Phase 2 Stomach Cancer Trial, Recruiting NCT04107077 Sponsor: University of Chicago Condition: Stomach Cancer
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Phase 2 Stomach Cancer Trial, Recruiting

NCT04107077
Recruiting Phase 2

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 been diagnosed with gastric cancer with peritoneal metastases (cancer that has spread to the lining of the abdomen), confirmed by a tissue sample, and/or have cancer cells found in fluid around the abdomen, and who have already completed at least 2 to 4 months of chemotherapy.
  • People aged 18 years or older.
  • People who are reasonably well and able to carry out some daily activities, as measured by a standard medical scale (confirm with trial site for exact threshold).
  • People whose blood counts and organ function (including white blood cells, platelets, liver, and kidneys) meet minimum levels set by the trial (confirm with trial site for exact values).
  • People living with HIV who are on effective treatment and whose virus levels in the blood have been undetectable within the past 6 months.
  • People with a history of hepatitis B who are on appropriate treatment and whose virus levels are undetectable.
  • People with a history of hepatitis C who have been successfully treated and cured, or who are currently on hepatitis C treatment with undetectable virus levels.
  • People who have had another cancer in the past, or who have one at the same time, as long as that cancer or its treatment is unlikely to affect the safety or results of this trial (confirm with trial site).
  • People with a history of heart disease or prior treatment with heart-affecting medicines, provided a standard heart function assessment rates them at a certain level or better (confirm with trial site for exact classification).
  • People with an expected survival of more than 3 months.
  • People who are able to use reliable contraception (such as hormonal methods, barrier methods, or abstinence) during the trial and for a set period afterward, given that the medicines used in this trial can harm an unborn baby.
  • People who are willing and able to understand and sign a written consent form.

Who may not be able to join:

  • People who currently have another untreated cancer (other than a common type of skin cancer called basal cell carcinoma) diagnosed within the last five years.
  • People whose cancer has spread to organs beyond the peritoneum and nearby lymph nodes — for example, to the liver, lungs, bones, or brain.
  • People who have not yet recovered from side effects of previous cancer treatment, where those side effects are still rated above a mild level (with the exception of hair loss).
  • People who are currently taking part in another clinical trial involving an experimental treatment.
  • People who have had a serious allergic reaction to medicines chemically similar to cisplatin or Mitomycin C, which are the drugs used in this trial.
  • People with other serious illnesses that are not well controlled.
  • People with psychiatric conditions or personal circumstances that would make it difficult to follow the trial requirements.
  • People who are pregnant, as the trial medicines carry a known risk of harm to unborn babies.
  • People who are breastfeeding, as it is unknown whether the trial medicines could affect a nursing infant.

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 23 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

Principal Investigator: Ardaman Shergill, University of Chicago

Phone: 1-855-702-8222

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
Registry
ClinicalTrials.gov
Start date
9 September 2025
Est. completion
1 June 2030

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

The PD-L1 expression can be upregulated after administration of HIPEC with greater frequency

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: 23 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