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Clinical Trial Summary

The main objective of this project is to perform a longitudinal monitoring of BRAF and NRAS cell-free DNA in a large cohort of metastatic melanomas patients before treatment and during the follow-up. Results will be compared with clinical data as imaging (based on RECIST criteria) and the activity of lactate dehydrogenase in serum (LDH).


Clinical Trial Description

During a consultation of follow-up for an advanced malignant melanoma (stage IIIb or IIIC or IV), an investigator presents the study to the patient and give him the note of information and the informed consent.

The patient can benefit from a reflexion period of of 7 days.

In case of agreement, a first blood draw will take place before initiation of any treatment. Between D15 and D30 a second blood draw will be taken. Then a blood draw will be necessary every two months until recurrence or progression of the disease for a maximum of 22 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03493230
Study type Interventional
Source Centre Hospitalier Universitaire de Nice
Contact Elodie LONG-MIRA, MD
Phone 04 92 03 88 55
Email long-mira.e@chu-nice.fr
Status Not yet recruiting
Phase N/A
Start date April 2018
Completion date December 2022

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