drugset / Trial / NCT02895945
BAX 802 in CHA With Inhibitors
Phase 3
Terminated
8 enrolled
Baxalta now part of Shire
Baxalta Innovations GmbH, now part of Shire · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | BAX 802 | Protein / enzyme biologic | — | — |