Melanoma Trial, Recruiting NCT04576429 Sponsor: Assistance Publique - Hôpitaux de Paris Condition: Melanoma
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Melanoma Trial, Recruiting

NCT04576429
Recruiting Not Applicable

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 years or older
  • People who have had stage III or IV melanoma fully removed by surgery and are being treated with an immunotherapy drug (such as pembrolizumab, nivolumab, or a similar type of drug called an immune checkpoint inhibitor) as a follow-up treatment after surgery
  • People with advanced stage IIIC/D or IV melanoma that cannot be surgically removed, who are being treated with immunotherapy (such as pembrolizumab, nivolumab, or a similar immune checkpoint inhibitor) combined with radiotherapy
  • People who have been informed about the study and have signed a consent form agreeing to take part
  • People enrolled in the French social security system

Who may not be able to join:

  • Women who are pregnant or breastfeeding
  • People who do not wish to take part
  • People currently taking immunosuppressant medication (drugs that lower the immune system's activity)
  • People who have been taking high-dose steroid tablets (more than 10 mg/kg/day) for more than 7 days
  • People currently participating in another clinical trial where they are receiving a blinded (unknown) treatment
  • People who do not have any form of social security or health protection coverage

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 22 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Elisa FUNCK-BRENTANO, MD, Dermato-oncology department, Ambroise Paré hospital, APHP

Phone: +33 (0)1 71 16 77 21

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
Not Applicable
Registry
ClinicalTrials.gov
Start date
27 January 2021
Est. completion
1 January 2031

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Rate of relapse/progression-free survival

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: 22 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