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A Phase 1, Subjects- and Investigator-Blinded, Sponsor-Unblinded, Placebo-Controlled, Randomized, Sequential Cohort Study to Assess the Safety and Pharmacokinetics of Single Ascending Subcutaneous and Intravenous Doses of DS-2325a in Healthy Subjects

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Trial Profile

A Phase 1, Subjects- and Investigator-Blinded, Sponsor-Unblinded, Placebo-Controlled, Randomized, Sequential Cohort Study to Assess the Safety and Pharmacokinetics of Single Ascending Subcutaneous and Intravenous Doses of DS-2325a in Healthy Subjects

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 21 Feb 2024

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At a glance

  • Drugs DS-2325a (Primary) ; DS-2325a (Primary)
  • Indications Netherton Syndrome
  • Focus Adverse reactions; First in man
  • Sponsors Daiichi Sankyo Inc

Most Recent Events

  • 02 Mar 2023 Status changed from recruiting to completed.
  • 28 Jun 2022 Status changed from not yet recruiting to recruiting.
  • 30 May 2022 New trial record

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