From Mdwiki - Reading time: 7 min| Monoclonal antibody | |
|---|---|
| Type | Whole antibody |
| Source | Humanized (from mouse) |
| Target | CD125 |
| Names | |
| Pronunciation | ben" ra liz' ue mab |
| Trade names | Fasenra |
| Clinical data | |
| Main uses | Eosinophilic asthma[1] |
| Side effects | Headache, sore throat[1] |
| Pregnancy category |
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| Routes of use | Subcutaneous |
| Typical dose | 30 mg[2] |
| External links | |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a618002 |
| Legal | |
| License data |
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| Legal status | |
| Chemical and physical data | |
| Formula | C6492H10060N1724O2028S42 |
| Molar mass | 146056.45 g·mol−1 |
Benralizumab, sold under the brand name Fasenra, is a medication used to treat eosinophilic asthma.[1] It may be used in those not controlled with inhaled corticosteroids and a long-acting beta-agonist.[1] It is given by injection under the skin.[2]
Common side effects include headache and sore throat.[1] Other side effects may include anaphylaxis or hives.[2] Safety in pregnancy is unclear.[2] It is a monoclonal antibody that binds to interleukin-5 receptors (CD125) on eosinophils, resulting in their destruction.[1]
Benralizumab was approved for medical use in the United States in 2017 and Europe in 2018.[2][1] In the United Kingdom it costs the NHS about £2,000 per dose as of 2021.[3] This amount is about 5,200 USD in the United States.[4]
It is give at a dose of 30 mg every 4 weeks for three doses, than every 8 weeks.[2]

In terms of the mode of action we find that Benralizumab binds with the α-chain of IL-5R1, this impedes IL-5 from binding to its receptor. Due to the aforementioned inhibition, Benralizumab blocks the hetero-oligomerization of alpha/beta subunits of IL-5R, as a consequence signal transduction is stopped.[5]
Two phase III clinical trials of benralizumab reported meeting their primary endpoints in 2016.[6][7]
It was approved by the US Food and Drug Administration in November 2017 for the treatment of severe eosinophilic asthma.[8]
It was granted designation as an orphan drug by the Food and Drug Administration for treatment of eosinophilic oesophagitis in August 2019.[9]
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