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Phases of drug trials: from animals to Phase IV

Walks through the sequence a new drug follows: preclinical animal testing, Phase I (safety), Phase II (does it work, what dose), Phase III (large RCTs), FDA approval, and Phase IV (open-label post-marketing surveillance).

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FDA approval runs from pre-clinical – lab animals – to clinical human trials. Phase I: small numbers (<100) of healthy volunteers, not placebo controlled. Phase II: larger numbers (~200) of volunteers with the to-be-treated disorder, placebo controlled. Phase III: much larger numbers (>1000), placebo controlled. Phase IV occurs after approval and is open-label.

Términos del curso

Las palabras de tu profesor, tal cual aparecen en las diapositivas. Aprende el término y esta definición; la explicación de abajo solo ayuda a entenderla.

Pre-clinical
“Pre-clinical – lab animals”Diapositivas 07, p. 23

Developing the drug, determining therapeutic index, safety, toxicity, primary effects and side effects.

Phase I
“Small numbers (<100) of healthy volunteers to examine effects in humans. Not placebo controlled”Diapositivas 07, p. 23

Is it safe in people?

Phase II
“Larger numbers (~200) of volunteers with to-be-treated disorder to determine efficacy. Placebo controlled”Diapositivas 07, p. 23

Does it work in people who have the disorder?

Phase III
“Much larger numbers (>1000) with broadened sample characteristics, different doses, etc. Placebo controlled”Diapositivas 07, p. 23

Confirms efficacy across a wider range of people and doses.

Phase IV
“Occurs after approval – continued monitoring for safety and efficacy in real world setting. Open-label”Diapositivas 07, p. 23

Where rare and long-term effects show up.

De tu curso: Course slides 07, p. 23 · Midterm study guide: Clinical Trials and Policy · Course slides 05, p. 45 (animal testing)

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