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Efficacy and Safety of Triazavirin Therapy for Coronavirus Disease 2019: A Pilot Randomized Controlled Trial
Xiaoke Wu1,2,3, Kaijiang Yu4, Yongchen Wang5
1College of Pharmacology, Harbin Medical University, Harbin 150001, China.
Abstract:
No therapeutics have been proven effective yet for the treatment of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). To assess the efficacy and safety of Triazavirin therapy for COVID-19, we conducted a randomized, double-blinded controlled trial involving hospitalized adult patients with COVID-19. Participants were enrolled from ten sites, and were randomized into two arms of the study with a ratio of 1:1. Patients were treated with Triazavirin 250 mg versus a placebo three or four times a day for 7 d. The primary outcome was set as the time to clinical improvement, defined as normalization of body temperature, respiratory rate, oxygen saturation, cough, and absorption of pulmonary infection by chest computed tomography (CT) until 28 d after randomization. Secondary outcomes included individual components of the primary outcome, the mean time and proportion of inflammatory absorption in the lung, and the conversion rate to a repeated negative SARS-CoV-2 nucleic acid test of throat swab sampling. Concomitant therapeutic treatments, adverse events, and serious adverse events were recorded. Our study was halted after the recruitment of 52 patients, since the number of new infections in the participating hospitals decreased greatly. We randomized 52 patients for treatment with Triazavirin (n = 26) or a placebo (n = 26). We found no differences in the time to clinical improvement (median, 7 d versus 12 d; risk ratio (RR), 2.0; 95% confidence interval (CI), 0.7-5.6; p = 0.2), with clinical improvement occurring in ten patients in the Triazavirin group and six patients in the placebo group (38.5% versus 23.1%; RR, 2.1; 95% CI, 0.6-7.0; p = 0.2). All components of the primary outcome normalized within 28 d, with the exception of absorption of pulmonary infection (Triazavirin 50.0%, placebo 26.1%). Patients in the Triazavirin group used less frequent concomitant therapies for respiratory, cardiac, renal, hepatic, or coagulation supports. Although no statistically significant evidence was found to indicate that Triazavirin benefits COVID-19 patients, our observations indicated possible benefits from its use to treat COVID-19 due to its antiviral effects. Further study is required for confirmation.
Insights
This study found no significant difference in clinical improvement for COVID-19 patients treated with Triazavirin compared to placebo. However, Triazavirin showed potential antiviral benefits, warranting further investigation for coronavirus disease 2019 treatment.
Area of Science:
- Virology
- Infectious Diseases
- Clinical Trials
Background:
- No definitive therapeutics exist for COVID-19.
- Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes COVID-19.
- Assessing novel antiviral agents is crucial.
Purpose of the Study:
- To evaluate the efficacy and safety of Triazavirin for treating COVID-19.
- To compare Triazavirin therapy against a placebo in hospitalized adult patients.
- To determine the time to clinical improvement and other key outcomes.
Main Methods:
- Randomized, double-blinded, placebo-controlled trial.
- 52 hospitalized adult COVID-19 patients randomized 1:1 to Triazavirin or placebo.
- Primary outcome: time to clinical improvement within 28 days.
Main Results:
- No statistically significant difference in time to clinical improvement between groups (7 vs. 12 days).
- Clinical improvement observed in 38.5% of Triazavirin group vs. 23.1% of placebo group.
- Triazavirin group required less concomitant supportive therapy.
Conclusions:
- Triazavirin did not demonstrate statistically significant benefits for COVID-19 clinical improvement.
- Observed trends suggest potential antiviral effects of Triazavirin.
- Further research is needed to confirm Triazavirin's efficacy in COVID-19 treatment.
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