Ombitasvir
Appearance
Clinical data | |
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Trade names | Viekira Pak (with ombitasvir, paritaprevir, ritonavir and dasabuvir), Technivie (with ombitasvir, paritaprevir, and ritonavir) |
Other names | ABT-267 |
Routes of administration | Oral |
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Pharmacokinetic data | |
Bioavailability | not determined |
Protein binding | ~99.9% |
Metabolism | amide hydrolysis followed by oxidation |
Onset of action | ~4 to 5 hours |
Elimination half-life | 21 to 25 hours |
Excretion | mostly with feces (90.2%) |
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Chemical and physical data | |
Formula | C50H67N7O8 |
Molar mass | 894.11 g/mol g·mol−1 |
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Ombitasvir is an antiviral drug for the treatment of hepatitis C virus (HCV) infection. In the United States, it is approved by the Food and Drug Administration for use in combination with paritaprevir, ritonavir and dasabuvir in the product Viekira Pak for the treatment of HCV genotype 1[1][2], and with paritaprevir and ritonavir in the product Technivie for the treatment of HCV genotype 4[3][4].
Ombitasvir acts by inhibiting the HCV protein NS5A.[5]
References
- ^ "VIEKIRA PAK™ (ombitasvir, paritaprevir and ritonavir tablets; dasabuvir tablets), for Oral Use. Full Prescribing Information" (PDF). AbbVie Inc., North Chicago, IL 60064. Retrieved 30 July 2015.
- ^ "FDA approves Viekira Pak to treat hepatitis C". Food and Drug Administration. December 19, 2014.
- ^ "TECHNIVIE™ (ombitasvir, paritaprevir and ritonavir) Tablets, for Oral Use. Full Prescribing Information" (PDF). AbbVie Inc., North Chicago, IL 60064. Retrieved 28 July 2015.
- ^ "FDA approves Technivie for treatment of chronic hepatitis C genotype 4". Food and Drug Administration. July 24, 2015.
- ^ Jordan J. Feld, Kris V. Kowdley, Eoin Coakley, Samuel Sigal, David R. Nelson, Darrell Crawford, Ola Weiland, Humberto Aguilar, Junyuan Xiong, Tami Pilot-Matias, Barbara DaSilva-Tillmann, Lois Larsen, Thomas Podsadecki, and Barry Bernstein (2014). "Treatment of HCV with ABT-450/r–Ombitasvir and Dasabuvir with Ribavirin". N Engl J Med. 370: 1594–1603. doi:10.1056/NEJMoa1315722.
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