drugset / Trial / NCT06941870
Efanesoctocog Alfa Prophylaxis in Patients With Hemophilia A With Synovial Hypertrophy
Non-randomizedSingle-groupOpen-labelTreatment
Summary
The objective of the study is to assess the improvement of synovial hypertrophy during the 12 months of efanesoctocog alfa prophylaxis once per week (QW) in joints with existing evidence of synovial hypertrophy in participants with hemophilia A. The study duration for each participant is approximately 12 months.
Timeline
- Start
- 2025-09-23
- Primary completion
- 2027-10-25
- Completion
- 2027-10-25
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Efanesoctocog alfa | Protein / enzyme biologic | 50 iu/kg | Intravenous |