drugset / Trial / NCT02895945

BAX 802 in CHA With Inhibitors

NCT02895945 ↗

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of BAX 802 in males with congenital hemophilia A (CHA) with inhibitors who are undergoing major or minor elective surgical, dental, or other invasive procedures.

Timeline

Start
2016-12-22
Primary completion
2021-01-22
Completion
2021-01-22

Outcome

Outcome not reported

Stopped: “Takeda has determined that the benefit/risk profile does not support continuation of the surgery Study for this specific Congenital Hemophilia A with Inhibitors patient population.”

Drugs

EvaluationDrugModalityDoseRoute
Subject BAX 802 Protein / enzyme biologic — —

Indications