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JAEB CENTER FOR HEALTH RESEARCH FOUNDATION, INC. - Florida Company Profile

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Company Details

Entity Name: JAEB CENTER FOR HEALTH RESEARCH FOUNDATION, INC.
Jurisdiction: FLORIDA
Filing Type: Domestic Non-Profit
Status: Active

The business entity is active. This status indicates that the business is currently operating and compliant with state regulations, suggesting a lower risk profile for lenders and potentially better creditworthiness.

Date Filed: 01 Jun 1998 (27 years ago)
Last Event: AMENDED AND RESTATED ARTICLES
Event Date Filed: 23 Jan 2024 (a year ago)
Document Number: N98000003298
FEI/EIN Number 593187624

Federal Employer Identification (FEI) Number assigned by the IRS.

Address: 15310 Amberly Dr, SUITE 350, Tampa, FL, 33647, US
Mail Address: 15310 AMBERLY DR., SUITE 350, TAMPA, FL, 33647, US
ZIP code: 33647
County: Hillsborough
Place of Formation: FLORIDA

Key Officers & Management

Name Role Address
BECK ROY W Chairman 15310 AMBERLY DR. STE 350, TAMPA, FL, 33647
Glassman Adam R President 15310 Amberly Dr, Tampa, FL, 33647
Vogt Erica Secretary 15310 Amberly Dr, Tampa, FL, 33647
GLASSMAN ADAM R Agent 15310 AMBERLY DR., TAMPA, FL, 33647

Unique Entity ID

A UEI is a government-provided number, like a tax ID number, that’s used to identify businesses eligible for federal grants, awards and contracts.

Note: In April 2022, the federal government replaced its old identifier of choice, the Data Universal Numbering System (DUNS) number, with a government-issued UEI. Now all the federal government’s Integrated Award Environment systems use UEI numbers instead of DUNS numbers. So any entity doing business with the federal government must register for a UEI.

Unique Entity ID:
RRCZRDT5DHP1
CAGE Code:
451A9
UEI Expiration Date:
2026-03-25

Business Information

Activation Date:
2025-03-27
Initial Registration Date:
2005-09-20

Commercial and government entity program

The The Commercial And Government Entity Code (CAGE) is assigned by the Department of Defense's Defense Logistics Agency (DLA) and represents your company's physical address for GSA's mailings, payments, and administrative records.

Note: A CAGE Code enables a company to contract with the U.S. government, allowing bid on government contracts and to receive government payments. Also for business this means that it's a Verified business entity and Has a validated physical address.

CAGE number:
451A9
Status:
Obsolete
Type:
Non-Manufacturer
CAGE Update Date:
2025-03-27
SAM Expiration:
2026-03-25

Contact Information

POC:
RACHEL WALDROP-HOLZHAUSER
Corporate URL:
http://www.jaeb.org

Events

Event Type Filed Date Value Description
REGISTERED AGENT NAME CHANGED 2024-01-19 GLASSMAN, ADAM R -
AMENDED AND RESTATEDARTICLES 2024-01-19 - -
REGISTERED AGENT ADDRESS CHANGED 2024-01-19 15310 AMBERLY DR., SUITE 350, TAMPA, FL 33647 -
CHANGE OF PRINCIPAL ADDRESS 2016-01-26 15310 Amberly Dr, SUITE 350, Tampa, FL 33647 -
AMENDMENT 2015-07-21 - -
CHANGE OF MAILING ADDRESS 2004-02-02 15310 Amberly Dr, SUITE 350, Tampa, FL 33647 -
CONVERSION 1998-06-01 - CORPORATION WAS A CONVERSION RESULT. CONVERTING CORPORATION WAS P93000043536. CONVERSION NUMBER 700000018387

Documents

Name Date
ANNUAL REPORT 2024-02-05
Amended and Restated Articles 2024-01-23
ANNUAL REPORT 2023-01-27
ANNUAL REPORT 2022-04-19
ANNUAL REPORT 2021-01-27
ANNUAL REPORT 2020-01-20
ANNUAL REPORT 2019-02-12
ANNUAL REPORT 2018-01-16
ANNUAL REPORT 2017-01-09
ANNUAL REPORT 2016-01-26

USAspending Awards / Financial Assistance

Date:
2022-09-08
Awarding Agency Name:
Department of Health and Human Services
Transaction Description:
GYRATE ATROPHY OCULAR AND SYSTEMIC STUDY (GYROS) - 1 PROJECT SUMMARY/ABSTRACT FOR GYROS 2 GYRATE ATROPHY IS A RARE INHERITED CHORIORETINAL DEGENERATION THAT IS ASSOCIATED WITH 3 HYPERORNITHINEMIA CAUSED BY AUTOSOMAL RECESSIVE MUTATIONS IN THE ORNITHINE AMINOTRANSFERASE 4 (OAT) GENE AND LEADS TO SEVERE LOSS OF VISION. THE CURRENT STANDARD OF CARE TREATMENT IS A 5 HIGHLY BURDENSOME ARGININE-RESTRICTED DIET (ARD) FRAUGHT WITH MANAGEMENT COMPLICATIONS. THE 6 PRINCIPAL INVESTIGATORS ARE CURRENTLY DEVELOPING A GENE AUGMENTATION THERAPY, A POTENTIAL 7 TREATMENT STRATEGY THAT MAY PRESERVE OR IMPROVE VISION WHILE AVOIDING OR REDUCING THE 8 NEED FOR ARD. TO FACILITATE A FUTURE INTERVENTIONAL CLINICAL TRIAL, THERE IS A NEED TO CHARACTERIZE 9 THE NATURAL HISTORY OF OAT-RELATED OCULAR AND SYSTEMIC DISEASE PROGRESSION. THE STUDY AIMS ARE: 10 1. NATURAL HISTORY – CHARACTERIZE THE NATURAL HISTORY OF ORNITHINE LEVELS AND RETINAL 11 DEGENERATION (RD) ASSOCIATED WITH DISEASE-CAUSING OAT VARIANTS IN THE PRESENCE OF 12 STANDARD DIETARY TREATMENT REGIMENS OVER 4 YEARS, USING METABOLIC MEASURES OF FASTING 13 PLASMA AND BLOOD SPOT AMINO ACIDS PANELS, FUNCTIONAL AND STRUCTURAL MEASURES OF RD, 14 AND PATIENT-REPORTED OUTCOME MEASURES. 15 2. METABOLIC-STRUCTURE-FUNCTION RELATIONSHIPS – EXPLORE THE RELATIONSHIPS BETWEEN 16 STRUCTURAL AND FUNCTIONAL RD OUTCOME MEASURES AND PLASMA ORNITHINE LEVELS. 17 3. IDENTIFY RAPID PROGRESSORS – EXPLORE THE RELATIONSHIP OF POSSIBLE RISK FACTORS 18 (GENOTYPE, PHENOTYPE, ENVIRONMENTAL, STANDARD CARE DIETARY REGIMEN) WITH SEVERITY AND 19 PROGRESSION OF OUTCOME MEASURES. 20 THIS NATURAL HISTORY STUDY WILL INFORM THE FUTURE INTERVENTIONAL CLINICAL TRIAL DESIGN AS FOLLOWS: 21 DETERMINE WITHIN-PATIENT VARIABILITY OF ORNITHINE LEVELS 22 DEVELOP QUANTITATIVE MEASURES OF PROGRESSION OF THE AREA OF PRESERVED RETINA AND 23 ESTABLISH ITS REPRODUCIBILITY, SENSITIVITY TO CHANGE, AND RELATIONSHIP WITH OTHER MEASURES 24 ESTABLISH RATES OF PROGRESSION OF FUNCTIONAL RD, STRUCTURAL RD, AND PATIENT-REPORTED 25 OUTCOME MEASURES, AND DETERMINE WHICH MEASURES ARE MOST SENSITIVE TO CHANGE 26 DETERMINE PRIMARY TIME POINTS AND DURATION FOR A PLANNED FUTURE TREATMENT TRIAL 27 USE VARIABILITY AND INTER-EYE CORRELATION OF OUTCOMES FOR TRIAL SAMPLE SIZE CALCULATIONS 28 IDENTIFY CANDIDATES FOR THE FUTURE TRIAL, INCLUDING ELIGIBILITY CRITERIA BASED ON RISK FACTORS 29 AND CUT POINTS FOR SEVERITY OF DISEASE MOST LIKELY TO BENEFIT FROM TREATMENT 30 ESTABLISH STUDY PROCEDURES AND WORKFLOWS
Obligated Amount:
800000.00
Face Value Of Loan:
0.00
Total Face Value Of Loan:
0.00
Date:
2021-04-21
Awarding Agency Name:
Department of Health and Human Services
Transaction Description:
DIABETES ENDOTHELIAL KERATOPLASTY STUDY: IMPACT OF DIABETES ON CORNEAL TRANSPLANT SUCCESS AND CELL LOSS - PROJECT SUMMARY THIS PROPOSAL ADDRESSES A SIGNIFICANT PUBLIC HEALTH QUESTION: DOES DIABETES, THE 3RD LEADING CAUSE OF DEATH IN THE UNITED STATES (US), IMPACT SUITABILITY OF DONOR CORNEAL TISSUE FOR TRANSPLANTATION? THIS QUESTION TAKES ON INCREASING URGENCY AS RECENT EYE BANK DATA SUGGESTS DONORS WITH DIABETES NOW COMPRISE ABOUT 30-35% OF THE CORNEA DONOR POOL, A 50-72% INCREASE IN JUST OVER A DECADE. THE IMPACT OF DIABETES ON KERATOPLASTY OUTCOMES REMAINS UNKNOWN, WITH CONFLICTING EVIDENCE FROM SECONDARY OR RETROSPECTIVE ANALYSES OF MULTIPLE CLINICAL STUDIES. PREVIOUS LARGE CLINICAL STUDIES DID NOT SHOW A DIABETIC DONOR EFFECT ON PENETRATING KERATOPLASTY (PKP) AND DESCEMET MEMBRANE ENDOTHELIAL KERATOPLASTY (DMEK) GRAFT SUCCESS, YET OUR RECENT CORNEA PRESERVATION TIME STUDY (CPTS) FOUND THE DIABETIC DONOR ADVERSELY AFFECTED GRAFT OUTCOMES FOLLOWING DESCEMET STRIPPING AUTOMATED ENDOTHELIAL KERATOPLASTY (DSAEK). ALTHOUGH CURRENT STANDARD OF CARE IS TO USE DIABETIC DONOR CORNEAS FOR ALL TYPES OF KERATOPLASTIES, SOME EYE BANKS AND SURGEONS ARE INCREASINGLY AVOIDING THEM FOR DMEK. AS BOTH THE DIABETIC DONOR POPULATION AND DMEK DEMAND INCREASES, A DEFINITIVE SUPERIORITY STUDY EVALUATING EFFECT OF DONOR DIABETES STATUS ON GRAFT OUTCOMES WILL ALLAY AND/OR DEFINE THESE CONCERNS. THE DIABETES ENDOTHELIAL KERATOPLASTY STUDY (DEKS) WILL ADDRESS THESE IMPORTANT QUESTIONS THROUGH A PROSPECTIVE MASKED CLINICAL TRIAL ENROLLING 1420 PARTICIPANT-EYES AT 30 CLINICAL SITES AND 15 EYE BANKS ACROSS THE US. THE DEKS WILL DETERMINE IF THE 3-YEAR GRAFT SUCCESS RATE FOLLOWING DMEK PERFORMED WITH CORNEAS FROM DONORS WITHOUT DIABETES IS SUPERIOR TO THE GRAFT SUCCESS RATE WITH CORNEAS FROM DONORS WITH DIABETES. IT WILL ALSO DETERMINE IF THE 3-YEAR CENTRAL ENDOTHELIAL CELL LOSS (ECL) AFTER DMEK WITH CORNEAS FROM DONORS WITHOUT DIABETES IS LESS THAN THE CENTRAL ECL WHEN CORNEAS FROM DONORS WITH DIABETES ARE USED. LASTLY, THE DEKS WILL EXPLORE THE RELATIONSHIP OF DONOR DIABETES SEVERITY, AS MEASURED BY EYE BANK-DETERMINED DIABETES RISK CATEGORIZATION SCORES, POST- MORTEM HBA1C, AND SKIN ADVANCED GLYCATION ENDPRODUCTS AND OXIDATION MARKERS, WITH DMEK GRAFT OUTCOMES 3 YEARS POSTOPERATIVELY IN CORNEAS FROM DIABETIC DONORS. THE DEKS COULD HAVE A MAJOR IMPACT ON THE TARGETED USE OF CORNEAS FROM AN INCREASING NUMBER OF DONORS WITH DIABETES WITH A RANGE OF DISEASE SEVERITY IN A DONOR POOL THAT MUST CONTINUE TO EXPAND TO MEET THE CLINICAL DEMANDS OF AN AGING POPULATION AND DMEK GROWTH.
Obligated Amount:
4053339.00
Face Value Of Loan:
0.00
Total Face Value Of Loan:
0.00
Date:
2020-04-28
Awarding Agency Name:
Small Business Administration
Transaction Description:
TO AID SMALL BUSINESSES IN MAINTAINING WORK FORCE DURING COVID-19 PANDEMIC.
Obligated Amount:
0.00
Face Value Of Loan:
2425077.00
Total Face Value Of Loan:
0.00
Date:
2019-09-19
Awarding Agency Name:
Department of Health and Human Services
Transaction Description:
DATA COORDINATING CENTER FOR ARTIFICIAL PANCREAS STUDIES
Obligated Amount:
1296392.72
Face Value Of Loan:
0.00
Total Face Value Of Loan:
0.00
Date:
2019-08-19
Awarding Agency Name:
Department of Health and Human Services
Transaction Description:
A RANDOMIZED CROSS-OVER TRIAL EVALUATING AUTOMATED INSULIN DELIVERY TECHNOLOGIES ON GLYCEMIC OUTCOMES AND QUALITY OF LIFE IN OLDER ADULTS WITH TYPE 1 DIABETES
Obligated Amount:
2760978.00
Face Value Of Loan:
0.00
Total Face Value Of Loan:
0.00

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Date of last update: 03 Jun 2025

Sources: Florida Department of State