Locally Advanced Unresectable or Metastatic Gastric Cancer

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Review clinical trials related to Locally Advanced Unresectable or Metastatic Gastric Cancer. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Long-term Follow-up Study of Subjects Enrolled in Clinical Trials of Cadonilimab (AK104)

This is an observational and non-interventional clinical study that only collects long-term follow-up data of the subjects. As the world's first approved PD-1/CTLA-4 bispecific antibody for marketing, Cadonilimab may confer long-term survival benefits.

Participants needed: 610
Trial details
Biological sex: AllType: ObservationalSponsor: AkesoUpdated: Apr 23, 2026Locations: 1Duration: 5 Years
Eligibility criteria

Ability to understand and voluntarily sign a written informed consent form (ICF)... [+3]

None

Status: Recruiting

M108 Plus CAPOX Versus Placebo Plus CAPOX as First-line Treatment for Claudin (CLDN) 18.2-Positive, HER2-Negative, PD-L1 CPS<5, Locally Advanced Unresectable or Metastatic Gastric or Gastroesophageal Junction (GEJ) Adenocarcinoma.

Gastric/GEJ adenocarcinoma, which is one of the major leading causes of cancer-related deaths worldwide, is a global challenge to human health. However, standard chemotherapy has limited efficacy in advanced gastric cancer, and there is an urgent need to explore and develop new therapeutic targets and combination therapy modalities. The main purpose of this study is to explore the efficacy of M108 monoclonal antibody plus capecitabine and oxaliplatin (CAPOX) versus placebo plus CAPOX as first-line treatment measured by progression free survival (PFS). This study will also evaluate safety, tolerability, pharmacokinetics and the immunogenicity profile of M108 monoclonal antibody, as well as its effects on quality of life.

Participants needed: 486
Trial details
Phase: Phase 3Age: 18-75Biological sex: AllType: InterventionalSponsor: FutureGen Biopharmaceutical (Beijing) Co., LtdUpdated: Feb 28, 2024Locations: 1
Eligibility criteria

Written informed consent [+9]

Previous radiotherapy within 4 weeks prior to the start of study treatment. (if... [+6]