Printed from Voxsanity (voxsanity.com.au) — NCT06112314 — Data sourced from ClinicalTrials.gov. Verify directly with the trial site before attending. Not medical advice.
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.
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.
Voxsanity
Clinical trials and treatments, explained plainly · voxsanity.com.au
Date:
To: My Doctor
Re: Clinical trial enquiry
I am writing to enquire about the following clinical trial which may be relevant to my care:
Trial: NCT06112314
Sponsor: Immunocore Ltd
Phase: Phase 3
Status: Recruiting
Condition: Melanoma
Trial contact: 844-466-8661
More information: https://clinicaltrials.gov/study/NCT06112314
Eligibility summary (AI generated)
Written by an AI model from ClinicalTrials.gov eligibility criteria and checked on a sample basis. Please confirm against the original criteria.
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.
Access in Australia: A treatment being studied in a clinical trial is generally not yet listed on the PBS. Where a medicine is not approved or not available through a trial, the TGA Special Access Scheme may allow a doctor to access unapproved therapeutic goods for individual patients. See voxsanity.com.au/sas-navigator/ for a plain English explainer.
This information was sourced from ClinicalTrials.gov via Voxsanity (data last synced 26 July 2026). It is not medical advice. Please verify the trial's current status directly with the trial site before acting.
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.
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.