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

Emily Boozalis, Yevgeniy R. Semenov, Shawn Kwatra

Research output: Contribution to journalArticlepeer-review

Abstract

Aim: The purpose of this review is to elucidate the steps involved in the FDA’s approval of new dermatology drugs. Methods: To help illustrate the process of drug approval, we use examples from the recent approval of dupilumab (REGN668; Regeneron Pharmaceuticals). Results: 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. Conclusions: The drug development process is enhanced by clinician input during all stages of development.

Original languageEnglish (US)
Pages (from-to)536-538
Number of pages3
JournalJournal of Dermatological Treatment
Volume29
Issue number6
DOIs
StatePublished - Aug 18 2018

Keywords

  • approval
  • dermatology
  • drugs
  • Food and Drug Administration
  • process
  • therapies
  • treatments

ASJC Scopus subject areas

  • Dermatology

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