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A Multi-Dose, Randomized, Multicenter Phase II Clinical Trial to Evaluate the Efficacy, Safety, and Pharmacokinetic Profile of SR604 Injection in Patients With Von Willebrand Disease
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 20, 2026
NCT ID
NCT07640893
Status
RECRUITING
Phase
Phase 2
Sponsor
Shanghai RAAS Blood Products Co., Ltd.
Executive brief
Investment-Ready Snapshot
SR604, developed by Shanghai RAAS Blood Products Co., Ltd., is currently undergoing a Phase II clinical trial targeting von Willebrand disease (VWD), a prevalent bleeding disorder. The trial aims to establish the drug's efficacy, safety, and pharmacokinetic profile. The global market for VWD treatments is expanding, with increasing awareness and diagnosis rates. Competitive products include existing therapies such as DDAVP and plasma-derived VWF preparations. Successful outcomes from this trial could position SR604 as a significant player in the VWD treatment landscape, potentially capturing market share from established therapies. The trial's recruitment across multiple centers in China indicates a robust operational strategy, but the company must navigate regulatory pathways and market access challenges to ensure commercial viability.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT07640893
Indication
Von Willebrand Disease (VWD)
Modality
small molecule
Target
Von Willebrand factor (VWF) modulation
Intervention
SR604
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.