Access to innovation through the national early access program and clinical trials for patients with malignant melanoma.
Claire ChristenLaetitia BelgodèreBernard GuillotCéline JumeauAnnie LorenceGhania Kerouani-LafayeLiora BrunelFlorence TurcryAdrien MonardFrancoise GrudéGaëlle GuyaderLotfi BoudaliNicolas AlbinPublished in: Cancer (2021)
Several tools allow the use of innovative drugs in France, even if they are not yet authorized or used off-label. From December 1, 2017 to September 1, 2019, 45 clinical trials have been authorized for metastatic melanoma, mostly using immunotherapy (63%) and targeted therapy (24%) at an early phase (51%). Since 2010, the national early access program has treated 6538 patients, including 28% under nominative temporary authorizations for use and 72% under cohort temporary authorizations for use. Fourteen drugs are available through nominative temporary authorizations for use, and 5 are available through cohort temporary authorizations for use, and all of these drugs were granted marketing authorization.