Sponsor or institution
Clinical trials and research at National Marrow Donor Program
As of November 12, 2026, Find a Trial lists 7 NIH-funded research projects at this institution, with $2.7 million in listed awards. Every study is explained in plain English. Data from ClinicalTrials.gov and NIH RePORTER, updated November 12, 2026.
- 7NIH research projects
NIH-funded research (7)
Early-stage science funded by the US National Institutes of Health. Most of these projects don't enroll patients, but they show what is being worked on.
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Optimizing busulfan dosing for infants with SCID undergoing stem cell transplant
This grant tests the safest busulfan dosing levels in infants with SCID to help achieve good T and B cell recovery after a stem cell transplant.
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Providing Pediatric Transplant Access and Personalized Conditioning for Children
A national program helps kids with life-threatening blood diseases access allogeneic hematopoietic cell transplantation and tailors pre-transplant chemotherapy to each child.
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Optimizing busulfan dosing for infants with SCID undergoing donor stem cell transplant
A study tests different busulfan doses in babies with SCID to see which helps transplant success and immune recovery.
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Choosing the right busulfan dose before transplant for infants with IL2RG, JAK3, or RAG1/2 SCID
This project compares two chemotherapy (busulfan) dosing strategies to help infants with certain genetic forms of SCID regain their immune cells after a stem cell transplant.
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Expanding access to bone marrow and cellular therapies for children with life‑threatening diseases
This program helps children with serious blood and genetic conditions get personalized bone marrow and cellular therapies through a network of transplant centers and trials.
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Finding the best busulfan dose for infants with SCID
This project compares lower versus moderate doses of the chemotherapy drug busulfan to help infants with IL2RG-, JAK3-, or RAG1/2-related SCID rebuild their immune systems after a donor bone marrow transplant.
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Access to clinical trials for children with life-threatening diseases through transplantation.
This study is all about making bone marrow transplants better for kids with blood diseases by using DNA tests to personalize their treatment and find the right chemotherapy dose just for them.
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