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A Randomized, Double-Blind, Placebo-Controlled Multicenter Study to Evaluate the Safety, Tolerability and Efficacy of ATI-501 Oral Suspension Compared to Placebo in Adult Subjects With Alopecia Areata, Alopecia Universalis or Alopecia Totalis

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Trial Profile

A Randomized, Double-Blind, Placebo-Controlled Multicenter Study to Evaluate the Safety, Tolerability and Efficacy of ATI-501 Oral Suspension Compared to Placebo in Adult Subjects With Alopecia Areata, Alopecia Universalis or Alopecia Totalis

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 16 Sep 2020

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At a glance

  • Drugs ATI 501 (Primary)
  • Indications Alopecia areata
  • Focus Therapeutic Use
  • Sponsors Aclaris Therapeutics

    • Most Recent Events

    • 30 Jul 2019 Results presented in the Aclaris Therapeutics media release.
    • 30 Jul 2019 Primary endpoint (The primary efficacy variable will be the mean change from Baseline in the SALT score at end of study) has been met, according to an Aclaris Therapeutics media release.
    • 01 Jul 2019 Status changed from active, no longer recruiting to completed.
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