Favipiravir for the treatment of patients with COVID-19: a systematic review and meta-analysis
- PMID: 34044777
- PMCID: PMC8159019
- DOI: 10.1186/s12879-021-06164-x
Favipiravir for the treatment of patients with COVID-19: a systematic review and meta-analysis
Abstract
Background: Favipiravir possesses high utility for treating patients with COVID-19. However, research examining the efficacy and safety of favipiravir for patients with COVID-19 is limited.
Methods: We conducted a systematic review of published studies reporting the efficacy of favipiravir against COVID-19. Two investigators independently searched PubMed, the Cochrane Database of Systematic Reviews, MedRxiv, and ClinicalTrials.gov (inception to September 2020) to identify eligible studies. A meta-analysis was performed to measure viral clearance and clinical improvement as the primary outcomes.
Results: Among 11 eligible studies, 5 included a comparator group. Comparing to the comparator group, the favipiravir group exhibited significantly better viral clearance on day 7 after the initiation of treatment (odds ratio [OR] = 2.49, 95% confidence interval [CI] = 1.19-5.22), whereas no difference was noted on day 14 (OR = 2.19, 95% CI = 0.69-6.95). Although clinical improvement was significantly better in the favipiravir group on both days 7 and 14, the improvement was better on day 14 (OR = 3.03, 95% CI = 1.17-7.80) than on day 7 (OR = 1.60, 95% CI = 1.03-2.49). The estimated proportions of patients with viral clearance in the favipiravir arm on days 7 and 14 were 65.42 and 88.9%, respectively, versus 43.42 and 78.79%, respectively, in the comparator group. The estimated proportions of patients with clinical improvement on days 7 and 14 in the favipiravir group were 54.33 and 84.63%, respectively, compared with 34.40 and 65.77%, respectively, in the comparator group.
Conclusions: Favipiravir induces viral clearance by 7 days and contributes to clinical improvement within 14 days. The results indicated that favipiravir has strong possibility for treating COVID-19, especially in patients with mild-to-moderate illness. Additional well-designed studies, including examinations of the dose and duration of treatment, are crucial for reaching definitive conclusions.
Keywords: COVID-19; Clinical improvement; Favipiravir; SARS-CoV-2; Viral clearance.
Conflict of interest statement
The authors declare that they have no competing interests.
Figures






Similar articles
-
A Trial of Favipiravir and Hydroxychloroquine combination in Adults Hospitalized with moderate and severe Covid-19: A structured summary of a study protocol for a randomised controlled trial.Trials. 2020 Oct 31;21(1):904. doi: 10.1186/s13063-020-04825-x. Trials. 2020. PMID: 33129363 Free PMC article.
-
The efficacy and safety of Favipiravir in treatment of COVID-19: a systematic review and meta-analysis of clinical trials.Sci Rep. 2021 May 26;11(1):11022. doi: 10.1038/s41598-021-90551-6. Sci Rep. 2021. PMID: 34040117 Free PMC article.
-
The Mechanism and Clinical Outcome of patients with Corona Virus Disease 2019 Whose Nucleic Acid Test has changed from negative to positive, and the therapeutic efficacy of Favipiravir: A structured summary of a study protocol for a randomised controlled trial.Trials. 2020 Jun 5;21(1):488. doi: 10.1186/s13063-020-04430-y. Trials. 2020. PMID: 32503657 Free PMC article.
-
An adaptive randomised placebo controlled phase II trial of antivirals for COVID-19 infection (VIRCO): A structured summary of a study protocol for a randomised controlled trial.Trials. 2020 Oct 13;21(1):847. doi: 10.1186/s13063-020-04766-5. Trials. 2020. PMID: 33050947 Free PMC article. Clinical Trial.
-
Favipiravir versus other antiviral or standard of care for COVID-19 treatment: a rapid systematic review and meta-analysis.Virol J. 2020 Sep 24;17(1):141. doi: 10.1186/s12985-020-01412-z. Virol J. 2020. PMID: 32972430 Free PMC article.
Cited by
-
Basis to Aid Crisis: Favipiravir Oral Solution for Hospital Compounding During COVID-19 Drug Shortage.J Pharm Sci. 2023 Feb;112(2):610-617. doi: 10.1016/j.xphs.2022.10.026. Epub 2022 Nov 2. J Pharm Sci. 2023. PMID: 36334809 Free PMC article.
-
Antivirals and the Potential Benefits of Orally Inhaled Drug Administration in COVID-19 Treatment.J Pharm Sci. 2022 Oct;111(10):2652-2661. doi: 10.1016/j.xphs.2022.06.004. Epub 2022 Jun 9. J Pharm Sci. 2022. PMID: 35691607 Free PMC article. Review.
-
Roles of host mitochondria in the development of COVID-19 pathology: Could mitochondria be a potential therapeutic target?Mol Biomed. 2021 Nov 23;2:38. doi: 10.1186/s43556-021-00060-1. eCollection 2021 Dec. Mol Biomed. 2021. PMID: 34841263 Free PMC article. Review.
-
Review on fluorinated nucleoside/non-nucleoside FDA-approved antiviral drugs.RSC Adv. 2022 Oct 31;12(48):31032-31045. doi: 10.1039/d2ra05370e. eCollection 2022 Oct 27. RSC Adv. 2022. PMID: 36348998 Free PMC article. Review.
-
Pyrazine and Phenazine Heterocycles: Platforms for Total Synthesis and Drug Discovery.Molecules. 2022 Feb 7;27(3):1112. doi: 10.3390/molecules27031112. Molecules. 2022. PMID: 35164376 Free PMC article. Review.
References
-
- Huang C, Wang Y, Li X, Ren L, Zhao J, Hu Y, Zhang L, Fan G, Xu J, Gu X, Cheng Z, Yu T, Xia J, Wei Y, Wu W, Xie X, Yin W, Li H, Liu M, Xiao Y, Gao H, Guo L, Xie J, Wang G, Jiang R, Gao Z, Jin Q, Wang J, Cao B. Clinical features of patients infected with 2019 novel coronavirus in Wuhan. China Lancet. 2020;395(10223):497–506. doi: 10.1016/S0140-6736(20)30183-5. - DOI - PMC - PubMed
-
- World Health Organization. WHO Director-General’s opening remarks at the media briefing on COVID-19 - 11 March 2020. Available at https://www.who.int/dg/speeches/detail/who-director-general-s-opening-re... (Accessed April 5, 2020).
-
- World Health Organization. Weekly epidemiological update-1 December 2020. Available at https://www.who.int/publications/m/item/weekly-epidemiological-update%2D... (Accessed December 5, 2020).
-
- FUJIFILM Toyama Chemical Co., Ltd. Drug Interview form. Avigan® http://fftc.fujifilm.co.jp/med/abigan/pack/pdf/abigan_if_01.pdf. Accessed 5 Apr 2020.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous