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trial · primary record

KM-023

Pachyonychia Congenita

PhasePhase 2
StatusRECRUITING
SponsorUnknown
Enrolment10
Primary completion2027-11
Primary endpointTo assess the safety of repeated doses of oral KM-023 in individuals with PC.
Registry IDNCT07893483

Provenance

  • Source: ClinicalTrials.gov
  • Fetched at: 2026-10-28T02:31:55.199Z
  • Licence class: attribution-required
  • Verdict: primary-source
  • Entity id: NCT07893483

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KM-023 — trial | AEaH