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Purpose

In this trial patients will be treated with either a combination of therapies to treat COVID-19 or a placebo. Treatment will last 10 days, and patients will be followed for 6 months.

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  1. Signed informed consent, demonstrating that the subject understands the procedures required for the study and the purpose of the study 2. Healthy male or female subjects at least 18 years of age 3. Diabetic and obese (BMI > 30) patients will be included in the Trial but randomization will be stratified. 4. Positive test for COVID-19 by RT-PCR or rapid antigen test at screening 5. Subjects must agree to practice at least two highly effective methods of birth control for the duration of the study. One of these must be a barrier method. Exceptions for females and partners of females that are not of childbearing potential. (e.g. surgically sterilized, post-menopausal) 6. Subjects must agree they will attend the treatment facility daily for 10d in the event of failure to attend, the patient will be visited at their home to collect the nasal swab and review data.

Exclusion Criteria

  1. Refusal to sign informed consent form 2. Negative test for COVID-19 by RT-PCR at screening 3. Severe disease symptomatically including pneumonia, respiratory distress, tachypnea, shortness of breath, temperature > 104.0 degrees F, pleuritic pain, or frequent cough. 4. Known drug allergy to any of the investigational medications 5. Currently taking medication with known drug interactions with investigational medications, found in Appendix II 6. Prescription or other antiviral medications 7. Any comorbidities which constitute health risk for the subject including known cardiac arrhythmias - but will be limited to those on hydroxychloroquine 8. Inability to attend daily for 10 days

Study Design

Phase
Phase 1
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Active Arm 		Patients will be treated with a combination of Ivermectin, Doxycycline, Zinc, Vitamin D3 and Vitamin C
  • Drug: Ivermectin
    Treatment days 1, 4, and 8
    Other names:
    • Soolantra, Stromectol, Sklice
  • Drug: Doxycycline Hcl
    10 day treatment
    Other names:
    • Doxy-100, Monodox, Oracea, Targadox, Acticlate, Morgidox, Avidoxy, Doryx MPC, Mondoxyne NL, Dory
  • Dietary Supplement: Zinc
    10 Day treatment
    Other names:
    • Zinc sulphate
  • Dietary Supplement: Vitamin D3
    10 day treatment
    Other names:
    • cholecalciferol-D3
  • Dietary Supplement: Vitamin C
    10 day treatment
    Other names:
    • L-ascorbic acid
Placebo Comparator
Placebo 		Placebo and Vitamin D3, Vitamin C, and Zinc
  • Dietary Supplement: Zinc
    10 Day treatment
    Other names:
    • Zinc sulphate
  • Dietary Supplement: Vitamin D3
    10 day treatment
    Other names:
    • cholecalciferol-D3
  • Dietary Supplement: Vitamin C
    10 day treatment
    Other names:
    • L-ascorbic acid

Recruiting Locations

More Details

NCT ID
NCT04482686
Status
Completed
Sponsor
ProgenaBiome

Detailed Description

Patients in this trial will undergo treatment for 10 days with either a combination of therapies or placebo. They will then be followed for an additional 20 days.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.