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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 19, 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 positioned to address the unmet medical need in the treatment of von Willebrand disease (VWD), a prevalent bleeding disorder. The market for VWD treatments is expanding, with increasing awareness and diagnosis leading to a growing patient population. The competitive landscape includes existing 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 facilitate market entry and establish SR604 as a preferred treatment option, potentially capturing significant market share. Diligence should focus on the robustness of clinical data, regulatory pathways, and potential reimbursement scenarios.
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.