Phase 1 Melanoma 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 18 years of age or older
- People who have voluntarily agreed to take part by signing a consent form before any study procedures begin
- People who are able and willing to follow all study procedures for the full duration of the trial
- People who have an advanced solid tumour cancer that has been confirmed through a tissue sample (biopsy), has continued to grow or spread, and has already been treated with standard therapies — either without success or with intolerable side effects
- People whose general physical health and ability to carry out daily activities meets a certain standard (rated 0 or 1 on a medical scale called ECOG) at the start of the trial
- People who have been free of any other active cancer for at least 2 years
- People whose recent blood and lab test results fall within the ranges required by the trial
- Women who could become pregnant, and men, who agree to use adequate contraception during the trial
Who may not be able to join:
- People who have acute leukaemia or a type of blood cancer called chronic lymphocytic leukaemia (CLL)
- People who have significant heart disease, have had a heart attack in the past 6 months, or have an unstable irregular heartbeat
- People with certain heart rhythm abnormalities detected on a heart tracing (ECG), including a prolonged QT interval, a condition called congenital long QT syndrome, or other ECG abnormalities that the study doctor considers a safety concern
- People who have an active, uncontrolled bacterial, viral, or fungal infection that requires treatment with systemic medication within 7 days before the trial starts
- People who have an active autoimmune disease or another medical condition that requires ongoing use of steroid or immune-suppressing medications
- People with a known HIV, hepatitis B, or hepatitis C infection, unless certain specific conditions are met (confirm with trial site)
- People who have had a major organ transplant or a bone marrow transplant
- People who have cancer that has spread to the brain or spinal cord and is causing symptoms
- People with serious non-cancer illnesses (confirm with trial site for specifics)
- Women who are pregnant or currently breastfeeding
- People who have had major surgery within 28 days before the first dose of the study drug
- People who have received other cancer treatments within 4 weeks, or within 5 half-lives of the treatment (whichever is the shorter period), before starting this trial — though some exceptions may apply (confirm with trial site)
- People who have had a severe allergic reaction to a biological therapy in the past, which the study doctor believes may pose a safety risk
- People who have received radiation therapy to treat symptoms within 14 days before the trial starts
- People with an active substance abuse problem
- People who have previously had a severe immune-related side effect (Grade 3 or higher) from cancer immunotherapy
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: +8618980600172
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
Evaluate GV20-0251 safety
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.