GLS-1027 for the Prevention of Severe Pneumonitis Caused by SARS-CoV-2 Infection (COVID-19)

    Not Recruiting
  • days left to enroll
  • participants needed
  • sponsor
    GeneOne Life Science, Inc.
Updated on 7 July 2022


This clinical trial will evaluate the safety, tolerability and efficacy of GLS-1027 in the prevention of severe pneumonitis caused by SARS-CoV-2 infection


This Phase II randomized, double-blind, placebo-controlled, study will assess 2 different doses of GLS-1027 in the prevention of severe pneumonitis among those hospitalized with PCR confirmed SARS-CoV-2 infection. Subjects will be randomized at a 1:1:1 ratio to either Standard of Care (SOC) plus placebo, or SOC plus GLS-1027 at either 120 mg or 360 mg daily. Clinical status will be monitored through 56 days from the initiation of treatment.

Condition Pneumonitis, SARS-CoV Infection
Treatment Placebo, GLS-1027
Clinical Study IdentifierNCT04590547
SponsorGeneOne Life Science, Inc.
Last Modified on7 July 2022

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