RecruitingPhase 2NCT05886816

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

Sponsor

University of Texas Southwestern Medical Center

Enrollment

112 participants

Start Date

Mar 1, 2024

Study Type

INTERVENTIONAL

Conditions

COVID-19 SARS-CoV Infection

Summary

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.

Eligibility

Min Age: 18 YearsMax Age: 65 Years

Inclusion Criteria1

Age 18-65 years old Asymptomatic (no symptoms of viral infection) on study entry High risk exposure without use of masks to confirmed case of COVID-19 Members in a household one of which is a confirmed case of COVID-19 Negative baseline SARS-COV-2 diagnostic test

Exclusion Criteria15

Women with variations in physiological functions due to hormones that may effect immune function and (transgender, pregnant, breastfeeding)
Specific significant clinical diseases \[cardiovascular disease (such as coronary artery/vascular disease), heart disease (such as congestive heart failure, cardiomyopathy, atrial fibrillation), lung disease (such as chronic obstructive pulmonary disease, asthma, bronchiectasis, pulmonary fibrosis, pleural effusions), kidney disease (glomerular filtration rate or GFR less than 60 ml/min/1.73 m2), liver disease (such as cirrhosis, hepatitis), major immunosuppression (such as history of transplantation, uncontrolled HIV infection, cancer on active chemotherapy\] based on history. Participants with well controlled HIV (CD4 count \> 500 cells/mm\^3 and HIV viral load \< 50 copies/ml) and people with remote history of cancer not on active treatment will be allowed to participate.
History of known gastrointestinal disease (such as gastroparesis) that may predispose patients to nausea
History of auto-immune diseases
Chronic viral hepatitis
Use of systemic immunomodulatory medications (e.g. steroids) within 4 weeks of enrollment
Any participant who has received any investigational drug within 30 days of dosing
History of underlying cardiac arrhythmia
History of severe recent cardiac or pulmonary event
A history of a hypersensitivity reaction to any components of the study drug or structurally similar compounds including Coenzyme Q10 and idebenone
Unable to swallow tablets
Use of any investigational products within 4 weeks of enrollment
Any other clinical condition or prior therapy that, in the opinion of the investigator, would make the patient unsuitable for the study or unable to comply with the study requirements.
Eligible for other FDA approved treatment for post-exposure prophylaxis against SARS-CoV-2
Use of Coenzyme Q10 or Vitamin E \< 120 days from enrollment