Phase 3 trial of coronavir (favipiravir) in patients with mild to moderate COVID-19
American Journal of Translational Research
; 13(11):12575-12587, 2021.
Article
in English
| EMBASE | ID: covidwho-1567690
ABSTRACT
Favipiravir has demonstrated efficacy against the SARS-CoV-2 virus in several preliminary studies. This study aimed to evaluate the efficacy and safety of favipiravir for treatment of mild to moderate COVID-19 in outpatients and hospitalized patients. We conducted an open-label, randomized, active-controlled trial of a generic form of favipiravir in patients with COVID-19 confirmed by PCR-test. Eligible patients (18-60 years) after stratification were randomly assigned (in a 21 ratio) to receive either favipiravir (1800 mg BID on day 1, followed by 800 mg BID for up to 9 days), or standard of care (SOC) treatment (umifenovir + intranasal interferon alpha-2b, or hydroxychloroquine) for up to 10 days. The co-primary outcomes were the time to clinical improvement and the time to viral clearance. Among 190 patients assessed for eligibility 168 were randomized to favipiravir (n=112) or to SOC (n=56) group. The median time to clinical improvement was 6.0 days (IQR 4.0;9.3) in the favipiravir group and 10.0 (IQR 5.0;21.0) days in the SOC group;the median difference was 4 days (HR 1.63;95% CI 1.14-2.34;P=0.007). The statistically significant difference in the median time to viral clearance was observed only for hospitalized patients 3.0 (IQR 3.0;3.0) days in the favipiravir group vs. 5.0 (IQR 4.5;5.5) days in the SOC group (HR 2.11;95% CI 1.04-4.31;P=0.038). The rate of viral elimination on Day 5 in the favipiravir group was significantly higher than in SOC group 81.2% vs. 67.9% (RR 1.22;05% CI 1.00-1.48;P=0.022). The rate of clinical improvement on Day 7 in the favipiravir group was 1.5-fold higher than in SOC group 52.7% vs. 35.8% (RR 1.50;95% CI 1.02-2.22;P=0.020). Favipiravir was well-tolerated and the most common adverse reactions were asymptomatic hyperuricemia, transient elevation of ALT & AST, and mild gastrointestinal disorders. Favipiravir was superior to the SOC in shortening the time to clinical improvement in patients with mild to moderate COVID-19.
NCT04501783; alanine, aminotransferase; albinterferon, alpha2b; antibiotic, agent; anticoagulant, agent; antipyretic, agent; aspartate, aminotransferase; creatine, kinase; favipiravir; hydroxychloroquine; umifenovir; vasoconstrictor, agent; abdominal, pain; abnormally, high, substrate, concentration, in, blood; adult; article; artificial, ventilation; clinical, outcome; computer, assisted, tomography; controlled, study; coronavirus, disease, 2019; diarrhea; disease, severity; drug, efficacy; drug, safety; drug, withdrawal; epigastric, pain; female; follow, up; fracture; hospitalization; human; hyperglycemia; hypertransaminasemia; hyperuricemia; loading, drug, dose; major, clinical, study; male; nasopharyngeal, swab; nausea; noninvasive, ventilation; oxygen, saturation; platelet, count; pneumonia; polymerase, chain, reaction; randomized, controlled, trial; telemedicine; viral, clearance
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Collection:
Databases of international organizations
Database:
EMBASE
Type of study:
Randomized controlled trials
Language:
English
Journal:
American Journal of Translational Research
Year:
2021
Document Type:
Article
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