Partnership0ForeignPartnershipInd
Boycott Countries0BoycottCountriesInd

Supplemental Information Detail SupplementalInformationDetail (4 entries)

Form And Line ReferenceFormAndLineReferenceDescExplanationExplanationTxt
PART I, LINE 2:BRIGHTFOCUS INTERACTS WITH ALL GRANTEES AT LEAST QUARTERLY BY E-MAIL OR AT SCIENTIFIC MEETINGS. IN ADDITION TO THESE INTERACTIONS, EACH GRANT RECIPIENT IS REQUIRED TO SUBMIT SEPARATE DETAILED ANNUAL SCIENTIFIC PROGRESS AND FINANCIAL REPORTS TO BRIGHTFOCUS. THESE ARE RECEIVED BY THE BRIGHTFOCUS SCIENTIFIC AFFAIRS DEPARTMENT, AND REVIEWED BY SCIENTIFIC STAFF WITH BROAD EXPERTISE, INCLUDING IMAGING, MOLECULAR BIOLOGY AND SIGNALING PATHWAYS, CELL BIOLOGY, ANGIOGENESIS, BIOCHEMISTRY, NEUROSCIENCE, AND GENETICS. SENIOR STAFF REVIEWS EACH PROGRESS REPORT AND EVALUATES THE PROJECT FOR SUFFICIENT PROGRESS TOWARDS THE SPECIFIC AIMS PROPOSED IN THE ORIGINAL APPLICATION OR ANY BUDGETARY CONCERNS. THIS EFFORT IS SUPPORTED BY ADDITIONAL SCIENTIFIC COUNSEL FROM MEMBERS OF THE BRIGHTFOCUS SCIENTIFIC REVIEW COMMITTEES, WHEN REQUIRED. IN ADDITION TO STATEMENTS OF EXPERIMENTAL PROGRESS, ALL GRANTEES ARE ASKED TO REPORT ANY TECHNICAL PUBLICATIONS, MEDIA REPORTS, OR PATENT APPLICATIONS IN WHICH BRIGHTFOCUS-SPONSORED RESEARCH IS DESCRIBED. IF SIGNIFICANT CONCERNS RELATED TO PROGRESS ON THE AWARDS ARE DISCOVERED, AND NOT RESOLVED AFTER INTERACTION WITH THE AWARD GRANTEE, THE BRIGHTFOCUS STAFF RECOMMENDS APPROPRIATE ACTIONS TO THE CHAIR OF THE SCIENTIFIC AFFAIRS COMMITTEE OF THE BOARD OF DIRECTORS. IN ACCORDANCE WITH THE GRANT AGREEMENT TERMS AND CONDITIONS, BRIGHTFOCUS MAY WITHHOLD FUNDING, OR DISCONTINUE AN AWARD, FOR ANY GRANTEE THAT FAILS TO ACHIEVE SUFFICIENT PROGRESS OR SUBMIT REQUIRED REPORTS. AT THE CONCLUSION OF THE GRANT AWARD PERIOD, EACH GRANTEE MUST COMPLETE AND SUBMIT A FINAL REPORT THAT IS ALSO REVIEWED BY THE BRIGHTFOCUS SENIOR SCIENTIFIC STAFF. EVALUATION OF THE WORK OF EACH GRANTEE IS QUALITATIVELY AND QUANTITATIVELY ASSESSED THROUGH VARIOUS METRICS RELATED TO THE IMPACT OF THE GRANT ON ITS TARGETED DISEASE FIELD. SUCH IMPACT METRICS HAVE REVEALED THAT 95% OF BRIGHTFOCUS-SUPPORTED RESEARCH RESULTS IN RESEARCH PUBLICATIONS THAT ADVANCE THE FIELDS SERVED BY BRIGHTFOCUS. THIS IMPACT IS FURTHER SUPPORTED BY ANNUAL CATEGORY NORMALIZED CITATION IMPACT ANALYSIS THAT COMPARES BRIGHTFOCUS-SUPPORTED WORKS TO AN UNBIASED COMPARISON OF IMPACT PERFORMANCE VERSUS THE WORLD AVERAGE. BRIGHTFOCUS-SUPPORTED PUBLICATIONS WERE RECENTLY CITED AT 2 TIMES THE FREQUENCY OF THE WORLD AVERAGE. A FINAL EXAMPLE OF IMPACT ASSESSMENT REVEALED THAT THE SUCCESSES OF BRIGHTFOCUS GRANTEES CONTINUE LONG AFTER THE GRANT EXPIRES. ON AVERAGE, EACH GRANTEE RECEIVES ADDITIONAL GRANTS FOR FOLLOW-ON PROJECTS SPAWNED BY THE BRIGHTFOCUS GRANT, WITH VALUES UP TO 10 TIMES THE LEVEL OF THE INITIAL BRIGHTFOCUS INVESTMENT. BRIGHTFOCUS SOLICITS FEEDBACK FROM ITS GRANTEES, AND PROVIDES AN ANONYMOUS FORUM FOR COLLECTING SUCH INFORMATION. THROUGH THE BRIGHTFOCUS FOUNDATION WEBSITE AND WITHIN THE SCIENTIFIC PROGRESS REPORTS, THERE ARE DESIGNATED SECTIONS WHERE AWARDEES ARE ASKED TO PROVIDE FEEDBACK TO THE FOUNDATION. THROUGH THIS MECHANISM, THEY ARE GIVEN THE ABILITY TO ANONYMOUSLY PROVIDE FEEDBACK OR COMMUNICATE THEIR CONCERNS TO PROGRAM STAFF OR THE BRIGHTFOCUS' COMPLIANCE OFFICE. ANY SUGGESTIONS, CONCERNS, COMPLAINTS, OR POSITIVE EXPERIENCES CAN BE OUTLINED AND BROUGHT TO THE ATTENTION OF BRIGHTFOCUS IN THIS MANNER, SO THAT BRIGHTFOCUS CAN ADDRESS ANY AREAS NEEDING IMPROVEMENT, REAFFIRM PRAISE-WORTHY POLICIES, OR OTHERWISE ASSESS NEEDS FOR PROGRAMMATIC CHANGE. THE SENIOR LEADERSHIP PRESENTS AND SUMMARIZES THE STATUS AND PROGRESS ON GRANTS TO THE BRIGHTFOCUS BOARD OF DIRECTORS AT EACH OF THEIR QUARTERLY BOARD MEETINGS.
PART I, LINE 3:BRIGHTFOCUS REPORTED THE EXPENDITURES BASED ON THE ACCOUNTING METHOD USED IN ITS AUDITED FINANCIAL STATEMENTS WHICH IS ON AN ACCRUAL BASIS.
PART II, LINE 1:BRIGHTFOCUS REPORTED THE EXPENDITURES BASED ON THE ACCOUNTING METHOD USED IN ITS AUDITED FINANCIAL STATEMENTS WHICH IS ON AN ACCRUAL BASIS.
PART II, LINE 1, COLUMN (D)REGION: EUROPE (INCLUDING ICELAND AND GREENLAND) (D) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY MARTIN J. DAHL, PHD, ENTITLED: (A2024006F) SHINING A LIGHT ON HOW EARLY TAU-RELATED BRAIN CHANGES AFFECT MEMORY LOSS. INVESTIGATOR'S SUMMARY: THIS PROJECT SPOTLIGHTS PREVIOUSLY UNDERSTUDIED BRAIN REGIONSTINY NUCLEI IN THE BRAINSTEMTHAT ARE THE STARTING POINT OF ALZHEIMER'S-RELATED TAU ACCUMULATION AND INVESTIGATES HOW THEIR CHANGES CONTRIBUTE TO MEMORY LOSS. USING INNOVATIVE BRAIN IMAGING TECHNIQUES, BLOOD-BASED BIOMARKERS, AND MEMORY ASSESSMENTS COLLECTED OVER A DECADE FROM A LARGE NUMBER OF PARTICIPANTS, THIS PROJECT IMPROVES OUR UNDERSTANDING OF THE TIME COURSE OF NEURAL CHANGES IN LATER LIFE AND THEIR MECHANISTIC ROLE IN THE EARLIEST STAGES OF ALZHEIMER'S DEVELOPMENT. GRANT AWARDED: $199,130, MAX PLANCK INSTITUTE FOR HUMAN DEVELOPMENT, BERLIN, GERMANY. REGION: EUROPE (INCLUDING ICELAND AND GREENLAND) (D) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY GEMMA SALVAD, PHD, ENTITLED: (A2024007F) STAGING ALZHEIMER'S DISEASE WITH BLOOD-BASED MEASURES. INVESTIGATOR'S SUMMARY: RESEARCHERS WILL DEVELOP A STAGING MODEL FOR ALZHEIMER'S DISEASE BASED ON PLASMA BIOMARKERS, WHICH WILL HELP CHARACTERIZE PEOPLE ACROSS THE DIFFERENT PHASES OF THE DISEASE. THE STUDY WILL ALSO INVESTIGATE HOW MULTIPLE PROTEIN LEVELS CHANGE ACROSS THESE STAGES TO BETTER UNDERSTAND THE COMPLEX BIOLOGICAL PROCESSES THAT OCCUR DURING THE DISEASE. RESEARCHERS ENVISION THAT THE STAGING MODEL MAY HELP DECIDE, IN AN EASY AND COST-EFFECTIVE WAY, WHO WOULD BENEFIT FROM A TREATMENT AGAINST ALZHEIMER'S DISEASE AND PERFORM A MORE PERSONALIZED MANAGEMENT OF THE INDIVIDUAL. STUDYING PROTEIN CHANGES MAY ALSO UNVEIL NEW DRUG TARGETS FOR ALZHEIMER'S. GRANT AWARDED: $200,000, LUND UNIVERSITY, LUND, SWEDEN. REGION: NORTH AMERICA (D) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY JULIE OTTOY, PHD, ENTITLED: (A2024012F) THE ROLE OF BRAIN VASCULAR-IMMUNE PROCESSES IN ALZHEIMER'S DISEASE. INVESTIGATOR'S SUMMARY: DAMAGE TO THE BRAIN'S BLOOD VESSELS CAN TRIPLE THE RISK OF DEVELOPING ALZHEIMER'S DISEASE, AND OVERACTIVE IMMUNE CELLS MAY FURTHER EXACERBATE THIS DAMAGE. HERE, RESEARCHERS WILL STUDY HOW THESE VASCULAR-IMMUNE RESPONSES AFFECT ALZHEIMER'S PROGRESSION BY ANALYZING BRAIN SCANS AND BLOOD SAMPLES FROM 500+ INDIVIDUALS OVER TIME. STUDY OUTCOMES WILL PRESENT A UNIQUE AND MORE DETAILED PICTURE OF KEY AND UNDERSTUDIED MECHANISMS DRIVING ALZHEIMER'S, THEREBY OPENING NEW PERSPECTIVES ON THE DEVELOPMENT OF PERSONALIZED BIOMARKERS AND TREATMENT STRATEGIES THAT TARGET THE INTERFACE BETWEEN THE VASCULAR SYSTEM, BRAIN IMMUNE CELLS, AND ALZHEIMER'S. GRANT AWARDED: $200,000, SUNNYBROOK RESEARCH INSTITUTE, TORONTO, CANADA. REGION: EUROPE (INCLUDING ICELAND AND GREENLAND) (D) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY HELENA GELLERSEN, PHD, ENTITLED: (A2024013F) IDENTIFYING NEW MEMORY AND BRAIN MARKERS FOR EARLY ALZHEIMER'S DISEASE. INVESTIGATOR'S SUMMARY: DESPITE NEWLY AVAILABLE TREATMENTS FOR ALZHEIMER'S DISEASE, DEMENTIA SUBTYPE SPECIFICITY IS IMPORTANT TO DETERMINE PRIOR TO TREATMENT TO ENSURE SAFE AND EFFICACIOUS OUTCOMES. OPTIMIZED COGNITIVE ASSESSMENTS AND IMAGING BIOMARKERS ARE ALSO ESSENTIAL FOR EARLY DETECTION AND TO MONITOR DISEASE PROGRESSION. THIS PROJECT WILL ADDRESS THESE CHALLENGES BY DEVELOPING NEW COGNITIVE AND NEURAL MARKERS SENSITIVE TO THE EARLY EFFECTS OF ALZHEIMER'S. THESE MARKERS CAN BE USED TO SCREEN FOR SUBTLE MEMORY CHANGES, CLASSIFY BY SUBTYPE, AND IDENTIFY SIGNATURES OF HEALTHY BRAIN FUNCTION THAT CAN CLARIFY MECHANISMS OF DISEASE-MODIFYING EFFECTS ON MEMORY IN EARLY-PHASE CLINICAL TRIALS. GRANT AWARDED: $199,967, GERMAN CENTER FOR NEURODEGENERATIVE DISEASES, MAGDEBURG, GERMANY. REGION: EUROPE (INCLUDING ICELAND AND GREENLAND) (D) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY RAFFAELLA NATIVIO, PHD, ENTITLED: (A2024018S) UNCOVERING HOW GENE REGULATORS PROTECT NEURONS AGAINST ALZHEIMER'S. INVESTIGATOR'S SUMMARY: THIS STUDY WILL FOCUS ON UNDERSTANDING HOW EPIGENETIC FACTORS, ESPECIALLY TRANSCRIPTIONAL REPRESSORS, INFLUENCE GENE EXPRESSION IN NEURONS AND CONTRIBUTE TO ALZHEIMER'S DISEASE. THE RESEARCH AIMS TO IDENTIFY HOW THESE TRANSCRIPTIONAL REPRESSORS PROTECT NEURONS FROM ALZHEIMER'S-RELATED STRESS, POTENTIALLY LEADING TO NEW TREATMENTS FOR ENHANCING BRAIN RESILIENCE AGAINST ALZHEIMER'S. GRANT AWARDED: $299,943, IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY, AND MEDICINE, LONDON, UNITED KINGDOM. REGION: EAST ASIA AND THE PACIFIC (D) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY GUOJUN BU, PHD, ENTITLED: (A2024019S) PERIPHERAL APOE IN ALZHEIMER'S DISEASE. INVESTIGATOR'S SUMMARY: DESPITE ENCOURAGING NEWS ON ANTI-AMYLOID DRUGS, RESEARCHERS ARE STILL FAR FROM DEVELOPING SAFE AND EFFECTIVE THERAPIES TO PREVENT OR CURE ALZHEIMER'S DISEASE. THE APOE GENE IS A STRONG RISK FACTOR, WITH APOE4 INCREASING AND APOE2 REDUCING RISK. THIS PROJECT WILL STUDY THE PROTECTIVE EFFECT OF APOE2 USING NEW MODEL SYSTEMS AND ADVANCED TECHNOLOGIES. THESE STUDIES WILL ADDRESS HOW APOE2 IN THE BLOOD AFFECTS BRAIN COGNITION AND ALZHEIMER'S DISEASE PATHOLOGY. OUTCOMES FROM THESE STUDIES SHOULD PROVIDE NEW KNOWLEDGE ON HOW DIFFERENT FORMS OF APOE AFFECT ALZHEIMER'S DISEASE AND HOW APOE EXPRESSED IN THE PERIPHERY AFFECTS BRAIN FUNCTION AND NEUROPATHOLOGY. MORE IMPORTANTLY, THE STUDY OUTCOMES WILL GUIDE US TO DESIGN APOE-TARGETED THERAPIES TO DELAY THE ONSET OR SLOW THE PROGRESSION OF ALZHEIMER'S DISEASE. GRANT AWARDED: $300,000, THE HONG KONG UNIVERSITY OF SCIENCE AND TECHNOLOGY, KOWLOON, HONG KONG. REGION: EUROPE (INCLUDING ICELAND AND GREENLAND) (D) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY EMANUELA PASCIUTO, PHD, ENTITLED: (A2024020S) MODULATION OF MICROGLIA-T CELLS CROSS TALK IN ALZHEIMER'S DISEASE. INVESTIGATOR'S SUMMARY: WHILE MICROGLIA ARE IN THE SPOTLIGHT, RESEARCHERS KNOW LITTLE ABOUT HOW ADAPTIVE IMMUNE CELLS INTERACT WITH ALZHEIMER'S AMYLOID PLAQUES. MHCII IS A MICROGLIA-ASSOCIATED ALZHEIMER'S RISK GENE THAT FUNCTIONS TO MEDIATE INTERACTION WITH T CELLS. THE RELEVANCE OF THE MICROGLIA-T CELL INTERACTION IN ALZHEIMER'S IS UNKNOWN. TO STUDY THE CONTRIBUTION OF THIS INTERACTION TO ALZHEIMER'S PATHOLOGY, DR. PASCIUTO AND HER TEAM WILL USE GENETIC MODELS TO MANIPULATE MHC II EXPRESSION IN MICE AND TEST EFFICACY OF T CELL-BASED IMMUNOTHERAPY IN ALZHEIMER'S MICE LACKING MHCII. DR. PASCIUTO'S RESEARCH WILL EXTEND THE CURRENT KNOWLEDGE OF HOW THE IMMUNE SYSTEM CHANGES IN ALZHEIMER'S DISEASE. BY UNCOVERING THESE MECHANISMS, THIS STUDY BUILDS THE BASIS TOWARD MORE PRECISE THERAPIES THAT TARGET THE IMMUNE SYSTEM TO PROTECT AGAINST THE PROGRESSION OF ALZHEIMER'S. ADDITIONALLY, THIS RESEARCH WILL ESTABLISH HOW THE ALZHEIMER'S RISK GENE MHCII INFLUENCES THE DEVELOPMENT OF ALZHEIMER'S AND THE RESPONSE TO POTENTIAL IMMUNE-BASED TREATMENTS, OFFERING HOPE FOR MORE PERSONALIZED APPROACHES TO COMBATING THE DISEASE. GRANT AWARDED: $300,000, FLANDERS INSTITUTE FOR BIOTECHNOLOGY, ANTWERP, BELGIUM. REGION: EUROPE (INCLUDING ICELAND AND GREENLAND) (D) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY MARIA LLORENS-MARTN, PHD, ENTITLED: (A2024021S) DOES ALZHEIMERS DISEASE ACCELERATE BRAIN AGING? INVESTIGATOR'S SUMMARY: THE HIPPOCAMPUS, A BRAIN REGION CRUCIAL FOR LEARNING AND MEMORY, GENERATES NEW NEURONS THROUGHOUT LIFE. THIS PROCESS IS DAMAGED IN PEOPLE WITH ALZHEIMER'S DISEASE, BUT THE CAUSE OF THESE ALTERATIONS IS UNKNOWN. DR. LLORENS-MARTN AND HER TEAM WILL USE HIGH-QUALITY HUMAN BRAIN SAMPLES AND CUTTING-EDGE GENOMIC AND MICROSCOPY METHODOLOGIES TO ASSESS THE TOXICITY OF THE ENVIRONMENT THAT SURROUNDS NEW NEURONS. STUDY FINDINGS WILL IDENTIFY NOVEL MECHANISMS RESPONSIBLE FOR HIPPOCAMPAL PERTURBATION IN ALZHEIMER'S AND GENERATE NOVEL RESOURCES THAT ALLOW FASTER AND MORE ACCURATE DIAGNOSIS OF THIS CONDITION. GRANT AWARDED: $300,000, SPANISH NATIONAL RESEARCH COUNCIL, MADRID, SPAIN. REGION: EUROPE (INCLUDING ICELAND AND GREENLAND) (D) PURPOSE OF GRANT: MACULAR DEGENERATION RESEARCH BY MAXIMILIAN PFAU, PHD, ENTITLED: (M2024009N) INNOVATIVE VISION TESTS TO MONITOR TREATMENT EFFECTS IN AMD. INVESTIGATOR'S SUMMARY: AGE-RELATED MACULAR DEGENERATION (AMD) CAUSES DEVASTATING VISION LOSS OVER TIME. HOWEVER, BEST-CORRECTED VISUAL ACUITYTHE MOST COMMON VISION TESTDOES NOT REVEAL DYSFUNCTION IN EARLY AMD. THUS, CLINICAL TRIALS FOCUS MOSTLY ON LATE AMD, DESPITE THE LIMITED TREATMENT POTENTIAL. THIS PROJECT WILL ESTABLISH VISION TESTS THAT EVALUATE DARK ADAPTATION FOLLOWING EXPOSURE TO BRIGHT LIGHT. USING RETINA TRACKING, RESEARCHERS WILL TEST SMALL RETINAL REGIONS PRONE TO SUBTLE PHOTORECEPTOR DYSFUNCTION IN AN UNPRECEDENTEDLY ACCURATE MANNER, MAKING DISEASE PROGRESSION MEASURABLE AT THE EARLIEST STAGE. GRANT AWARDED: $330,400, INSTITUTE OF MOLECULAR AND CLINICAL OPHTHALMOLOGY BASEL, BASEL, SWITZERLAND.

Schedule G IRS990ScheduleG

FieldValueIRS element (for citing)
Mail SolicitationsYes (X)MailSolicitationsInd
Email SolicitationsYes (X)EmailSolicitationsInd
Solicitation Of Non Govt GrantsYes (X)SolicitationOfNonGovtGrantsInd
Special Fundraising EventsYes (X)SpecialFundraisingEventsInd
Agrmt Prof Fundraising ActyYes (1)AgrmtProfFundraisingActyInd

Fundraiser Activity Info FundraiserActivityInfoGrp (2 entries)

Address Line1USAddress/AddressLine1TxtCityUSAddress/CityNmState AbbreviationUSAddress/StateAbbreviationCdZIPUSAddress/ZIPCdActivityActivityTxtFundraiser Control Of FundsFundraiserControlOfFundsIndGross ReceiptsGrossReceiptsAmtRetained By ContractorRetainedByContractorAmtNet To OrganizationNetToOrganizationAmt
RKD GROUP
35 PARKWOOD DRIVE STE 160HOPKINTONMA01748FUNDRAISING AND COMMUNICATIONS CONSULTANT0$30,452,088$499,942$29,952,146
BEACONFIRE REDENGINE
2300 CLARENDON BLVD STE 925ARLINGTONVA22201FUNDRAISING AND COMMUNICATIONS CONSULTANT0$2,368,623$452,839$1,915,784
FieldValueIRS element (for citing)
Total Gross Receipts$32,820,711TotalGrossReceiptsAmt
Total Retained By Contractors$952,781TotalRetainedByContractorsAmt
Total Net To Organization$31,867,930TotalNetToOrganizationAmt
Licensed StatesAKLicensedStatesCd
Licensed StatesALLicensedStatesCd
Licensed StatesARLicensedStatesCd
Licensed StatesAZLicensedStatesCd
Licensed StatesCALicensedStatesCd
Licensed StatesCOLicensedStatesCd
Licensed StatesCTLicensedStatesCd
Licensed StatesDCLicensedStatesCd
Licensed StatesFLLicensedStatesCd
Licensed StatesGALicensedStatesCd
Licensed StatesHILicensedStatesCd
Licensed StatesILLicensedStatesCd
Licensed StatesKSLicensedStatesCd
Licensed StatesKYLicensedStatesCd
Licensed StatesLALicensedStatesCd
Licensed StatesMALicensedStatesCd
Licensed StatesMDLicensedStatesCd
Licensed StatesMELicensedStatesCd
Licensed StatesMILicensedStatesCd
Licensed StatesMNLicensedStatesCd
Licensed StatesMOLicensedStatesCd
Licensed StatesMSLicensedStatesCd
Licensed StatesNCLicensedStatesCd
Licensed StatesNDLicensedStatesCd
Licensed StatesNHLicensedStatesCd
Licensed StatesNJLicensedStatesCd
Licensed StatesNMLicensedStatesCd
Licensed StatesNVLicensedStatesCd
Licensed StatesNYLicensedStatesCd
Licensed StatesOHLicensedStatesCd
Licensed StatesOKLicensedStatesCd
Licensed StatesORLicensedStatesCd
Licensed StatesPALicensedStatesCd
Licensed StatesRILicensedStatesCd
Licensed StatesSCLicensedStatesCd
Licensed StatesTNLicensedStatesCd
Licensed StatesUTLicensedStatesCd
Licensed StatesVALicensedStatesCd
Licensed StatesWALicensedStatesCd
Licensed StatesWILicensedStatesCd
Licensed StatesWVLicensedStatesCd

Fundraising Event Information FundraisingEventInformationGrp

FieldValueIRS element (for citing)
Event1BRIGHTFOCUS 50TH ANNIVERSARY CELEBREvent1Nm
Gross Receipts Event1$314,290GrossReceiptsEvent1Amt
Charitable Contri Event1$250,290CharitableContriEvent1Amt
Gross Revenue Event1$64,000GrossRevenueEvent1Amt
Rent Facility Costs Event1$17,300RentFacilityCostsEvent1Amt
Food And Beverage Event1$149,677FoodAndBeverageEvent1Amt
Entertainment Event1$157,317EntertainmentEvent1Amt
Other Direct Expenses Event1$74,176OtherDirectExpensesEvent1Amt
Gross Receipts Total$314,290GrossReceiptsTotalAmt
Charitable Contributions Tot$250,290CharitableContributionsTotAmt
Gross Revenue Total Events$64,000GrossRevenueTotalEventsAmt
Rent Fclty Costs Total Events$17,300RentFcltyCostsTotalEventsAmt
Food And Beverage Total Events$149,677FoodAndBeverageTotalEventsAmt
Entertainment Total Events$157,317EntertainmentTotalEventsAmt
Oth Direct Expnss Total Events$74,176OthDirectExpnssTotalEventsAmt
Direct Expense Summary Events$398,470DirectExpenseSummaryEventsAmt
Net Income Summary-$334,470NetIncomeSummaryAmt

Supplemental Information Detail SupplementalInformationDetail

FieldValueIRS element (for citing)
Form And Line ReferenceSCHEDULE G, PART I, LINE 2B, COLUMN (V)FormAndLineReferenceDesc
ExplanationIN THE CONTRACT WITH RKD GROUP, THE MANAGEMENT FEES ARE FIXED AMOUNTS PER MONTH FOR IN-SCOPE SERVICES THAT TOTALS $1,151,196 PER YEAR OF WHICH $606,941 HAS BEEN ALLOCATED UNDER PART IX, LINE 11(G) TO PROGRAM AND MANAGEMENT AND ARE NOT CONSIDERED TO BE THE PROFESSIONAL FUNDRAISING CONSULTANT FEE.ExplanationTxt

Schedule I IRS990ScheduleI

FieldValueIRS element (for citing)
Grant Records MaintainedYes (1)GrantRecordsMaintainedInd

Recipient Table RecipientTable (35 entries)

Address Line1USAddress/AddressLine1TxtCityUSAddress/CityNmState AbbreviationUSAddress/StateAbbreviationCdZIPUSAddress/ZIPCdRecipient EINRecipientEINIRC SectionIRCSectionDescCash GrantCashGrantAmtNon Cash AssistanceNonCashAssistanceAmtPurpose Of GrantPurposeOfGrantTxtAddress Line2USAddress/AddressLine2Txt
BOSTON CHILDREN'S HOSPITAL
300 LONGWOOD AVENUEBOSTONMA02115042774441501(C)(3)$200,000$0MACULAR DEGENERATION RESEARCH BY NEETU KUSHWAH, PHD, ENTITLED: (M2024002F)
COLUMBIA UNIVERSITY
535 W 116TH STREETNEW YORKNY10027135598093501(C)(3)$166,667$0NATIONAL GLAUCOMA RESEARCH BY SIMON JOHN, PHD, ENTITLED: (CG2020004)
DUKE UNIVERSITY
2200 WEST MAIN STREET SUITE 820DURHAMNC27705560532129501(C)(3)$52,325$0NATIONAL GLAUCOMA RESEARCH BY W. DANIEL STAMER, PHD, ENTITLED: (CG2020002)
EMORY UNIVERSITY
SCHOOL OF NURSING 1520 CLIFTON RDATLANTAGA30322580566256501(C)(3)$300,000$0ALZHEIMER'S DISEASE RESEARCH BY BRITTANY BUTTS, PHD, ENTITLED: (A2024024S)
GEORGIA INSTITUTE OF TECHNOLOGY
FERST DRIVE ROOM 230ATLANTAGA30332586002023501(C)(3)$85,561$0NATIONAL GLAUCOMA RESEARCH BY C. ROSS ETHIER, PHD, ENTITLED: (CG2020001)
GEORGIA TECH RESEARCH CORPORATION
BIOMEDICAL ENGINEERING 315 FERSTATLANTAGA30332580603146501(C)(3)$150,000$0NATIONAL GLAUCOMA RESEARCH BY HAIYAN LI, PHD, ENTITLED: (G2024003F)DRIVE
GEORGIA TECH RESEARCH CORPORATION
SCHOOL OF CHEMISTRY ANDATLANTAGA30332580603146501(C)(3)$150,000$0NATIONAL GLAUCOMA RESEARCH BY HANNAH YOUNGBLOOD, PHD, ENTITLED: (G2024001F)BIOCHEMISTRY 311 FERST DRIVE
HEBREW REHABILITATION CENTER
1200 CENTRE STREETROSLINDALEMA02131042104298501(C)(3)$297,336$0ALZHEIMER'S DISEASE RESEARCH BY DAVIDE CAPPON, PHD, ENTITLED: (A2024027S)
ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
GENETICS AND GENOMIC SCIENCES 1425NEW YORKNY10029136171197501(C)(3)$300,000$0ALZHEIMER'S DISEASE RESEARCH BY ANNA PODLESNY-DRABINIOK, PHD, ENTITLED: (A2024025S)MADISON AVENUE
ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
NEUROSCIENCE 1425 MADISON AVENUENEW YORKNY10029136171197501(C)(3)$193,526$0ALZHEIMER'S DISEASE RESEARCH BY TATSUHIKO NAITO, MD, PHD, ENTITLED: (A2024004F)ICAHN 10-52
INDIANA UNIVERSITY
MEDICAL AND MOLECULAR GENETICS 320INDIANAPOLISIN46202356001673501(C)(3)$150,000$0NATIONAL GLAUCOMA RESEARCH BY SHRUTI PATIL, PHD, ENTITLED: (G2024002F)W 15TH ST NB 408
JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE
DEPARTMENT OF OPHTHALMOLOGY 400 NBALTIMOREMD21231520595110501(C)(3)$200,000$0MACULAR DEGENERATION RESEARCH BY KRISHNA SINGH, PHD, ENTITLED: (M2024003F)BROADWAY
MASSACHUSETTS GENERAL HOSPITAL
55 FRUIT STBOSTONMA02145042697983501(C)(3)$200,000$0ALZHEIMER'S DISEASE RESEARCH BY MD JOYNAL ABEDIN, PHD, ENTITLED: (A2024010F)
MASSACHUSETTS GENERAL HOSPITAL
114 16TH STREETBOSTONMA02145042697983501(C)(3)$300,000$0ALZHEIMER'S DISEASE RESEARCH BY JAEHONG SUH, PHD, ENTITLED: (A2024022S)
MAYO CLINIC JACKSONVILLE
4500 SAN PABLO ROADJACKSONVILLEFL32224593337028501(C)(3)$299,997$0ALZHEIMER'S DISEASE RESEARCH BY MERCEDES PRUDENCIO, PHD, ENTITLED: (A2024017S)
OREGON HEALTH & SCIENCE UNIVERSITY
3181 SW SAM JACKSON PARK ROADPORTLANDOR97239931176109501(C)(3)$200,000$0ALZHEIMER'S DISEASE RESEARCH BY PAULA SANCHEZ-MOLINA, PHD, ENTITLED: (A2024011F)
OREGON HEALTH & SCIENCE UNIVERSITY
3181 SW SAM JACKSON PARK ROADPORTLANDOR97239931176109501(C)(3)$200,000$0NATIONAL GLAUCOMA RESEARCH BY DIANA LOZANO, PHD, ENTITLED: (G2024009S)
SAINT LOUIS UNIVERSITY
INTERNAL MEDICINE 1402 S GRAND BLVDST LOUISMO63104430654872501(C)(3)$300,000$0ALZHEIMER'S DISEASE RESEARCH BY ANDREW D. NGUYEN, PHD, ENTITLED: (A2024028S)
SCHEPENS EYE RESEARCH INSTITUTE INC
20 STANIFORD STREETBOSTONMA02114042129889501(C)(3)$200,000$0MACULAR DEGENERATION RESEARCH BY SHINTARO SHIRAHAMA, MD, PHD, ENTITLED: (M2024004F)
STANFORD UNIVERSITY
NEUROLOGY 1201 WELCH RDPALO ALTOCA94305941156365501(C)(3)$200,000$0ALZHEIMER'S DISEASE RESEARCH BY HANNAH ENNERFELT, PHD, ENTITLED: (A2024005F)
STANFORD UNIVERSITY
2452 WATSON CTPALO ALTOCA94305941156365501(C)(3)$62,531$0NATIONAL GLAUCOMA RESEARCH BY JEFFREY GOLDBERG, PHD, ENTITLED: (CG2022001)
SUNY UPSTATE MEDICAL UNIVERSITY
505 IRVING AVE NEUROSCIENCESYRACUSENY13210141368361501(C)(3)$200,000$0NATIONAL GLAUCOMA RESEARCH BY SAMUEL HERBERG, PHD, ENTITLED: (G2024006S)RESEARCH BLDG ROOM4609
THE PENNSYLVANIA STATE UNIVERSITY COLLEGE OF MEDICINE
CELLULAR AND MOLECULAR PHYSIOLOGYHERSHEYPA17033246000376501(C)(3)$200,000$0MACULAR DEGENERATION RESEARCH BY SANDEEP MOOTHEDATH SUBRAHMANIAN, PHD, ENTITLED: (M2024006F)500 UNIVERSITY DRIVE
TUFTS UNIVERSITY
NEUROSCIENCE 136 HARRISON AVENUEBOSTONMA02111042103634501(C)(3)$300,000$0ALZHEIMER'S DISEASE RESEARCH BY GIUSEPPINA TESCO, MD, PHD, ENTITLED: (A2024016S)
UNIVERSITY OF CALIFORNIA BERKELEY
1608 FOURTH STREETBERKELEYCA94710946002123501(C)(3)$200,000$0ALZHEIMER'S DISEASE RESEARCH BY SANKALP SHUKLA, PHD, ENTITLED: (A2024008F)
UNIVERSITY OF CALIFORNIA SAN FRANCISCO
OPHTHALMOLOGY 490 ILLINOIS STREETSAN FRANCISCOCA94143946036493501(C)(3)$150,000$0NATIONAL GLAUCOMA RESEARCH BY MENGYA ZHAO, PHD, ENTITLED: (G2024005F)4TH FLOOR
UNIVERSITY OF CALIFORNIA SAN FRANCISCO
513 PARNASSUS AVESAN FRANCISCOCA94143946036493501(C)(3)$200,000$0ALZHEIMER'S DISEASE RESEARCH BY SARAH KAUFMAN, MD, PHD, ENTITLED: (A2024001F)
UNIVERSITY OF COLORADO
1800 GRANT STREETDENVERCO80203846000555501(C)(3)$428,935$0MACULAR DEGENERATION RESEARCH BY MIGUEL FLORES-BELIVER, PHD, ENTITLED: (M2024008N)
UNIVERSITY OF GEORGIA RESEARCH FOUNDATION INC
310 E CAMPUS ROADATHENSGA30602581353149501(C)(3)$449,985$0MACULAR DEGENERATION RESEARCH BY HEIKE KROEGER, PHD, ENTITLED: (M2024010N)
UNIVERSITY OF MICHIGAN MEDICAL CENTER
KELLOGG EYE CENTER DEPARTMENT OFANN ARBORMI48105386006309501(C)(3)$200,000$0MACULAR DEGENERATION RESEARCH BY JOHN HAN, PHD, ENTITLED: (M2024001F)OPHTHALMOLOGY 1000 WALL STREET
UNIVERSITY OF PITTSBURGH
OPHTHALMOLOGY 1622 LOCUST STPITTSBURGHPA15260250965591501(C)(3)$150,000$0NATIONAL GLAUCOMA RESEARCH BY BINGRUI WANG, PHD, ENTITLED: (G2024004F)
UNIVERSITY OF VIRGINIA
1001 N EMMET STREETCHARLOTTESVILLEVA22903546001796501(C)(3)$200,000$0NATIONAL GLAUCOMA RESEARCH BY XIARONG LIU, PHD, ENTITLED: (G2024008S)
UNIVERSITY OF WASHINGTON
BIOLOGICAL STRUCTURE 4333 BROOKLYNSEATTLEWA98195916001537501(C)(3)$191,339$0MACULAR DEGENERATION RESEARCH BY JULIETTE WOHLSCHLEGEL, PHD, ENTITLED: (M2024005F)AVE NE BOX 359472
WASHINGTON UNIVERSITY IN ST LOUIS
PSYCHIATRY 4370 DUNCAN AVENUEST LOUISMO63130430653611501(C)(3)$200,000$0ALZHEIMER'S DISEASE RESEARCH BY DANIRA TORAL-RIOS, PHD, ENTITLED: (A2024002F)
WEILL MEDICAL COLLEGE OF CORNELL UNIVERSITY
1300 YORK AVENEW YORKNY10065131623978C CORP$200,000$0ALZHEIMER'S DISEASE RESEARCH BY WENHUI QU, PHD, ENTITLED: (A2024003F)
FieldValueIRS element (for citing)
Total501c3 Org34Total501c3OrgCnt
Total Other Org1TotalOtherOrgCnt

Supplemental Information Detail SupplementalInformationDetail (5 entries)

Form And Line ReferenceFormAndLineReferenceDescExplanationExplanationTxt
PART I, LINE 2:BRIGHTFOCUS INTERACTS WITH ALL GRANTEES AT LEAST QUARTERLY BY E-MAIL OR AT SCIENTIFIC MEETINGS. IN ADDITION TO THESE INTERACTIONS, EACH GRANT RECIPIENT IS REQUIRED TO SUBMIT SEPARATE DETAILED ANNUAL SCIENTIFIC PROGRESS AND FINANCIAL REPORTS TO BRIGHTFOCUS. THESE ARE RECEIVED BY THE BRIGHTFOCUS SCIENTIFIC AFFAIRS DEPARTMENT, AND REVIEWED BY SCIENTIFIC STAFF WITH BROAD EXPERTISE, INCLUDING IMAGING, MOLECULAR BIOLOGY AND SIGNALING PATHWAYS, CELL BIOLOGY, ANGIOGENESIS, BIOCHEMISTRY, NEUROSCIENCE, AND GENETICS. SENIOR STAFF REVIEWS EACH PROGRESS REPORT AND EVALUATES THE PROJECT FOR SUFFICIENT PROGRESS TOWARDS THE SPECIFIC AIMS PROPOSED IN THE ORIGINAL APPLICATION OR ANY BUDGETARY CONCERNS. THIS EFFORT IS SUPPORTED BY ADDITIONAL SCIENTIFIC COUNSEL FROM MEMBERS OF THE BRIGHTFOCUS SCIENTIFIC REVIEW COMMITTEES, WHEN REQUIRED. IN ADDITION TO STATEMENTS OF EXPERIMENTAL PROGRESS, ALL GRANTEES ARE ASKED TO REPORT ANY TECHNICAL PUBLICATIONS, MEDIA REPORTS, OR PATENT APPLICATIONS IN WHICH BRIGHTFOCUS-SPONSORED RESEARCH IS DESCRIBED. IF SIGNIFICANT CONCERNS RELATED TO PROGRESS ON THE AWARDS ARE DISCOVERED, AND NOT RESOLVED AFTER INTERACTION WITH THE AWARD GRANTEE, THE BRIGHTFOCUS STAFF RECOMMENDS APPROPRIATE ACTIONS TO THE CHAIR OF THE SCIENTIFIC AFFAIRS COMMITTEE OF THE BOARD OF DIRECTORS. IN ACCORDANCE WITH THE GRANT AGREEMENT TERMS AND CONDITIONS, BRIGHTFOCUS MAY WITHHOLD FUNDING, OR DISCONTINUE AN AWARD, FOR ANY GRANTEE THAT FAILS TO ACHIEVE SUFFICIENT PROGRESS OR SUBMIT REQUIRED REPORTS. AT THE CONCLUSION OF THE GRANT AWARD PERIOD, EACH GRANTEE MUST COMPLETE AND SUBMIT A FINAL REPORT THAT IS ALSO REVIEWED BY THE BRIGHTFOCUS SENIOR SCIENTIFIC STAFF. EVALUATION OF THE WORK OF EACH GRANTEE IS QUALITATIVELY AND QUANTITATIVELY ASSESSED THROUGH VARIOUS METRICS RELATED TO THE IMPACT OF THE GRANT ON ITS TARGETED DISEASE FIELD. SUCH IMPACT METRICS HAVE REVEALED THAT 95% OF BRIGHTFOCUS-SUPPORTED RESEARCH RESULTS IN RESEARCH PUBLICATIONS THAT ADVANCE THE FIELDS SERVED BY BRIGHTFOCUS. THIS IMPACT IS FURTHER SUPPORTED BY ANNUAL CATEGORY NORMALIZED CITATION IMPACT ANALYSIS THAT COMPARES BRIGHTFOCUS-SUPPORTED WORKS TO AN UNBIASED COMPARISON OF IMPACT PERFORMANCE VERSUS THE WORLD AVERAGE. BRIGHTFOCUS-SUPPORTED PUBLICATIONS WERE RECENTLY CITED AT 2 TIMES THE FREQUENCY OF THE WORLD AVERAGE. A FINAL EXAMPLE OF IMPACT ASSESSMENT REVEALED THAT THE SUCCESSES OF BRIGHTFOCUS GRANTEES CONTINUE LONG AFTER THE GRANT EXPIRES. ON AVERAGE, EACH GRANTEE RECEIVES ADDITIONAL GRANTS FOR FOLLOW-ON PROJECTS SPAWNED BY THE BRIGHTFOCUS GRANT, WITH VALUES UP TO 10 TIMES THE LEVEL OF THE INITIAL BRIGHTFOCUS INVESTMENT. BRIGHTFOCUS SOLICITS FEEDBACK FROM ITS GRANTEES, AND PROVIDES AN ANONYMOUS FORUM FOR COLLECTING SUCH INFORMATION. THROUGH THE BRIGHTFOCUS FOUNDATION WEBSITE AND WITHIN THE SCIENTIFIC PROGRESS REPORTS, THERE ARE DESIGNATED SECTIONS WHERE AWARDEES ARE ASKED TO PROVIDE FEEDBACK TO THE FOUNDATION. THROUGH THIS MECHANISM, THEY ARE GIVEN THE ABILITY TO ANONYMOUSLY PROVIDE FEEDBACK OR COMMUNICATE THEIR CONCERNS TO PROGRAM STAFF OR THE BRIGHTFOCUS' COMPLIANCE OFFICE. ANY SUGGESTIONS, CONCERNS, COMPLAINTS, OR POSITIVE EXPERIENCES CAN BE OUTLINED AND BROUGHT TO THE ATTENTION OF BRIGHTFOCUS IN THIS MANNER, SO THAT BRIGHTFOCUS CAN ADDRESS ANY AREAS NEEDING IMPROVEMENT, REAFFIRM PRAISE-WORTHY POLICIES, OR OTHERWISE ASSESS NEEDS FOR PROGRAMMATIC CHANGE. THE SENIOR LEADERSHIP PRESENTS AND SUMMARIZES THE STATUS AND PROGRESS ON GRANTS TO THE BRIGHTFOCUS BOARD OF DIRECTORS AT EACH OF THEIR QUARTERLY BOARD MEETINGS.
PART II, LINE 1(H)NAME OF ORGANIZATION OR GOVERNMENT: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO (H) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY SARAH KAUFMAN, MD, PHD, ENTITLED: (A2024001F) IDENTIFYING MECHANISMS OF TAU AGGREGATION & TOXICITY ACROSS TAUOPATHIES. INVESTIGATOR'S SUMMARY: ALZHEIMER'S DISEASE AND FRONTOTEMPORAL DEMENTIA FEATURE THE ACCUMULATION OF MISFOLDED, AGGREGATED TAU PROTEIN IN NEURONS THAT ARE LOST EARLY IN THE COURSE OF THESE DISEASES. THE MECHANISMS THAT UNDERLIE TAU MISFOLDING AND ACCUMULATION, AND ITS ASSOCIATED NEUROTOXICITY, ARE NOT KNOWN. THIS PROJECT EMPLOYS WHOLE-GENOME SCREENING TECHNIQUES TO IDENTIFY THE CELLULAR PATHWAYS THAT REGULATE TAU AGGREGATION AND TOXICITY IN HUMAN-INDUCED PLURIPOTENT STEM CELL-DERIVED NEURONS. THIS WORK WILL PROVIDE CRITICAL INSIGHT INTO TAU-ASSOCIATED DISEASE MECHANISMS AND IDENTIFY POTENTIAL THERAPEUTIC TARGETS FOR ALZHEIMER'S AND FRONTOTEMPORAL DEMENTIA. NAME OF ORGANIZATION OR GOVERNMENT: WASHINGTON UNIVERSITY IN ST. LOUIS (H) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY DANIRA TORAL-RIOS, PHD, ENTITLED: (A2024002F) OXYSTEROLS IN INNATE AND ADAPTIVE IMMUNITY IN A TAUOPATHY MOUSE MODEL. INVESTIGATOR'S SUMMARY: NEURONAL LOSS IN ALZHEIMER'S DISEASE IS LINKED TO BRAIN INFILTRATION OF BLOOD-DERIVED IMMUNE CELLS IN A NEUROTOXIC CASCADE OF TAU PROTEIN ACCUMULATION AND INFLAMMATION IN THE BRAIN. PRELIMINARY STUDIES SHOW EVIDENCE FOR ALTERED BRAIN CHOLESTEROL METABOLISM IN MEDIATING TAU PATHOLOGY AND INFILTRATION OF BLOOD IMMUNE CELLS INTO THE BRAIN. THIS PROJECT AIMS TO INVESTIGATE THIS PATHWAY WITH THE LONG-TERM GOAL OF PHARMACOLOGICAL INTERVENTION TO BLOCK NEURONAL LOSS IN ALZHEIMER'S. NAME OF ORGANIZATION OR GOVERNMENT: WEILL MEDICAL COLLEGE OF CORNELL UNIVERSITY (H) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY WENHUI QU, PHD, ENTITLED: (A2024003F) UNLOCKING TAU'S SECRETS: HUMAN BRAIN CELLS IN THE LIVING MOUSE BRAIN. INVESTIGATOR'S SUMMARY: DR. QU HAS PIONEERED MODELING TAU BUILDUP IN HUMAN NEURONS USING DIFFERENT TYPES OF NEURAL CELLS FROM STEM CELLS DERIVED FROM SKIN BIOPSY. THIS STUDY PROPOSES TRANSPLANTING BOTH HUMAN NEURONS AND MICROGLIATHE BRAIN'S IMMUNE CELLSINTO MOUSE BRAINS TO GENERATE A GROUNDBREAKING CHIMERA HUMAN-MOUSE MODEL THAT DEVELOPS TAU ACCUMULATION. USING THIS MODEL, THE STUDY WILL ALSO EXAMINE HOW HUMAN SPECIFIC MOLECULAR PATHWAYS AFFECT THE DISEASE'S PROGRESSION. THIS RESEARCH COULD LEAD TO BREAKTHROUGHS IN UNDERSTANDING AND TREATING ALZHEIMER'S AND OTHER TAU-RELATED DISEASES. NAME OF ORGANIZATION OR GOVERNMENT: ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI (H) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY TATSUHIKO NAITO, MD, PHD, ENTITLED: (A2024004F) DECODING ALZHEIMER'S DISEASE GENOMES WITH DEEP LEARNING. INVESTIGATOR'S SUMMARY: DR. NAITO'S RESEARCH AIMS TO UNRAVEL THE GENETIC COMPLEXITIES OF ALZHEIMER'S DISEASE. THIS PROJECT HAS TWO PRIMARY OBJECTIVES: TO DEVELOP A PIPELINE TO PREDICT THE IMPACT OF GENETIC MUTATIONS ON RNA PROCESSING IN BRAIN CELLS BY STATE-OF-THE-ART MACHINE-LEARNING TECHNOLOGIES AND TO INVESTIGATE HOW GENETIC MUTATIONS HAVE AN IMPACT ON INDIVIDUALS WITH ALZHEIMER'S VIA RNA PROCESSING BY APPLYING THIS PIPELINE TO HUGE GENOMIC DATA. A BETTER UNDERSTANDING OF GENETIC ASSOCIATIONS OF ALZHEIMER'S WILL HELP IN DEVELOPING NEW TREATMENTS AND IDENTIFYING BIOMARKERS. NAME OF ORGANIZATION OR GOVERNMENT: STANFORD UNIVERSITY (H) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY HANNAH ENNERFELT, PHD, ENTITLED: (A2024005F) THE ROLE OF THE IMMUNE SYSTEM IN DRIVING COGNITIVE DECLINE. INVESTIGATOR'S SUMMARY: DURING AGING AND ALZHEIMER'S DISEASE, CERTAIN INFLAMMATORY RESPONSES REGULATED BY THE IMMUNE SYSTEM FURTHER EXACERBATE THE DISEASE AND CONTRIBUTE TO IMPAIRED COGNITION AND MEMORY. THIS STUDY FOCUSES ON DELINEATING THE MACHINERY NECESSARY FOR IMMUNE CELLS TO AMPLIFY DAMAGING INFLAMMATION IN THE BODY AND, ULTIMATELY, THE BRAIN. USING A NOVEL METHOD TO TARGET A SPECIFIC IMMUNE CELL MECHANISM, DR. ENNERFELT AND COLLEAGUES WILL ASSESS HOW IMPEDING ITS ASSOCIATED INFLAMMATORY PATHWAYS CAN CURB COGNITIVE DECLINE AND ALZHEIMER'S PROGRESSION. NAME OF ORGANIZATION OR GOVERNMENT: UNIVERSITY OF CALIFORNIA, BERKELEY (H) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY SANKALP SHUKLA, PHD, ENTITLED: (A2024008F) UNDERSTANDING THE ROLE OF PROTEIN CLUMPS ON MEMBRANE IN ALZHEIMER'S DISEASE. INVESTIGATOR'S SUMMARY: NEURODEGENERATIVE DISEASES LIKE ALZHEIMER'S DISEASE ARE CAUSED BY THE BUILDUP OF CLUMPS OF PROTEINS THAT SPREAD FROM ONE PART OF THE BRAIN TO ANOTHER, CAUSING PROGRESSIVE BRAIN DAMAGE. THESE PROTEIN CLUMPS CAN INTERACT AND DISRUPT THE MEMBRANES RESPONSIBLE FOR CONTAINING AND DESTROYING THEM, CAUSING PROTEIN CLUMP LEAKAGE AND SPREAD. THIS PROJECT AIMS TO UNDERSTAND THE UNDERLYING CAUSE OF THIS MEMBRANE LEAKAGE FOR THE DEVELOPMENT OF THERAPIES TO COUNTERACT PROTEIN CLUMP ESCAPE BY PROMOTING THE REPAIR OF THE MEMBRANES DAMAGED BY THESE PROTEIN CLUMPS. NAME OF ORGANIZATION OR GOVERNMENT: MASSACHUSETTS GENERAL HOSPITAL (H) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY MD JOYNAL ABEDIN, PHD, ENTITLED: (A2024010F) THE EFFECT OF ALZHEIMER'S DISEASE ON NEURONS ACROSS THE SLEEP/WAKE CYCLE. INVESTIGATOR'S SUMMARY: IN ALZHEIMER'S DISEASE, BUILDUP OF AMYLOID BETA (A) PROTEIN CAN RESULT IN SLEEP DISTURBANCES. DR. ABEDIN AND HIS TEAM WILL INVESTIGATE THE ACTIVITY OF SPECIFIC NEURONAL TYPES IN A GENETICALLY ENGINEERED MOUSE MODEL OF ALZHEIMER'S DISEASE TO UNDERSTAND HOW A AFFECTS NEURONAL ACTIVITY DURING THE SLEEP/WAKE CYCLE. THIS RESEARCH COULD PAVE THE WAY FOR THERAPEUTIC DEVELOPMENT AIMED AT RESTORING ABNORMAL NEURONAL ACTIVITY AND POTENTIALLY LEADING TO A CURE FOR ALZHEIMER'S DISEASE. NAME OF ORGANIZATION OR GOVERNMENT: OREGON HEALTH & SCIENCE UNIVERSITY (H) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY PAULA SANCHEZ-MOLINA, PHD, ENTITLED: (A2024011F) ROLE OF THE IMMUNE SYSTEM IN ALZHEIMER'S DISEASE. INVESTIGATOR'S SUMMARY: ALZHEIMER'S DISEASE HAS TRADITIONALLY BEEN CONSIDERED A NEURONAL PATHOLOGY, BUT NOW IT IS KNOWN THAT A SPECIFIC TYPE OF BRAIN IMMUNE CELL, CALLED MICROGLIA, PLAYS A CRUCIAL ROLE IN THE PATHOGENESIS OF THE DISEASE. THIS PROJECT AIMS TO UNDERSTAND HOW IMMUNE CELLS FROM THE BLOOD IMPACT MICROGLIA AND CONTRIBUTE TO THE DEVELOPMENT OF ALZHEIMER'S DISEASE. THIS PROJECT WILL USE HUMAN SAMPLES, ENABLING RESEARCHERS TO OBTAIN POTENTIAL TRANSLATIONAL RESULTS FOR THE CLINIC. THE CHARACTERIZATION AND VALIDATION OF A PERIPHERAL IMMUNE MECHANISM THAT CONTRIBUTES TO ALZHEIMER'S PATHOLOGY COULD OFFER IMPORTANT BIOMARKERS FOR DISEASE DIAGNOSIS AND THE DESIGN OF NEW THERAPIES. NAME OF ORGANIZATION OR GOVERNMENT: TUFTS UNIVERSITY (H) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY GIUSEPPINA TESCO, MD, PHD, ENTITLED: (A2024016S) ROLE OF GGA3 IN ALZHEIMER'S DISEASE. INVESTIGATOR'S SUMMARY: DR. TESCO'S LAB RECENTLY FOUND A NOVEL GENETIC VARIANT ASSOCIATED WITH LATE-ONSET ALZHEIMER'S DISEASE IN AFRICAN AMERICAN FAMILIES, CALLED GGA3 . HER RESEARCH PREVIOUSLY DEMONSTRATED THAT GGA3 PLAYS A CRITICAL ROLE IN THE TRANSPORT AND REGULATION OF BACE1, A KEY ENZYME RESPONSIBLE FOR AMYLOID-BETA PRODUCTION. THE STUDY AIMS TO DETERMINE HOW THIS NOVEL GENETIC VARIANT LEADS TO ALZHEIMER'S DISEASE. RESULTS MAY CONTRIBUTE TO A BETTER UNDERSTANDING OF GENETIC RISK FACTORS IN THE AFRICAN AMERICAN POPULATION, WHICH IS CURRENTLY UNDERSTUDIED. NAME OF ORGANIZATION OR GOVERNMENT: MAYO CLINIC JACKSONVILLE (H) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY MERCEDES PRUDENCIO, PHD, ENTITLED: (A2024017S) UNDERSTANDING THE CONTRIBUTION OF TDP-43 LOSS OF FUNCTION IN AD. INVESTIGATOR'S SUMMARY: TDP-43 PROTEINS ABNORMALLY ACCUMULATE IN THE BRAIN OF UP TO 70% OF PEOPLE WITH ALZHEIMER'S DISEASE AND ARE CHARACTERIZED BY WORSE MEMORY AND GREATER BRAIN ATROPHY COMPARED TO THOSE WITH ALZHEIMER'S LACKING TDP-43 PATHOLOGY. THIS PROPOSAL AIMS TO CHARACTERIZE THE ROLE OF TDP-43 DYSFUNCTION IN THE PATHOGENESIS OF ALZHEIMER'S BY EVALUATING: 1) WHETHER TDP-43 DYSFUNCTION EXACERBATES BEHAVIOR AND PATHOLOGICAL ALZHEIMER'S PHENOTYPES, AS WELL AS INDUCES NEURONAL LOSS IN AN ALZHEIMER'S MOUSE MODEL, AND 2) THE RELATIONSHIPS BETWEEN ALZHEIMER'S PATHOLOGIES AND TDP-43 DYSFUNCTION IN ALZHEIMER'S HUMAN BRAINS. THESE STUDIES ARE EXPECTED TO ALSO HIGHLIGHT THE IMPORTANCE OF TDP-43 PATHOLOGY IN THERAPEUTIC TARGET AND BIOMARKER DESIGN AND IN PARTICIPANT EVALUATIONS DURING CLINICAL TRIALS.
PART II, LINE 1(H) CONTINUEDNAME OF ORGANIZATION OR GOVERNMENT: MASSACHUSETTS GENERAL HOSPITAL (H) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY JAEHONG SUH, PHD, ENTITLED: (A2024022S) INCREASE OF BRAIN ADAM10 EXPRESSION AS ALZHEIMER'S DISEASE THERAPEUTIC. INVESTIGATOR'S SUMMARY: ADAM10 IS AN ENZYME THAT PREVENTS THE GENERATION OF AMYLOID-BETA, THE MAIN COMPONENT OF SENILE PLAQUES IN ALZHEIMER'S DISEASE BRAINS. PREVIOUS STUDIES CONSISTENTLY SHOWED THAT LOSS OF ADAM10 FUNCTION INCREASES ALZHEIMER'S RISK, SUGGESTING THAT INCREASING ADAM10 EXPRESSION CAN BE A PROMISING THERAPEUTIC TARGET. THIS STUDY WILL TEST IF BRAIN-SELECTIVE MODULATION OF ADAM10 EXPRESSION AFFECTS ALZHEIMER'S PATHOGENESIS AND DEVELOP AN EXPERIMENTAL ANTISENSE OLIGONUCLEOTIDE DRUG THAT INCREASES ADAM10 EXPRESSION FOR ALZHEIMER'S TREATMENT. IF SUCCESSFUL, DR. SUH AND OTHERS COULD SCREEN FDA-APPROVED DRUGS OR OTHER MEDICINAL LIBRARIES TO IDENTIFY SMALL MOLECULE COMPOUNDS THAT INCREASE ADAM10 EXPRESSION AND DEVELOP THEM AS ALZHEIMER'S DRUGS. IN ADDITION, ADAM10 ANTISENSE OLIGONUCLEOTIDES IDENTIFIED FROM THE PROPOSED STUDY CAN BE OPTIMIZED FOR HUMAN SEQUENCES AND FURTHER TESTED AND DEVELOPED FOR ALZHEIMER'S TREATMENT. NAME OF ORGANIZATION OR GOVERNMENT: EMORY UNIVERSITY (H) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY BRITTANY BUTTS, PHD, ENTITLED: (A2024024S) ALZHEIMER'S DISEASE RISK AND IMMUNE FUNCTION IN HEART DISEASE. INVESTIGATOR'S SUMMARY: THIS STUDY EXPLORES HOW THE IMMUNE SYSTEM RELATES TO MEMORY, COGNITION, AND ALZHEIMER'S RISK IN MIDDLE-AGED ADULTS WITH HEART CONDITIONS. AS HEART PROBLEMS SURGE IN THE UNDER-65 POPULATION, THE CONNECTION TO COGNITIVE DECLINE AND ALZHEIMER'S REMAINS UNCLEAR. SURVEYS, BLOOD TESTS, AND MEMORY ASSESSMENTS WILL BE USED TO BETTER UNDERSTAND HOW FACTORS LIKE HIGH BLOOD PRESSURE AFFECT COGNITION AND MAY ELEVATE ALZHEIMER'S RISK. INSIGHTS INTO HEART HEALTH, IMMUNITY, AND ALZHEIMER'S CAN BENEFIT AT-RISK INDIVIDUALS AND SHAPE FUTURE TREATMENTS. NAME OF ORGANIZATION OR GOVERNMENT: ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI (H) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY ANNA PODLESNY-DRABINIOK, PHD, ENTITLED: (A2024025S) MICROGLIAL REPROGRAMMING IN ALZHEIMER'S DISEASE. INVESTIGATOR'S SUMMARY: HUMAN GENETIC STUDIES IMPLICATE MICROGLIA, THE BRAIN'S "TRASH COLLECTOR" CELLS, AS KEY PLAYERS IN ALZHEIMER'S DISEASE. DR. PODLESNY-DRABINIOK AND COLLEAGUES NOMINATED CANDIDATE FACTORS THAT MAY BOOST THE ABILITY OF MICROGLIA TO DISPOSE OF THE WASTE THAT ACCUMULATES DURING ALZHEIMER'S. HERE, THE STUDY AIMS TO VALIDATE COMPUTATIONAL PREDICTIONS AND CHARACTERIZE THE ROLE OF TWO CANDIDATE FACTORS IN HUMAN MICROGLIA AT BASELINE AND IN THE CONTEXT OF AMYLOIDS. RESEARCHERS WILL ALSO TARGET THESE FACTORS IN MICROGLIA DERIVED FROM PEOPLE CARRYING TWO COPIES OF APOE4 TO HELP THESE CELLS OVERCOME THE DEFICITS ASSOCIATED WITH THIS MAJOR GENETIC FACTOR FOR ALZHEIMER'S. DR. PODLESNY-DRABINIOK'S RESEARCH HOLDS THE POTENTIAL TO EXPLORE NOVEL THERAPEUTIC STRATEGIES AIMING TO INDUCE WASTE CLEARANCE PROCESSES IN MICROGLIA. NAME OF ORGANIZATION OR GOVERNMENT: HEBREW REHABILITATION CENTER (H) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY DAVIDE CAPPON, PHD, ENTITLED: (A2024027S) SYMPTOM-SPECIFIC NEUROSTIMULATION FOR DEMENTIA. INVESTIGATOR'S SUMMARY: THIS PROJECT WILL COMBINE TWO TYPES OF TRANSCRANIAL ELECTRICAL STIMULATION, A NONINVASIVE TECHNOLOGY THAT ALLOWS FOR THE MODULATION OF BRAIN NETWORK ACTIVITY TO ADDRESS DEPRESSIVE AND MEMORY SYMPTOMS IN OLDER ADULTS WITH DEPRESSION AND ALZHEIMER'S DEMENTIA. BY USING CUTTING-EDGE TECHNOLOGY TO STUDY THE ELECTRICAL FIELDS GENERATED IN THE TARGETED BRAIN CIRCUITS AND DELIVERING THE INTERVENTION AT HOME, THIS PROJECT WILL HELP DEVELOP A SCALABLE, ACCESSIBLE, NONINVASIVE INTERVENTION WITH THE GREATEST IMPACT ON ALLEVIATING DEPRESSION AND ALZHEIMER'S SYMPTOMS. NAME OF ORGANIZATION OR GOVERNMENT: SAINT LOUIS UNIVERSITY (H) PURPOSE OF GRANT: ALZHEIMER'S DISEASE RESEARCH BY ANDREW D. NGUYEN, PHD, ENTITLED: (A2024028S) PROGRANULIN AS A POTENTIAL THERAPEUTIC TARGET FOR ALZHEIMER'S DISEASE. INVESTIGATOR'S SUMMARY: PREVIOUS STUDIES SUGGEST THAT PROGRANULIN CONFERS A PROTECTIVE EFFECT ON ALZHEIMER'S DISEASE IN MOUSE MODELS AND IN HUMANS, BUT SEVERAL IMPORTANT GAPS IN KNOWLEDGE EXIST. THIS PROJECT AIMS TO DETERMINE HOW PROGRANULIN EXERTS ITS EFFECTS IN THE CENTRAL NERVOUS SYSTEM TO ENHANCE MEMORY AND TO TEST IF PHARMACOLOGICALLY INCREASING PROGRANULIN LEVELS CAN PROTECT AGAINST ALZHEIMER'S DISEASE. NAME OF ORGANIZATION OR GOVERNMENT: UNIVERSITY OF MICHIGAN MEDICAL CENTER (H) PURPOSE OF GRANT: MACULAR DEGENERATION RESEARCH BY JOHN HAN, PHD, ENTITLED: (M2024001F) TARGETING LIPID STORAGE FOR TREATING AGE-RELATED MACULAR DEGENERATION. INVESTIGATOR'S SUMMARY: AGE-RELATED MACULAR DEGENERATION (AMD) IS CHARACTERIZED BY THE BUILDUP OF FATTY DEPOSITS OUTSIDE A CELL LAYER IN THE BACK OF THE EYE CALLED THE RETINAL PIGMENT EPITHELIUM (RPE). AS PART OF ITS NORMAL FUNCTION, THE RPE CONSUMES ENORMOUS AMOUNTS OF FAT EACH DAY, AND THIS FAT IS TEMPORARILY STORED INSIDE THE CELL IN SPHERES CALLED LIPID DROPLETS. THE RESEARCHERS' GOAL IS TO UNDERSTAND HOW THE RPE FORMS LIPID DROPLETS AND MANIPULATE THOSE LIPID DROPLETS IN SUCH A WAY THAT LESS FAT IS SECRETED FROM THE RPE TO FORM THE TOXIC FATTY DEPOSITS OUTSIDE THE CELL THAT CHARACTERIZE AMD. TARGETING ENZYMES GOVERNING LIPID DROPLET FORMATION AND DEGRADATION HAS BECOME A VIABLE THERAPEUTIC STRATEGY IN OTHER DISEASES. RPE LIPID DROPLETS MAY BE CRITICAL GUARDIANS AGAINST THE ONSET OF AMD. LIPID DROPLETS ARE HIGHLY DRUGGABLE, WITH AVAILABLE SMALL MOLECULES THAT ARE HIGHLY SPECIFIC TO TARGET ENZYMES REQUIRED FOR LIPID DROPLET FORMATION AND LIPID RELEASE, PROVIDING AN INNOVATIVE NEW THERAPEUTIC APPROACH FOR AMD. NAME OF ORGANIZATION OR GOVERNMENT: BOSTON CHILDREN'S HOSPITAL (H) PURPOSE OF GRANT: MACULAR DEGENERATION RESEARCH BY NEETU KUSHWAH, PHD, ENTITLED: (M2024002F) ROLE OF NUCLEAR RECEPTOR RORA IN LIPID DYSREGULATION. INVESTIGATOR'S SUMMARY: AGE-RELATED MACULAR DEGENERATION (AMD) IS A LEADING CAUSE OF BLINDNESS AMONG PEOPLE AGED 60 AND OLDER. IT IS A MULTIFACTORIAL DISEASE INVOLVING MULTIPLE CELLULAR PATHWAYS, AMONG WHICH LIPID DYSREGULATION AND INFLAMMATION ARE MAJOR PATHOGENIC FACTORS. RESEARCHERS WILL INVESTIGATE THE ROLE OF A LIPID-SENSING NUCLEAR RECEPTOR RETINOIC ACID-RELATED ORPHAN RECEPTOR ALPHA (RORA) IN REGULATING CHRONIC SUBRETINAL INFLAMMATION TO ELUCIDATE AMD PATHOGENESIS. THEY WILL ASSESS IF GENETIC DELETION OF RORA IN A TYPE OF INFLAMMATORY CELLS MAY LEAD TO LIPID DYSREGULATION AND CHRONIC INFLAMMATION. NAME OF ORGANIZATION OR GOVERNMENT: JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE (H) PURPOSE OF GRANT: MACULAR DEGENERATION RESEARCH BY KRISHNA SINGH, PHD, ENTITLED: (M2024003F) NRF2 PROTEIN ENHANCES NATURAL ANTIOXIDANT DEFENSES BY CELLULAR ACETYLATION. INVESTIGATOR'S SUMMARY: IN AGE-RELATED MACULAR DEGENERATION (AMD), RETINAL PIGMENT EPITHELIAL (RPE) CELLS ARE DAMAGED BY OXIDATIVE STRESS. NRF2 IS A PROTEIN THAT PROTECTS AGAINST OXIDATIVE STRESS; HOWEVER, NRF2 SIGNALING DECLINES IN AMD. DR. SINGH AND HIS TEAM PROPOSE TO FIND A CAUSE FOR NRF2 SIGNALING DECLINE, CALLED ACETYLATION, A PROCESS THAT MODIFIES PROTEINS TO CHANGE HOW GENES ARE PRODUCED. RESEARCHERS WILL TREAT RPE CELLS WITH SMOKE AND VERIFY IF THE ACETYLATING NRF2 WILL PREVENT ITS DECLINE. IF SUCCESSFUL, THEY WILL HAVE A FAVORABLE STRATEGY FOR TREATING AMD. NAME OF ORGANIZATION OR GOVERNMENT: SCHEPENS EYE RESEARCH INSTITUTE, INC. (H) PURPOSE OF GRANT: MACULAR DEGENERATION RESEARCH BY SHINTARO SHIRAHAMA, MD, PHD, ENTITLED: (M2024004F) DEVELOPMENT OF A TRANSPLANT-INDEPENDENT THERAPY FOR RPE DYSFUNCTION. INVESTIGATOR'S SUMMARY: AGING IS A CRITICAL RISK FACTOR FOR DEVELOPING AGE-RELATED MACULAR DEGENERATION (AMD), WHICH IMPLIES THAT YOUNG RETINAL PIGMENT EPITHELIUM (RPE) CELLS CAN SUCCESSFULLY COMBAT THE UNDERLYING CAUSES OF AMD. CONVERSELY, AS RPE CELLS AGE, THEY UNDERGO ALTERATIONS, RENDERING THEM MORE SUSCEPTIBLE TO AMD PATHOGENESIS. DR. SHIRAHAMA'S TEAM FOUND THAT EPIGENETIC REPROGRAMMING THROUGH OSK (OCT4, SOX2, AND KLF4) TRANSDUCTION COULD REVERSE THE CELLULAR BIOLOGICAL AGE AND RESTORE FUNCTION. THEREFORE, IF THEY CAN REVERSE THE BIOLOGICAL AGE OF RPE CELLS, THESE YOUNGER CELLS COULD SUCCESSFULLY COMBAT THE DISEASE, STOPPING FURTHER PROGRESSION AND RESTORING FUNCTIONAL VISION.
PART II, LINE 1(H) CONTINUEDNAME OF ORGANIZATION OR GOVERNMENT: UNIVERSITY OF WASHINGTON (H) PURPOSE OF GRANT: MACULAR DEGENERATION RESEARCH BY JULIETTE WOHLSCHLEGEL, PHD, ENTITLED: (M2024005F) REGENERATING THE HUMAN RETINA. INVESTIGATOR'S SUMMARY: THE HUMAN RETINA CANNOT REGENERATE AFTER DISEASES LIKE AGE-RELATED MACULAR DEGENERATION, WHICH OFTEN LEADS TO BLINDNESS. HOWEVER, A FEW SPECIES INCLUDING FISH CAN REGENERATE NEW RETINAL CELLS THAT EVENTUALLY RESTORE VISUAL FUNCTION. THE REGENERATIVE PROCESS IS DRIVEN BY THE MLLER GLIA, A SUPPORT CELL IN THE RETINA. RESEARCHERS ARE NOW PARTIALLY ABLE TO RECAPITULATE THIS PHENOMENON IN THE HUMAN RETINA. USING THIS NEW STRATEGY, THEY PLAN TO TEST THE REGENERATIVE CAPACITY OF A SPECIFIC ZONE OF THE HUMAN RETINA: THE MACULA. DR. WOHLSCHLEGEL AND HER TEAM NEXT PROPOSE TO TEST DIFFERENT FACTORS TO SPECIFICALLY STIMULATE CONE PHOTORECEPTOR REGENERATION FROM MLLER GLIA. NAME OF ORGANIZATION OR GOVERNMENT: THE PENNSYLVANIA STATE UNIVERSITY COLLEGE OF MEDICINE (H) PURPOSE OF GRANT: MACULAR DEGENERATION RESEARCH BY SANDEEP MOOTHEDATH SUBRAHMANIAN, PHD, ENTITLED: (M2024006F) UNDERSTANDING EARLY EVENTS IN AGE-RELATED MACULAR DEGENERATION. INVESTIGATOR'S SUMMARY: AGE-RELATED MACULAR DEGENERATION (AMD) IS A LEADING CAUSE OF VISION LOSS AMONG THE ELDERLY POPULATION. A SIGNIFICANT CHALLENGE IN ADDRESSING AMD IS THE LACK OF UNDERSTANDING OF THE EARLY MOLECULAR EVENTS THAT CONTRIBUTE TO ITS DEVELOPMENT. THIS PROJECT AIMS TO EXPLORE A NOVEL MOLECULAR SWITCH THAT PLAYS A ROLE IN THE FAILED ANTIOXIDANT AND INFLAMMATORY RESPONSES IN RETINAL PIGMENT EPITHELIUM WITH AGING. THE FINDINGS ARE EXPECTED TO IDENTIFY NEW TARGETS FOR THERAPEUTICS THAT ARE PREVENTATIVE OR PROVIDE INTERVENTIONS EARLY IN THE DEVELOPMENT OF AMD. NAME OF ORGANIZATION OR GOVERNMENT: UNIVERSITY OF COLORADO (H) PURPOSE OF GRANT: MACULAR DEGENERATION RESEARCH BY MIGUEL FLORES-BELIVER, PHD, ENTITLED: (M2024008N) EXOSOMES & AUTOPHAGY: SUSPICIOUS PARTNERS IN DRUSEN BIOGENESIS AND AMD. INVESTIGATOR'S SUMMARY: THE RESEARCH TEAM SEEKS TO UNDERSTAND HOW LITTLE VESICLES, CALLED EXOSOMES, THAT RETINAL PIGMENT EPITHELIUM (RPE) AND RETINAL CELLS SECRETE AND CONTAIN MANY CELLULAR BIOPRODUCTS CONTRIBUTE TO DRUSEN FORMATION AND THE PROGRESSION OF AMD. THEY WILL ALSO IDENTIFY BIOACTIVE MOLECULES RELEASED IN EXOSOMES THAT COULD SERVE AS POTENTIAL BIOMARKERS FOR AMD. THE GOAL IS TO BRIDGE BASIC RESEARCH ON AMD WITH CLINICAL APPLICATION BY TRANSFORMING OUR UNDERSTANDING OF AMD PATHOPHYSIOLOGY AND DRUSEN FORMATION. THIS INVOLVES PRECLINICAL VALIDATION, INVESTIGATING INTERVENTIONS TARGETING AUTOPHAGY AND EXOSOMES, BIOMARKER DEVELOPMENT, DIAGNOSTIC TOOL INTEGRATION, THERAPEUTIC DEVELOPMENT, AND PATIENT STRATIFICATION FOR PERSONALIZED TREATMENTS. THROUGH THESE STRATEGIES, WE AIM TO IMPROVE AMD DIAGNOSIS, TREATMENT, AND PATIENT OUTCOMES. NAME OF ORGANIZATION OR GOVERNMENT: UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (H) PURPOSE OF GRANT: MACULAR DEGENERATION RESEARCH BY HEIKE KROEGER, PHD, ENTITLED: (M2024010N) DECODING VISION: CONE DEVELOPMENT IN RETINAL ORGANOIDS AND ANOLE LIZARD. INVESTIGATOR'S SUMMARY: THE LOSS OF CONE PHOTORECEPTOR CELLS DURING AGE-RELATED MACULAR DEGENERATION (AMD) CAN LEAD TO IRREVERSIBLE VISION LOSS. REPAIRING THESE SPECIALIZED CELLS COULD CHANGE THE OVERALL APPROACH OF AMD THERAPIES AND COMPLEMENT CURRENT TREATMENT OPTIONS. THIS RESEARCH INVESTIGATES HOW CONE PHOTORECEPTOR OUTER SEGMENTS ARE FORMED AND REGENERATED USING STEM CELL ORGANOIDS AND THE BROWN ANOLE LIZARD, A NOVEL RESEARCH MODEL FOR CONE PHOTORECEPTOR DISEASES. FINDINGS WILL IDENTIFY A NEW STRATEGY AND POTENTIAL NEW THERAPEUTIC TARGETS TO IMPROVE AND PREVENT LOSS OF CONE PHOTORECEPTOR CELL FUNCTION DURING AMD. NAME OF ORGANIZATION OR GOVERNMENT: GEROGIA TECH RESEARCH CORPORATION (H) PURPOSE OF GRANT: NATIONAL GLAUCOMA RESEARCH BY HANNAH YOUNGBLOOD, PHD, ENTITLED: (G2024001F) EFFECTS OF PSEUDOEXFOLIATION GLAUCOMA VARIANTS IN LOXL1. INVESTIGATOR'S SUMMARY: GENETIC VARIANTS IN LOXL1 CAN ALTER RISK FOR PSEUDOEXFOLIATION GLAUCOMA (XFG), A BLINDING DISEASE THAT AFFECTS MORE THAN 10 MILLION PEOPLE. THIS PROJECT SEEKS TO DETERMINE HOW THESE VARIANTS ALTER THE STRUCTURE AND FUNCTION OF THE LOXL1 PROTEIN. SUCCESSFUL COMPLETION OF THIS PROJECT WILL PROVIDE A BETTER UNDERSTANDING OF HOW LOXL1 VARIANTS CONTRIBUTE TO XFG AND PROVIDE GROUNDWORK FOR THERAPEUTIC DEVELOPMENT. THIS PROJECT WOULD BE THE FIRST TO CHARACTERIZE THE PROTEIN STRUCTURE OF LOXL1 WITH AND WITHOUT PSEUDOEXFOLIATION GLAUCOMA-ASSOCIATED VARIANTS. RESULTS WILL OFFER NOVEL INSIGHT INTO HOW PSEUDOEXFOLIATION GLAUCOMA-ASSOCIATED VARIANTS CONTRIBUTE TO THE DISEASE BY ALTERING INTERACTIONS WITH FIBULIN-5, A PROTEIN NECESSARY FOR PROPER LOXL1 LOCALIZATION. NAME OF ORGANIZATION OR GOVERNMENT: INDIANA UNIVERSITY (H) PURPOSE OF GRANT: NATIONAL GLAUCOMA RESEARCH BY SHRUTI PATIL, PHD, ENTITLED: (G2024002F) RGC AXON DEGENERATION IN A 3D MICROFLUIDIC HYDROGEL MODEL. INVESTIGATOR'S SUMMARY: RETINAL GANGLION CELL (RGC) AXONS TRAVERSING THE OPTIC NERVE HEAD ARE HIGHLY SUSCEPTIBLE TO GLAUCOMATOUS DAMAGE, YET THE LINK BETWEEN OPTIC NERVE HEAD BIOMECHANICS AND RGC AXONAL DEGENERATION REMAINS POORLY UNDERSTOOD. TO ADDRESS THIS, RESEARCHERS WILL IMPLEMENT 3D PLATFORMS INTEGRATING MICROFLUIDICS AND HYDROGELS WITH TUNABLE STIFFNESS TO MODEL BIOMECHANICAL ASPECTS AFFECTING RGC AXONS IN THE OPTIC NERVE HEAD. UPON COMPLETION, THE STUDY WILL UNCOVER INSIGHTS INTO RGC AXONAL DYSFUNCTION DUE TO BIOMECHANICAL CHANGES IN CONTEXT OF HUMAN TISSUE USING A STEM CELL MODEL. BY TARGETING THE BIOMECHANICAL ASPECTS OF THE LAMINA CRIBROSA, THE STUDY COULD LEAD TO NOVEL THERAPEUTIC INTERVENTIONS BEYOND TRADITIONAL APPROACHES REGULATING INTRAOCULAR PRESSURE. INCORPORATING HYDROGELS IN THE MICROFLUIDIC SYSTEM ALLOWS STUDY OF COMPLEX CELLULAR INTERACTIONS IN A 3D MICROENVIRONMENT, APPLICABLE TO OTHER AGE-ASSOCIATED OPTIC NERVE DEGENERATION. THIS OFFERS HOPE FOR MORE EFFECTIVE GLAUCOMA TREATMENTS. NAME OF ORGANIZATION OR GOVERNMENT: GEROGIA TECH RESEARCH CORPORATION (H) PURPOSE OF GRANT: NATIONAL GLAUCOMA RESEARCH BY HAIYAN LI, PHD, ENTITLED: (G2024003F) THE ROLE OF MICROTUBULES IN GLAUCOMATOUS SCHLEMM'S CANAL MECHANOBIOLOGY. INVESTIGATOR'S SUMMARY: INTRAOCULAR PRESSURE IS LARGELY CONTROLLED BY TISSUES AT OR NEAR SCHLEMM'S CANAL INNER WALL ENDOTHELIUM, WHERE REDUCED FLUID CONDUCTIVITY OCCURS IN GLAUCOMA. THIS PROJECT AIMS TO INVESTIGATE THE IMPACT OF MICROTUBULES, CRUCIAL COMPONENTS OF THE CYTOSKELETON, ON SCHLEMM'S CANAL CELL MECHANOBIOLOGY AND INTRAOCULAR PRESSURE, A KEY RISK FACTOR FOR GLAUCOMA. THIS WORK WILL IMPROVE OUR UNDERSTANDING OF SCHLEMM'S CANAL CELL MECHANOBIOLOGY, CREATING A FOUNDATION FOR FUTURE STUDIES INVESTIGATING HOW MICROTUBULES IN SCHLEMM'S CANAL CELLS INFLUENCE OUTFLOW FACILITY AND OCULAR HYPERTENSION. ADDITIONALLY, IT WILL OPEN AVENUES FOR BOTH EX VIVO AND IN VIVO INVESTIGATIONS OF CANDIDATE DRUGS TARGETING THE HYDRAULIC CONDUCTIVITY OF SCHLEMM'S CANAL INNER WALL CELLS AS TREATMENTS FOR OCULAR HYPERTENSION IN PRIMARY OPEN-ANGLE GLAUCOMA. NAME OF ORGANIZATION OR GOVERNMENT: UNIVERSITY OF PITTSBURGH (H) PURPOSE OF GRANT: NATIONAL GLAUCOMA RESEARCH BY BINGRUI WANG, PHD, ENTITLED: (G2024004F) HOW PRESSURE DEFORMS THE EYE AND LEADS TO GLAUCOMA VISION LOSS. INVESTIGATOR'S SUMMARY: BLINDNESS IN GLAUCOMA IS CAUSED BY DAMAGE TO AXONS THAT CARRY VISUAL INFORMATION TO THE BRAIN. DAMAGE OFTEN STARTS IN THE BACK OF THE EYE AND IS DUE TO HIGH EYE PRESSURE WHICH MECHANICALLY DEFORMS AXONS. HOWEVER, THE LINK BETWEEN AXON DEFORMATION AND LONG-TERM DAMAGE IS UNCLEAR. USING ANIMAL MODELS, RESEARCHERS WILL INVESTIGATE AXON DEFORMATION AND ITS LINK TO DAMAGE TO UNDERSTAND GLAUCOMA'S CAUSES. NAME OF ORGANIZATION OR GOVERNMENT: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO (H) PURPOSE OF GRANT: NATIONAL GLAUCOMA RESEARCH BY MENGYA ZHAO, PHD, ENTITLED: (G2024005F) WHY CERTAIN RETINA GANGLION CELLS STAY STRONG IN GLAUCOMA. INVESTIGATOR'S SUMMARY: THIS PROJECT FOCUSES ON UNDERSTANDING THE MECHANISMS UNDERLYING NEURONAL LOSS IN GLAUCOMA, WHICH CAN LEAD TO IRREVERSIBLE BLINDNESS. THIS DISEASE VARIABLY IMPACTS MANY EYE NEURONS. USING A COMBINATION OF CUTTING-EDGE TECHNIQUES, RESEARCHERS WILL INVESTIGATE WHY CERTAIN NEURONS ARE MORE RESILIENT THAN OTHERS. THIS WORK COULD UNLOCK NEW TREATMENTS, OFFERING A BREAKTHROUGH IN GLAUCOMA THERAPY AND EYE CARE.
PART II, LINE 1(H) CONTINUEDNAME OF ORGANIZATION OR GOVERNMENT: SUNY UPSTATE MEDICAL UNIVERSITY (H) PURPOSE OF GRANT: NATIONAL GLAUCOMA RESEARCH BY SAMUEL HERBERG, PHD, ENTITLED: (G2024006S) INVESTIGATE HOW THE MICROENVIRONMENT AFFECTS SCHLEMM'S CANAL CELL BEHAVIOR. INVESTIGATOR'S SUMMARY: HIGH-PRESSURE GLAUCOMA IS A LEADING CAUSE OF BLINDNESS WORLDWIDE, BUT THE CAUSAL MECHANISMS ARE UNCLEAR. USING OUR UNIQUE 3D FLUID DRAINAGE TISSUE MODEL SYSTEM, WE SEEK TO INVESTIGATE THE CONTRIBUTIONS OF GLAUCOMATOUS BIOMECHANICAL CUES IN DRIVING SCHLEMM'S CANAL CELL MECHANO-DYSFUNCTION. THIS WORK WILL SET THE STAGE FOR IDENTIFICATION OF FUTURE GLAUCOMA THERAPIES TARGETING CELLULAR BIOMECHANICS. NAME OF ORGANIZATION OR GOVERNMENT: UNIVERSITY OF VIRGINIA (H) PURPOSE OF GRANT: NATIONAL GLAUCOMA RESEARCH BY XIARONG LIU, PHD, ENTITLED: (G2024008S) LIGHT-MEDIATED SLEEP AND MOOD DISORDERS IN GLAUCOMA. INVESTIGATOR'S SUMMARY: A SMALL POPULATION OF RETINAL GANGLION CELLS, THE IPRGCS, COMMUNICATES LIGHT INFORMATION FROM THE EYES TO THE BRAIN FOR PURPOSES OTHER THAN VISION SUCH AS THE REGULATION OF SLEEP AND MOOD. BECAUSE GLAUCOMA PATIENTS OFTEN SUFFER FROM LIGHT-MEDIATED SLEEP AND MOOD DISORDERS, WE AIM TO UNDERSTAND HOW IPRGCS CONTROL LIGHT'S EFFECTS ON MOOD AND SLEEP. THIS STUDY REPRESENTS A FIRST ATTEMPT TO EXPLORE THE CHANGES DUE TO GLAUCOMA IN THE IPRGC-BASED NEURAL CIRCUITRY RESPONSIBLE FOR NON-VISUAL RESPONSES TO LIGHT. THIS RESEARCH WILL CONTRIBUTE TO OUR UNDERSTANDING OF THE NEURAL PATHWAYS UNDERLYING MOOD AND BEHAVIORAL CHANGES EXPERIENCED BY GLAUCOMA PATIENTS. SUCH INSIGHTS ARE CRUCIAL FOR ENHANCING PATIENT CARE AND DEVELOPING BETTER TREATMENTS AS GLAUCOMA ADVANCES AND EVOLVES. NAME OF ORGANIZATION OR GOVERNMENT: OREGON HEALTH & SCIENCE UNIVERSITY (H) PURPOSE OF GRANT: NATIONAL GLAUCOMA RESEARCH BY DIANA LOZANO, PHD, ENTITLED: (G2024009S) IOP-RELATED GENE RESPONSES IN GLAUCOMA TISSUES. INVESTIGATOR'S SUMMARY: ELEVATED INTRAOCULAR PRESSURE (IOP) IS A LEADING RISK FACTOR FOR PRIMARY OPEN-ANGLE GLAUCOMA. YET, THE CELLULAR EVENTS THAT COMPRISE PROTECTIVE HOMEOSTATIC IOP RESPONSES, OR DELETERIOUS EVENTS LEADING TO TISSUE INJURY, ARE CURRENTLY POORLY UNDERSTOOD. WE WILL INVESTIGATE HOW MILD AND REPEAT IOP ELEVATIONS MODIFY THE MOLECULAR MECHANISMS IN OCULAR TISSUES IMPLICATED IN GLAUCOMA PATHOGENESIS. NAME OF ORGANIZATION OR GOVERNMENT: GEORGIA INSTITUTE OF TECHNOLOGY (H) PURPOSE OF GRANT: NATIONAL GLAUCOMA RESEARCH BY C. ROSS ETHIER, PHD, ENTITLED: (CG2020001) NEXT-GENERATION GLAUCOMA DRUGS TO SELECTIVELY RELEASE THE PRESSURE-BUILDING BLOCK IN SCHLEMM'S CANAL. INVESTIGATOR'S SUMMARY: WE NOW UNDERSTAND THAT ENDOTHELIAL CELLS OF THE INNER WALL OF SCHLEMM'S CANAL (SC) PLAY A KEY ROLE IN HOMEOSTATIC CONTROL MECHANISMS THAT MAINTAIN IOP WITHIN A TARGET RANGE. THE LONG-TERM GOAL OF THIS PROJECT IS TO DEVELOP NOVEL THERAPIES THAT DIRECTLY TARGET SC CELLS TO IMPROVE IOP CONTROL. THESE TARGETED THERAPIES WILL BE HIGHLY EFFECTIVE DUE TO THEIR SPECIFICITY AND WILL THUS GREATLY BENEFIT GLAUCOMA PATIENTS. NAME OF ORGANIZATION OR GOVERNMENT: DUKE UNIVERSITY (H) PURPOSE OF GRANT: NATIONAL GLAUCOMA RESEARCH BY W. DANIEL STAMER, PHD, ENTITLED: (CG2020002) NEXT-GENERATION GLAUCOMA DRUG DEVELOPMENT. INVESTIGATOR'S SUMMARY: FOR THE PROJECT, WE WILL SCREEN CANDIDATE ADENO-ASSOCIATED VIRUSES AND ENGINEERED PROMOTERS CLONED INTO LENTIVIRUSES OBTAINED FROM COLLABORATORS IN HUMAN SCHLEMM'S CANAL CELLS IN VITRO AND ANTERIOR SEGMENTS EX VIVO FOR SELECTIVE TROPISM TO/ACTIVITY IN TRABECULAR MESHWORK VERSUS SCHLEMM'S CANAL. NAME OF ORGANIZATION OR GOVERNMENT: COLUMBIA UNIVERSITY (H) PURPOSE OF GRANT: NATIONAL GLAUCOMA RESEARCH BY SIMON JOHN, PHD, ENTITLED: (CG2020004) NOVEL GENE-THERAPY APPROACH FOR GLAUCOMA. INVESTIGATOR'S SUMMARY: THE PROJECT AIMS TO DEVELOP AND TEST RESOURCES FOR SCHLEMM'S CANAL SPECIFIC TARGETING AND EXPRESSION OF GENES FOR GENE THERAPY. SUCCESSFUL DEVELOPMENT OF THIS TARGETED THERAPY WILL HELP CONTROL EYE PRESSURE MORE EFFECTIVELY AND PROVIDE BETTER TREATMENT OPTIONS FOR GLAUCOMA PATIENTS. NAME OF ORGANIZATION OR GOVERNMENT: STANFORD UNIVERSITY (H) PURPOSE OF GRANT: NATIONAL GLAUCOMA RESEARCH BY JEFFREY GOLDBERG, PHD, ENTITLED: (CG2022001) NEUROPROTECTION AND NEUROENHANCEMENT IN GLAUCOMA. INVESTIGATOR'S SUMMARY: THE GOAL OF THIS PROJECT IS TO EVALUATE SAFETY AND PROOF OF CONCEPT FOR WHETHER CILIARY NEUROTROPHIC FACTOR (CNTF) CAN ENHANCE VISION OR PROTECT AGAINST VISION LOSS IN GLAUCOMA.

Schedule J IRS990ScheduleJ

FieldValueIRS element (for citing)
Compensation CommitteeYes (X)CompensationCommitteeInd
Independent ConsultantYes (X)IndependentConsultantInd
Form990 Of Other OrganizationsYes (X)Form990OfOtherOrganizationsInd
Compensation SurveyYes (X)CompensationSurveyInd
Board Or Committee ApprovalYes (X)BoardOrCommitteeApprovalInd
Severance Payment0SeverancePaymentInd
Supplemental Nonqual Rtr Plan0SupplementalNonqualRtrPlanInd
Equity Based Comp Arrngm0EquityBasedCompArrngmInd
Comp Based On Revenue Of Flng Org0CompBasedOnRevenueOfFlngOrgInd
Comp Bsd On Rev Related Orgs0CompBsdOnRevRelatedOrgsInd
Comp Bsd Net Earns Flng Org0CompBsdNetEarnsFlngOrgInd
Comp Bsd Net Earns Rltd Orgs0CompBsdNetEarnsRltdOrgsInd
Any Non Fixed Payments0AnyNonFixedPaymentsInd
Initial Contract Exception0InitialContractExceptionInd

Rltd Org Officer Trst Key Empl RltdOrgOfficerTrstKeyEmplGrp (11 entries)

TitleTitleTxtBase Compensation Filing OrgBaseCompensationFilingOrgAmtCompensation Based On Rltd OrgsCompensationBasedOnRltdOrgsAmtBonus Filing OrganizationBonusFilingOrganizationAmountBonus Related OrganizationsBonusRelatedOrganizationsAmtOther Compensation Filing OrgOtherCompensationFilingOrgAmtOther Compensation Rltd OrgsOtherCompensationRltdOrgsAmtDeferred Compensation Flng OrgDeferredCompensationFlngOrgAmtDeferred Comp Rltd OrgsDeferredCompRltdOrgsAmtNontaxable Benefits Filing OrgNontaxableBenefitsFilingOrgAmtNontaxable Benefits Rltd OrgsNontaxableBenefitsRltdOrgsAmtTotal Compensation Filing OrgTotalCompensationFilingOrgAmtTotal Compensation Rltd OrgsTotalCompensationRltdOrgsAmtComp Report Prior990 Filing OrgCompReportPrior990FilingOrgAmtComp Report Prior990 Rltd OrgsCompReportPrior990RltdOrgsAmt
STACY PAGOS HALLER
PRESIDENT/CEO$408,714$0$0$0$1,693$0$29,700$0$27,785$0$467,892$0$0$0
NANCY LYNN
SR. VP STRATEGIC PARTNERSHIPS$259,564$0$0$0$1,584$0$24,465$0$37,027$0$322,640$0$0$0
R BRIAN ELDERTON
SR. VP, DEVELOPMENT$252,137$0$0$0$1,715$0$23,361$0$24,967$0$302,180$0$0$0
DIANE BOVENKAMP PHD
VP, SCIENTIFIC AFFAIRS$189,665$0$0$0$552$0$17,075$0$5,165$0$212,457$0$0$0
DAVID F MARKS CPA CMA
VP, FINANCE & ADMIN TILL 10/2023$155,687$0$0$0$1,254$0$15,151$0$39,533$0$211,625$0$0$0
KACI BAEZ
VP, INTEGRATED MKTING & COMM.$172,402$0$0$0$200$0$4,650$0$21,999$0$199,251$0$0$0
SHARYN ROSSI PHD DIR OF
SCIENT. PROGRAMS, NEUROSCIENCE$125,121$0$0$0$240$0$8,775$0$35,057$0$169,193$0$0$0
LISA MORGAN
DIRECTOR OF ANNUAL GIVING$127,764$0$0$0$552$0$12,139$0$21,508$0$161,963$0$0$0
AYO ABRAHAM CPA CGMA
CONTROLLER UNTIL 8/2023$138,238$0$0$0$688$0$9,371$0$11,985$0$160,282$0$0$0
JEFFREY HONAKER
SR. MGR. OPS AND BUILDING$111,125$0$0$0$1,032$0$10,271$0$34,133$0$156,561$0$0$0
PREETI SUBRAMANIAN PHD DIR
OF SCIENT. PROGRAMS, VISION SCIENCE$134,875$0$0$0$240$0$12,139$0$3,518$0$150,772$0$0$0

Supplemental Information Detail SupplementalInformationDetail

FieldValueIRS element (for citing)
Form And Line ReferencePART I, LINE 3FormAndLineReferenceDesc
ExplanationTHE LAST COMPENSATION SURVEY WAS COMPLETED ON 3/9/2022.ExplanationTxt

Schedule M IRS990ScheduleM

Securities Publicly Traded SecuritiesPubliclyTradedGrp

FieldValueIRS element (for citing)
Non Cash CheckboxYes (X)NonCashCheckboxInd
Contribution20ContributionCnt
Noncash Contributions Rpt F990$87,848NoncashContributionsRptF990Amt
Method Of Determining RevenuesFMVMethodOfDeterminingRevenuesTxt
FieldValueIRS element (for citing)
Any Property That Must Be Held0AnyPropertyThatMustBeHeldInd
Review Process Unusual NC GiftsYes (1)ReviewProcessUnusualNCGiftsInd
Third Parties Used0ThirdPartiesUsedInd

Supplemental Information Detail SupplementalInformationDetail

FieldValueIRS element (for citing)
Form And Line ReferencePART I, COLUMN (B):FormAndLineReferenceDesc
ExplanationBRIGHTFOCUS REPORTS THE NUMBER OF CONTRIBUTIONS IN PART I, COLUMN B.ExplanationTxt

Schedule O IRS990ScheduleO

Supplemental Information Detail SupplementalInformationDetail (9 entries)

Form And Line ReferenceFormAndLineReferenceDescExplanationExplanationTxt
FORM 990, PART III, LINE 1, DESCRIPTION OF ORGANIZATION MISSION:BRIGHTFOCUS FOUNDATION FUNDS EXCEPTIONAL RESEARCH WORLDWIDE TO DEFEAT ALZHEIMER'S DISEASE, MACULAR DEGENERATION, AND GLAUCOMA AND PROVIDES EXPERT INFORMATION ON THESE HEARTBREAKING DISEASES. OUR VISION IS: A WORLD FREE FROM DISEASES OF MIND AND SIGHT. COLLECTIVELY, MORE THAN 300 MILLION PEOPLE WORLDWIDE SUFFER FROM THESE DISEASES. BRIGHTFOCUS HAS A PROVEN TRACK RECORD OF SUPPORTING THE MOST INNOVATIVE, EARLY-STAGE RESEARCH SEEKING TO FOSTER A BETTER UNDERSTANDING OF, TREATMENTS FOR, AND ULTIMATELY, A CURE FOR, THESE AGE-RELATED DISEASES WITH NO CURE. SINCE 1973, BRIGHTFOCUS HAS AWARDED MORE THAN $297 MILLION IN RESEARCH GRANTS TO THOUSANDS OF SCIENTISTS IN 25 COUNTRIES THROUGH ITS THREE PROGRAMS: ALZHEIMER'S DISEASE RESEARCH, MACULAR DEGENERATION RESEARCH, AND NATIONAL GLAUCOMA RESEARCH. THE RESEARCH WE SUPPORT IS CAREFULLY CHOSEN BY OUR SCIENTIFIC REVIEW COMMITTEES, COMPRISING WORLD-RENOWNED RESEARCHERS AND LEADERS IN THEIR FIELDS. OUR RESEARCH FUNDING HAS LED TO MAJOR CONTRIBUTIONS TO UNDERSTANDING THESE DISEASES AND SUPPORT FOR SCIENTISTS WHO HAVE RECEIVED PRESTIGIOUS AWARDS, INCLUDING TWO NOBEL PRIZES. AN INDICATOR OF OUR ABILITY TO PUSH NEW BOUNDARIES OF KNOWLEDGE IS THAT BRIGHTFOCUS-SUPPORTED RESEARCH WAS FOUND TO HAVE HAD 10 TIMES THE IMPACT ON DRIVING FUTURE SCIENCE THAN WORK SUPPORTED BY MANY OTHER ORGANIZATIONS. THE WORLD-CLASS RESEARCH IDENTIFIED AND SUPPORTED BY BRIGHTFOCUS IS ON THE CUTTING EDGE OF THE FIGHT TO SAVE MIND AND SIGHT. OUR FUNDING ACTS AS A CATALYST IN EARLY-STAGE RESEARCH, AND BRIGHTFOCUS RESEARCH PROGRAMS ARE DESIGNED TO PROVIDE INITIAL FUNDING FOR HIGHLY INNOVATIVE EXPERIMENTAL IDEAS. DUE TO THE STRUCTURED GRANT REVIEW AND APPROVAL PROCESS, THE RESEARCH IMPACT OF BRIGHTFOCUS IS VERY HIGH. MOST RECIPIENTS OF BRIGHTFOCUS FUNDING GO ON TO RECEIVE FUTURE GRANTS FROM OTHER SOURCES THAT ARE UP TO 10 TIMES LARGER THAN THE ORIGINAL BRIGHTFOCUS AWARD. THIS HIGH RETURN ON BRIGHTFOCUS INVESTMENT SPEAKS TO OUR ABILITY TO IDENTIFY PROMISING RESEARCH IN ITS EARLIEST STAGES AND SPAWN FUTURE SCIENTIFIC DISCOVERIES. IT IS OUR FIRM BELIEF THAT HAVING THE COURAGE TO INVEST IN INNOVATIVE IDEAS WILL LEAD TO REVOLUTIONARY APPROACHES AND LIFE-SAVING BREAKTHROUGHS. ALONG WITH FUNDING CUTTING-EDGE RESEARCH TO FIND CURES FOR SOME OF THE WORLD'S COSTLIEST DISEASES, BRIGHTFOCUS ALSO PROVIDES FREE, EXPERT-VETTED EDUCATIONAL MATERIALS AND SUPPORT TO HUNDREDS OF THOUSANDS OF PEOPLE IMPACTED BY THESE DISEASES NATIONWIDE. WE GROUND THESE EDUCATIONAL MATERIALS IN THE LATEST RESEARCH FINDINGS AND BREAKTHROUGHS. BRIGHTFOCUS ALSO INCREASES PUBLIC AWARENESS OF ALZHEIMER'S, MACULAR DEGENERATION, AND GLAUCOMA, AND COMMUNICATES WITH THOUGHT LEADERS AND ELECTED OFFICIALS ABOUT THE IMPORTANCE OF SCIENTIFIC RESEARCH IN THESE AREAS. BRIGHTFOCUS' AWARD-WINNING PUBLIC SERVICE ANNOUNCEMENTS (PSAS) HAVE APPEARED ON TELEVISION, RADIO, AND IN PRINT THROUGHOUT THE NATION. THE IMPACT OF ALZHEIMER'S, MAKE A PLAN TODAY: GET YOUR EYES CHECKED, AND FINDING ANSWERS IN THE FIGHT AGAINST ALZHEIMER'S SEEK TO RAISE AWARENESS ABOUT THESE DISEASES AND THE IMPORTANCE OF EARLY DETECTION. SIMILAR MESSAGES HAVE BEEN DELIVERED THROUGH DONATED PRINT PSA SPACE IN AIRPORTS AND TRAIN STATIONS, AS WELL AS AT PHARMACIES, SUPERMARKETS AND DIGITALLY. IN FISCAL YEAR 2024, THESE PSA MESSAGES GENERATED $24,713,985 IN DONATED MEDIA SERVICES AND GARNERED OVER 405 MILLION IMPRESSIONS. WE CONTINUE TO INCREASE OUR PRINT PUBLICATIONS, MANY IN SPANISH, THAT PROVIDE HELPFUL INFORMATION TO PATIENTS AND CAREGIVERS, AND REGULARLY PRODUCE NEW VIDEO AND AUDIO RESOURCES IN CONJUNCTION WITH ALLIES IN THE MEDICAL AND SCIENTIFIC COMMUNITIES. PARTNERING WITH SEVERAL HIGH-PROFILE PUBLIC AND PRIVATE ORGANIZATIONS, BRIGHTFOCUS IS HELPING TO BETTER EDUCATE THE PUBLIC ON THE LATEST RESEARCH DEVELOPMENTS PERTAINING TO ALZHEIMER'S, MACULAR DEGENERATION, AND GLAUCOMA, AS WELL AS THE IMPORTANCE OF EQUITABLE PARTICIPATION IN CLINICAL RESEARCH TO ACCELERATE THE PATH TO CURES FOR NEURODEGENERATIVE DISEASES. SPECIFICALLY, BRIGHTFOCUS PRODUCES AND DISSEMINATES FREE PROGRAMS INCLUDING: BRIGHTFOCUS VISION CHATS. SINCE 2014, THESE AUDIO DISCUSSIONS HAVE BROUGHT TOGETHER PATIENTS AND CAREGIVERS FOR INTERACTIVE MONTHLY TELEPHONE FORUMS TO LEARN FROM AND ASK QUESTIONS OF LEADING VISION DISEASE EXPERTS. THE CHATS ARE ARCHIVED ON OUR WEBSITE, WITH AUDIO AND PRINT TRANSCRIPTS AVAILABLE IN SEVERAL ACCESSIBLE FORMATS ONLINE, INCLUDING AS PODCASTS ON SPOTIFY AND APPLE ITUNES. ZOOM IN ON DEMENTIA AND ALZHEIMER'S, A MONTHLY VIRTUAL DISCUSSION OPEN TO THE PUBLIC FEATURING WORLD-RENOWNED RESEARCH SCIENTISTS WHO SHARE THE LATEST BREAKTHROUGHS AND FINDINGS IN THE FIELD. ALL EPISODES ARE RECORDED AND AVAILABLE TO WATCH ON DEMAND ON OUR WEBSITE AND YOUTUBE. WE REGULARLY PUBLISH ARTICLES AND RESOURCES PROVIDING LAY-PERSON INFORMATION ABOUT COMMONLY ASKED DISEASE QUESTIONS. OVER THREE MILLION VISITORS EACH YEAR TO OUR WEBSITE, WWW.BRIGHTFOCUS.ORG, FIND A WEALTH OF INFORMATION ON RESEARCH, SYMPTOMS, TREATMENTS, AND CAREGIVER SUPPORT. BRIGHTFOCUS IS A PRESENTING PARTNER OF SEVERAL DOCUMENTARY FILMS, INCLUDING REMEMBERING GENE WILDER AND GLEN CAMPBELL: I'LL BE ME, AND EXECUTES ASSOCIATED EDUCATIONAL IMPACT CAMPAIGNS. THESE FILMS ARE SHOWN IN COMMUNITY SETTINGS ACROSS THE COUNTRY TO INCREASE AWARENESS OF, AND PARTICIPATION IN, ALZHEIMER'S CLINICAL RESEARCH. BRIGHTFOCUS HAS A LONG-RUNNING AND ROBUST DIRECT MAIL PROGRAM ACROSS THE THREE RESEARCH AREAS IT SUPPORTS. BRIGHTFOCUS SHARES MAILS AWARENESS-RAISING MATERIALS ACROSS ITS THREE PROGRAM AREAS TO OVER 520,000 NATIONAL HOUSEHOLDS, WITH MESSAGES FOCUSING ON: RISK FACTORS AND SYMPTOM RECOGNITION THROUGH PUBLIC AWARENESS AND STEPS THE PUBLIC SHOULD TAKE THAT MAY HELP REDUCE THEIR RISK. LIFESTYLE CHOICES THAT PROMOTE GOOD HEALTH, ENCOURAGING READERS TO TAKE ACTION TO REDUCE THE LIKELIHOOD OF THE ONSET OF THE DISEASE. RESEARCH RESULTS AND TREATMENTS AVAILABLE TO ADDRESS THE DISEASE. BRIGHTFOCUS REGULARLY INTERACTS WITH ADVOCACY ORGANIZATIONS, GOVERNMENTS AT ALL LEVELS, AND MEMBERS OF THE MEDIA, TO CALL GREATER ATTENTION TO DISEASES OF MIND AND SIGHT AND SHARE THE LATEST RESEARCH AND BEST PRACTICES WITH PUBLIC FIGURES AND KEY STAKEHOLDERS. THROUGH OUR OWN OUTREACH EFFORTS, AS WELL AS VIA ACTIVE ROLES IN ADVOCACY COALITIONS, WE HELP ADVANCE THE CAUSE OF PIONEERING SCIENCE AND BETTER POSITION BRIGHTFOCUS AS A RESOURCE FOR THOSE STRUGGLING WITH AND SEARCHING FOR CURES FOR THESE TERRIBLE DISEASES. BRIGHTFOCUS IS THE PRESENTING SPONSOR OF THE HELEN KELLER PRIZE FOR VISION RESEARCH, ONE OF THE MOST PRESTIGIOUS RECOGNITIONS IN THE FIELD. SELECTED BY A PANEL OF THE WORLD'S FOREMOST VISION SCIENTISTS, EACH YEAR'S LAUREATE IS HONORED FOR A GROUNDBREAKING CONTRIBUTION OR DISCOVERY TO SAVE SIGHT. BRIGHTFOCUS BEGAN ITS SPONSORSHIP IN 2015 TO CALL GREATER ATTENTION TO VISION RESEARCH ACROSS THE PRIVATE AND PUBLIC SECTORS. BRIGHTFOCUS WAS HONORED IN 2023 FOR ITS CONTRIBUTIONS TO ADVANCING GLOBAL VISION RESEARCH BY THE ASSOCIATION FOR RESEARCH IN VISION AND OPHTHALMOLOGY (ARVO) FOUNDATION.
FORM 990, PART III, LINE 4A, DESCRIPTION OF PROGRAM SERVICE:ALZHEIMER'S DISEASE RESEARCH (ADR) ALZHEIMER'S DISEASE IS THE ONLY CAUSE OF DEATH AMONG THE TOP 10 IN AMERICA WITHOUT A WAY TO PREVENT, CURE, OR EVEN SLOW ITS PROGRESSION. IT IS AN IRREVERSIBLE DEGENERATION OF THE BRAIN THAT CAUSES DISRUPTIONS IN MEMORY, COGNITION, PERSONALITY, AND OTHER FUNCTIONS AND INEVITABLY LEADS TO DEATH. AN ESTIMATED 55 MILLION PEOPLE WORLDWIDE HAVE ALZHEIMER'S DISEASE OR OTHER DEMENTIAS, WITH WOMEN AND BLACK AND HISPANIC ADULTS MOST AT RISK. ALZHEIMER'S DISEASE RESEARCH (ADR), A BRIGHTFOCUS FOUNDATION PROGRAM, FUNDS RESEARCH FOCUSED ON UNDERSTANDING THE CAUSES OF ALZHEIMER'S DISEASE, EARLY DETECTION, TREATMENTS TO HELP SLOW OR STOP ITS PROGRESSION, AND ULTIMATELY TO PREVENT THE DISEASE ALTOGETHER. ADR ANNUALLY AWARDS PEER-REVIEWED GRANTS TO SCIENTISTS FROM INSTITUTIONS WORLDWIDE WHO ARE CONDUCTING BIOMEDICAL AND CLINICAL RESEARCH ON ALZHEIMER'S DISEASE. SINCE INCEPTION, ADR HAS CONTRIBUTED MORE THAN $180 MILLION TO DEFEATING ALZHEIMER'S DISEASE. DURING THE FISCAL YEAR ENDING MARCH 31, 2024, ADR AWARDED $5,689,899 IN PEER-REVIEWED GRANT AWARDS TO 23 NEW RESEARCH PROJECTS . NOTABLE PROJECTS INCLUDE: HYPERTENSION AND LIFESTYLE EFFECTS ON RISK OF ALZHEIMER'S (INCLUDING LIPIDS); DRUG DISCOVERY AND BIOMARKERS; THE ROLE OF INFLAMMATION, MICROGLIA AND VASCULAR HEALTH IN DISEASE RISK; LOOKING AT THE MITOCHONDRIA AND CELL ENERGY DEFICIENCIES; ROLE OF SLEEP DISTURBANCES CAUSING INCREASED RISK OF COGNITIVE ISSUES; DIFFERENCES IN GENETICS AND DISEASE RISK FOR UNDERREPRESENTED POPULATIONS; AND BETTER USE OF MODERN TECHNOLOGIES, INCLUDING BIG DATA/AI AND SYSTEMS GENETICS ANALYSIS FOR INCREASED AND DECREASED RISKS. ADDITIONAL INFORMATION ABOUT SPECIFIC PROJECTS IS INCLUDED IN SCHEDULES F & I. BRIGHTFOCUS IS HONORED TO HAVE SUPPORTED THE EARLY RESEARCH OF TWO NOBEL PRIZE WINNERS: DR. STANLEY PRUSINER AND DR. PAUL GREENGARD, WHOSE WORK HAS BEEN INSTRUMENTAL TO OUR CURRENT UNDERSTANDING OF ALZHEIMER'S DISEASE. BRIGHTFOCUS CONTINUES ITS PARTNERSHIP WITH THE ACADEMIC JOURNAL MOLECULAR NEURODEGENERATION AS THE OFFICIAL JOURNAL OF BRIGHTFOCUS FOUNDATION. THE JOURNAL PUBLISHES TECHNICAL PAPERS RELATED TO NEURODEGENERATION IN THE THREE DISEASE AREAS. TO ACCELERATE SCIENTIFIC PROGRESS, IT IS AN OPEN-ACCESS JOURNAL, AND ALL CONTENT IS FREE OF CHARGE. THIS OPEN ACCESS ENSURES MAXIMAL REACH OF JOURNAL CONTENTS TO SCIENTISTS AND CARE PROVIDERS WORLDWIDE. MOLECULAR NEURODEGENERATION IS CURRENTLY THE HIGHEST IMPACT OPEN ACCESS JOURNAL IN THE NEUROSCIENCES. IN ADDITION TO SUPPORTING CUTTING-EDGE RESEARCH, ALZHEIMER'S DISEASE RESEARCH PROVIDES EXPERT-VETTED RESOURCES ON DETECTING, TREATING, AND LIVING WITH THE DISEASE. THESE ARE AVAILABLE IN BOTH PRINT AS WELL AS ON OUR WEBSITE, WWW.BRIGHTFOCUS.ORG.
FORM 990, PART III, LINE 4B, DESCRIPTION OF PROGRAM SERVICE:MACULAR DEGENERATION RESEARCH (MDR) AGE-RELATED MACULAR DEGENERATION IS A LEADING CAUSE OF VISION LOSS IN THE UNITED STATES. IT DESTROYS THE MACULA, THE PART OF THE EYE THAT PROVIDES SHARP, CENTRAL VISION NEEDED FOR SEEING OBJECTS CLEARLY. THE MOST COMMON EYE CONDITION IN PEOPLE AGE 60 AND OLDER, IT CAN LEAD TO VISION LOSS IN ONE OR BOTH EYES, MAKING IT DIFFICULT TO RECOGNIZE FACES, DRIVE A CAR, OR READ. AT LEAST 20 MILLION AMERICANS HAVE SOME TYPE OF MACULAR DEGENERATION, INCLUDING BOTH THE EARLY AND LATER STAGES OF THE WET AND DRY TYPES. MACULAR DEGENERATION RESEARCH (MDR), A BRIGHTFOCUS FOUNDATION PROGRAM, HAS AWARDED NEARLY $53 MILLION TO SCIENTISTS STUDYING THE DISEASE. THE LATEST RESEARCH IS FOCUSED ON NOVEL TREATMENTS, UNDERSTANDING THE CAUSES AND DISEASE PROGRESSION, PREDICTION METHODS AND DISEASE MODELING, DRUG THERAPIES, THE ROLE OF METABOLISM AND IMMUNE RESPONSE IN DISEASE RISK, GENES, AND NEW IMAGING, MACHINE LEARNING, AND SCREENING TECHNIQUES. MDR GRANTS ARE AVAILABLE TO MACULAR DEGENERATION RESEARCHERS WORLDWIDE. MDR PLACES SPECIAL EMPHASIS ON ENCOURAGING APPLICATIONS FROM YOUNG SCIENTISTS AND THOSE WITH CUTTING-EDGE IDEAS. ANNUAL GRANT APPLICATIONS ARE PEER-REVIEWED, AND RECIPIENT SELECTIONS ARE BASED ON SCIENTIFIC MERIT. DURING THE FISCAL YEAR ENDING MARCH 31, 2024, MDR AWARDED $3,839,035 IN PEER-REVIEWED GRANT AWARDS TO 10 NEW RESEARCH PROJECTS, A TOTAL FUNDING AMOUNT OF $2,850,660. DETAILS ABOUT SPECIFIC PROJECTS ARE INCLUDED IN SCHEDULES F & I. IN ADDITION TO SUPPORTING CUTTING-EDGE RESEARCH, MACULAR DEGENERATION RESEARCH PROVIDES EXPERT-VETTED RESOURCES ON DETECTING, TREATING, AND LIVING WITH THIS DISEASE. THESE ARE AVAILABLE IN BOTH PRINT AS WELL AS ON OUR WEBSITE, WWW.BRIGHTFOCUS.ORG.
FORM 990, PART III, LINE 4C, DESCRIPTION OF PROGRAM SERVICE:NATIONAL GLAUCOMA RESEARCH (NGR) GLAUCOMA IS THE SECOND LEADING CAUSE OF BLINDNESS WORLDWIDE, ACCORDING TO A RECENT REPORT FROM THE WORLD HEALTH ORGANIZATION, APPROXIMATELY 80 MILLION PEOPLE AROUND THE WORLD HAVE GLAUCOMA. MORE THAN THREE MILLION AMERICANS, OVER THE AGE OF 40 ARE LIVING WITH GLAUCOMA, WITH AN ESTIMATED 2.7 MILLION HAVE OPEN-ANGLE GLAUCOMA, THE MOST COMMON TYPE. IN THE UNITED STATES, GLAUCOMA IS A LEADING CAUSE OF BLINDNESS AMONG BLACK AND HISPANIC AMERICANS. WITH EARLY DETECTION AND TREATMENT, GLAUCOMA OFTEN CAN BE MANAGED TO PROTECT EYES FROM MORE SERIOUS VISION LOSS. IT IS ESTIMATED THAT ONLY HALF OF THE PEOPLE LIVING WITH GLAUCOMA ARE AWARE THAT THEY HAVE THE DISEASE. NATIONAL GLAUCOMA RESEARCH (NGR), A BRIGHTFOCUS FOUNDATION PROGRAM, HAS AWARDED NEARLY $51 MILLION WORLDWIDE IN RESEARCH GRANTS TOWARD THE STUDY OF GLAUCOMA. NGR-SUPPORTED RESEARCH HAS FOCUSED ON THE EYE-BRAIN CONNECTION, HOW PRESSURE BUILDUP IN THE EYE CAN AFFECT SYNAPTIC NERVE COMMUNICATIONS, NEUROPROTECTION AND OPTIC NERVE REGENERATION, DISCOVERING GLAUCOMA RISK GENES, AI/DEEP LEARNING AND ADAPTIVE OPTICS, SLEEP DISTURBANCE AND GLAUCOMA RISK, DEVELOPING EARLY GLAUCOMA SCREENING, AND PURSUING NOVEL GENETIC COUNSELING AND COMMUNICATION STRATEGIES, AMONGST OTHER INNOVATIVE PURSUITS. NGR GRANTS ARE AVAILABLE TO GLAUCOMA RESEARCHERS WORLDWIDE. NGR PLACES SPECIAL EMPHASIS ON ENCOURAGING APPLICATIONS FROM YOUNG SCIENTISTS AND THOSE WITH CUTTING-EDGE IDEAS. ANNUAL GRANT APPLICATIONS ARE PEER-REVIEWED, AND RECIPIENT SELECTIONS ARE BASED ON SCIENTIFIC MERIT. DURING THE FISCAL YEAR ENDING MARCH 31, 2024, NGR AWARDED $1,549,923 IN PEER-REVIEWED GRANT AWARDS FOR 9 NEW PROJECTS. DETAILS ABOUT SPECIFIC PROJECTS ARE INCLUDED IN SCHEDULES F & I. IN ADDITION TO SUPPORTING CUTTING-EDGE RESEARCH, NATIONAL GLAUCOMA RESEARCH PROVIDES EXPERT-VETTED RESOURCES ON DETECTING, TREATING, AND LIVING WITH THE DISEASE. THESE ARE AVAILABLE IN BOTH PRINT AS WELL AS ON OUR WEBSITE, WWW.BRIGHTFOCUS.ORG.
FORM 990, PART VI, SECTION B, LINE 11BA DRAFT OF THE FEDERAL FORM 990 IS DISTRIBUTED TO THE AUDIT COMMITTEE FOR REVIEW PRIOR TO BEING SUBMITTED TO THE INTERNAL REVENUE SERVICE. THE DRAFT FEDERAL FORM 990 IS DISTRIBUTED EARLY ENOUGH TO PROVIDE EACH COMMITTEE MEMBER WITH A REASONABLE AMOUNT OF TIME FOR REVIEW AND SUBMISSION OF QUESTIONS OR COMMENTS PRIOR TO THE FILING DEADLINE. THE FINAL FEDERAL FORM 990 IS DISTRIBUTED TO EACH MEMBER OF THE FULL BOARD OF DIRECTORS PRIOR TO BEING FILED WITH THE INTERNAL REVENUE SERVICE. THE DRAFT OR FINAL FEDERAL FORM 990 MAY BE DISTRIBUTED IN PERSON, BY REGULAR MAIL, E-MAIL, OR FAX.
FORM 990, PART VI, SECTION B, LINE 12CBRIGHTFOCUS HAS ALL EMPLOYEES, OFFICERS, AND DIRECTORS AGREE TO THE CODE OF CONDUCT THAT INCLUDES ADHERENCE TO THE CONFLICT OF INTEREST AND IMPLEMENTATION POLICY. EACH BOARD DIRECTOR, OFFICER, AND EMPLOYEE IS REQUIRED TO COMPLETE A CONFLICT OF INTEREST DISCLOSURE STATEMENT ANNUALLY. EMPLOYEES MEET ANNUALLY WITH THE BRIGHTFOCUS' CHIEF COMPLIANCE OFFICER TO REVIEW THEIR CONFLICT OF INTEREST STATEMENTS, AND GIVE AN ANNUAL CONFLICT OF INTEREST COMPLIANCE REPORT TO THE BOARD CHAIR AND VICE CHAIR. IF A CONFLICT IS REPORTED, IT IS THEN REFERRED TO THE PRESIDENT/CEO AND/OR BRIGHTFOCUS' LEGAL COUNSEL AND, IF APPROPRIATE AND NECESSARY, THEN TO THE BOARD OF DIRECTORS OR ITS APPOINTED COMMITTEE FOR FURTHER ACTION. THE DIRECTOR'S AND OFFICER'S STATEMENTS ARE REVIEWED BY THE BRIGHTFOCUS LEGAL COUNSEL. IF A CONFLICT IS REPORTED, IT IS THEN REFERRED TO THE BOARD OF DIRECTORS OR ITS APPOINTED COMMITTEE FOR FURTHER ACTION. AT THE TIME OF THE BRIGHTFOCUS DISCUSSION AND DECISION CONCERNING A CONFLICT OF INTEREST, THE CONFLICTED PARTY IS NOT PRESENT IN THE MEETING.
FORM 990, PART VI, SECTION B, LINE 15BRIGHTFOCUS' BOARD OF DIRECTORS HAS OVERALL AUTHORITY AND RESPONSIBILITY FOR APPROVING THE ANNUAL BUDGET WHICH INCLUDES SALARY AND BENEFITS FOR ALL EMPLOYEES AT EVERY LEVEL INCLUDING NON-DIRECTOR OFFICERS AND KEY EMPLOYEES. ALL PAY ADJUSTMENTS ARE MADE ON A YEARLY BASIS EFFECTIVE APRIL 1ST, THE BEGINNING OF THE BRIGHTFOCUS FISCAL YEAR. BEFORE APPROVING THE COMPENSATION OF THE PRESIDENT/CEO, THE BOARD DETERMINES THE TOTAL COMPENSATION TO BE PROVIDED BY BRIGHTFOCUS TO THE PRESIDENT/CEO IS REASONABLE CONSIDERING THE POSITION, RESPONSIBILITY AND QUALIFICATION OF THE POSITION HELD, INCLUDING THE RESULT OF AN EVALUATION OF PRIOR PERFORMANCE FOR BRIGHTFOCUS, IF APPLICABLE. THE PRESIDENT/CEO IS EVALUATED YEARLY BY THE BOARD OF DIRECTORS USING AN IN-DEPTH GOAL ATTAINMENT STRUCTURE, THAT INCLUDES A SELF-ASSESSMENT AND A BOARD OF DIRECTOR'S ASSESSMENT AND EVALUATION AGAINST SET GOALS, OUTCOMES, AND DELIVERABLES. IN ADDITION, THE BOARD OF DIRECTORS PERIODICALLY ENGAGES AN OUTSIDE CONSULTANT TO OBTAIN AND CONSIDER APPROPRIATE DATA, INCLUDING A SALARY SURVEY, WHICH INCLUDES INFORMATION COMPILED FROM THE FEDERAL FORM 990 OF OTHER ORGANIZATIONS, CONCERNING COMPENSATION PAID TO CEOS IN SIMILAR CIRCUMSTANCES. IN MAKING THE DETERMINATION, THE BOARD OF DIRECTORS CONSIDERS TOTAL COMPENSATION TO INCLUDE THE SALARY AND VALUE OF ALL BENEFITS PROVIDED BY BRIGHTFOCUS TO THE INDIVIDUAL IN PAYMENT FOR SERVICES. AT THE TIME OF THE BRIGHTFOCUS BOARD DISCUSSION AND DECISION CONCERNING THE PRESIDENT/CEO'S COMPENSATION, THE PRESIDENT/CEO IS NOT PRESENT IN THE MEETING. THE BOARD OF DIRECTORS SHALL SET FORTH THE BASIS FOR ITS DECISIONS WITH RESPECT TO COMPENSATION IN THE MINUTES OF THE MEETING AT WHICH THE DECISIONS ARE MADE, INCLUDING THE CONCLUSIONS OF THE EVALUATION AND THE BASIS FOR DETERMINING THAT THE INDIVIDUAL'S COMPENSATION WAS REASONABLE CONSIDERING THE EVALUATION AND COMPARABILITY DATA. THE PRESIDENT/CEO IS CHARGED WITH SETTING THE SALARIES OF ALL OTHER EMPLOYEES IN ACCORDANCE WITH A COMPENSATION STRUCTURE AND BUDGET APPROVED BY THE BOARD OF DIRECTORS. THE PRESIDENT/CEO AND HUMAN RESOURCES REVIEW EMPLOYEE COMPENSATION AND BENEFITS THAT INCLUDE KEY EMPLOYEES, BY PERIODICALLY ENGAGING AN OUTSIDE CONSULTANT TO CONDUCT COMPENSATION AND BENEFIT BENCHMARKING STUDIES THAT INCLUDE VARIOUS REGIONAL AND NATIONAL NON-PROFIT COMPENSATION REPORTS AND SURVEYS. COMPENSATION DELIBERATIONS AND DECISIONS INCLUDE THE REVIEW OF SELF AND SUPERVISORY EVALUATIONS OF EMPLOYEE PERFORMANCE COMPARED TO SET INDIVIDUAL AND ORGANIZATIONAL GOALS.
FORM 990, PART VI, SECTION C, LINE 19BRIGHTFOCUS MAKES ITS GOVERNING DOCUMENTS INCLUDING ITS ARTICLES OF INCORPORATION AND BYLAWS, THE FEDERAL FORM 1023, THE 501(C)(3) LETTER OF DETERMINATION FROM THE INTERNAL REVENUE SERVICE, CONFLICT OF INTEREST POLICY, AUDITED FINANCIAL STATEMENTS AND FEDERAL FORM 990 AVAILABLE TO THE PUBLIC UPON REQUEST. IN ADDITION, THE PUBLIC ALSO HAS ACCESS TO THE ANNUAL REPORT, AUDITED FINANCIAL STATEMENTS, THE 501(C)(3) LETTER OF DETERMINATION FROM THE INTERNAL REVENUE SERVICE, AND FEDERAL FORM 990 ON ITS WEBSITE AT WWW.BRIGHTFOCUS.ORG.
FORM 990, PART XI, LINE 9:RECOVERIES OF PRIOR YEAR GRANTS 435,223. CHANGE IN PRESENT VALUE OF GRANTS -129,218.

Schedule R IRS990ScheduleR

Id Disregarded Entities IdDisregardedEntitiesGrp (2 entries)

Address Line1USAddress/AddressLine1TxtCityUSAddress/CityNmState AbbreviationUSAddress/StateAbbreviationCdZIPUSAddress/ZIPCdEINEINPrimary ActivitiesPrimaryActivitiesTxtLegal Domicile StateLegalDomicileStateCdTotal IncomeTotalIncomeAmtEnd Of Year AssetsEndOfYearAssetsAmtBusiness Name Line1DirectControllingEntityName/BusinessNameLine1Txt
NATIONAL DEVELOPMENT LLC
22512 GATEWAY CENTER DRIVECLARKSBURGMD20871237337229PROPERTY RENTAL AND MANAGEMENTMD$450,765$4,729,697BRIGHTFOCUS FOUNDATION
AMERICAN HEALTH ASSISTANCE LLC
22512 GATEWAY CENTER DRIVECLARKSBURGMD20871237337229OWNER OF BRIGHTFOCUS HEADQUARTERSMD$0$3,114,398BRIGHTFOCUS FOUNDATION