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NCT07640893RECRUITINGanonymous

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

Sponsor

Source record

Shanghai RAAS Blood Products Co., Ltd.

Phase

Source record

Phase 2

Modality

AI-normalized

small molecule

Target

AI-normalized

Von Willebrand factor (VWF) modulation

Indication / condition

AI-normalized

Von Willebrand Disease (VWD)

Intervention

Source record

SR604

Source & freshness

Source record

NCT ID

NCT07640893

Original source

ClinicalTrials.gov

Source last updated

Jun 11, 2026

Ingested at

Jun 17, 2026

Internal sync

Jun 17, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

Open original registry record
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NCT ID

NCT07640893

Title

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

Sponsor

Shanghai RAAS Blood Products Co., Ltd.

Status

RECRUITING

Phase

Phase 2

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

Interventions

SR604

Public preview

Source record

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-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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