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Antioxidant
Active Treatment for Coronavirus
Phase 2 & 3
Waitlist Available
Research Sponsored by Adamis Pharmaceuticals Corporation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 7,14 and 21 days from the date randomization/first dosing.
Awards & highlights
Study Summary
This trial will test whether the drug Tempol can help people with COVID-19. The trial is double-blind, meaning that neither the participants nor the researchers will know who is receiving the drug or the placebo.
Eligible Conditions
- Coronavirus
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 7,14 and 21 days from the date randomization/first dosing.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~7,14 and 21 days from the date randomization/first dosing.
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Difference in the rate of sustained clinical resolution1 of symptoms of COVID-19
Secondary outcome measures
Changes in functional status: Post COVID Functional Scale (PCFS)
Efficacy of Tempol on preventing hospitalization: Odds ratio of the rate of hospitalization
Safety of Tempol + SOC vs placebo + SOC: Occurrence of Adverse Events/All cause of mortality
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: Active TreatmentActive Control1 Intervention
Tempol (MMB-02) 800 mg per Day (n=124)
Group II: PlaceboPlacebo Group1 Intervention
Placebo (n=124)
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Who is running the clinical trial?
Adamis Pharmaceuticals CorporationLead Sponsor
3 Previous Clinical Trials
60 Total Patients Enrolled
Ronald B Moss, MDStudy DirectorAdamis Pharmaceutical Corporation
Frequently Asked Questions
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