Tenofovir alafenamide
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Systematic (IUPAC) name | |
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Isopropyl (2S)-2-[[[(1R)-2-(6-aminopurin-9-yl)-1-methyl-ethoxy]methyl-phenoxy-phosphoryl]amino]propanoate
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Clinical data | |
Trade names | Genvoya (with elvitegravir, cobicistat and emtricitabine |
Legal status |
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Routes of administration |
Oral (tablets) |
Pharmacokinetic data | |
Protein binding | ~80%[1] |
Biological half-life | 0.51 hours |
Excretion | Feces (31.7%), urine (<1%) |
Identifiers | |
CAS Number | 379270-37-8 |
ATC code | J05AR17 (WHO) J05AR18 J05AR19 (combination codes) |
PubChem | CID: 9574768 |
DrugBank | DB09299 |
ChemSpider | 7849225 |
UNII | EL9943AG5J ![]() |
KEGG | D10428 |
ChEBI | CHEBI:90926 ![]() |
ChEMBL | CHEMBL2107825 |
Chemical data | |
Formula | C21H29N6O5P |
Molecular mass | 476.466 g/mol |
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Tenofovir alafenamide (INN/USAN, formerly GS-7340) is a nucleotide reverse transcriptase inhibitor and a prodrug of tenofovir. It is under development by Gilead Sciences for use in the treatment of HIV infection and chronic hepatitis B, and is applied in the form of tenofovir alafenamide fumarate (TAF). Closely related to the commonly used reverse-transcriptase inhibitor tenofovir disoproxil, TAF has greater antiviral activity and better distribution into lymphoid tissues than that agent.[2][3]
Gilead announced a phase 3 clinical trial evaluating a single-tablet regimen combining tenofovir alafenamide with cobicistat, emtricitabine and elvitegravir[4] and developed a coformulation of the drug with cobicistat, emtricitabine and the protease inhibitor darunavir.[5][6][7] In a 48 week study comparing elvitegravir/cobicistat/emtricitabine/tenofovir disoproxil to elvitegravir/cobicistat/emtricitabine/tenofovir alafenamide (trade name Genvoya), the results showed the newer drug to be noninferior to the established agent, but at much lower dosages and with lower incidence of adverse side effects such as impaired kidney function.[8][9][10] The FDA approved the TAF-based treatment regimen for treatment of HIV-1 in November 2015.[11] Genvoya is the first TAF-based regimen to receive approval.[11]
Fixed-dose combinations containing tenofovir alafenamide
- Elvitegravir/cobicistat/emtricitabine/tenofovir alafenamide (trade name Genvoya) — approved November 5, 2015
- Emtricitabine/rilpivirine/tenofovir alafenamide (trade name Odefsey)[12] — approved March 1, 2016
- Emtricitabine/tenofovir alafenamide (trade name Descovy)[13] — approved April 4, 2016
See also
- Sofosbuvir — an HCV RNA polymerase (NS5B) inhibitor bearing structural similarity (phosphoramidate side chain metabolized by cathepsin A, carboxylesterase 1 and histidine triad nucleotide-binding protein 1)[14][15]
References
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- ↑ M Markowitz, A Zolopa, et al. GS-7340 Demonstrates Greater Declines in HIV-1 RNA than Tenofovir Disoproxil Fumarate During 14 Days of Monotherapy in HIV-1 Infected Subjects. 18th Conference on Retroviruses and Opportunistic Infections 2 Mar 2011. Paper # 152LB
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- ↑ GS-7340 Packs Greater HIV Punch, Potentially Better Safety, Versus Viread Horn, Tim. 15 Mar 2012. AIDSmeds.com
- ↑ Pharmacokinetics of a Novel EVG/COBI/FTC/GS-7340 Single Tablet Regimen. 13th International Workshop on Clinical Pharmacology of HIV Therapy. Barcelona, Spain. April 16–18, 2012.
- ↑ Once-Daily Tenofovir Prodrug Combo Pill as Effective as Stribild. AIDSmeds.com 1 Nov 2012.
- ↑ CROI 2013: New Pro-drug Tenofovir Alafenamide Appears Equally Effective but Better Tolerated. Highleyman, Liz. HIVandHepatitis.com. 6 March 2013.
- ↑ Horn, T. et al. Tenefovir Alafenamide Fumarate (TAF) Sign-On Letter to Gilead. 13 June 2013. Treatment Action Group.
- ↑ 11.0 11.1 Lua error in package.lua at line 80: module 'strict' not found.
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