Phase 2 Melanoma Trial, Recruiting NCT06940739 Sponsor: Iovance Biotherapeutics, Inc. Condition: Melanoma
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Phase 2 Melanoma Trial, Recruiting

NCT06940739
Recruiting Phase 2 🇦🇺 Australian site

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 15 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Iovance Biotherapeutics Study Team, Iovance Biotherapeutics

Phone: 1-844-845-4682

Australian sites

Greenslopes Private Hospital, Greenslopes, Queensland
Hollywood Private Hospital Ramsay, Nedlands, Western Australia

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

Status
Recruiting
Phase
Phase 2
Sponsor
Iovance Biotherapeutics, Inc.
Registry
ClinicalTrials.gov
Start date
11 March 2025
Est. completion
1 June 2032

Where this trial is recruiting

🇦🇺 Australia 🇺🇸 United States

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?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov