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A Phase I, Parallel-group, Multi-center, Open-label, Investigation of the Pharmacokinetics, Safety and Tolerability of a Single Subcutaneous Injection of Cotadutide in Participants With Mild, Moderate or Severe Hepatic Impairment Compared to Participants With Normal Hepatic Function

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A Phase I, Parallel-group, Multi-center, Open-label, Investigation of the Pharmacokinetics, Safety and Tolerability of a Single Subcutaneous Injection of Cotadutide in Participants With Mild, Moderate or Severe Hepatic Impairment Compared to Participants With Normal Hepatic Function

Status: Discontinued
Phase of Trial: Phase I

Latest Information Update: 27 Mar 2023

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At a glance

  • Drugs Cotadutide (Primary)
  • Indications Non-alcoholic fatty liver disease; Non-alcoholic steatohepatitis; Obesity; Type 2 diabetes mellitus
  • Focus Pharmacokinetics
  • Sponsors AstraZeneca

    • Most Recent Events

    • 17 Mar 2023 Status changed from recruiting to discontinued. Discontinuing the development of cotadutide, a daily injectable GLP-1/glucagon co-agonist, is based on strategic pipeline considerations.The premature closure is not due to any newly observed safety signals or a change in therisk/benefit profile.
    • 17 Feb 2023 Planned End Date changed from 29 Mar 2023 to 26 Jun 2023.
    • 17 Feb 2023 Planned primary completion date changed from 29 Mar 2023 to 26 Jun 2023.

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