R44HL174138
Project Grant
Overview
Grant Description
Nourexal™: A novel bioenergetic drug to increase donor heart utilization - Project summary
In the U.S., over 20,000 heart transplants are needed each year, but fewer than 4,000 procedures are performed despite the yearly availability of more than 12,000 donors.
This gap exists because 6 hearts from every 10 organ donors are unused.
The vast majority of eligible donor hearts are rejected because the transport time is limited to 4 hours.
To address this unmet need, Nour Heart developed and patented the bioenergetic cardioprotective drug, Nourexal™ (Cyclocreatine Phosphate (CCRP)), which was recently granted FDA orphan drug designation for “prevention of ischemic injury to enhance cardiac graft recovery and survival in heart transplantation” (DRU-2015-4951).
CCRP enhances myocardial energy stores during ischemia, reduces cell injury, inhibits inflammation and fibrosis, and restores normal cardiac function after extended cold storage of rat and dog hearts.
Further, injection of CCRP (1.2 gm/kg) into rat donors protected hearts during harvesting and allowed prolonged storage for 22 hours with full recovery of surgically grafted hearts for 3 days.
In this two-year Direct-to-Phase II SBIR project, Nour Heart, Inc. (NHI) will prepare and file an Investigational New Drug (IND) for FDA approval to initiate CCRP Phase I safety trial in human healthy volunteers.
Based on the FDA response to NHI’s pre-IND application (PIND 125867), we will:
1) Produce Good Manufacturing Practice (GMP) grade CCRP and determine its chemistry manufacturing and controls (CMC) (Aim 1);
2) Conduct FDA-recommended, IND-enabling CCRP preclinical safety studies in rats, dogs, and human unused cadaver donors (UCDs) (Aim 2) (initial rat studies indicated that CCRP is a safe drug);
3) Conduct a pilot in vivo efficacy study in pigs to confirm the ability of CCRP to safely extend cold storage time of pig hearts to 6 hours before surgically transplanting the graft into recipient pigs (Aim 3).
This pig study will be overseen by Dr. O.H. Frazier at the Texas Heart Institute to test the therapeutic benefits of our patented “three-step clinical protocol” where CCRP will be administered only once to heart donors and not to recipients;
and 4) Prepare CCRP Phase I safety protocol, investigational brochure, as well as assemble and file Nour Heart’s IND application to the FDA for an indication for end-stage heart failure patients scheduled for heart transplantation procedures (Aim 4).
We expect CCRP to be safe in rats, dogs, and human unused cadaver donors and can preserve cardiac function in the pig heart transplantation model.
As a novel bioenergetic cardioprotective drug, CCRP will potentially increase the time and distance that the hearts can be transported, thus extending transplantation to eligible recipient candidates located outside the current 4-hour transport limit.
Upon successful completion of this project, Nour Heart plans to commercialize CCRP by raising capital to conduct CCRP Phase I safety trial, via two venture capital groups, who have indicated interest, or to partner with Rallybio Pharmaceuticals.
Future broader use of CCRP that can safely extend transport time (>4 hours) could significantly reduce the number of unused donor hearts and expand supply of usable human donor hearts, thus, potentially increase heart transplant cases by over 3,000 yearly.
In the U.S., over 20,000 heart transplants are needed each year, but fewer than 4,000 procedures are performed despite the yearly availability of more than 12,000 donors.
This gap exists because 6 hearts from every 10 organ donors are unused.
The vast majority of eligible donor hearts are rejected because the transport time is limited to 4 hours.
To address this unmet need, Nour Heart developed and patented the bioenergetic cardioprotective drug, Nourexal™ (Cyclocreatine Phosphate (CCRP)), which was recently granted FDA orphan drug designation for “prevention of ischemic injury to enhance cardiac graft recovery and survival in heart transplantation” (DRU-2015-4951).
CCRP enhances myocardial energy stores during ischemia, reduces cell injury, inhibits inflammation and fibrosis, and restores normal cardiac function after extended cold storage of rat and dog hearts.
Further, injection of CCRP (1.2 gm/kg) into rat donors protected hearts during harvesting and allowed prolonged storage for 22 hours with full recovery of surgically grafted hearts for 3 days.
In this two-year Direct-to-Phase II SBIR project, Nour Heart, Inc. (NHI) will prepare and file an Investigational New Drug (IND) for FDA approval to initiate CCRP Phase I safety trial in human healthy volunteers.
Based on the FDA response to NHI’s pre-IND application (PIND 125867), we will:
1) Produce Good Manufacturing Practice (GMP) grade CCRP and determine its chemistry manufacturing and controls (CMC) (Aim 1);
2) Conduct FDA-recommended, IND-enabling CCRP preclinical safety studies in rats, dogs, and human unused cadaver donors (UCDs) (Aim 2) (initial rat studies indicated that CCRP is a safe drug);
3) Conduct a pilot in vivo efficacy study in pigs to confirm the ability of CCRP to safely extend cold storage time of pig hearts to 6 hours before surgically transplanting the graft into recipient pigs (Aim 3).
This pig study will be overseen by Dr. O.H. Frazier at the Texas Heart Institute to test the therapeutic benefits of our patented “three-step clinical protocol” where CCRP will be administered only once to heart donors and not to recipients;
and 4) Prepare CCRP Phase I safety protocol, investigational brochure, as well as assemble and file Nour Heart’s IND application to the FDA for an indication for end-stage heart failure patients scheduled for heart transplantation procedures (Aim 4).
We expect CCRP to be safe in rats, dogs, and human unused cadaver donors and can preserve cardiac function in the pig heart transplantation model.
As a novel bioenergetic cardioprotective drug, CCRP will potentially increase the time and distance that the hearts can be transported, thus extending transplantation to eligible recipient candidates located outside the current 4-hour transport limit.
Upon successful completion of this project, Nour Heart plans to commercialize CCRP by raising capital to conduct CCRP Phase I safety trial, via two venture capital groups, who have indicated interest, or to partner with Rallybio Pharmaceuticals.
Future broader use of CCRP that can safely extend transport time (>4 hours) could significantly reduce the number of unused donor hearts and expand supply of usable human donor hearts, thus, potentially increase heart transplant cases by over 3,000 yearly.
Awardee
Funding Goals
TO FOSTER HEART AND VASCULAR RESEARCH IN THE BASIC, TRANSLATIONAL, CLINICAL AND POPULATION SCIENCES, AND TO FOSTER TRAINING TO BUILD TALENTED YOUNG INVESTIGATORS IN THESE AREAS, FUNDED THROUGH COMPETITIVE RESEARCH TRAINING GRANTS. SMALL BUSINESS INNOVATION RESEARCH (SBIR) PROGRAM: TO STIMULATE TECHNOLOGICAL INNOVATION, USE SMALL BUSINESS TO MEET FEDERAL RESEARCH AND DEVELOPMENT NEEDS, FOSTER AND ENCOURAGE PARTICIPATION IN INNOVATION AND ENTREPRENEURSHIP BY SOCIALLY AND ECONOMICALLY DISADVANTAGED PERSONS, AND INCREASE PRIVATE-SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT FUNDING. SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM: TO STIMULATE TECHNOLOGICAL INNOVATION, FOSTER TECHNOLOGY TRANSFER THROUGH COOPERATIVE R&D BETWEEN SMALL BUSINESSES AND RESEARCH INSTITUTIONS, AND INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL R&D.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Vienna,
Virginia
221805709
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 119% from $1,658,923 to $3,632,845.
Nour Heart was awarded
Bioenergetic Drug Nourexal™: Enhancing Heart Utilization Transplantation
Project Grant R44HL174138
worth $3,632,845
from National Heart Lung and Blood Institute in September 2024 with work to be completed primarily in Vienna Virginia United States.
The grant
has a duration of 1 year 9 months and
was awarded through assistance program 93.837 Cardiovascular Diseases Research.
The Project Grant was awarded through grant opportunity PHS 2023-2 Omnibus Solicitation of the NIH, CDC and FDA for Small Business Innovation Research Grant Applications (Parent SBIR [R43/R44] Clinical Trial Not Allowed).
SBIR Details
Research Type
SBIR Phase II
Title
Nourexal™: A Novel Bioenergetic Drug to Increase Donor Heart Utilization
Abstract
PROJECT SUMMARY In the U.S., over 20,000 heart transplants are needed each year, but fewer than 4,000 procedures are performed despite the yearly availability of more than 12,000 donors. This gap exists because 6 hearts from every 10 organ donors are unused. The vast majority of eligible donor hearts are rejected because the transport time is limited to 4 hours. To address this unmet need, Nour Heart developed and patented the bioenergetic cardioprotective drug, Nourexal™ (Cyclocreatine Phosphate (CCrP)), which was recently granted FDA Orphan Drug Designation for “Prevention of Ischemic Injury to Enhance Cardiac Graft Recovery and Survival in Heart Transplantation” (DRU-2015-4951). CCrP enhances myocardial energy stores during ischemia, reduces cell injury, inhibits inflammation and fibrosis, and restores normal cardiac function after extended cold storage of rat and dog hearts. Further, injection of CCrP (1.2 gm/kg) into rat donors, protected hearts during harvesting and allowed prolonged storage for 22 hours with full recovery of surgically grafted hearts for 3 days. In this two-year Direct-to-Phase II SBIR project, Nour Heart, Inc. (NHI) will prepare and file an Investigational New Drug (IND) for FDA approval to initiate CCrP Phase I safety trial in human healthy volunteers. Based on the FDA response to NHI’s Pre-IND application (PIND 125867), we will: 1) produce Good Manufacturing Practice (GMP) grade CCrP and determine its Chemistry Manufacturing and Controls (CMC) (Aim 1); 2) conduct FDA- recommended, IND-enabling CCrP preclinical safety studies in rats, dogs, and human unused cadaver donors (UCDs) (Aim 2) (initial rat studies indicated that CCrP is a safe drug); 3) conduct a pilot in vivo efficacy study in pigs to confirm the ability of CCrP to safely extend cold storage time of pig hearts to 6 hours before surgically transplanting the graft into recipient pigs (Aim 3). This pig study will be overseen by Dr. O.H. Frazier at the Texas Heart Institute to test the therapeutic benefits of our patented “three-step clinical protocol” where CCrP will be administered only once to heart donors and not to recipients; and 4) prepare CCrP Phase I safety protocol, investigational brochure, as well as assemble and file Nour Heart’s IND application to the FDA for an indication for end-stage heart failure patients scheduled for heart transplantation procedures (Aim 4). We expect CCrP to be safe in rats, dogs, and human unused cadaver donors and can preserve cardiac function in the pig heart transplantation model. As a novel bioenergetic cardioprotective drug, CCrP will potentially increase the time and distance that the hearts can be transported, thus extending transplantation to eligible recipient candidates located outside the current 4-hour transport limit. Upon successful completion of this project, Nour Heart plans to commercialize CCrP by raising capital to conduct CCrP Phase I safety trial, via two venture capital groups, who have indicated interest, or to partner with Rallybio pharmaceuticals. Future broader use of CCrP that can safely extend transport time (>4 hours), could significantly reduce the number of unused donor hearts & expand supply of useable human donor hearts, thus, potentially increase heart transplant cases by over 3,000 yearly.
Topic Code
NHLBI
Solicitation Number
PA23-230
Status
(Ongoing)
Last Modified 9/5/25
Period of Performance
9/20/24
Start Date
6/30/26
End Date
Funding Split
$3.6M
Federal Obligation
$0.0
Non-Federal Obligation
$3.6M
Total Obligated
Activity Timeline
Transaction History
Modifications to R44HL174138
Additional Detail
Award ID FAIN
R44HL174138
SAI Number
R44HL174138-462394149
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Small Business
Awarding Office
75NH00 NIH National Heart, Lung, and Blood Institute
Funding Office
75NH00 NIH National Heart, Lung, and Blood Institute
Awardee UEI
ZNSWMA88N9J5
Awardee CAGE
4JD73
Performance District
VA-11
Senators
Mark Warner
Timothy Kaine
Timothy Kaine
Modified: 9/5/25