ClinicalTrials.Veeva

Menu

Personalized Circulating DNA Follow-up in Melanoma (PERCIMEL)

I

Institut de Cancérologie de Lorraine

Status

Enrolling

Conditions

Melanoma

Treatments

Procedure: Personalized Circulating DNA follow-up

Study type

Interventional

Funder types

Other

Identifiers

NCT04866680
2022-A01904-39

Details and patient eligibility

About

PERCIMEL is an open multicentric study. The purpose of this study is to assess the interest of molecular analysis on circulating tumor DNA in the follow-up of the disease.

Enrollment

165 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • locally advanced, operable melanoma
  • treated by immunotherapy or anti-BRAF and anti-MEK targeted therapies (stage IIIb, IIIc) or exclusive immunotherapy (stage IV) in an adjuvant situation.

Exclusion criteria

  • second cancer
  • woman who is pregnant, likely to be pregnant or breastfeeding

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

165 participants in 1 patient group

Personalized Circulating DNA follow-up
Experimental group
Description:
FFPE tissue sample + blood sample (20ml)
Treatment:
Procedure: Personalized Circulating DNA follow-up

Trial contacts and locations

8

Loading...

Central trial contact

MERLIN JEAN-LOUIS, PharmD, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems