Phase 2 Colorectal 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 who are willing to take part voluntarily and agree to sign a consent form
- People aged between 18 and 80 years old who are generally active and able to care for themselves (PS score 0–1)
- People who have been confirmed by tissue testing to have colorectal adenocarcinoma at a specific stage of disease, including some cases where cancer has spread to limited areas that surgeons assess as removable; the cancer must also have specific molecular features: a type called PMMR/MSS, a gene mutation called KRAS G12C, and no mutations in the NRAS or BRAF genes
- People with locally advanced colorectal cancer who have not previously received systemic (whole-body) treatment, or people with removable spread of cancer who have not previously received targeted therapy — though people who developed new spread after earlier adjuvant (preventive) chemotherapy may still be considered
- People whose blood test results meet minimum levels for red blood cells, white blood cells, and platelets (confirm with trial site for exact values)
- People whose liver and kidney function blood tests fall within acceptable ranges (confirm with trial site for exact values)
- People whose blood clotting and thyroid function tests fall within acceptable ranges (confirm with trial site for exact values)
- People whose heart pumping function, measured by an ultrasound of the heart, shows the heart pumping at least 50% of its capacity
Who may not be able to join:
- People whose cancer has a specific molecular feature called MSI-H or dMMR
- People whose cancer has spread to multiple areas in the body that cannot be surgically removed
- People who have had another cancer in the past 3 years (some exceptions may apply for certain early-stage or fully cured cancers such as cervical carcinoma in situ, certain skin cancers, or superficial bladder tumours — confirm with trial site)
- People who have had active inflammatory bowel disease in the 4 weeks before joining
- People with fluid build-up around the lungs, heart, or abdomen that cannot be controlled and requires repeated draining
- People who still have unresolved significant side effects from a previous cancer treatment (with some exceptions for hair loss or mild nerve-related side effects from a drug called oxaliplatin)
- People who have had a serious bleeding event, an unhealed wound, an active ulcer, or an unhealed fracture in the 4 weeks before the study starts
- People who have had a blood clot event in the past 6 months, such as a stroke, mini-stroke, deep vein clot, or a blood clot in the lungs
- People with a history of substance misuse involving mind-affecting drugs who are unable to stop
- People with serious uncontrolled health conditions, including: very high blood pressure that does not respond to treatment; significant heart disease including heart attack, irregular heart rhythm, or heart failure; serious active infection; liver cirrhosis or active hepatitis B or C (note: people with hepatitis B or C markers in their blood may still be considered if they are on continuous antiviral treatment — confirm with trial site); kidney failure requiring dialysis; HIV or other immune system conditions; organ transplant history; poorly controlled diabetes; significant protein in the urine; or a confirmed neurological or psychiatric condition requiring ongoing treatment, such as epilepsy or dementia
- People who have previously received targeted drug treatments, including KRAS G12C inhibitors or a drug called bevacizumab
- People who, in the opinion of the medical team running the trial, have other serious health concerns that could affect their safety or their ability to complete 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: Kefeng Ding, PhD, Second Affiliated Hospital, Zhejiang University School of Medicine
Phone: 86-571-87784720
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
overall response rate
Can't join this trial?
Data last synced from ClinicalTrials.gov: 20 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.