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:
- Adults aged 18 or older
- People whose physical fitness is rated as good (a performance score of 0–1 on a standard medical scale), and this rating has been stable for at least 7 days
- People who have been confirmed through a tissue biopsy to have stomach cancer or cancer of the junction between the stomach and oesophagus that has spread to other parts of the body or cannot be surgically removed
- People who have received one prior chemotherapy treatment for this cancer and the cancer has since grown, OR people who completed adjuvant (post-surgery) chemotherapy but whose cancer returned or grew within 6 months of finishing that treatment
- People whose first treatment included a PD-1 immunotherapy drug, and whose cancer did not progress for more than 9 months during that first treatment
- People who have at least one tumour that can be measured on a scan, according to standard medical guidelines (RECIST 1.1)
- People whose blood, liver, and kidney function results meet the specific levels required by the trial (confirm details with trial site)
- People whose blood clotting results are within the normal range required by the trial
- Women of childbearing age for whom a pregnancy test taken within 14 days before joining comes back negative, and who agree to use contraception during the trial and for 8 weeks after the last dose
- Men who are surgically sterilised or who agree to use contraception during the trial and for 8 weeks after the last dose
- People with a life expectancy of at least 3 months
- People who have voluntarily agreed to take part and have signed a consent form
- People expected to be able to attend all required follow-up visits and comply with the trial schedule
Who may not be able to join:
- People who have previously been treated with a type of drug called a VEGFR inhibitor
- People who have previously received paclitaxel chemotherapy — unless it was given before or after surgery and finished more than 6 months before the cancer progressed
- People who have received a live vaccine within 4 weeks before joining, or who may need one during the trial
- People who have an active autoimmune disease, or who have had one within the 4 weeks before joining
- People who have previously had a bone marrow transplant or an organ transplant from another person
- People with high blood pressure that cannot be controlled with medication (specifically, readings at or above 150/90 mmHg)
- People who have a condition that affects how they absorb medication, or who are unable to swallow and take tablets by mouth
- People with active stomach or bowel conditions such as ulcers, ulcerative colitis, active bleeding from a tumour, or other conditions that may increase the risk of bleeding or a hole forming in the digestive tract
- People who have had significant bleeding (more than 30 mL), vomiting blood, or blood in the stool within the past 3 months, or a blood clot, stroke, or mini-stroke within the past 12 months
- People who have had a serious heart-related condition within the past 6 months, including heart attack, severe chest pain, or bypass surgery; or who have moderate-to-severe heart failure, certain irregular heartbeats requiring medication, or a heart pumping function below 50%
- People with an active or uncontrolled serious infection
- People known to have HIV, active hepatitis B (with virus levels above a certain threshold), or hepatitis C with detectable virus levels
- People with any other significant medical condition, abnormal test results, or health concern that, in the treating doctor's judgement, would make participation unsafe or affect the trial results
- People whom the trial investigators consider unsuitable for any other reason
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: Ting Deng, MD, Tianjin Medical University Cancer Institute and Hospital
Phone: 022-23340123
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
Progression Free Survival
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.