COVID-OUT: Early Outpatient Treatment for SARS-CoV-2 Infection (COVID-19)

• Status: Recruiting
• Trial end date: 2021-12-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this trial is to understand whether:

1. Metformin vs fluvoxamine vs ivermectin vs metformin+fluvoxamine vs metformin+ivermectin is superior to placebo in non-hospitalized adults with SARS-CoV-2 disease for preventing Covid-19 disease progression.

2. To understand if the active treatment arms are superior to placebo in improving viral load, serologic markers associated with Covid-19, and gut microbiome in non-hospitalized adults with SARS-CoV-2 infection.

3. To understand if any of the active treatment arms prevent long-covid syndrome, PASC (post-acute sequelae of SARS-CoV-2 infection).

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: University of Minnesota
• Collaborators: Hennepin County Medical Center, Minneapolis; Northwestern University; Olive View-UCLA Education & Research Institute; UnitedHealth Group; University of Colorado, Denver
• Treatments: Fluvoxamine; Ivermectin; Metformin

Criteria

Inclusion Criteria:

• Positive laboratory test for active SARS-CoV-2 viral infection based on local laboratory standard (i.e. +PCR) within 3 days of randomization.

• No known history of confirmed SARS-CoV-2 infection

• BMI >= 25kg/m2 by self-report height/weight or >= 23kg/m2 in patients who self-identify in South Asian or Latinx background.

• Willing and able to comply with study procedures (i.e. swallow pills)

• Has an address and electronic device for communication

• GFR>45ml/min within 2 weeks for patients >75 years old, or with history of heart, kidney, or liver failure.

Exclusion Criteria:

• Hospitalized, for COVID-19 or other reasons.

• Symptom onset greater than 7 days before randomization (symptoms not required for inclusion).

• Immune compromised state (solid organ transplant, bone marrow transplant, AIDS, on high dose steroids)

• Hepatic impairment (Child-Pugh B and C) or other condition that, in the opinion of the investigator, would affect safety

• Inability to obtain informed consent

• Enrollment in another blinded Randomized Controlled Trial for COVID-19

• Already received an effective (FDA approved/EUA*) therapy for COVID-19 (currently monoclonal antibody treatment)

• Alcohol use disorder

• Other unstable medical condition or combination of home medications that in the view of the PI make it unsafe for the individual to participate

• History of severe kidney disease i.e.:

1. Stage 4 or 5 CKD, or Estimated Glomerular Filtration Rate (eGFR) of < 45ml/min/1.73 m2

2. Other kidney disease that in the opinion of the investigator would affect clearance

• Unstable heart failure (Stage 3 or 4 heart failure)

• Allergic reaction to metformin, fluvoxamine, or ivermectin in the past

• Bipolar disease: individuals who report they have bipolar disorder or are taking medication for bipolar disorder (lithium, valproate, high-dose antipsychotic), unless the investigator concludes that the risk for mania is unlikely

• Current loa loa or onchocerciasis infection

• Typhoid, BCG, or cholera vaccination within the 14-days or 3 days after

Medication Exclusions:

• Cimetidine, hydroxychloroquine, insulin, sulfonylurea, dolutegravir, patiromer, ranolazine, tafenoquine.

• Rasagiline, selegiline, or monoamine oxidase inhibitors, linezolid, methadone

• Duloxetine, methylene blue

• Tizanidine, ramelteon, sodium picosulfate

• Alosetron, agomelatine, bromopride, dapoxetine, tamsimelteon, thioridazine, urokinase, pimozide

The following medications may not need to be excluded when dose for that individual is considered alongside the low dose of fluvoxamine being used and other medications being used. The PI or site PI may review and decide if the patient should be excluded from the fluvoxamine arms:

1. Taking SSRIs, SNRIs, or tricyclic antidepressants, unless these are at a low dose such that a study investigator concludes that a clinically significant interaction with fluvoxamine (ie either serotonin syndrome or TCA overdose) is unlikely (examples: participant takes escitalopram but only at 10mg daily; that dose plus 100mg fluvoxamine would be insufficient to cause serotonin syndrome; or, participant takes amitriptyline but only at 25mg nightly; even if fluvoxamine inhibits its metabolism, it would be an insufficient dose to cause QTc prolongation or problematic side effects). Risk Class C, monitor therapy.

2. Individuals who take alprazolam or diazepam and are unwilling to cut the medication by 20% (rationale: fluvoxamine modestly inhibits the metabolism of these drugs). Risk Class C, monitor therapy

3. Participants taking theophylline, clozapine, or olanzapine (drugs with a narrow therapeutic index that are primarily metabolized by CYP 1A2, which is inhibited by fluvoxamine) will be reviewed with a study investigator and excluded unless the investigator concludes that the risk to the participant is low (this would be unlikely; example: participant takes clozapine only as needed and is willing to avoid it for the 14 days of the study).

4. Patients will be advised that there is a small risk that the following substances will be affected by fluvoxamine, but that significant effects are not likely at the low dose being used: caffeine, nicotine, melatonin. Risk Class C, monitor therapy

5. Taking warfarin-also known as Coumadin, NSAIDs, and Aspirin (rationale: increased risk of bleeding), phenytoin (rationale: fluvoxamine inhibits its metabolism), clopidogrel (rationale: fluvoxamine inhibits its metabolism from pro-drug to active drug which raises risk of cardiovascular events), and St John's wort (rationale: fluvoxamine + St John's wort are considered contraindicated because of the risk of serotonin syndrome) Risk C, monitor therapy.