R01HL166254
Project Grant
Overview
Grant Description
The Darbepoetin Kindergarten Development Study - Project Summary/Abstract
Improved survival of very preterm infants has not translated into improved neurodevelopment at school age. One promising neuroprotective therapy is the use of erythropoiesis stimulating agents (ESAs) such as Darbepoetin.
Preclinical and preliminary clinical data suggest that Darbepoetin treatment will lead to improved neurodevelopmental outcomes in high-risk preterm infants.
The NHLBI-funded "Darbepoetin Trial to Improve Red Cell Mass and Neurodevelopment in Preterms" (DARBE Trial) is a multicenter masked, randomized trial to test the hypothesis that Darbepoetin leads to improved neurodevelopment at 2 years in very preterm infants.
In the current application, we propose the Darbepoetin Kindergarten Development Study (DARBE-KIDS) in which we will evaluate neurodevelopment in the same children at preschool and school age.
The specific aims of DARBE-KIDS are to (1) test the impact of neonatal exposure to Darbepoetin on neurodevelopment and behavior at 4.0-5.0 and 6.0-7.0 years corrected age; (2) test the impact of neonatal exposure to Darbepoetin on longitudinal neurodevelopment and behavior from 2.0 to 7.0 years corrected age; and (3) evaluate mediating and moderating factors on the effects of Darbepoetin on school functioning at 6.0-7.0 years corrected age.
We hypothesize that preschool children treated with Darbepoetin will have better cognitive, motor, and behavior outcomes at each time point and over time, as compared to those treated with placebo.
Further, we hypothesize that executive function and cognition will be significant mediators and biological sex and family socioeconomic status will be significant moderators of the effects of Darbepoetin on pre-academic skills and teacher-reported behavior and social skills.
DARBE-KIDS builds on the collective expertise in follow-up of preterm infants among our core group of investigators and at the 16 clinical sites that enrolled children in the DARBE Trial and capitalizes on the existing infrastructure that supports both the DARBE Trial and other ongoing school-age studies funded by NHLBI.
The study is led by a highly collaborative, interdisciplinary multi-PI team with extensive relevant experience studying the impacts of ESAs in preterm infants and a long history of successful collaborations in conducting high-quality developmental follow-up through school-age in large cohorts of high-risk infants.
DARBE-KIDS will be the first comprehensive evaluation of developmental impacts over time and school functioning at school age in a large, multicenter cohort of school-age children treated with Darbepoetin.
In addition to providing critical data about the multidimensional effects of Darbepoetin on outcomes through school age, DARBE-KIDS will yield novel and important data on school functioning in a large contemporary cohort of preterm infants treated in U.S. neonatal intensive care units.
Results of this study will directly impact interpretation of the DARBE Trial and influence whether Darbepoetin should be adopted as a neuroprotective therapy to improve outcomes for preterm infants.
Improved survival of very preterm infants has not translated into improved neurodevelopment at school age. One promising neuroprotective therapy is the use of erythropoiesis stimulating agents (ESAs) such as Darbepoetin.
Preclinical and preliminary clinical data suggest that Darbepoetin treatment will lead to improved neurodevelopmental outcomes in high-risk preterm infants.
The NHLBI-funded "Darbepoetin Trial to Improve Red Cell Mass and Neurodevelopment in Preterms" (DARBE Trial) is a multicenter masked, randomized trial to test the hypothesis that Darbepoetin leads to improved neurodevelopment at 2 years in very preterm infants.
In the current application, we propose the Darbepoetin Kindergarten Development Study (DARBE-KIDS) in which we will evaluate neurodevelopment in the same children at preschool and school age.
The specific aims of DARBE-KIDS are to (1) test the impact of neonatal exposure to Darbepoetin on neurodevelopment and behavior at 4.0-5.0 and 6.0-7.0 years corrected age; (2) test the impact of neonatal exposure to Darbepoetin on longitudinal neurodevelopment and behavior from 2.0 to 7.0 years corrected age; and (3) evaluate mediating and moderating factors on the effects of Darbepoetin on school functioning at 6.0-7.0 years corrected age.
We hypothesize that preschool children treated with Darbepoetin will have better cognitive, motor, and behavior outcomes at each time point and over time, as compared to those treated with placebo.
Further, we hypothesize that executive function and cognition will be significant mediators and biological sex and family socioeconomic status will be significant moderators of the effects of Darbepoetin on pre-academic skills and teacher-reported behavior and social skills.
DARBE-KIDS builds on the collective expertise in follow-up of preterm infants among our core group of investigators and at the 16 clinical sites that enrolled children in the DARBE Trial and capitalizes on the existing infrastructure that supports both the DARBE Trial and other ongoing school-age studies funded by NHLBI.
The study is led by a highly collaborative, interdisciplinary multi-PI team with extensive relevant experience studying the impacts of ESAs in preterm infants and a long history of successful collaborations in conducting high-quality developmental follow-up through school-age in large cohorts of high-risk infants.
DARBE-KIDS will be the first comprehensive evaluation of developmental impacts over time and school functioning at school age in a large, multicenter cohort of school-age children treated with Darbepoetin.
In addition to providing critical data about the multidimensional effects of Darbepoetin on outcomes through school age, DARBE-KIDS will yield novel and important data on school functioning in a large contemporary cohort of preterm infants treated in U.S. neonatal intensive care units.
Results of this study will directly impact interpretation of the DARBE Trial and influence whether Darbepoetin should be adopted as a neuroprotective therapy to improve outcomes for preterm infants.
Awardee
Funding Goals
THE DIVISION OF BLOOD DISEASES AND RESOURCES SUPPORTS RESEARCH AND RESEARCH TRAINING ON THE PATHOPHYSIOLOGY, DIAGNOSIS, TREATMENT, AND PREVENTION OF NON-MALIGNANT BLOOD DISEASES, INCLUDING ANEMIAS, SICKLE CELL DISEASE, THALASSEMIA, LEUKOCYTE BIOLOGY, PRE-MALIGNANT PROCESSES SUCH AS MYELODYSPLASIA AND MYELOPROLIFERATIVE DISORDERS, HEMOPHILIA AND OTHER ABNORMALITIES OF HEMOSTASIS AND THROMBOSIS, AND IMMUNE DYSFUNCTION. FUNDING ENCOMPASSES A BROAD SPECTRUM OF HEMATOLOGIC INQUIRY, RANGING FROM STEM CELL BIOLOGY TO MEDICAL MANAGEMENT OF BLOOD DISEASES AND TO ASSURING THE ADEQUACY AND SAFETY OF THE NATION'S BLOOD SUPPLY. PROGRAMS ALSO SUPPORT THE DEVELOPMENT OF NOVEL CELL-BASED THERAPIES TO BRING THE EXPERTISE OF TRANSFUSION MEDICINE AND STEM CELL TECHNOLOGY TO THE REPAIR AND REGENERATION OF HUMAN TISSUES AND ORGANS. 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
North Carolina
United States
Geographic Scope
State-Wide
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 190% from $2,254,823 to $6,538,886.
Research Triangle Institute was awarded
DARBE-KIDS Study: Impact of Darbepoetin on School-Age Neurodevelopment
Project Grant R01HL166254
worth $6,538,886
from National Heart Lung and Blood Institute in September 2023 with work to be completed primarily in North Carolina United States.
The grant
has a duration of 5 years and
was awarded through assistance program 93.837 Cardiovascular Diseases Research.
The Project Grant was awarded through grant opportunity NIH Research Project Grant (Parent R01 Clinical Trial Not Allowed).
Status
(Ongoing)
Last Modified 8/6/25
Period of Performance
9/1/23
Start Date
8/31/28
End Date
Funding Split
$6.5M
Federal Obligation
$0.0
Non-Federal Obligation
$6.5M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for R01HL166254
Transaction History
Modifications to R01HL166254
Additional Detail
Award ID FAIN
R01HL166254
SAI Number
R01HL166254-1381146337
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Nonprofit With 501(c)(3) IRS Status (Other Than An Institution Of Higher Education)
Awarding Office
75NH00 NIH National Heart, Lung, and Blood Institute
Funding Office
75NH00 NIH National Heart, Lung, and Blood Institute
Awardee UEI
JJHCMK4NT5N3
Awardee CAGE
3A730
Performance District
NC-90
Senators
Thom Tillis
Ted Budd
Ted Budd
Budget Funding
| Federal Account | Budget Subfunction | Object Class | Total | Percentage |
|---|---|---|---|---|
| National Heart, Lung, and Blood Institute, National Institutes of Health, Health and Human Services (075-0872) | Health research and training | Grants, subsidies, and contributions (41.0) | $2,254,823 | 100% |
Modified: 8/6/25