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
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.
Indication: Von Willebrand Disease (VWD)
Modality: small molecule
Target: Von Willebrand factor (VWF) modulation
Sponsor: Shanghai RAAS Blood Products Co., Ltd.
Source URL: ClinicalTrials.gov
Source updated: Jun 11, 2026
Ingested: Jun 17, 2026
Model: trialsignal-ai-v1
Validation: validated
Matched by target_normalized: Von Willebrand factor (VWF) modulation
View original source fields
Condition raw: Von Willebrand Disease (VWD)
Condition normalized: Von Willebrand Disease (VWD)
Modality raw: small molecule
Modality normalized: small molecule
Target raw: Von Willebrand factor (VWF) modulation
Target normalized: Von Willebrand factor (VWF) modulation