Stomach Cancer Trial, Recruiting NCT06128252 Sponsor: Tang-Du Hospital Condition: Stomach Cancer
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Stomach Cancer Trial, Recruiting

NCT06128252
Recruiting Not Applicable

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 between 18 and 75 years old (any gender)
  • You have been diagnosed through a lab test (biopsy) with stomach cancer or cancer at the junction of the stomach and food pipe (gastroesophageal junction), at a specific intermediate-to-advanced stage (stage II or III, meaning the cancer has grown into the stomach wall or nearby areas but has not spread to distant parts of the body)
  • Your doctors expect you to live for at least 3 months
  • Your tumor tissue has tested positive for a protein called PD-L1 (with a score of 1 or higher)
  • You have a measurable tumor that doctors believe could potentially be fully removed by surgery
  • You are generally well enough to carry out light daily activities (rated 0 or 1 on a standard health scale used in cancer research)
  • You have been fully informed about the trial and have signed a written agreement to take part

Who may not be able to join:

  • You have taken a substance called a "taurine agent" in the month before the trial starts or plan to use it during the study (confirm with trial site)
  • Your cancer tests positive for a protein called HER-2
  • You have a blockage in your digestive tract, active bleeding in your stomach or gut, a hole (perforation) in your digestive tract, or difficulty swallowing
  • You have serious problems with your heart, lungs, liver, kidneys, hormones, blood, or mental health that the doctors feel make it unsafe to join
  • You have HIV, AIDS, an autoimmune disease, or are taking medications that suppress your immune system
  • You have any other serious or complex health conditions that the trial doctors believe would make it unsafe or unsuitable for you to participate

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
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Xin Wang, MD, PhD, Tang-Du Hospital

Phone: 17702979587

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
Not Applicable
Sponsor
Tang-Du Hospital
Registry
ClinicalTrials.gov
Start date
1 September 2024
Est. completion
30 June 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Pathological complete response

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