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A Phase I, Single-center, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety and Tolerability of ILB-202 Administered Intravenously as Single Ascending Doses to Healthy Participants

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A Phase I, Single-center, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety and Tolerability of ILB-202 Administered Intravenously as Single Ascending Doses to Healthy Participants

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 10 Oct 2023

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At a glance

  • Drugs ILB-202 (Primary)
  • Indications Acute kidney injury; Inflammation; Preterm labour; Sepsis
  • Focus Adverse reactions; First in man; Therapeutic Use
  • Sponsors ILIAS Biologics

    • Most Recent Events

    • 07 Sep 2023 Status changed from recruiting to completed.
    • 29 May 2023 Status changed from not yet recruiting to recruiting.
    • 02 May 2023 Status changed from planning to not yet recruiting.

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