Pegvaliase: Difference between revisions
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| ATCvet = |
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| ATC_prefix = A16 |
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| ATC_suffix = AB19 |
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| PubChem = 86278362 |
| PubChem = 86278362 |
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| DrugBank = DB12839 |
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==References== |
==References== |
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{{Other alimentary tract and metabolism products}} |
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[[Category:Recombinant proteins]] |
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Revision as of 19:24, 24 December 2019
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| Trade names | Palynziq |
| Other names | Pegvaliase-pqpz; PEG-PAL; RAvPAL-PEG |
| Routes of administration | Subcutaneous injection |
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Pegvaliase (trade name Palynziq) is a medication for the treatment of the genetic disease phenylketonuria.[2] Chemically, it is a pegylated derivative of the enzyme phenylalanine ammonia-lyase that metabolizes phenylalanine to reduce its blood levels.[3]
It was approved by the Food and Drug Administration for use in the United States in 2018.[2]
References
- ^ "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved 22 Oct 2023.
- ^ a b "FDA approves a new treatment for PKU, a rare and serious genetic disease". Food and Drug Administration. May 24, 2018.
- ^ "Palynziq". BioMarin Pharmaceutica.
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