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A Phase 1 and 2 Randomized, Double-Blind, Vehicle-Controlled, Parallel-Group Study to Evaluate the Safety, Tolerability, Efficacy, and Exposure of up to 12 Weeks of XPF-005 Treatment in Healthy Volunteers and Subjects With Acne Vulgaris

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A Phase 1 and 2 Randomized, Double-Blind, Vehicle-Controlled, Parallel-Group Study to Evaluate the Safety, Tolerability, Efficacy, and Exposure of up to 12 Weeks of XPF-005 Treatment in Healthy Volunteers and Subjects With Acne Vulgaris

Status: Completed
Phase of Trial: Phase I/II

Latest Information Update: 29 Jan 2019

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At a glance

  • Drugs XEN 801 (Primary)
  • Indications Acne vulgaris
  • Focus Therapeutic Use
  • Sponsors Xenon Pharmaceuticals

    • Most Recent Events

    • 27 Jun 2017 Status changed from active, no longer recruiting to completed.
    • 24 Mar 2017 Results published in the Xenon Pharmaceuticals Media Release
    • 24 Mar 2017 Primary endpoint has not been met. (Change from Baseline in acne lesion count), as reported in a Xenon Pharmaceuticals media release.

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