For Healthcare Professionals

An Umbrella Study Evaluating the Efficacy and Safety of Multiple Treatment Combinations in Patients With Gastric or Gastroesophageal Junction Carcinoma

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About the study

This is a Phase Ib/II, open-label, multicenter, randomized umbrella study in participants with advanced gastric carcinoma (GC) or gastroesophageal junction carcinoma (GEJC). The study is designed with the flexibility to open new treatment arms as new treatments become available, close existing treatment arms that demonstrate minimal clinical activity or unacceptable toxicity, and modify the participant population. Cohort 1 will enroll participants with inoperable locally advanced, metastatic, or advanced GC or GEJC, with adenocarcinoma confirmed as the predominant histology, who have not received prior systemic therapy for advanced or metastatic disease. Eligible participants will initially be randomly assigned to one of treatment arms (Stage 1). Participants who experience loss of clinical benefit or unacceptable toxicity during Stage 1 may be eligible to receive treatment with a different treatment combination (Stage 2). When a Stage 2 treatment combination is available, this will be introduced by amending the protocol.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria for Stage 1:


  1. ECOG Performance Status of 0 or 1
  2. Inoperable locally advanced, metastatic, or advanced GC or GEJC, with adenocarcinoma confirmed as the predominant histology
  3. No prior systemic treatment for advanced or metastatic disease
  4. Life expectancy >= 3 months, as determined by the investigator
  5. Human epidermal growth factor receptor 2 (HER2)-negative tumors
  6. Measurable disease according to RECIST v1.1
  7. Adequate hematologic and end-organ function
  8. Patients without hepatitis B virus (HBV) infection at screening
  9. Negative hepatitis C virus (HCV) antibody test at screening, or positive HCV antibody test followed by a negative HCV RNA test at screening
  10. Negative HIV test at screening
  11. For women of childbearing potential: agreement to remain abstinent or use contraception, and agreement to refrain from donating eggs, as outlined for each specific treatment arm
  12. For men: agreement to remain abstinent or use contraception, and agreement to refrain from donating sperm, as outlined for each specific treatment arm

EXCLUSION CRITERIA

Exclusion Criteria for Stage 1:


  1. Prior treatment with CD137 agonists or immune checkpoint blockade therapies
  2. Treatment with investigational therapy within 28 days prior to initiation of study treatment
  3. Any contraindications to any of the study drugs of the chemotherapy regimen
  4. Eligible only for the control arm
  5. Patients with a signet ring cells dominant carcinoma
  6. Symptomatic, untreated, or actively progressing CNS metastases
  7. History of leptomeningeal disease
  8. Active or history of autoimmune disease or immune deficiency
  9. Significant cardiovascular disease within 3 months prior to initiation of study treatment, unstable arrhythmia, or unstable angina
  10. History of malignancy other than GC or GEJC within 2 years prior to initiation of study treatment, with the exception of malignancies with a negligible risk of metastasis or death

Exclusion Criteria for Tiragolumab-Containing Arm:


  1. Prior treatment with an anti-TIGIT agent
  2. Active Epstein-Barr virus (EBV) infection or known or suspected chronic active EBV infection at screening

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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.

Study’s details


Contition

Gastric and Gastroesophageal Junction Carcinoma

Age (in years)

18+

Phase

Phase 1/Phase 2

Participants needed

255

Est. Completion Date

Jun 22, 2025

Treatment type

Interventional


Sponsor

Hoffmann-La Roche

ClinicalTrials.gov identifier

NCT05251948

Study number

YO43408

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