Phase 2 Melanoma Trial, Recruiting NCT07230613 Sponsor: UNICANCER Condition: Melanoma
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Phase 2 Melanoma Trial, Recruiting

NCT07230613
Recruiting Phase 2

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 aged 18 or older.
  • People who have a type of melanoma (skin or mucosal) that is at stage III, can be surgically removed, and is measurable using standard imaging guidelines.
  • People who previously received a type of immunotherapy called anti-PD-1 treatment, as long as that treatment stopped more than 6 months before joining this trial.
  • People who previously received targeted therapy for melanoma, as long as that treatment stopped more than 3 months before joining this trial.

Who may not be able to join:

  • People whose melanoma has spread to distant parts of the body, as detected by clinical examination or imaging scans.
  • People who have a type of melanoma that started in the eye (uveal melanoma).
  • People who have had a serious allergic reaction or sensitivity to nivolumab or ipilimumab, or to any of the ingredients in these medicines.
  • People whose disease cannot be properly measured or assessed using standard imaging guidelines (confirm with trial site).

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 23 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

Phone: +33(0)662536043

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
UNICANCER
Registry
ClinicalTrials.gov
Start date
12 January 2026
Est. completion
1 December 2027

Where this trial is recruiting

🇫🇷 France

Primary endpoints

The primary objective is to evaluate the efficacy of the intratumoral combination of ipilimumab and nivolumab in terms of pCR or MPR in patients with resectable stage III cutaneous or mucosal melanoma.; The primary objective is to evaluate the tolerability of the intratumoral combination of ipilimumab and nivolumab in patients with resectable stage III cutaneous or mucosal melanoma.

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: 23 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