Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Phase I Study of BC008-1A Injection in Patients With Advanced Solid Tumors

The goal of this study is to learn if BC008-1A given 900mg or 1200mg intravenously once every 3 weeks is safe and effective to treat patients with advanced esophageal cancer or advanced non-small cell lung cancer. It will also learn about the safety and pharmacokinetics of BC008-1A.

Participants needed: 80
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Sichuan Luzhou Buchang Biopharmaceutical Co., Ltd.Updated: Jul 9, 2025Locations: 1
Eligibility criteria

Sign a written informed consent form before any study-specific procedures and be... [+5]

Having been previously exposed to any anti-TIGIT drugs. [+19]

Status: Recruiting

BC008-1A Injection for Recurrent CNS WHO G4 Glioma

The purpose of this Phase I clinical study is to evaluate the safety, preliminary efficacy and pharmacokinetic characteristics of BC008-1A injection in subjects with recurrent CNS WHO grade 4 glioma. This is a randomized and open-label study, with two dose groups set up, and 10 to 20 subjects will be enrolled in each group.

Participants needed: 40
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Sichuan Luzhou Buchang Biopharmaceutical Co., Ltd.Updated: Jul 9, 2025Locations: 1
Eligibility criteria

Voluntarily sign the informed consent form; [+10]

Having been previously exposed to any anti-TIGIT, PD-1, PD-L1 or CTLA-4 drugs; [+17]

Status: Recruiting

BC001 in Combination with Sintilimab and XELOX in the Treatment of HER-2 Negative Advanced or Metastatic Gastric Cancer or Gastroesophageal Junction Adenocarcinoma.

The goal of this clinical trial is to learn the efficaty and safety of BC001 in combination with Sintilimab and XELOX in treating patients with advanced or metastatic GC/GEJ. Participants will: Be administered with BC001, Sintilimab and Oxaliplatin once every three weeks for up to 24 months or until disease progression as per RECIST 1.1 or withdrawal from this study. Take Capecitabine once daily in the first two weeks of each three-week treatment cycle for up to 24 months or until disease progression as per RECIST 1.1 or withdrawal from this study.

Participants needed: 80
Trial details
Phase: Phase 1Age: 18-75Biological sex: AllType: InterventionalSponsor: Sichuan Luzhou Buchang Biopharmaceutical Co., Ltd.Updated: Mar 10, 2025Locations: 1
Eligibility criteria

Subjects must be able to understand and voluntarily sign the written informed co... [+9]

Subjects who have undergone major organ surgical operations (excluding needle bi... [+24]