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A Phase 1 Single Intravenous Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of ASP5354 in Healthy Adult Japanese Male Participants

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Trial Profile

A Phase 1 Single Intravenous Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of ASP5354 in Healthy Adult Japanese Male Participants

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 13 Oct 2024

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At a glance

  • Drugs Pudexacianinium (Primary)
  • Indications Unspecified
  • Focus Adverse reactions
  • Sponsors Astellas Pharma

    • Most Recent Events

    • 06 Aug 2021 Status changed from recruiting to completed.
    • 21 Jun 2021 Planned End Date changed from 24 Jul 2021 to 22 Jul 2021.
    • 21 Jun 2021 Planned primary completion date changed from 24 Jul 2021 to 22 Jul 2021.

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