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An Phase I, Open-label, Multi-center, Parallel, Single Oral Dose Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety, and Tolerability of ADC189 in Subjects With Hepatic Impairment (Child-Pugh A and B) Compared With Subjects With Normal Hepatic Function

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Trial Profile

An Phase I, Open-label, Multi-center, Parallel, Single Oral Dose Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety, and Tolerability of ADC189 in Subjects With Hepatic Impairment (Child-Pugh A and B) Compared With Subjects With Normal Hepatic Function

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 22 Jan 2025

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At a glance

  • Drugs ADC 189 (Primary)
  • Indications Influenza virus infections
  • Focus Pharmacokinetics
  • Sponsors Jiaxing AnDiCon Biotech

Most Recent Events

  • 20 Jan 2025 Status changed from recruiting to completed.
  • 15 Jul 2024 New trial record

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