An Evaluation Of The Safety And Efficacy Of On-Demand Treatment With Xyntha (B Domain Deleted Recombinant Factor VIII, Albumin Free) In Chinese Subjects With Hemophilia A
Abstract
This study will evaluate the safety and efficacy of on-demand treatment with Xyntha in Chinese hemophilia A subjects.
Conditions: Hemophilia A.
Primary outcome: Investigator Hemostatic Efficacy Assessment 8 Hours Post Infusion; Investigator Hemostatic Efficacy Assessment 24 Hours Post Infusion; Number of Participants With Factor VIII (FVIII) Inhibitor Development.
Enrollment: 53 participants.
How strong is the evidence?
Evidence Hub reads this as a clinical trial, done in people. Its evidence level is 3 of 5 (Moderate · trial / cohort / secondary analysis). Trials without a large randomized design, cohorts and secondary analyses give moderate evidence. Reported size: 53 participants or records.
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