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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: Discontinued
Phase of Trial: Phase I

Latest Information Update: 25 Jun 2020

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At a glance

  • Drugs CSL 730 (Primary)
  • Indications Autoimmune disorders; Epidermolysis bullosa; Idiopathic thrombocytopenic purpura
  • Focus Adverse reactions
  • Sponsors CSL Behring

    • Most Recent Events

    • 22 Jun 2020 Status changed from active, no longer recruiting to discontinued.
    • 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.

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