Chemistry:Taliglucerase alfa

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Taliglucerase alfa
Clinical data
Trade namesElelyso, Uplyso (Latin America)
AHFS/Drugs.comMonograph
Pregnancy
category
  • AU: B1
Routes of
administration
Intravenous infusion
ATC code
Legal status
Legal status
  • AU: S4 (Prescription only) [1]
  • US: ℞-only
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Elimination half-life18.9-28.7 minutes
Identifiers
CAS Number
DrugBank
ChemSpider
  • none
UNII
KEGG
ChEMBL
Chemical and physical data
FormulaC2580H3918N680O727S17
Molar mass56638.78 g·mol−1

Taliglucerase alfa, sold under the brand name Elelyso among others, is a biopharmaceutical medication developed by Protalix and Pfizer.[2][3][full citation needed] The drug, a recombinant glucocerebrosidase used to treat Gaucher's disease, is the first plant-made pharmaceutical to win approval by the U.S. Food and Drug Administration (FDA).[4][5] Each vial has 200 units of taliglucerase alfa.

Approval history

The U.S. FDA New Drug Application (NDA) was granted approval in May 2012, for use in adults.[6][7] The U.S. FDA Supplemental New Drug Application (sNDA) for pediatric use was granted approved in August 2014.[8] In Israel, the Israeli Ministry of Health granted approval in September 2012.[9] In Brazil, the Brazilian Health Surveillance Agency (ANVISA) granted approval in March 2013. In Canada, Health Canada issued a Notice of Compliance in May 2014, for both adults and pediatric patients.[10]

Taliglucerase alfa is made by the Israeli biotherapeutics company Protalix and sold by the American pharmaceutical company Pfizer.[citation needed]

Society and culture

Economics

For 2016, Elelyso was ranked third for pharmaceuticals with the highest cost-per-patient, with an average cost of $483,242 per year.[11]

References

  1. "Prescription medicines: registration of new chemical entities in Australia, 2014". 21 June 2022. https://www.tga.gov.au/resources/resource/guidance/prescription-medicines-registration-new-chemical-entities-australia-2014. 
  2. "A plant-derived recombinant human glucocerebrosidase enzyme--a preclinical and phase I investigation". PLOS ONE 4 (3): e4792. 2009. doi:10.1371/journal.pone.0004792. PMID 19277123. Bibcode2009PLoSO...4.4792A. 
  3. Clinical trial number NCT00962260 for "Expanded Access Trial of Plant Expressed Recombinant Glucocerebrosidase (prGCD) in Patients With Gaucher Disease" at ClinicalTrials.gov
  4. "Is the drought over for pharming?". Science 320 (5875): 473–5. April 2008. doi:10.1126/science.320.5875.473. PMID 18436771. 
  5. Maxmen, Amy (2 May 2012). "First plant-made drug on the market". Nature, Biology & Biotechnology, Industry. http://blogs.nature.com/news/2012/05/first-plant-made-drug-on-the-market.html. 
  6. Beitz, Julie. "Elenyso (taliglucerase alfa) NDA Approval". Center for Drug Evaluation and Research. U.S. Food and Drug Administration. http://www.accessdata.fda.gov/drugsatfda_docs/appletter/2012/022458s000ltr.pdf. 
  7. "Elenyso (taliglucerase alfa): Highlights of Prescribing Information". U.S. Food and Drug Administration. http://www.accessdata.fda.gov/drugsatfda_docs/label/2012/022458lbl.pdf. 
  8. "Supplement Approval Fulfillment of Postmarketing Requirement". U.S. Food and Drug Administration. http://www.accessdata.fda.gov/drugsatfda_docs/appletter/2014/022458Orig1s003,022458Orig1s006ltr.pdf. 
  9. "מאגר התרופות (Drug details for Elelyso)". Ministry of Health Israel. https://www.old.health.gov.il/units/pharmacy/trufot/PerutTrufa.asp?Reg_Number=148%2067%2033413%2000&safa=e. 
  10. "Summary Basis of Decision (SBD): Elelyso". Health Canada. 2014-08-01. http://www.hc-sc.gc.ca/dhp-mps/prodpharma/sbd-smd/drug-med/sbd_smd_2014_elelyso_140854-eng.php. 
  11. "Medical Pharmacy Trend Report". Magellan Rx Management. 2016. https://www1.magellanrx.com/media/604882/2016mrxtrendreport_final.pdf. 

External links