drugset / Trial / NCT05345197

Emicizumab in Patients With Acquired Hemophilia A

NCT05345197

Phase 2 Active not recruiting 51 enrolled University of Washington Genentech, Inc. · collab
NaSingle-groupOpen-labelTreatment

Summary

This is a phase II multicenter open-label, single-arm prospective study to evaluate the efficacy of prophylactic emicizumab administered on a scheduled basis to prevent bleeds in patients with acquired hemophilia A (AHA).

Timeline

Start
2022-08-31
Primary completion
2026-07
Completion
2026-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Emicizumab Monoclonal antibody 1.5 mg/kg Subcutaneous

Indications