Phase 2/3 Study Evaluating the Safety and Efficacy of PTX-022 in Treatment of Adults With Pachyonychia Congenita
Trial details
- Registry ID
- NCT03920228
- Phase
- Phase 2, Phase 3
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Research sample: selected versions from May 2023 onward plus a preceding baseline where available. Only selected fields were retained; endpoint measures were truncated to 300 characters. This is not complete trial or sponsor history. Daily snapshots begin when collection starts.
NCT06653842 · Palvella Therapeutics, Inc.
Estimated
Actual
Dec 2025
21 Nov 2025
Recruiting
Active not recruiting
NCT06239480 · Palvella Therapeutics, Inc.
Estimated
Actual
40 participants (planned)
51 participants (actual)
Estimated
Actual
Jan 2026
14 Jan 2026
Recruiting
Active not recruiting