Food and drug administration approval process for dermatology drugs in the United States.

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Food and drug administration approval process for dermatology drugs in the United States.

J Dermatolog Treat. 2018 Jan 05;:1-16

Authors: Boozalis E, Semenov YR, Kwatra SG

Abstract
The process by which dermatology drugs are approved in the United States is not well understood by many clinicians. In general, new dermatology drugs must undergo pre-clinical studies on non-human subjects and three phases of clinical trials in humans before undergoing review by the Food and Drug Administration (FDA). This review process involves an interdisciplinary team of scientists that determines if the drug should be brought to market based on its efficacy, risk-to-benefit ratio, and ability to be labeled. The team that specifically reviews dermatology drugs within the Center for Drug Evaluation and Research (CDER) at the FDA is the Division of Dermatologic and Dental Drug Products. The purpose of this review is to elucidate the steps involved in the FDA's approval of new dermatology drugs. To help illustrate this process, we use examples from the recent approval of dupilumab (REGN668; Regeneron Pharmaceuticals).

PMID: 29304565 [PubMed - as supplied by publisher]

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