NCT05180708Phase 3Completed

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

Study sponsor: Palvella Therapeutics, Inc. · PVLA

Compare the available registry edits below. Primary completion is the date data collection ends for the main study measures; it does not tell you when results will be published.

Primary completion2023-06-30Actual
Enrollment · participants87Actual
Source updated2024-08-29Last update listed in the registry record
Version history

Changes to this trial

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