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Single-Ascending Dose Phase 1 Study to Assess the Safety, Tolerability, and Pharmacokinetics of DS-6016a After Subcutaneous Injection in Healthy Japanese Subjects

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Trial Profile

Single-Ascending Dose Phase 1 Study to Assess the Safety, Tolerability, and Pharmacokinetics of DS-6016a After Subcutaneous Injection in Healthy Japanese Subjects

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 10 Oct 2024

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At a glance

  • Drugs DS-6016 (Primary)
  • Indications Fibrodysplasia ossificans progressiva
  • Focus Adverse reactions
  • Sponsors Daiichi Sankyo Company

Most Recent Events

  • 02 Aug 2022 Status changed from active, no longer recruiting to completed.
  • 02 Nov 2021 Status changed from recruiting to active, no longer recruiting.
  • 20 Apr 2021 Status changed from not yet recruiting to recruiting.

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