Comparer des méthodes

	Essai clinique de phase II	Essai clinique de phase III
Domaine	Épidémiologie	Épidémiologie
Famille	Process / pipeline	Process / pipeline
Année d'origine	1960s–1970s (formalised in US federal drug regulation)	1962 (Kefauver-Harris Amendment formalised phased drug development)
Auteur d'origine	U.S. Food and Drug Administration / ICH E8 guidelines (institutionalised framework)	FDA regulatory framework / ICH guidelines
Type	Interventional clinical study design	Confirmatory randomised controlled trial
Source fondatrice	Friedman, L. M., Furberg, C. D., DeMets, D. L., Reboussin, D. M., & Granger, C. B. (2015). Fundamentals of Clinical Trials (5th ed.). Springer. ISBN: 978-3319185392	Friedman, L. M., Furberg, C. D., DeMets, D. L., Reboussin, D. M., & Granger, C. B. (2015). Fundamentals of Clinical Trials (5th ed.). Springer. ISBN: 978-3319185385
Alias	Phase 2 trial, Phase II study, early efficacy trial, proof-of-concept trial	Phase 3 trial, confirmatory trial, pivotal trial, Phase III RCT
Apparentées	6	6
Résumé	A Phase II clinical trial is the second stage in the drug or intervention development pipeline, conducted after Phase I safety testing. Its primary goal is to assess whether the intervention shows preliminary efficacy signals in a relevant patient population at the dose established in Phase I, while continuing to characterise the safety and tolerability profile. Phase II trials are generally smaller than Phase III confirmatory trials and serve as critical go/no-go decision points before large-scale investment.	A Phase III clinical trial is a large-scale, confirmatory randomised controlled trial designed to establish the efficacy and safety of an intervention in the target patient population before regulatory submission. It builds on the signal identified in Phase II, tests the intervention at its proposed dose under controlled conditions, and provides the primary evidence base for marketing authorisation or guideline adoption.