U.S. License Holder:
Rocket Pharmaceuticals, Inc.
Date of License:
March-26-2026
Last Update:
Mar-31-2026
FDA-Approved Indications
KRESLADI (marnetegragene autotemcel) is indicated for the treatment of pediatric patients with severe leukocyte adhesion deficiency-I (LAD-I) due to biallelic variants in ITGB2 without an available human leukocyte antigen (HLA)-matched sibling donor for allogeneic hematopoietic stem cell transplant.
