Favipiravir
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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
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL221722 |
| Name | Favipiravir |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 492405 |
| ChEBI | CHEBI:134722 |
| ATC | J05AX27 |
| Molecular formula | C5H4FN3O2 |
| Molecular weight | 157.1 |
| InChIKey | ZCGNOVWYSGBHAU-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).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| viral infectious disease | 3 | MONDO:0005108 | EFO:0000763 |
| influenza | 3 | MONDO:0005812 | EFO:0007328 |
| severe acute respiratory syndrome | 3 | MONDO:0005091 | EFO:0000694 |
| Ebola hemorrhagic fever | 2 | MONDO:0005737 | EFO:0007243 |
| Lassa fever | 2 | MONDO:0005820 | EFO:0007338 |
| liver disorder | 1 | MONDO:0005154 | EFO:0001421 |
| viral pneumonia | 1 | MONDO:0006012 | EFO:0007541 |
| infectious disease | 1 | MONDO:0005550 | EFO: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
| Phase | Trials |
|---|---|
| PHASE3 | 21 |
| PHASE2 | 18 |
| PHASE2/PHASE3 | 7 |
| Not specified | 6 |
| PHASE1/PHASE2 | 4 |
| PHASE1 | 3 |
| PHASE4 | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT04359615 | PHASE4 | UNKNOWN | Favipiravir in Hospitalized COVID-19 Patients |
| NCT05502081 | PHASE4 | COMPLETED | Clinical Study to Compare Efficacy and Safety of Casirivimab and Imdevimab Combination, Remdesivir and Favipravir in Hospitalized COVID-19 Patients |
| NCT06212336 | PHASE2/PHASE3 | RECRUITING | ISTH/ANRS 0409s INTEGRATE Lassa Fever Study |
| NCT02008344 | PHASE3 | COMPLETED | Phase 3 Efficacy and Safety Study of Favipiravir for Treatment of Uncomplicated Influenza in Adults |
| NCT02026349 | PHASE3 | COMPLETED | Phase 3 Efficacy and Safety Study of Favipiravir for Treatment of Uncomplicated Influenza in Adults - T705US316 |
| NCT04319900 | PHASE2/PHASE3 | UNKNOWN | Clinical Trial of Favipiravir Tablets Combine With Chloroquine Phosphate in the Treatment of Novel Coronavirus Pneumonia |
| NCT04336904 | PHASE3 | UNKNOWN | Clinical Study To Evaluate The Performance And Safety Of Favipiravir in COVID-19 |
| NCT04349241 | PHASE3 | COMPLETED | Efficacy and Safety of Favipiravir in Management of COVID-19 |
| NCT04351295 | PHASE2/PHASE3 | COMPLETED | Efficacy of Faviprevir in COVID-19 Treatment |
| NCT04373733 | PHASE3 | COMPLETED | Early Intervention in COVID-19: Favipiravir Verses Standard Care |
| NCT04402203 | PHASE2/PHASE3 | UNKNOWN | Study on Safety and Efficacy of Favipiravir (Favipira) for COVID-19 Patient in Selected Hospitals of Bangladesh |
| NCT04425460 | PHASE3 | UNKNOWN | A Multi-center,Randomized,Double-blind,Placebo-controlled,Phase 3 Study Evaluating Favipiravir in Treatment of COVID19 |
| NCT04434248 | PHASE2/PHASE3 | UNKNOWN | An Adaptive Study of Favipiravir Compared to Standard of Care in Hospitalized Patients With COVID-19 |
| NCT04464408 | PHASE2/PHASE3 | COMPLETED | Favipiravir Therapy in Adults With Mild COVID-19 |
| NCT04501783 | PHASE3 | COMPLETED | Study of Efficacy and Safety of TL-FVP-t vs. SOC in Patients With Mild to Moderate COVID-19 |
| NCT04529499 | PHASE3 | TERMINATED | Clinical Trial Evaluating the Efficacy and Safety of Favipiravir in Moderate to Severe COVID-19 Patients |
| NCT04542694 | PHASE3 | COMPLETED | Study of Favipiravir Compared to Standard of Care in Hospitalized Patients With COVID-19 |
| NCT04558463 | PHASE3 | UNKNOWN | The Effectivity and Safety of Favipiravir Compared to Oseltamivir as Adjuvant Therapy for COVID-19 |
| NCT04600895 | PHASE3 | COMPLETED | The Prevent Severe COVID-19 (PRESECO) Study |
| NCT04600999 | PHASE3 | COMPLETED | Clinical Trial of Favipiravir Treatment of Patients With COVID-19 |
| NCT04613271 | PHASE3 | COMPLETED | Efficacy and Safety of Favipiravir in Covid-19 Patients in Indonesia |
| NCT04694612 | PHASE3 | UNKNOWN | Efficacy of Favipiravir in Treatment of Mild & Moderate COVID-19 Infection in Nepal |
| NCT04784559 | PHASE3 | TERMINATED | Trial to Determine the Efficacy/Safety of Plitidepsin vs Control in Patients With Moderate COVID-19 Infection |
| NCT04818320 | PHASE3 | COMPLETED | Favipiravir in High-risk COVID-19 Patients |
| NCT04828564 | PHASE2/PHASE3 | UNKNOWN | Efficacy and Safety of Favipiravir and Ribavirin Formulation for Treatment of COVID-19 |
| NCT04981379 | PHASE3 | COMPLETED | Clinical Trial For Early SARS-CoV-2 (COVID-19) Treatment |
| NCT05014373 | PHASE3 | UNKNOWN | Philippine Trial to Determine Efficacy and Safety of Favipiravir for COVID-19 |
| NCT05185284 | PHASE3 | COMPLETED | Randomized Multicenter Study on the Efficacy and Safety of Favipiravir for Parenteral Administration Compared to Standard of Care in Hospitalized Patients With COVID-19 |
| NCT05279235 | PHASE3 | TERMINATED | Efficacy and Safety of JT001 (VV116) Compared With Favipiravir |
| NCT05417997 | PHASE3 | COMPLETED | Effect of Kunamin in SARS-CoV-2 RT-PCR Positive Covid-19 Patients |
| NCT04746183 | PHASE1/PHASE2 | RECRUITING | AGILE (Early Phase Platform Trial for COVID-19) |
| NCT05041907 | PHASE2 | RECRUITING | Finding Treatments for COVID-19: A Trial of Antiviral Pharmacodynamics in Early Symptomatic COVID-19 (PLATCOV) |
| NCT05648448 | PHASE2 | RECRUITING | A Phase 2 Trial Comparing Antiviral Treatments in Early Symptomatic Influenza |
| NCT06488300 | PHASE2 | RECRUITING | Assessing Antiviral Treatments in Early Symptomatic RSV |
| NCT06860334 | PHASE2 | NOT_YET_RECRUITING | UMIT-2 - Adaptive Phase IIb Platform Trial to Determine the Efficacy and Safety of Therapeutics for CCHF |
| NCT01068912 | PHASE2 | COMPLETED | Dose-Finding Study of Favipiravir in the Treatment of Uncomplicated Influenza |
| NCT01728753 | PHASE1/PHASE2 | COMPLETED | T-705a Multicenter Study in Adults Subjects With Uncomplicated Influenza |
| NCT02329054 | PHASE2 | COMPLETED | Efficacy of Favipiravir Against Ebola (JIKI) |
| NCT02662855 | PHASE2 | COMPLETED | Efficacy of Favipiravir Against Severe Ebola Virus Disease |
| NCT02739477 | PHASE2 | TERMINATED | Tolerance 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.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).