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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 Albin
Published 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.
Keyphrases
  • quality improvement
  • clinical trial
  • end stage renal disease
  • newly diagnosed
  • ejection fraction
  • chronic kidney disease
  • prognostic factors
  • randomized controlled trial
  • open label
  • study protocol