drugset / Trial / NCT05203679

Evaluation of the Safety and Efficacy of Hemophilia B Gene Therapy Drug

NCT05203679 ↗

Phase 2/3 Active not recruiting 32 enrolled Shanghai Xinzhi BioMed Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

This is a multi-center, Phase 1/2/3, single-arm, open-label, single-dose treatment clinical study to evaluate the safety, tolerability and efficacy of BBM-H901 injection in Hemophilia B subjects with ≤2 International unit per deciliter (IU/dl) residual factor IX (FIX) levels. BBM-H901 is an adeno-associated virus (AAV) vector derived from recombinant DNA techniques to contain an expression cassette of the human factor IX (hFIX) transgene and raises circulating levels of endogenous FIX.

Timeline

Start
2021-12-30
Primary completion
2024-04-16
Completion
2028-06-30

Outcome

Met primary endpoint

paper The primary endpoint was met with no DLT observed in the 10 weeks postinfusion. PMID 41266685 ↗

paper The study met its primary endpoint PMID 41266685 ↗

paper the upper limit of the 95% CI (1.99) was lower than the predefined superiority margin of 5.0 PMID 41266685 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject BBM-H901 Gene therapy (AAV / viral vector) 5e+12 vg/kg Intravenous

Indications