Methoden vergelijken

	Fase III Klinische Studie	Fase II Klinische Studie
Vakgebied	Epidemiologie	Epidemiologie
Familie	Process / pipeline	Process / pipeline
Jaar van ontstaan	1962 (Kefauver-Harris Amendment formalised phased drug development)	1960s–1970s (formalised in US federal drug regulation)
Grondlegger	FDA regulatory framework / ICH guidelines	U.S. Food and Drug Administration / ICH E8 guidelines (institutionalised framework)
Type	Confirmatory randomised controlled trial	Interventional clinical study design
Oorspronkelijke bron	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	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
Aliassen	Phase 3 trial, confirmatory trial, pivotal trial, Phase III RCT	Phase 2 trial, Phase II study, early efficacy trial, proof-of-concept trial
Verwant	6	6
Samenvatting	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.	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.