Mitoquinone/Mitoquinol Mesylate as Oral and Safe Postexposure Prophylaxis for Covid-19
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Mitoquinone/mitoquinol mesylate, Placebo.
- Who it may be relevant to
- Registry conditions: SARS-CoV Infection, COVID-19. Basic parameters: 18 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
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.
Detailed description
The overall goal of the study is to determine the efficacy of the treatment with mito-MES 20 mg daily versus placebo for 14 days to prevent confirmed SARS-CoV-2 infection in high-risk close contacts of confirmed COVID-19 cases. Primary measure will be confirmed COVID-19 infection based on a diagnostic test within 14 days after exposure. Secondary measures of efficacy will be symptomatic viral infection, hospitalization, respiratory failure requiring ventilatory support attributable to COVID-19 disease, mortality. The secondary objective is to determine the safety of mito-MES for 14 days as post-exposure prophylaxis against SARS-CoV-2 in healthy adults.
Interventions
- Drug Mitoquinone/mitoquinol mesylate
Mitochondrial antioxidant - Other Placebo
Placebo pills
Primary outcome measures
- SARS-CoV-2 infection [Time frame: Within 14 days after exposure to SARS-CoV-2]
Secondary outcome measures (4)
- Safety of mito-MES [Time frame: Within 14 days since initiation of the pills]
- Symptomatic SARS-CoV-2 infection [Time frame: Within 14 days after exposure to SARS-CoV-2]
- Severity of symptoms of SARS-CoV-2 infection [Time frame: Within 14 days after exposure to SARS-CoV-2]
- Duration of symptoms of SARS-CoV-2 infection [Time frame: Within 14 days after exposure to SARS-CoV-2]
Eligibility criteria
Inclusion criteria
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 criteria
- 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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Single group
- Masking
- Triple blind
- Primary purpose
- Treatment
Study locations
United States · 1 center
- University of Texas Southwestern Medical Center — Dallas
Identifiers
NCT: NCT05886816 · STU-2023-0524