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A Multicenter, Phase 3 Randomized, Double-Blind, Vehicle-controlled Study Evaluating the Safety and Efficacy of QTORIN 3.9% Rapamycin Anhydrous Gel in the Treatment of Pachyonychia Congenita

Trial Profile

A Multicenter, Phase 3 Randomized, Double-Blind, Vehicle-controlled Study Evaluating the Safety and Efficacy of QTORIN 3.9% Rapamycin Anhydrous Gel in the Treatment of Pachyonychia Congenita

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 03 Sep 2024

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At a glance

  • Drugs Sirolimus (Primary)
  • Indications Pachyonychia congenita
  • Focus Registrational; Therapeutic Use
  • Acronyms VAPAUS
  • Sponsors Palvella Therapeutics

Most Recent Events

  • 29 Aug 2024 Status changed from active, no longer recruiting to completed.
  • 20 Jul 2023 According to Palvella media release, the company plans to further analyze and share the Phase 3 VAPAUS study results with key stakeholders, including PC Project, physicians, and scientists.
  • 20 Jul 2023 Primary endpoint has not been met. (Patient Global Assessment of Activities Difficulty Scale)

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