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A Phase 2a, Proof of Concept, 24-Week, Parallel Group, Double Blind, Vehicle-Controlled Study of the Safety and Efficacy of ARQ-252 Cream 0.3% in Subjects With Non-Segmental Facial Vitiligo

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Trial Profile

A Phase 2a, Proof of Concept, 24-Week, Parallel Group, Double Blind, Vehicle-Controlled Study of the Safety and Efficacy of ARQ-252 Cream 0.3% in Subjects With Non-Segmental Facial Vitiligo

Status: Discontinued
Phase of Trial: Phase II

Latest Information Update: 22 Jul 2024

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At a glance

  • Drugs ARQ 252 (Primary)
  • Indications Vitiligo
  • Focus Proof of concept; Therapeutic Use
  • Sponsors Arcutis Biotherapeutics

    • Most Recent Events

    • 01 Jul 2021 Results published in the Arcutis Biotherapeutics Media Release.
    • 01 Jul 2021 According to an Arcutis Biotherapeutics media release, the company announced its decision to terminate this study based on further analyses of the ARQ-252 drug formulation used in both this vitiligo study and the recently completed Phase 2b study(ARQ-252-205). The study is not being terminated for any safety or tolerability reasons.
    • 01 Jul 2021 Status changed from recruiting to discontinued, according to an Arcutis Biotherapeutics media release.

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