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A Phase 1, Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Intravenous CSL730 in Healthy Caucasian and Japanese Subjects

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Trial Profile

A Phase 1, Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Intravenous CSL730 in Healthy Caucasian and Japanese Subjects

Status: Active, no longer recruiting
Phase of Trial: Phase I

Latest Information Update: 14 Oct 2019

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At a glance

  • Drugs M-230 (Primary)
  • Indications Autoimmune disorders; Epidermolysis bullosa; Idiopathic thrombocytopenic purpura
  • Focus Adverse reactions
  • Sponsors CSL Behring

    • Most Recent Events

    • 08 Oct 2019 Planned End Date changed from 22 Sep 2019 to 1 May 2020.
    • 08 Oct 2019 Planned primary completion date changed from 22 Sep 2019 to 1 May 2020.
    • 02 Aug 2019 Status changed from recruiting to active, no longer recruiting.
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