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Study identifier: NCT04576429 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: RecruitingEPITHEM

Immune Profiles Evolution Under Immunotherapy for Melanoma

Condition: Melanoma  ·  Sponsor: Assistance Publique - Hôpitaux de Paris

PhaseNA
Planned participants360
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
WhereBoulogne-Billancourt, France

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

The primary objective of the study aims to compare the immune profiles (circulating cytokines and lymphocytes) before and after (6 to 8 weeks) the first infusion of immune checkpoint inhibitors in patients with melanoma treated in the adjuvant setting(cohort A) or in metastatic setting(cohort B); and to study the association of these immune profiles with relapse- or progression-free survival.

This description comes directly from the study's public registry record.

Talk to the study team

Elisa FUNCK-BRENTANO, MD  ·  +33 (0)1 71 16 77 21  ·  elisa.funck-brentano@aphp.fr

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Patient aged ≥ 18 years; * Totally resected stage III or IV melanoma totally resected, treated with a immune therapy (pembrolizumab or nivolumab ou other immune checkpoint inhibitors) as adjuvant treatment; * Unresectable stage IIIC/D or IV metastatic melanoma, treated with immune therapy (pembrolizumab or nivolumab or immune checkpoint inhibitors) which should be associated by a radiotherapy ; * Patient has been informed about the study and signed the consent; * Affiliated to the French social security scheme. Exclusion Criteria: * Pregnant or breastfeeding woman; * Patient refusal; * Patient receiving a immunosuppressor; * Undergo a general corticotherapy of \> 10 mg/kg/day since more than 7 days; * Patient who participate to another blind interventional study receiving blinded treatment; * Patient without any social protection by organization.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (1)

Dermato-oncology department, Ambroise Paré hospital, APHPBoulogne-Billancourt, FranceRecruiting

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

Boulogne-Billancourt

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