Trial Profile

Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics and Preliminary Efficacy of SI-B003, a PD-1/CTLA-4 Bispecific Antibody, in Patients With Advanced Solid Tumors

Status: Active, no longer recruiting

Phase of Trial: Phase I

Latest Information Update: 09 Oct 2025

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At a glance

Drugs Danvilostomig (Primary)
Indications Adenocarcinoma; Gastric cancer; Malignant-mesothelioma; Oesophageal cancer; Solid tumours
Focus Adverse reactions
Sponsors Sichuan Baili Pharmaceutical

26 Sep 2025 Status changed from recruiting to active, no longer recruiting.
18 Sep 2025 Planned End Date changed from 1 Jun 2025 to 1 Dec 2025.
18 Sep 2025 Planned primary completion date changed from 1 Jun 2025 to 1 Dec 2025.

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