Telbivudine

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Telbivudine
Systematic (IUPAC) name
1-(2-deoxy-β-L-erythro-pentofuranosyl)-5-methylpyrimidine-2,4(1H,3H)-dione
Clinical data
Trade names Tyzeka
AHFS/Drugs.com monograph
MedlinePlus a607045
Licence data EMA:Link, US FDA:link
Pregnancy cat. B (US)
Legal status POM (UK) -only (US)
Routes Oral
Pharmacokinetic data
Protein binding Low (3.3% in vitro)
Metabolism Nil
Half-life 40 to 49 hours (terminal phase)
Excretion Renal
Identifiers
CAS number 3424-98-4 YesY
ATC code J05AF11
PubChem CID 159269
DrugBank DB01265
ChemSpider 140081 YesY
UNII 2OC4HKD3SF YesY
ChEMBL CHEMBL374731 N
Synonyms 1-(2-deoxy-β-L-ribofuranosyl)-5-methyluracil
β-L-2-deoxythymidine
β-L-thymidine (LdT)
1-[(2S,4R,5S)-4-hydroxy-5-hydroxymethyltetrahydrofuran-2-yl]-5-methyl-1H-pyrimidine-2,4-dione
Chemical data
Formula C10H14N2O5 
Mol. mass 242.23 g/mol
 N (what is this?)  (verify)

Telbivudine is an antiviral drug used in the treatment of hepatitis B infection. It is marketed by Swiss pharmaceutical company Novartis under the trade names Sebivo (Europe) and Tyzeka (United States). Clinical trials have shown it to be significantly more effective than lamivudine or adefovir, and less likely to cause resistance.[1][2][3]

Telbivudine is a synthetic thymidine nucleoside analogue; it is the L-isomer of thymidine. It is taken once daily.

References

  1. Lai CL, Leung N, Teo EK, et al. (2005). "A 1-year trial of telbivudine, lamivudine, and the combination in patients with hepatitis B e antigen-positive chronic hepatitis B". Gastroenterology 129 (2): 528–36. doi:10.1016/j.gastro.2005.05.053. PMID 16083710. 
  2. Lai CL, Gane E, Liaw YF, et al. (2007). "Telbivudine versus lamivudine in patients with chronic hepatitis B". N Engl J Med 357 (25): 2576–88. doi:10.1056/NEJMoa066422. PMID 18094378. 
  3. Chan HL, Heathcote EJ, Marcellin P, et al. (4 December 2007). "Treatment of hepatitis B e antigen positive chronic hepatitis with telbivudine or adefovir: a randomized trial". Ann Intern Med 147 (11): 745–54. PMID 17909201. 

External links

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