Phase 3 Melanoma Trial, Recruiting NCT06112314 Sponsor: Immunocore Ltd Condition: Melanoma
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Phase 3 Melanoma Trial, Recruiting

NCT06112314
Recruiting Phase 3 🇦🇺 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 test positive for a specific genetic marker called HLA-A*02:01
  • People who have been diagnosed with Stage IV melanoma, or Stage III melanoma that cannot be removed by surgery, confirmed through a tissue biopsy
  • People who can provide a stored or fresh tumor tissue sample that meets the trial's quality requirements
  • People whose cancer can be measured using standard imaging scans
  • People who have had their tumor tested to find out whether a specific gene change called BRAF V600 mutation is present or absent
  • People who are in good enough general health to carry out daily activities with little to no limitation (rated 0 or 1 on a standard medical scale)
  • People of childbearing potential who are sexually active with a partner who has not been sterilised must agree to use highly effective contraception from the time of screening until 5 months after the last dose of the trial treatment

Who may not be able to join:

  • People who have had another type of cancer (other than the melanoma being studied in this trial)
  • People who have brain or spinal cord metastases that are untreated, currently active, or causing symptoms, or who have cancer that has spread to the lining of the brain or spinal cord
  • People who have had a serious allergic reaction to any of the trial drugs (IMC-F106C, nivolumab, or relatlimab) or their ingredients
  • People who have significant lung disease or seriously reduced lung function
  • People who have significant heart disease or seriously reduced heart function
  • People who have an active autoimmune disease that requires medication to suppress the immune system
  • People who have any other poorly controlled medical condition that, in the judgement of the trial doctors, could affect safety, the ability to follow trial procedures, or the reliability of results
  • People who have already received systemic (whole-body) drug treatment for melanoma that cannot be removed by surgery or has spread to other parts of the body
  • People who have previously had a life-threatening side effect related to certain immunotherapy drugs (anti-PD-(L)1 or anti-LAG-3 treatments)

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 26 July 2026
Phase 3: approximately ~65% 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

Phone: 844-466-8661

Australian sites

Calvary Mater Newcastle Hospital, Waratah, New South Wales
(02) 40143280
Gallipoli Medical Research Foundation (Greenslopes Private Hospital), Greenslopes, Queensland
Linear Clinical Research, Nedlands, Western Australia
61-8-6383 3189
One Clinical Research - Nedlands, Nedlands, Western Australia
+61 8 6279 9466
Austin Hospital, Heidelberg,
Peter MacCallum Cancer Centre, North Melbourne,
61385595000
University of Sydney - Melanoma Institute Australia (MIA) - The Poche Centre, Wollstonecraft,
The University of Queensland (UQ) - Princess Alexandra Hospital (PAH), Woolloongabba,

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 3
Sponsor
Immunocore Ltd
Registry
ClinicalTrials.gov
Start date
5 June 2024
Est. completion
16 October 2027

Where this trial is recruiting

🇦🇷 Argentina 🇦🇺 Australia 🇦🇹 Austria 🇧🇪 Belgium 🇧🇷 Brazil 🇧🇬 Bulgaria 🇨🇦 Canada 🇨🇿 Czechia 🇩🇰 Denmark 🇫🇮 Finland 🇫🇷 France 🇩🇪 Germany 🇭🇺 Hungary 🇮🇹 Italy 🇱🇹 Lithuania 🇲🇽 Mexico 🇳🇴 Norway 🇵🇱 Poland 🇵🇹 Portugal 🇷🇴 Romania 🇪🇸 Spain 🇸🇪 Sweden 🇨🇭 Switzerland Turkey (Türkiye) 🇬🇧 United Kingdom 🇺🇸 United States

8 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Progression-Free Survival (PFS)

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: 26 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