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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 Subcutaneous CSL730 in Healthy Adult 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 Subcutaneous CSL730 in Healthy Adult Subjects

Status: Discontinued
Phase of Trial: Phase I

Latest Information Update: 02 May 2023

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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

  • 26 Apr 2023 Status changed from recruiting to discontinued.
  • 28 Mar 2023 Planned End Date changed from 1 May 2023 to 1 Dec 2024.
  • 28 Mar 2023 Planned primary completion date changed from 1 May 2023 to 1 Dec 2024.

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