drugset / Trial / NCT06003387

Efficacy and Safety of CSL222 (Etranacogene Dezaparvovec) Gene Therapy in Adults With Hemophilia B With Pretreatment Adeno-associated Virus Serotype 5 (AAV5) Neutralizing Antibodies (Nabs)

NCT06003387 ↗

Phase 3 Recruiting 35 enrolled CSL Behring
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the risk of bleeding due to failure of expected pharmacological action of CSL222 in adults with severe or moderately severe hemophilia B with detectable pretreatment AAV5 Nabs.

Timeline

Start
2024-01-30
Primary completion
2028-10-04
Completion
2032-04-02

Drugs

EvaluationDrugModalityDoseRoute
Subject CSL222 Gene therapy (AAV / viral vector) 2e+13 vg/kg Intravenous

Indications