Velpatasvir
| Clinical data | |
|---|---|
| Trade names | Epclusa, Sofosvel, Velpanat (all in combination with sofosbuvir) |
| Routes of administration | Oral (tablets) |
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| Pharmacokinetic data | |
| Protein binding | >99.5% |
| Metabolism | Liver (CYP2B6, 2C8, 3A4) |
| Elimination half-life | 15 hours |
| Excretion | Feces (94%), urine (0.4%)[1] |
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| Chemical and physical data | |
| Formula | C49H54N8O8 |
| Molar mass | 883.019 g·mol−1 |
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Velpatasvir is an NS5A inhibitor (by Gilead) which is used together with sofosbuvir in the treatment of hepatitis C infection of all six major genotypes.[2][3]
- ^ "Epclusa (sofosbuvir and velpatasvir) Tablets, for Oral Use. Full Prescribing Information" (PDF). Gilead Sciences, Inc. Foster City, CA 94404. Retrieved 1 August 2016.
- ^ "FDA Approves Epclusa". Drugs.com.
- ^ Heo YA, Deeks ED (April 2018). "Sofosbuvir/Velpatasvir/Voxilaprevir: A Review in Chronic Hepatitis C". Drugs. 78 (5): 577–587. doi:10.1007/s40265-018-0895-5. PMID 29546556.