Gastric Cancer or Gastroesophageal Junction Adenocarcinoma

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Review clinical trials related to Gastric Cancer or Gastroesophageal Junction Adenocarcinoma. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Oral Paclitaxel Plus Fruquintinib Verus Investigator's Choice in Second-Line Advanced Gastric Cancer

The goal of this study is to evaluate the efficacy and safety of oral paclitaxel solution plus fruquintinib as second-line therapy in adult subjects with advanced or metastatic gastric (G) or gastroesophageal junction (GEJ) cancer.

Participants needed: 150
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Harbin Medical UniversityUpdated: Jul 1, 2026Locations: 3
Eligibility criteria

Age 18 to 75 years, regardless of sex; [+9]

Known HER2-positive status without prior anti-HER2 therapy (patients who progres... [+18]

Status: Recruiting

A Clinical Study of Sintilimab Combined With Chemothrapy Versus Chemotherapy as Adjuvant Therapy for Gastric/Gastroesophageal Junction Adenocarcinoma

This study aims to explore the efficacy and safety of sintilimab combined with SOX versus SOX alone as adjuvant therapy for patients with pIIIC stage or dMMR/MSI-H pIIIA/IIIB stage gastric/gastroesophageal junction adenocarcinoma. A total of 276 subjects are planned to be enrolled in this study. Patients will be randomly assigned in a 1:1 ratio to receive up to 8 cycles of sintilimab combined with SOX or SOX alone as adjuvant therapy.

Participants needed: 276
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Fudan UniversityUpdated: Mar 25, 2026Locations: 1
Eligibility criteria

Signed written informed consent. [+19]

Cancers involving the EGJ with the tumor center located in the proximal stomach... [+28]

Status: Not yet recruiting

First in Human Study of QLS5316 in Solid Tumors

This is a first-in-human (FIH) Phase I, multi-center, open-label, study of QLS5316, in patients with advanced solid tumors. The study aim to evaluating the safety, tolerability, preliminary efficacy, pharmacokinetics (PK), and immunogenicity of QLS5316 as monotherapy.

Participants needed: 300
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Qilu Pharmaceutical Co., Ltd.Updated: Jan 22, 2026
Eligibility criteria

Age ≥ 18 years [+6]

Prior treatment with antibody-drug conjugates (ADCs) containing topoisomerase I... [+8]