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Study identifier: NCT07640893 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Von Willebrand Disease (VWD)  ·  Sponsor: Shanghai RAAS Blood Products Co., Ltd.

PhasePhase 2
Planned participants24
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

The purpose of this study is to evaluate the efficacy, safety, pharmacokinetics (PK), and pharmacodynamic (PD) of SR604 in patients with von Willebrand disease.

This description comes directly from the study's public registry record.

Talk to the study team

Research and Development  ·  862122130888  ·  hanyu@raas-corp.com

Always discuss trial participation with your own doctor first.

Locations (9)

Xiangya Hospital of Central South UniversityChangsha, ChinaRecruiting
The First Affiliated Hospital of University of Science and Technology of ChinaHefei, ChinaRecruiting
Jinan Central HospitalJinan, ChinaRecruiting
The First Affiliated Hospital of Guangxi Medical UniversityNanning, ChinaRecruiting
The First Affiliated Hospital of Soochow UniversitySuzhou, ChinaRecruiting
The Second Hospital of Shanxi Medical UniversityTaiyuan, ChinaRecruiting
North China University of Science and Technology Affiliated HospitalTangshan, ChinaRecruiting
Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical SciencesTianjin, ChinaRecruiting
Henan Provincial People's HospitalZhengzhou, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07640893