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A Phase 1, Randomized, Double-Blind, Placebo-Controlled, SAD/MAD Adaptive-Design Study to Assess the Safety, Tolerability, PK, and PD of RLS-0071 in Healthy Adult Subjects in Support of a COVID-19 Development Program

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A Phase 1, Randomized, Double-Blind, Placebo-Controlled, SAD/MAD Adaptive-Design Study to Assess the Safety, Tolerability, PK, and PD of RLS-0071 in Healthy Adult Subjects in Support of a COVID-19 Development Program

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 01 Jun 2022

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At a glance

  • Drugs RLS 0071 (Primary)
  • Indications Acute lung injury; Brain hypoxia-ischaemia; Brain injuries
  • Focus Adverse reactions; First in man
  • Sponsors ReAlta Life Sciences

    • Most Recent Events

    • 26 Apr 2022 Results presented at the 74th Annual Meeting of the American Academy of Neurology 2022
    • 04 Apr 2022 Results presented in a ReAlta Life Sciences Media Release.
    • 25 Mar 2022 Status changed from recruiting to completed.

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