drugset / Trial / NCT05441553

A Study to Evaluate the Safety and Efficacy of VGB-R04 in Adult Hemophilia B Patients

NCT05441553 ↗

Phase 1/2 Unknown 26 enrolled Shanghai Vitalgen BioPharma Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

A multicenter, open, non-randomized, phase I/II, two-phase clinical study. The dose exploration phase was phase I, and the dose extension phase was phase II.

Timeline

Start
2022-07
Primary completion
2025-01
Completion
2025-01

Drugs

EvaluationDrugModalityDoseRoute
Subject VGB-R04 Gene therapy (AAV / viral vector) — Intravenous

Indications