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Etravirine: Difference between revisions

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| ChEMBL = 308954
| ChEMBL = 308954
| NIAID_ChemDB = 105156
| NIAID_ChemDB = 105156
| PDB_ligand = 65B


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*[http://www.aidsmap.com/cms1256807.asp AIDS map]
*[http://www.aidsmap.com/cms1256807.asp AIDS map]
*[http://www.aidsmeds.com/archive/etravirine_1618.shtml AIDS meds]
*[http://www.aidsmeds.com/archive/etravirine_1618.shtml AIDS meds]
* [http://www.ebi.ac.uk/pdbe-srv/PDBeXplore/ligand/?ligand=65B Etravirine bound to proteins] in the [[Protein Data Bank|PDB]]


==References==
==References==

Revision as of 11:02, 23 March 2014

Etravirine
Clinical data
Trade namesIntelence
AHFS/Drugs.comMonograph
MedlinePlusa608016
License data
Pregnancy
category
  • AU: B1
Routes of
administration		Oral
ATC code
Legal status
Legal status
Pharmacokinetic data
Protein binding99.9%
MetabolismHepatic (CYP3A4, CYP2C9 & CYP2C19-mediated)
Elimination half-life41±20 hours
ExcretionFaeces (93.7%), urine (1.2%)
Identifiers
  • 4-[6-Amino-5-bromo-2- [(4-cyanophenyl)amino] pyrimidin-4-yl]oxy-3,5-dimethylbenzonitrile
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
NIAID ChemDB
PDB ligand
CompTox Dashboard (EPA)
ECHA InfoCard100.207.546 Edit this at Wikidata
Chemical and physical data
FormulaC20H15BrN6O
Molar mass435.28 g/mol g·mol−1
3D model (JSmol)
  • N#Cc3cc(c(Oc1nc(nc(c1Br)N)Nc2ccc(C#N)cc2)c(c3)C)C
  • InChI=1S/C20H15BrN6O/c1-11-7-14(10-23)8-12(2)17(11)28-19-16(21)18(24)26-20(27-19)25-15-5-3-13(9-22)4-6-15/h3-8H,1-2H3,(H3,24,25,26,27) checkY
  • Key:PYGWGZALEOIKDF-UHFFFAOYSA-N checkY
  (verify)

Etravirine (ETR,[1] brand name Intelence, formerly known as TMC125) is a drug used for the treatment of HIV. Etravirine is a non-nucleoside reverse transcriptase inhibitor (NNRTI). Etravirine works by reducing the amount of HIV and increasing the number of CD4 or T cells in the blood. Unlike the currently available agents in the class, resistance to other NNRTIs does not seem to confer resistance to etravirine.[2] Etravirine is marketed by Tibotec, a subsidiary of Johnson & Johnson. In January 2008, the Food and Drug Administration approved its use for patients with established resistance to other drugs, making it the 30th anti-HIV drug approved in the United States and the first to be approved in 2008.[3] It was also approved for use in Canada on April 1, 2008.[4]

Etravirine is licensed in the United States, Canada, Israel, Russia and the European Union,[5] and is under regulatory review in Switzerland and Australia.[6]

Indications and dosage

Etravirine, in combination with other anti-retrovirals, is indicated for the treatment of human immunodeficiency virus type 1 (HIV-1) infection in antiretroviral treatment-experienced adult patients, who have evidence of viral replication and HIV-1 strains resistant to a non-nucleoside reverse transcriptase inhibitor (NNRTI) and other antiretroviral agents.

The recommended dose of etravirine is 200 mg (2 x 100 mg tablets, or 1 x 200 mg tablet as of 03/18/2011) taken twice daily following a meal. The type of food does not affect the exposure to etravirine.[7]

Contraindication

Each 100 mg etravirine tablet contains 160 mg of lactose. Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption should not take this medicine.[8]

Mechanism of action

Etravirine is a second-generation non-nucleoside reverse transcriptase inhibitor (NNRTI), designed to be active against HIV with mutations that confer resistance to the two most commonly prescribed first-generation NNRTIs, mutation K103N for efavirenz and Y181C for nevirapine.[9] This potency appears to be related to etravirine's flexibility as a molecule. Etravirine is a diarylpyrimidine (DAPY), a type of organic molecule with some conformational isomerism that can bind the enzyme reverse transcriptase in multiple conformations, allowing for a more robust interaction between etravirine and the enzyme, even in the presence of mutations.[10] Other diarylpyrimidine-analogues are currently being developed as potential anti-HIV agents, notably rilpivirine.

Warnings and risks

In 2009, the prescribing information for etravirine was modified to include "postmarketing reports of cases of Stevens–Johnson syndrome, toxic epidermal necrolysis and erythema multiforme, as well as hypersensitivity reactions characterized by rash, constitutional findings, and sometimes organ dysfunction, including hepatic failure. Intelence therapy should be immediately discontinued when signs and symptoms of severe skin or hypersensitivity reactions develop."[11]

References

  1. ^ "Appendix A: Key to Acronyms". Guidelines for the Use of Antiretroviral Agents in HIV-1-Infected Adults and Adolescents. Department of Health and Human Services.
  2. ^ Stellbrink HJ (October 2007). "Antiviral drugs in the treatment of AIDS: what is in the pipeline?". Eur. J. Med. Res. 12 (9): 483–95. PMID 17933730.
  3. ^ "FDA Approves HIV Drug Etravirine". Associated Press. January 18, 2008.[dead link]
  4. ^ "First New NNRTI in Nearly a Decade to Benefit Canadians with HIV/AIDS" (PDF) (Press release). Janssen-Ortho Inc. 2008-04-01. Retrieved 2008-07-09.
  5. ^ "Intelence receives marketing authorisation in the European Union for HIV combination therapy". Tibotec. Retrieved 2008-08-29.
  6. ^ "Etravirine (TMC125, Intelence) granted accelerated approval in US". aidsmap. Retrieved 2008-01-24.
  7. ^ "Intelence prescribing information" (pdf). FDA. Retrieved January 2012. {{cite web}}: Check date values in: |accessdate= (help)
  8. ^ "Etravine: Summary of product characteristics" (PDF). EMEA. p. 5. Retrieved July 2011. {{cite web}}: Check date values in: |accessdate= (help)
  9. ^ Evans, David (2008-01-15). "Etravirine—Countdown to Launch". AIDSmeds.com. Retrieved 2008-02-02. {{cite web}}: Cite has empty unknown parameter: |coauthors= (help)
  10. ^ Das K, Clark AD, Lewi PJ, Heeres J, De Jonge MR, Koymans LM, Vinkers HM, Daeyaert F, Ludovici DW, Kukla MJ, De Corte B, Kavash RW, Ho CY, Ye H, Lichtenstein MA, Andries K, Pauwels R, De Béthune MP, Boyer PL, Clark P, Hughes SH, Janssen PA, Arnold E; Clark (2004). "Roles of conformational and positional adaptability in structure-based design of TMC125-R165335 (etravirine) and related non-nucleoside reverse transcriptase inhibitors that are highly potent and effective against wild-type and drug-resistant HIV-1 variants". J. Med. Chem. 47 (10): 2550–60. doi:10.1021/jm030558s. PMID 15115397.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  11. ^ "FDA Medwatch Safety Information". Retrieved 2009-08-27.
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