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Glecaprevir
Clinical data | |
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Trade names | Mavyret (combination with pibrentasvir) |
Other names | ABT-493 |
Routes of administration |
By mouth |
ATC code |
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Pharmacokinetic data | |
Protein binding | 97.5% |
Metabolism | CYP3A |
Elimination half-life | 6 hours |
Excretion | Faeces (92.1%), urine (0.7%) |
Identifiers | |
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CAS Number | |
PubChem CID | |
DrugBank | |
ChemSpider | |
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KEGG | |
Chemical and physical data | |
Formula | C38H46F4N6O9S |
Molar mass | 838.87 g·mol−1 |
3D model (JSmol) | |
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Glecaprevir (INN,) is a hepatitis C virus (HCV) nonstructural (NS) protein 3/4A protease inhibitor that was identified jointly by AbbVie and Enanta Pharmaceuticals. It is being developed as a treatment of chronic hepatitis C infection in co-formulation with an HCV NS5A inhibitor pibrentasvir. Together they demonstrated potent antiviral activity against major HCV genotypes and high barriers to resistance in vitro.
On 19 December 2016, AbbVie submitted a new drug application to the U.S. Food and Drug Administration for the glecaprevir/pibrentasvir (trade name Mavyret) regimen for the treatment of all major genotypes (1–6) of chronic hepatitis C. On 3 August 2017 the FDA approved the combination for hepatitis C treatment. In Europe, it was approved on 17 August 2017 for the same indication, under the trade name Maviret.
See also
Hepatitis C |
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Hepatitis D | |||||||||
Picornavirus | |||||||||
Anti-influenza agents | |||||||||
Multiple/general |
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