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Open-label, Non-randomised, Parallel-group Study to Investigate the Pharmacokinetics, Safety and Tolerability Following Single Administration of CHF6001 in Subjects With Mild, Moderate and Severe Liver Impairment in Comparison With Matched Healthy Control Subjects

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Trial Profile

Open-label, Non-randomised, Parallel-group Study to Investigate the Pharmacokinetics, Safety and Tolerability Following Single Administration of CHF6001 in Subjects With Mild, Moderate and Severe Liver Impairment in Comparison With Matched Healthy Control Subjects

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 28 Jun 2024

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At a glance

  • Drugs Tanimilast (Primary)
  • Indications Chronic obstructive pulmonary disease
  • Focus Pharmacokinetics
  • Sponsors Chiesi Farmaceutici SpA

Most Recent Events

  • 22 May 2024 Results assessing systemic exposure and safety of tanimilast in subjects with mild, moderate and severe hepatic impairment ,presented at the 120th International Conference of the American Thoracic Society
  • 15 Jan 2024 Status changed from recruiting to completed.
  • 18 May 2022 New trial record

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