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von willebrand factor vwf modulation clinical trial intelligence

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NCT07640893
Source recordAI-normalized

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.

AI analysis

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

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