Phase 2 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 at the time of signing the consent form
- People who have melanoma that cannot be surgically removed or has spread to other parts of the body
- People who have melanoma (not originating in the eye/uvea) where the disease continued to grow or spread during or within 12 weeks after receiving a specific type of immunotherapy (a PD-1/PD-L1 blocking antibody); if the melanoma has a specific gene change called BRAF V600, prior treatment with a BRAF inhibitor (with or without a MEK inhibitor) must also have been received or refused
- For one specific part of the trial only (Phase 1, Part 1): People with uveal (eye) melanoma where a treatment called tebentafusp was received if it was available as a standard treatment for that person, or refused
- People whose general health and activity level is rated as 0 or 1 on a standard medical scale (meaning fully active or able to carry out light activity), and who are expected by their doctor to live more than 6 months
- For one specific part of the trial only (Phase 1, Part 2): People who, after a tumour removal procedure used to generate a treatment called lifileucel, still have at least one measurable tumour remaining
- People who have recovered from side effects of any previous cancer treatments
Who may not be able to join:
- People who have brain metastases (cancer that has spread to the brain) that are causing symptoms and have not been treated
- People who are considered at increased risk for serious infections, or who have seizure disorders, blood clotting disorders, or significant active illnesses affecting the heart, lungs, or immune system
- People who have active uveitis (inflammation inside the eye) that currently requires treatment
- People who have a primary immune system disorder (such as severe combined immunodeficiency or AIDS)
- People who have had an allergic reaction to any ingredient in the study treatment
- People who have had another separate cancer diagnosis within the past 3 years
- People who currently need daily steroid medication at a dose of 10 mg or more of prednisone (or an equivalent steroid)
- People who have a history of receiving an organ transplant from another person, or who have undergone any cell-based therapy that required chemotherapy preparation within the past 20 years
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: Iovance Biotherapeutics Study Team, Iovance Biotherapeutics
Phone: 1-844-845-4682
Australian sites
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
2 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Safety and Tolerability; Recommended Dose for Phase 2
Can't join this trial?
Data last synced from ClinicalTrials.gov: 15 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.