Amprenavir
| Clinical data | |
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| Trade names | Agenerase |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a699051 |
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| Routes of administration | Oral (capsules) |
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| Pharmacokinetic data | |
| Protein binding | 90% |
| Metabolism | Hepatic |
| Elimination half-life | 7.1–10.6 hours |
| Excretion | <3% renal |
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| ECHA InfoCard | 100.262.589 |
| Chemical and physical data | |
| Formula | C25H35N3O6S |
| Molar mass | 505.63 g·mol−1 |
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Amprenavir (original brand name Agenerase, GlaxoSmithKline) is a protease inhibitor used to treat HIV infection. It was approved by the Food and Drug Administration on April 15, 1999, for twice-a-day dosing instead of needing to be taken every eight hours. The convenient dosing came at a price, as the dose required is 1,200 mg, delivered in 8 (eight) very large 150 mg gel capsules or 24 (twenty-four) 50 mg gel capsules twice daily.[1]
It was patented in 1992 and approved for medical use in 1999.[2] Production of amprenavir was discontinued by the manufacturer on December 31, 2004; a prodrug version (fosamprenavir), is available.
- ^ "Agenerase (amprenavir) Capsules. Full Prescribing Information. Section Dosage and Administration" (PDF). US Food and Drug Administration. GlaxoSmithKline and Vertex Pharmaceuticals Inc. Archived from the original (PDF) on August 24, 2013. Retrieved 29 November 2015.
- ^ Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 509. ISBN 9783527607495.