Study Objective: To test if early preemptive hydroxychloroquine therapy can prevent disease progression in persons with known symptomatic COVID-19 disease, decreasing hospitalizations and symptom severity.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a rapidly emerging viral
infection causing COVID19. Therapy is generally not given to persons who are not
hospitalized.
Hydroxychloroquine may have antiviral effects against SARS-CoV2 which may decrease disease
severity when given early. This trial will use a modification of standard malaria dosing of
hydroxychloroquine to provide preemptive therapy for those with early symptoms.
This study is a continuation of NCT04308668 which looked at post-exposure prophylaxis (now
closed) and early treatment in the USA (now closed, data to be pooled) and Canada (which
continues in this study). On April 28, 2020 NCT04308668 changed its primary outcome to
symptomatic improvement in the preemptive therapy arm. This study continues enrollment for
the primary ordinal outcome of hospitalization; hospitalization with intensive care stay; or
death.
People in the participating Canadian provinces can help answer this critically important
question. No in-person visits are needed.
The doses of hydroxychloroquine being used have been approved by Health Canada.
This trial is targeting the following groups of people:
If you are symptomatic with a positive COVID-19 test within the first 4 days of symptoms and
are not hospitalized; OR If you have had occupational exposure with known exposure to someone
with lab-confirmed COVID-19 within the last 14 days AND have compatible symptoms starting
within the last 4 days;
You may participate if you live anywhere in the Canadian Provinces of Quebec, Manitoba,
Alberta, British Columbia, Newfoundland or Ontario.
For information on how to participate in the research trial, go to:
Drug: Hydroxychloroquine
200mg tablet; 800 mg orally once, followed in 6 to 8 hours by 600 mg, then 600mg once a day for 4 consecutive days
Drug: Placebo oral tablet
4 placebo tablets once, followed in 6 to 8 hours by 3 tablets, then 3 tablets once-a-day for 4 consecutive days
Inclusion Criteria:
Age 18 years of age or older AND provision of informed consent
WITH
Symptomatic COVID-19 disease with confirmed diagnosis with PCR+ SARS-CoV-2 within <= 4 days
of symptoms
OR
Healthcare worker with compatible symptoms with exposure to known PCR+ case <= 14 days (and
no available/pending testing for the individual).
Exclusion Criteria:
- Current hospitalization
- Allergy to chloroquine or hydroxychloroquine
- Severe diarrhea and/or vomiting
- Significant hepatic impairment defined as known cirrhosis with history of hepatic
encephalopathy or ascites.
- Prior retinal eye disease
- Concurrent malignancy requiring chemotherapy
- Known Chronic Kidney disease, Stage 4 or 5 or dialysis.
- Known glucose-6 phosphate dehydrogenase (G6PD) deficiency.
- Known ventricular arrythmia, known prolonged QTc interval, or any known episode of
sudden cardiac death
- Known Porphyria
- Weight <40 kg
- Known Pregnancy of Breastfeeding
- Current use of chloroquine or hydroxychloroquine
- Current use of Artemether, Dapsone, Lumefantrine or Mefloquine
- Current use of Cardiac medicines: amiodarone, digoxin, dofetilide, flecainide,
procainamide, sotalol, or propafenone
- Current use of the following antimicrobials: levofloxacin, ciprofloxacin,
moxifloxacin, azithromycin, clarithromycin, erythromycin, ketoconazole, or
itraconazole
- Current use of the following antidepressants: amitriptyline, citalopram, desipramine,
escitalopram, imipramine, doxepin, fluoxetine, sertraline, bupropion (Wellbutrin), or
venlafaxine
- Current use of the following antipsychotic or mood stabilizers: haloperidol,
droperidol, lithium, quetiapine, thioridazine, ziprasidone
- Current use of methadone
- Current use of Sumatriptan, Zolmitriptan other than "as needed"
- Current use of systemic chemotherapy
University of Minnesota
Minneapolis, Minnesota, United States
University of Alberta
Edmonton, Alberta, Canada
University of British Columbia
Vancouver, British Columbia, Canada
University of Manitoba
Winnipeg, Manitoba, Canada
Eastern Health
Saint John's, Newfoundland and Labrador, Canada
McMaster University
Hamilton, Ontario, Canada
Lawson Health Research Institute
London, Ontario, Canada
Research Institute of the McGill University Health Centre
Montréal, Quebec, Canada
Todd C Lee, MD MPH FIDSA, Principal Investigator
Research Institute of the McGill University Health Centre