Zinbryta (multiple sclerosis) Zenapax (acute transplant rejection, discontinued in 2009)
AHFS/Drugs.com
zinbryta
Pregnancy category
AU: B3
Routes of administration
Subcutaneous injection, Intravenous
ATC code
L04AC01 (WHO)
Legal status
Legal status
AU: S4 (Prescription only)[1]
CA: ℞-only[2]
US: ℞-only / Withdrawn[3]
In general: ℞ (Prescription only)
Pharmacokinetic data
Bioavailability
90%
Metabolism
Proteases
Elimination half-life
21 days (11–38 days)
Identifiers
CAS Number
152923-56-3Y
DrugBank
DB00111Y
ChemSpider
none
UNII
CUJ2MVI71Y
KEGG
D03639N
ChEMBL
ChEMBL1201605N
Chemical and physical data
Formula
C6332H9808N1678O1989S42
Molar mass
142612.39 g·mol−1
NY (what is this?)(verify)
Daclizumab (trade name Zinbryta) is a therapeutic humanized monoclonal antibody which was used for the treatment of adults with relapsing forms of multiple sclerosis (MS). Daclizumab works by binding to CD25, the alpha subunit of the IL-2 receptor of T-cells.
In March 2018, it was voluntarily withdrawn from the market by Biogen and Abbvie after reports of autoimmune encephalitis in Europe.[4][5][3]
^"Prescription medicines: registration of new chemical entities in Australia, 2016". Therapeutic Goods Administration (TGA). 21 June 2022. Retrieved 10 April 2023.
^"Health Canada New Drug Authorizations: 2016 Highlights". Health Canada. 14 March 2017. Retrieved 7 April 2024.
^ ab"FDA working with manufacturers to withdraw Zinbryta from the market in the United States". U.S. Food and Drug Administration (FDA). Retrieved 15 March 2018.
^"Biogen, AbbVie withdraw multiple sclerosis drug Zinbryta". Reuters. 2018.
^Loftus P (2 March 2018). "Biogen and Abbvie Take Multiple Sclerosis Drug Off Market". The Wall Street Journal.
Daclizumab (trade name Zinbryta) is a therapeutic humanized monoclonal antibody which was used for the treatment of adults with relapsing forms of multiple...
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colitis by their ability to bind to and inhibit TNF-α. Basiliximab and daclizumab inhibit IL-2 on activated T cells and thereby help preventing acute rejection...