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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
Aug 04, 2026
Report code
NCT07640893-Aug 04, 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 aimed at treating patients with von Willebrand disease (VWD). The market for VWD therapies is growing, driven by increasing awareness and diagnosis of bleeding disorders. The competitive landscape includes established therapies such as DDAVP and plasma-derived products, but SR604's unique pharmacokinetic and pharmacodynamic profile may offer advantages in terms of dosing frequency and efficacy. Successful trial outcomes could position SR604 as a significant player in the VWD treatment market, potentially leading to lucrative partnerships or acquisitions. Diligence should focus on the trial's recruitment progress and the robustness of safety and efficacy data as they emerge.
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.