drugset / Trial / NCT06941870

Efanesoctocog Alfa Prophylaxis in Patients With Hemophilia A With Synovial Hypertrophy

NCT06941870

Phase 4 Recruiting 35 enrolled Sanofi
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

EvaluationDrugModalityDoseRoute
Subject Efanesoctocog alfa Protein / enzyme biologic 50 iu/kg Intravenous