drugset / Trial / NCT03020160

A Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Emicizumab Given Every 4 Weeks in Participants With Hemophilia A

NCT03020160

Phase 3 Completed 48 enrolled Hoffmann-La Roche Chugai Pharmaceutical · collab
Non-randomizedParallel-groupOpen-labelPrevention

Summary

This multicenter, open-label, non-randomized study will assess the efficacy, safety, pharmacokinetics, and pharmacodynamics of emicizumab administered at a dose of 6 milligrams per kilogram (mg/kg) every 4 weeks in participants with hemophilia A with or without inhibitors against factor VIII (FVIII). The study consists of 2 parts: a pharmacokinetic (PK) run-in part followed by an expansion part.

Timeline

Start
2017-01-30
Primary completion
2017-12-15
Completion
2022-06-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Emicizumab Monoclonal antibody 1.5 mg/kg Subcutaneous
Subject Emicizumab Monoclonal antibody 3 mg/kg Subcutaneous
Subject Emicizumab Monoclonal antibody 6 mg/kg Subcutaneous

Indications