Phase 2 Stomach Cancer Trial, Recruiting NCT04891016 Sponsor: Henan Cancer Hospital Condition: Stomach Cancer
Back to Stomach Cancer

Phase 2 Stomach Cancer Trial, Recruiting

NCT04891016
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:

  • Adults between 18 and 70 years old, of any gender
  • People who have been diagnosed with stomach cancer (a specific type called gastric adenocarcinoma) confirmed by a lab test
  • People whose cancer has not spread to distant parts of the body, and whose surgical team considers the tumour removable or potentially removable
  • People who are relatively active and able to carry out daily activities (a medical scoring system called ECOG rates this as 0 or 1, meaning fully active or restricted in strenuous activity only)
  • People whose cancer is at a certain stage — specifically stage T3/4 or has spread to nearby lymph nodes, based on a standard staging system
  • People whose cancer cells test positive for a protein called PD-L1, with a score of 1 or higher on a specific lab test
  • People who are expected to live for more than 3 months
  • People whose heart, liver, kidney, and blood function meet certain minimum levels as measured by blood tests (confirm with trial site for specific numbers)
  • People whose blood pressure is normal, or is controlled within a normal range with medication
  • People with diabetes whose fasting blood sugar is controlled to a certain level with medication
  • People who have hepatitis B must have a low enough level of the hepatitis B virus in their blood, as measured by a specific test
  • People who have no other serious illnesses that would conflict with this study
  • People with no history of any other cancer
  • Women who could become pregnant must have a negative blood pregnancy test within 7 days before joining, and all people who could father or carry a child must use reliable contraception during the trial and for 6 months after it ends
  • People who have read, understood, and signed a consent form agreeing to take part

Who may not be able to join:

  • Women who are pregnant or breastfeeding
  • People who had a serious infection in the 4 weeks before joining the trial
  • People who have bronchial asthma that requires regular use of inhalers or other medical treatment
  • People who have been taking immune-suppressing medications (such as prednisone at a certain dose) for more than 2 weeks due to another condition (confirm with trial site for specific dose details)
  • People who have had significant heart or stroke-related conditions, including recent heart attack, severe chest pain, heart bypass surgery, heart failure, serious irregular heartbeat, reduced heart pumping ability, or a stroke within the past 6 months
  • People who are allergic to any of the study drugs or their ingredients, or who have a history of severe allergic reactions
  • People with severe mental health conditions
  • People who have problems with blood clotting, a tendency to bleed, or who are currently receiving blood-thinning or clot-dissolving treatment
  • People who have or have had lung scarring, lung inflammation, dust-related lung disease, radiation-related lung damage, or severely reduced lung function
  • People who are unable to swallow the study medication, or who have ongoing digestive conditions (such as irritable bowel syndrome, Crohn's disease, or ulcerative colitis) or bowel blockages that may affect how the medication is absorbed
  • People who have a weakened immune system, are HIV positive, have any other immune deficiency condition, or have had an organ transplant
  • People who the research team determines do not meet the entry requirements for other reasons

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 6 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: Quanli Gao, M.D, Department of Immunotherapy, Henan Provincial Cancer Hospital

Phone: +8637165587483

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
Henan Cancer Hospital
Registry
ClinicalTrials.gov
Start date
25 June 2021
Est. completion
31 December 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

pathological complete response rate

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: 6 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