Notice: This application will enforce Multi-factor authentication (MFA) for NIH users beginning the evening of Wed Aug 3rd.
NIH | National Cancer Institute | NCI Wiki  

When you specify trial data in CTRP, the system requires you to specify the phase of investigation, as defined by the US FDA for trials involving investigational new drugs. The following table provides a definition of each phase and maps the ClinicalTrials.gov values to the CTRP values:
CTRP Phase ValueClinicalTrials.gov Phase ValueDefinition
Early Phase IEarly Phase 1 (Formerly listed as "Phase 0")Exploratory trials, involving very limited human exposure, with no therapeutic or diagnostic intent (e.g., screening studies, microdose studies). See FDA guidance on exploratory IND studies for more information.
IPhase 1Includes initial studies to determine the metabolism and pharmacologic actions of drugs in humans, the side effects associated with increasing doses, and to gain early evidence of effectiveness; may include healthy participants and/or patients.
I/IIPhase 1/Phase 2Trials that are a combination of phases 1 and 2.
IIPhase 2Includes controlled clinical studies conducted to evaluate the effectiveness of the drug for a particular indication or indications in participants with the disease or condition under study and to determine the common short-term side effects and risks.
II/IIIPhase 2/Phase 3Trials that are a combination of phases 2 and 3.
IIIPhase 3Includes trials conducted after preliminary evidence suggesting effectiveness of the drug has been obtained, and are intended to gather additional information to evaluate the overall benefit-risk relationship of the drug.
IVPhase 4Studies of FDA-approved drugs to delineate additional information including the drug's risks, benefits, and optimal use.
NAN/ATrials without phases (for example, studies of devices or behavioral interventions).

  • No labels