Phase 1 Stomach Cancer Trial, Recruiting
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 have been diagnosed with an advanced solid tumor (confirmed by a tissue or lab test) that is one of the following cancer types: colorectal cancer, esophageal cancer, stomach cancer, pancreatic cancer, non-small cell lung cancer, breast cancer, or bile duct cancer
- Your cancer has gotten worse or you could not tolerate standard treatments, and surgery or local treatments are no longer suitable options — the number of prior treatments required before joining varies by cancer type (confirm with trial site for your specific cancer)
- A test on your tumor tissue taken within the last 3 months shows a protein called CEA at a high level (IHC score 3+), or your blood CEA level is at least twice the upper limit of normal if no tissue sample is available
- You have at least one measurable tumor that can be tracked during the trial
- Your general physical health is rated as good to moderately functional on a standard scale used by doctors (ECOG score 0–1 for most cancer types; 0–2 for pancreatic cancer) (confirm with trial site)
- Your doctors expect you to live for at least 12 more weeks
- You do not have serious mental health conditions
- Your blood counts, heart function, kidney function, liver function, and blood oxygen levels meet certain minimum health standards (confirm with trial site for specific values)
- You are able to have blood drawn or collected through a vein without other complications
- You agree to use effective contraception for 1 year after receiving the cell treatment, and agree not to donate eggs or sperm during that time
- You (or your legal guardian) are willing to sign a consent form agreeing to take part in the trial
Who may not be able to join:
- You have previously received CAR-T therapy or any other type of gene-modified cell therapy
- You have brain tumors or brain spread with symptoms, or brain lesions in critical areas (cases without symptoms in non-critical areas may be reviewed individually — confirm with trial site)
- You received an experimental drug or unapproved treatment within the 4 weeks before screening
- You received a live vaccine within the 4 weeks before screening
- You had a radioactive seed implant (iodine-125) within the 8 weeks before screening
- You took high-dose steroid tablets or injections (equivalent to more than 10mg/day of prednisone) within 2 weeks before the blood collection procedure, not including inhaled steroids
- You received certain immune checkpoint or chemotherapy drugs within 2–4 weeks before the blood collection procedure (confirm with trial site for specific timeframes)
- You have an active infection requiring treatment within 1 week before screening
- You have a bowel blockage, active bleeding in the gut, a history of major gastrointestinal bleeding in the past 3 months, severe stomach ulcers, or severe bowel inflammation
- You have a history of serious breathing or lung disease
- You have large fluid build-ups around the lungs, abdomen, or heart that cannot be controlled with treatment
- You have significant heart problems, including severe heart failure, a heart attack or heart bypass surgery within the past 6 months, serious heart rhythm problems, or a history of severe heart muscle disease
- You have an active autoimmune disease (such as Crohn's disease, rheumatoid arthritis, or lupus) that requires treatment with immune-suppressing medications
- You test positive for active hepatitis B, hepatitis C, HIV, syphilis, or cytomegalovirus (CMV) (confirm with trial site for exact testing requirements)
- You currently have a blood clot in a vein (such as a pulmonary embolism) and need blood-thinning medication
- You have had another type of cancer within the past 3 years (exceptions may apply for certain early-stage skin or cervical cancers — confirm with trial site)
- You are pregnant, currently breastfeeding, or plan to have a child within 1 year of receiving the cell treatment
- Your doctor determines there are other reasons you should not participate in the study
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.
Contact this trial
Principal Investigator: Ying Yuan, M.D, Second Affiliated Hospital, School of Medicine, Zhejiang University
Phone: 13858193601
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
Where this trial is recruiting
Primary endpoints
To determine the dose range and DLT of C-13-60 cells for CEA positive advanced malignant solid tumors [Safety and Tolerability]; To obtain the maximum tolerable dose of C-13-60 cells [Safety and Tolerability]
Can't join this trial?
Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.