Reduced Intensity Conditioning and Familial HLA-Mismatched BMT for Non-Malignant Disorders

PHASE1/PHASE2RecruitingINTERVENTIONAL
Enrollment

29

Participants

Timeline

Start Date

March 20, 2017

Primary Completion Date

April 30, 2026

Study Completion Date

April 30, 2031

Conditions
Severe Sickle Cell DiseaseBone Marrow Failure SyndromesMetabolic DisordersImmunologic DisordersHemoglobinopathiesNon-malignant Disorders
Interventions
DRUG

RIC regimen

Days -60 to -21: hydroxyurea (30mg/kg/day po) \>6hrs prior to 1st dose: alemtuzumab (3mg IV) Day -21: alemtuzumab (10mg IV or S/C) Day -20: alemtuzumab (15mg IV or S/C) (10mg if \< 10kg) Day -19: alemtuzumab (20mg IV or S/C) (10mg if \< 10kg) Days -8 to -4: fludarabine (30mg/m2/day IV) Day -4: thiotepa (8mg/kg IV) Day -3: melphalan (140mg/m2) Days -2 to -1: rest days/no therapy Day 0: bone marrow transplant

DRUG

GVHD prophylaxis regimen

Day +3 to +4: cyclophosphamide (50mg/kg/day IV) Day +5: Start of tacrolimus \& Start of mycophenolate mofetil (MMF) Days +5, +14, +30, +60, +90: abatacept (IND) (10mg/kg/day IV) Days +120 to +390: abatacept (IND) monthly (5mg/kg/day IV)

Trial Locations (3)

49503

RECRUITING

Helen DeVos Children's Hospital, Grand Rapids

63110

RECRUITING

Washington University School of Medicine, St Louis

06510

RECRUITING

Yale School of Medicine, New Haven

All Listed Sponsors
lead

Washington University School of Medicine

OTHER