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Clinical Trial ● Currently Recruiting Phase III NCT07043400

A Study to Investigate Tislelizumab Administered as Subcutaneous Injection Versus Intravenous Infusion Plus Chemotherapy in Patients With Unresectable or Metastatic Gastric or Gastroesophageal Junction Adenocarcinoma

A Study to Investigate Tislelizumab Administered as Subcutaneous Injection Versus Intravenous Infusion Plus Chemotherapy in Patients With Unresectable or Metastatic Gastric or Gastroesophageal Junction Adenocarcinoma — Recruiting •…

📅 14 Sep 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase III
NCT ID
NCT07043400
Start
2025-08-27
Completion
2027-10-30
ClinicaliQ Trial Snapshot
  • A Study to Investigate Tislelizumab Administered as Subcutaneous Injection Versus Intravenous Infusion Plus Chemotherapy in Patients With Unresectable or Metastatic Gastric or Gastroesophageal Junction Adenocarcinoma — Recruiting • Phase III • Oncology • NCT07043400.
  • Trial comparing subcutaneous versus intravenous tislelizumab plus chemotherapy for advanced gastric cancer in 351 patients.

Verify eligibility, endpoints and current status on the original ClinicalTrials.gov registry before acting on this summary.

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  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

This study is designed to assess the levels of drug exposure following treatment with tislelizumab administered as a subcutaneous (SC) injection compared to intravenous infusion (IV) as first-line therapy in adults with gastric or gastroesophageal junction (GEJ) that is locally advanced and cannot be surgically removed or has spread from the stomach to other areas of the body. Approximately 351 patients will be participating in this study. The study is composed of a screening period, a treatment period, and a follow-up period. Conditions: Metastatic Gastric Adenocarcinoma, Gastroesophageal Junction Adenocarcinoma Interventions:…

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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