Favipiravir

drug
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Also known as AviganT-705Favipiravir

Summary

Favipiravir (CHEMBL221722) is an approved small-molecule antiviral drug (ATC J05AX27); indicated across 9 conditions including viral infectious disease and influenza.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: J05AX27
  • Indications: 9 conditions
  • Clinical trials: 61
  • Chemistry: 157.1 Da · C5H4FN3O2

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL221722
NameFavipiravir
TypeSmall molecule
Max phase4
FDA approvedno
PubChem CID492405
ChEBICHEBI:134722
ATCJ05AX27
Molecular formulaC5H4FN3O2
Molecular weight157.1
InChIKeyZCGNOVWYSGBHAU-UHFFFAOYSA-N

SMILES: C1=C(N=C(C(=O)N1)C(=O)N)F

IUPAC name: 5-fluoro-2-oxo-1H-pyrazine-3-carboxamide

ChEBI definition: A member of the class of pyrazines that is pyrazine substituted by aminocarbonyl, hydroxy and fluoro groups at positions 2, 3 and 6, respectively. It is an anti-viral agent that inhibits RNA-dependent RNA polymerase of several RNA viruses and is approved for the treatment of influenza in Japan.

Pharmacological roles (ChEBI): antiviral drug, anticoronaviral agent, EC 2.7.7.48 (RNA-directed RNA polymerase) inhibitor.

Also known as: Avigan, Favipiravir, T-705, FAVIPIRAVIR, favipiravir, Favipiravir; Avigan

Patent coverage: 1,957 distinct patent families (4,309 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 3,609 (84%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 1 (assay-derived). Sample: RNA-directed RNA polymerase.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

9 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
viral infectious disease3MONDO:0005108EFO:0000763
influenza3MONDO:0005812EFO:0007328
severe acute respiratory syndrome3MONDO:0005091EFO:0000694
Ebola hemorrhagic fever2MONDO:0005737EFO:0007243
Lassa fever2MONDO:0005820EFO:0007338
liver disorder1MONDO:0005154EFO:0001421
viral pneumonia1MONDO:0006012EFO:0007541
infectious disease1MONDO:0005550EFO:0005741

1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 61.

Phase distribution

PhaseTrials
PHASE321
PHASE218
PHASE2/PHASE37
Not specified6
PHASE1/PHASE24
PHASE13
PHASE42

Top trials by phase / activity

NCTPhaseStatusTitle
NCT04359615PHASE4UNKNOWNFavipiravir in Hospitalized COVID-19 Patients
NCT05502081PHASE4COMPLETEDClinical Study to Compare Efficacy and Safety of Casirivimab and Imdevimab Combination, Remdesivir and Favipravir in Hospitalized COVID-19 Patients
NCT06212336PHASE2/PHASE3RECRUITINGISTH/ANRS 0409s INTEGRATE Lassa Fever Study
NCT02008344PHASE3COMPLETEDPhase 3 Efficacy and Safety Study of Favipiravir for Treatment of Uncomplicated Influenza in Adults
NCT02026349PHASE3COMPLETEDPhase 3 Efficacy and Safety Study of Favipiravir for Treatment of Uncomplicated Influenza in Adults - T705US316
NCT04319900PHASE2/PHASE3UNKNOWNClinical Trial of Favipiravir Tablets Combine With Chloroquine Phosphate in the Treatment of Novel Coronavirus Pneumonia
NCT04336904PHASE3UNKNOWNClinical Study To Evaluate The Performance And Safety Of Favipiravir in COVID-19
NCT04349241PHASE3COMPLETEDEfficacy and Safety of Favipiravir in Management of COVID-19
NCT04351295PHASE2/PHASE3COMPLETEDEfficacy of Faviprevir in COVID-19 Treatment
NCT04373733PHASE3COMPLETEDEarly Intervention in COVID-19: Favipiravir Verses Standard Care
NCT04402203PHASE2/PHASE3UNKNOWNStudy on Safety and Efficacy of Favipiravir (Favipira) for COVID-19 Patient in Selected Hospitals of Bangladesh
NCT04425460PHASE3UNKNOWNA Multi-center,Randomized,Double-blind,Placebo-controlled,Phase 3 Study Evaluating Favipiravir in Treatment of COVID19
NCT04434248PHASE2/PHASE3UNKNOWNAn Adaptive Study of Favipiravir Compared to Standard of Care in Hospitalized Patients With COVID-19
NCT04464408PHASE2/PHASE3COMPLETEDFavipiravir Therapy in Adults With Mild COVID-19
NCT04501783PHASE3COMPLETEDStudy of Efficacy and Safety of TL-FVP-t vs. SOC in Patients With Mild to Moderate COVID-19
NCT04529499PHASE3TERMINATEDClinical Trial Evaluating the Efficacy and Safety of Favipiravir in Moderate to Severe COVID-19 Patients
NCT04542694PHASE3COMPLETEDStudy of Favipiravir Compared to Standard of Care in Hospitalized Patients With COVID-19
NCT04558463PHASE3UNKNOWNThe Effectivity and Safety of Favipiravir Compared to Oseltamivir as Adjuvant Therapy for COVID-19
NCT04600895PHASE3COMPLETEDThe Prevent Severe COVID-19 (PRESECO) Study
NCT04600999PHASE3COMPLETEDClinical Trial of Favipiravir Treatment of Patients With COVID-19
NCT04613271PHASE3COMPLETEDEfficacy and Safety of Favipiravir in Covid-19 Patients in Indonesia
NCT04694612PHASE3UNKNOWNEfficacy of Favipiravir in Treatment of Mild & Moderate COVID-19 Infection in Nepal
NCT04784559PHASE3TERMINATEDTrial to Determine the Efficacy/Safety of Plitidepsin vs Control in Patients With Moderate COVID-19 Infection
NCT04818320PHASE3COMPLETEDFavipiravir in High-risk COVID-19 Patients
NCT04828564PHASE2/PHASE3UNKNOWNEfficacy and Safety of Favipiravir and Ribavirin Formulation for Treatment of COVID-19
NCT04981379PHASE3COMPLETEDClinical Trial For Early SARS-CoV-2 (COVID-19) Treatment
NCT05014373PHASE3UNKNOWNPhilippine Trial to Determine Efficacy and Safety of Favipiravir for COVID-19
NCT05185284PHASE3COMPLETEDRandomized Multicenter Study on the Efficacy and Safety of Favipiravir for Parenteral Administration Compared to Standard of Care in Hospitalized Patients With COVID-19
NCT05279235PHASE3TERMINATEDEfficacy and Safety of JT001 (VV116) Compared With Favipiravir
NCT05417997PHASE3COMPLETEDEffect of Kunamin in SARS-CoV-2 RT-PCR Positive Covid-19 Patients
NCT04746183PHASE1/PHASE2RECRUITINGAGILE (Early Phase Platform Trial for COVID-19)
NCT05041907PHASE2RECRUITINGFinding Treatments for COVID-19: A Trial of Antiviral Pharmacodynamics in Early Symptomatic COVID-19 (PLATCOV)
NCT05648448PHASE2RECRUITINGA Phase 2 Trial Comparing Antiviral Treatments in Early Symptomatic Influenza
NCT06488300PHASE2RECRUITINGAssessing Antiviral Treatments in Early Symptomatic RSV
NCT06860334PHASE2NOT_YET_RECRUITINGUMIT-2 - Adaptive Phase IIb Platform Trial to Determine the Efficacy and Safety of Therapeutics for CCHF
NCT01068912PHASE2COMPLETEDDose-Finding Study of Favipiravir in the Treatment of Uncomplicated Influenza
NCT01728753PHASE1/PHASE2COMPLETEDT-705a Multicenter Study in Adults Subjects With Uncomplicated Influenza
NCT02329054PHASE2COMPLETEDEfficacy of Favipiravir Against Ebola (JIKI)
NCT02662855PHASE2COMPLETEDEfficacy of Favipiravir Against Severe Ebola Virus Disease
NCT02739477PHASE2TERMINATEDTolerance and Activity Evaluation of High Doses of Favipiravir Against Ebola Virus in the Semen

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).