Phase 2 Pancreatic 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:
- People aged 18 to 75 years, of any gender
- People who have been diagnosed with locally advanced or metastatic pancreatic cancer through a tissue or cell sample test
- People who have not yet received any cancer treatment
- People who have at least one tumour that can be measured on a scan, according to standard measurement guidelines
- People with a good general level of physical functioning (able to carry out daily activities with little or no limitation)
- People with an expected survival of at least 3 months
- People without serious disease affecting the heart, lungs, brain, liver, kidneys, or other major organs
- Women of childbearing age who are willing to use contraception during treatment and for 6 months after treatment ends, who are not pregnant (confirmed by a blood or urine test within 7 days before joining), and who are not breastfeeding
- Men who are willing to use contraception during the study and for 6 months after it ends
Who may not be able to join:
- People who have already received or are currently receiving cancer treatments such as chemotherapy, radiotherapy, targeted therapy, immunotherapy, or traditional Chinese medicine for cancer
- People with a known allergy to any of the study drugs
- People with brain metastases causing symptoms, or whose brain metastases have only been controlled for less than 2 months
- People whose cancer has spread to more than 70% of the liver
- People with jaundice caused by a blockage where bilirubin levels cannot be adequately reduced even after treatment to relieve the blockage
- People with active autoimmune diseases, or conditions expected to flare up again (such as lung inflammation, bowel inflammation, liver inflammation, or other immune-related conditions)
- People with a history of immune system deficiency, or who are currently using medications that suppress the immune system, including steroids
- People with known bleeding disorders or blood clotting conditions (such as haemophilia), or those who have recently used full-dose blood-thinning or clot-dissolving medications within 10 days before starting the study (preventive low-dose aspirin or low molecular weight heparin is allowed)
- People who have had a serious infection within 4 weeks before starting the study, or who show signs of an active infection or are taking antibiotic treatment within 2 weeks before starting (unless antibiotics are being used only for prevention)
- People who have had another cancer in the past 5 years or currently have another cancer, except for certain treated skin cancers, cervical carcinoma in situ, or papillary thyroid carcinoma
- People with a mental illness, or a history of misuse of alcohol, recreational drugs, or psychoactive substances
- Women who are pregnant or breastfeeding
- People considered unsuitable for the trial by the research team for other reasons (confirm with trial site)
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
Phone: 0591-88217140
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
Objective response rate, ORR
Can't join this trial?
Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.