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Study identifier: NCT05886816 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Mitoquinone/Mitoquinol Mesylate as Oral and Safe Postexposure Prophylaxis for Covid-19

Condition: SARS-CoV Infection · COVID-19  ·  Sponsor: University of Texas Southwestern Medical Center

PhasePhase 2
Planned participants112
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersYes

About this study

Adults who do not have major health, kidney, gastrointestinal disease will be randomized to receive oral mitoquinone/mitoquinol mesylate (Mito-MES) versus placebo to prevent the development and progression of COVID-19 after high-risk exposure to a person with confirmed SARS-CoV-2 infection.

This description comes directly from the study's public registry record.

Talk to the study team

Theodoros Kelesidis, MD, PHD, Msc  ·  214-648-3486  ·  Theodoros.Kelesidis@UTSouthwestern.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Texas Southwestern Medical CenterDallas, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05886816