Retrospective Chart Review to Evaluate Safety and Tolerability of ADVATE Among Previously Untreated Patients in China With Moderate to Severe Hemophilia A
NCT02634723 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 21
Last updated 2021-03-17
Summary
The purpose of this post-marketing safety study is to evaluate the safety, immunogenicity, and effectiveness of ADVATE in previously untreated patients (PUPs) in China with moderate to severe hemophilia A.
Conditions
Interventions
- BIOLOGICAL
-
Octocog alfa (recombinant human coagulation factor VIII)
Sponsors & Collaborators
-
Baxalta now part of Shire
lead INDUSTRY
Principal Investigators
-
Study Director · Takeda
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-12-23
- Primary Completion
- 2016-06-30
- Completion
- 2016-06-30
Countries
- China
Study Locations
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