Phase 2 Stomach Cancer Trial, Recruiting NCT07115043 Sponsor: AstraZeneca Condition: Stomach Cancer
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Phase 2 Stomach Cancer Trial, Recruiting

NCT07115043
Recruiting Phase 2 🇦🇺 Australian site

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:

  • You are 18 years of age or older
  • You are generally able to carry out daily activities with little or no difficulty (your doctor can confirm your activity level score)
  • You can provide a stored sample of your tumor tissue
  • You have at least one tumor that can be measured on a scan
  • Your doctor estimates you have a life expectancy of at least 12 weeks
  • Your heart is functioning adequately and is stable
  • Your bone marrow, liver, and kidneys are functioning well enough (based on blood tests)
  • You weigh at least 35 kg (about 77 lbs)
  • You are able to understand and sign a consent form agreeing to take part

For one part of the trial (Module 1) only:

  • You have an advanced or spreading solid tumor of a specific type (such as melanoma, certain skin cancers, lung cancer, head and neck cancer, stomach cancer, kidney cancer, ovarian cancer, or triple-negative breast cancer) and have already received standard treatments

For another part of the trial (Module 2) only:

  • You have Stage IV non-small cell lung cancer (NSCLC) and have received at least one prior treatment for it, OR you have not yet received treatment for your NSCLC and your tumor shows a certain protein marker (PD-L1) at 1% or higher

Who may not be able to join:

  • You have serious or uncontrolled illnesses affecting your breathing, heart, or related to your cancer
  • You have had, or are planned to have, an organ transplant or a stem cell transplant from a donor
  • You have had or currently have an immune system disorder or inflammatory condition diagnosed within the last 3 years
  • A previous immunotherapy treatment had to be permanently stopped because of side effects you experienced
  • You are still experiencing significant side effects (moderate or worse) from a previous cancer treatment
  • You have cancer that has spread to the brain, unless it has been treated, is stable, causes no symptoms, and you do not need ongoing steroid medication for it
  • You have an untreated or symptomatic compression of your spinal cord caused by cancer, or cancer that has spread to the lining of the brain or spinal cord
  • You have an active, uncontrolled, or ongoing infection with hepatitis B or hepatitis C
  • You have previously had a serious (severe or life-threatening) lung inflammation not caused by infection
  • You need ongoing medication that suppresses your immune system, including steroids above a low daily dose
  • You have received a live vaccine within the last 30 days

For the Module 2 part of the trial only:

  • You have previously been treated with a type of therapy called anti-TIGIT
  • You have not yet received treatment for your NSCLC but your cancer has a specific genetic change (such as an EGFR mutation) for which a targeted therapy is available as a standard first treatment in your area

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 22 July 2026
Phase 2: approximately ~30% 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

Phone: 1-877-240-9479

Australian sites

Research Site, East Melbourne,

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 2
Sponsor
Registry
ClinicalTrials.gov
Start date
29 July 2025
Est. completion
2 October 2029

Where this trial is recruiting

🇦🇺 Australia 🇯🇵 Japan 🇰🇷 South Korea 🇺🇸 United States

1 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Safety- Part 1A & Part 2A (dose escalation) and Part 2B (dose expansion); Efficacy- Part 2B only (dose expansion)

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: 22 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