Phase 3 Stomach Cancer Trial, Recruiting NCT05078047 Sponsor: UNICANCER Condition: Stomach Cancer
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Phase 3 Stomach Cancer Trial, Recruiting

NCT05078047
Recruiting Phase 3

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have signed a written consent form before any trial-related procedures take place.
  • People aged 18 or older.
  • People with cancer that has spread to other parts of the body (or is locally advanced and not suitable for local treatment), where the cancer type has been confirmed by a tissue test, including: lung cancer, kidney cancer, head and neck cancer, bladder/urinary tract cancer, triple negative breast cancer, Merkel cell cancer, liver cancer, melanoma, bowel cancer with a specific genetic marker (MSI), oesophageal squamous cell cancer, uterine cancer, cervical cancer, stomach or stomach-oesophagus junction cancer, basal cell skin cancer, or squamous cell skin cancer.
  • People whose cancer has partially or completely responded to standard immunotherapy after at least 6 months of treatment, as confirmed by scans.
  • People with metastatic melanoma who have had a partial response to immunotherapy (note: complete responders with melanoma are not eligible — confirm with trial site).
  • People whose treating doctor considers them suitable to continue on the same immunotherapy treatment.
  • People who are relatively well and active, with a fitness score of 0 or 1 on a standard medical scale (meaning fully active or able to carry out light activity).
  • People with brain metastases that have been treated (with surgery or targeted radiation) and have been stable, with no signs of new or growing brain tumours before entering the trial.
  • People who previously received immunotherapy combined with chemotherapy, targeted therapy (TKI), pemetrexed, or bevacizumab.
  • Women who have gone through menopause, or women of childbearing age who have a negative pregnancy test.
  • People who agree to use adequate contraception during and after the study treatment, as directed by the treatment guidelines.
  • People who are willing and able to attend all required visits, treatments, and follow-up appointments for the full duration of the trial.
  • People who are enrolled in a national social security or health insurance system (this criterion is specific to the French healthcare system — confirm with trial site).

Who may not be able to join:

  • People with metastatic melanoma whose cancer has completely disappeared in response to immunotherapy.
  • People with metastatic kidney cancer classified as "favourable risk" (by a specific medical scoring system) who are being treated with a combination of targeted therapy and immunotherapy.
  • People with blood cancers such as leukaemia, myeloma, or lymphoma.
  • People with an active infection that requires systemic (whole-body) treatment, such as antibiotics given by mouth or through a drip.
  • People who are currently enrolled in another treatment-based clinical trial, or who have been in one within the 30 days before joining this trial.
  • People who are unable to follow the study requirements due to geographic, personal, social, or physical reasons, or who are unable to understand the study's purpose and procedures.
  • People who are in legal custody, under guardianship, or otherwise deprived of their liberty.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 15 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Gwenaëlle GRAVIS-MESCAM, MD, Institut Paoli Calmettes, Marseille

Phone: +33 (0) 1 73 79 79 11

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 3
Sponsor
UNICANCER
Registry
ClinicalTrials.gov
Start date
8 March 2022
Est. completion
7 March 2027

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Progression-free survival (PFS)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 15 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov