Phase 1 Stomach Cancer Trial, Recruiting NCT06043466 Sponsor: Chongqing Precision Biotech Co., Ltd Condition: Stomach Cancer
Back to Stomach Cancer

Phase 1 Stomach Cancer Trial, Recruiting

NCT06043466
Recruiting Phase 1

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.

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 16 July 2026
Phase 1: approximately ~10% 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: 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

Status
Recruiting
Phase
Phase 1
Sponsor
Chongqing Precision Biotech Co., Ltd
Registry
ClinicalTrials.gov
Start date
11 August 2023
Est. completion
31 December 2026

Where this trial is recruiting

🇨🇳 China

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?

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: 16 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