RecruitingPhase 3NCT05078047

Study Comparing the Standard Administration of IO Versus the Same IO Administered Each 3 Months in Patients in Response After 6 Months of Standard IO

Studying MITF-related melanoma and renal cell carcinoma predisposition syndrome

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Key facts

Sponsor
UNICANCER
Principal Investigator
Gwenaëlle GRAVIS-MESCAM, MD
Institut Paoli Calmettes, Marseille
Intervention
Reduced dose intensity of IO(drug)
Enrollment
646 enrolled
Eligibility
18 years · All sexes
Timeline
20222027

Study locations (30)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT05078047 on ClinicalTrials.gov

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