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trial · primary record

HRS-4642

Drug Interactions

PhasePhase 1
StatusRECRUITING
SponsorUnknown
Enrolment18
Primary completion2026-11
Primary endpointMaximum Observed Plasma Concentration (Cmax) of Total HRS-4642 Following Administration Alone
Registry IDNCT07894679

Provenance

  • Source: ClinicalTrials.gov
  • Fetched at: 2026-10-28T02:32:47.927Z
  • Licence class: attribution-required
  • Verdict: primary-source
  • Entity id: NCT07894679

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HRS-4642 — trial | AEaH