Nivolumab +/- Ipilimumab Immunomonitoring in Metastatic Melanoma

Study Purpose

This is an open bi-centric prospective non-randomized study in patients with metastatic melanoma treated with a first line treatment of Nivolumab +/- Ipilimumab. The aim of the study is to characterize the immune cells modulations under anti-PD-1 +/- anti-CTLA4 and identify the differences between responder and non-responder patients.

Recruitment Criteria

Accepts Healthy Volunteers

Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms

No
Study Type

An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.


An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes.


Searching Both is inclusive of interventional and observational studies.

Interventional
Eligible Ages 18 Years and Over
Gender All
More Inclusion & Exclusion Criteria

Inclusion Criteria:

  • - Men and women aged ≥ 18 years of age.
  • - Patient with metastatic or unresectable melanoma.
  • - Nivolumab or Nivolumab + Ipilimumab treatment indication.
  • - Skin biopsies available.
  • - Patient affiliated to or a beneficiary of a social security category.
  • - Signed Written Informed Consent.
  • - Patient who agrees to the storage of his biological samples.

Exclusion Criteria:

  • - Treated haematological malignancies Subjects with a condition requiring systemic treatment with either corticosteroids or other immunosuppressive medications.
  • - Patients with autoimmune disease.
- Ocular melanoma

Trial Details

Trial ID:

This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.

NCT03225365
Phase

Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans.

Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data.

Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.

Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.

N/A
Lead Sponsor

The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.

Hospices Civils de Lyon
Principal Investigator

The person who is responsible for the scientific and technical direction of the entire clinical study.

N/A
Principal Investigator Affiliation N/A
Agency Class

Category of organization(s) involved as sponsor (and collaborator) supporting the trial.

Other
Overall Status Not yet recruiting
Countries France
Conditions

The disease, disorder, syndrome, illness, or injury that is being studied.

Metastatic Melanoma
Arms & Interventions

Arms

Other: Nivolumab

Previous untreated patient with metastatic melanoma eligible for a Nivolumab treatment. 30 patients will be included in the arm.

Other: Nivolumab + Ipilimumab

Previous untreated patient with metastatic melanoma eligible for a Nivolumab + Ipilimumab treatment. 30 patients will be included in the arm.

Interventions

Biological: - Blood and biopsy sampling

Blood samples (52mL) will be taken at week 1, week 3, week 7, week 13, week 53 or at the progression. Skin biopsies will be taken at week 1, week 7, week 53 or at the progression.

Contact a Trial Team

If you are interested in learning more about this trial, find the trial site nearest to your location and contact the site coordinator via email or phone. We also strongly recommend that you consult with your healthcare provider about the trials that may interest you and refer to our terms of service below.

International Sites

Lyon, France

Status

Address

Plateforme immuno-monitoring, Centre Leon Berard

Lyon, , 69008

Site Contact

Sylvie Dr Négrier

sylvie.negrier@lyon.unicancer.fr

4 78 86 16 79

Pierre-Bénite, France

Status

Address

Service de Dermatologie, Centre Hospitalier Lyon Sud (HCL)

Pierre-Bénite, , 69310

Site Contact

DALLE Stephane

stephane.dalle@chu-lyon.fr

4 78 86 16 79 #+33

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