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Clinical Trial
. 2022 Nov 30;75(11):1883-1892.
doi: 10.1093/cid/ciac312.

Favipiravir for Treatment of Outpatients With Asymptomatic or Uncomplicated Coronavirus Disease 2019: A Double-Blind, Randomized, Placebo-Controlled, Phase 2 Trial

Marisa Holubar  1 , Aruna Subramanian  1 , Natasha Purington  2 , Haley Hedlin  2 , Bryan Bunning  2 , Katharine S Walter  1 , Hector Bonilla  1 , Athanasia Boumis  3 , Michael Chen  4 , Kimberly Clinton  3 , Liisa Dewhurst  3 , Carol Epstein  5 , Prasanna Jagannathan  1   6 , Richard H Kaszynski  4 , Lori Panu  3 , Julie Parsonnet  1   7 , Elizabeth L Ponder  8 , Orlando Quintero  1 , Elizabeth Sefton  8 , Upinder Singh  1   6 , Luke Soberanis  3 , Henry Truong  9 , Jason R Andrews  1 , Manisha Desai  2 , Chaitan Khosla  8   10 , Yvonne Maldonado  7   11
Affiliations
Clinical Trial

Favipiravir for Treatment of Outpatients With Asymptomatic or Uncomplicated Coronavirus Disease 2019: A Double-Blind, Randomized, Placebo-Controlled, Phase 2 Trial

Marisa Holubar et al. Clin Infect Dis. .

Abstract

Background: Favipiravir, an oral, RNA-dependent RNA polymerase inhibitor, has in vitro activity against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Despite limited data, favipiravir is administered to patients with coronavirus disease 2019 (COVID-19) in several countries.

Methods: We conducted a phase 2, double-blind, randomized controlled outpatient trial of favipiravir in asymptomatic or mildly symptomatic adults with a positive SARS-CoV-2 reverse-transcription polymerase chain reaction assay (RT-PCR) within 72 hours of enrollment. Participants were randomized to receive placebo or favipiravir (1800 mg twice daily [BID] day 1, 800 mg BID days 2-10). The primary outcome was SARS-CoV-2 shedding cessation in a modified intention-to-treat (mITT) cohort of participants with positive enrollment RT-PCRs. Using SARS-CoV-2 amplicon-based sequencing, we assessed favipiravir's impact on mutagenesis.

Results: We randomized 149 participants with 116 included in the mITT cohort. The participants' mean age was 43 years (standard deviation, 12.5 years) and 57 (49%) were women. We found no difference in time to shedding cessation overall (hazard ratio [HR], 0.76 favoring placebo [95% confidence interval {CI}, .48-1.20]) or in subgroups (age, sex, high-risk comorbidities, seropositivity, or symptom duration at enrollment). We detected no difference in time to symptom resolution (initial: HR, 0.84 [95% CI, .54-1.29]; sustained: HR, 0.87 [95% CI, .52-1.45]) and no difference in transition mutation accumulation in the viral genome during treatment.

Conclusions: Our data do not support favipiravir at commonly used doses in outpatients with uncomplicated COVID-19. Further research is needed to ascertain if higher favipiravir doses are effective and safe for patients with COVID-19.

Clinical trials registration: NCT04346628.

Keywords: COVID-19; SARS-CoV-2; clinical trial; favipiravir.

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Conflict of interest statement

Potential conflicts of interest. M. H. reports payment or honoraria for lectures, presentations, speaker’s bureaus, manuscript writing, or educational events from UpToDate. A. S. reports grants from Gilead Sciences, Regeneron Pharma, and Janssen Pharma. H. H. reports salary support from anonymous donors to Stanford University and grant support from the NIH (UL1 TR003142). C. E. reports financial support for the present manuscript from Fujifilm Pharmaceuticals USA (payments made to author’s consulting LLC). P. J. reports research support from anonymous donors to Stanford University to support clinical work. R. H. K. is currently the Chief Medical Officer for AiPharma Global Holdings LLC; is an unpaid consultant to Fujifilm Toyama Chemical Co Ltd and the Anti Viral Drug Development Alliance; and reports support for attending conferences and stock options from AiPharma Global Holdings LLC. J. P. reports grants from Heluna Health (seroepidemiological studies of SARS-CoV-2), Gauss Surgical (testing of an antigen test for SARS-CoV-2) and Ono Pharmaceuticals (clinical trial of Camostat for SARS-CoV-2). J. R. A. reports research support from anonymous donors to Stanford University. C. K. reports licenses from Clear Creek Bio and a patent assigned to Stanford University (“Use of a dihydroorotate dehydrogenase (DHODH) inhibitor in combination with an inhibitor of pyrimidine salvage,” US patent number 10,736,911; 2020). Y. M. reports grants from the NIH (U54 MD010724, U54 MD010724-05S1, R21AI148810, P30AG059307, 000522211-022), Pfizer (C3671008, C4591007), the Bill & Melinda Gates Foundation (OPP1113682), and the Chan Zuckerberg Foundation (12089sc); has received payment or honoraria for lectures, presentations, speaker’s bureaus, manuscript writing, or educational events from the American Academy of Pediatrics for the National Conference; and is on a Pfizer DSMB (non–COVID-19 vaccine trial). All other authors report no potential conflicts of interest. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

Figures

Figure 1.
Figure 1.
Consolidated Standards of Reporting Trials (CONSORT) diagram. Trial schematic showing participants screened, randomized, and followed through study completion. Two of the 3 participants randomized to receive favipiravir withdrew due to nausea and dizziness. Abbreviations: ITT, intention-to-treat; mITT, modified intention-to-treat; RT-PCR, reverse-transcription polymerase chain reaction; smITT, symptomatic modified intention-to-treat.
Figure 2.
Figure 2.
Kaplan-Meier analyses of the primary and key secondary outcomes in the modified intention-to-treat population. Time until shedding cessation of SARS-CoV-2 in RT-PCR from nasal swabs (A), initial symptom resolution (B), and sustained symptom resolution (C), stratified by treatment arm: favipiravir (red) vs placebo (gray). Participants who did not experience the endpoint were censored (+ symbols) at their last positive swab for the primary outcome or at the last completed symptom questionnaire for the key secondary outcomes. Solid lines represent Kaplan-Meier survival probability; shading represents 95% confidence intervals. Abbreviations: CI, confidence interval; HR, hazard ratio; NA, not applicable.
Figure 3.
Figure 3.
Symptom prevalence in the symptomatic modified intention-to-treat (smITT) population. Mirrored bar plots of percentage of smITT participants reporting symptoms by treatment arm and study day, colored by symptom severity. Numerator is the number of participants reporting the symptom severity per study day and treatment arm; denominator is the number of overall participants in the treatment arm (n = 70 in placebo and n = 65 in favipiravir). Symptoms are ordered by day 1 relative frequency within their respective organ systems (lower respiratory, upper respiratory, systemic, gastrointestinal, other). Bars to the right of the centered black line represent favipiravir symptom distributions, while those on the left are representative of placebo.
Figure 4.
Figure 4.
Trajectory of nasal cycle threshold (Ct) in the modified intention-to-treat population. Line plots of nasal Ct values over time by treatment arm. Each dot represents the mean Ct value on that study day by treatment arm; bars represent the standard error around the mean. Lines are slightly jittered to avoid overlap. The red horizontal line at y = 40 represents the limit of detection. The y-axis is reversed so that lower values of Ct represent more virus detected.
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