Clinical Trial

A Phase II Clinical Trial to Evaluate the Efficacy, Safety, and Pharmacokinetics of SR604 Injection in Patients With Von Willebrand Disease

Recruiting Phase 2
View on ClinicalTrials.gov →
Summary
The purpose of this study is to evaluate the efficacy, safety, pharmacokinetics (PK), and pharmacodynamic (PD) of SR604 in patients with von Willebrand disease.
Trial Details
NCT Number NCT07640893
Lead Sponsor Shanghai RAAS Blood Products Co., Ltd.
Conditions Von Willebrand Disease (VWD)
Enrollment 24 participants
Start Date 2025-11-26
Primary Completion 2027-12-31 (estimated)
Study Completion 2027-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-06-11