NCT03920228Phase 2, phase 3Completed

Phase 2/3 Study Evaluating the Safety and Efficacy of PTX-022 in Treatment of Adults With 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 completion2020-09-19Actual
Enrollment · participants73Actual
Source updated2024-08-29Last update listed in the registry record
Version history

Changes to this trial

Last 12 months
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