Clin2
NCT05903365Worth exploringNot yet recruiting

Follow-up after half-matched bone marrow transplant for fanconi anemia

Fanconi Syndrome

Treatments studied

Part of Genetic & congenital, Kidney & urinary, Women’s health & pregnancy clinical trials.

This study follows patients with Fanconi anemia who receive a bone marrow transplant from a half-matched donor. The goal is to monitor their health and outcomes after the transplant to learn more about how well this treatment works.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
18 people
Ages
6 months to 60 years
Study type
Observational

Who can take part

  • Diagnosis of Fanconi anemia confirmed by a chromosome test or genetic testing
  • Age between 6 months and 60 years
  • Severely low blood counts (for example, needing many transfusions or having very low platelets, white cells, or red cells)
  • Signs of bone marrow problems, like a blood disorder or leukemia
  • Access to a half-matched (haploidentical) donor who is not affected by Fanconi anemia
  • Must have health insurance (French social security) and give consent (for minors, parent or guardian consent)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

Similar studies

Other trials that look related to this one.

NCT02143830Recruiting· Phase 2
Stem cell transplant chemotherapy for Fanconi anemia

This Phase 2 study tests a stem cell transplant approach using adjusted chemotherapy doses for people with Fanconi anemia. It may help replace damaged bone marrow and treat blood problems like severe aplastic anemia, MDS, or leukemia.

New York, New York
NCT04784052Recruiting· Phase 1/Phase 2
Briquilimab with reduced donor stem cell transplant for Fanconi anemia

This study tests whether a reduced-intensity donor stem cell transplant (with briquilimab as part of the conditioning) can safely treat bone marrow failure in people with Fanconi anemia. It may help by lowering how much intensive treatment is needed before the transplant, while still helping the donor cells grow.

Stanford, California
NCT07408583Not yet recruiting· Phase 1/Phase 2
Prenatal bone marrow transplant for fetuses with Fanconi anemia

This trial tests giving a bone marrow transplant to a fetus diagnosed with Fanconi anemia while still in the womb. The goal is to help the baby's body make healthy blood cells before birth, potentially reducing complications after birth.

San Francisco, California
NCT03579875Recruiting· Phase 2
Testing an inherited bone marrow transplant approach for rare blood disorders

This Phase 2 study tests a special “T-cell depleted” transplant plan for people with inherited bone marrow failure disorders (Fanconi anemia or T-Beta-thalassemia—or “TBD”). It may help restore healthy blood production while lowering the chance of certain transplant complications.

Minneapolis, Minnesota
NCT01995305AVAILABLE
Genetic testing for children with fanconi anemia

This study uses advanced genetic testing to look at the DNA of children with Fanconi anemia and their parents. The goal is to learn more about the genetic causes of the condition, which might help guide future care.

Tianjin, Tianjin Municipality
NCT05687149Recruiting
Study of mouth and throat cancer patterns in Fanconi anemia

This study looks at how squamous cell carcinoma (a type of cancer) naturally develops over time in people with Fanconi anemia. It may help doctors better recognize warning signs and plan care in the future.

Bethesda, Maryland

Hear when a new Fanconi Syndrome trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.