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Fremanezumab
Pharmaceutical biological monoclonal antibody From Wikipedia, the free encyclopedia
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Fremanezumab, sold under the brand name Ajovy, is a medication used to prevent migraines in adults.[8][6] It is given by subcutaneous injection (injection under the skin).[8][6]
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The most common side effect is pain and redness at the site of injection.[8] Other side effects include allergic reactions.[8] It is in the calcitonin gene-related peptide antagonist class of medications.[8]
It was approved for medical use in the United States in 2018,[8] the European Union in 2019,[7] the United Kingdom in 2020,[4] and Argentina by September 2021.[9]
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Medical uses
Fremanezumab was shown to be effective in adults with four or more attacks per month.[10] It comes in Monthly and Quarterly injection dosages.
Adverse effects
The most common adverse reactions are located at the injection site, which occurred in 43 to 45% of people in studies (as compared to 38% under placebo). Hypersensitivity reactions occurred in fewer than 1% of patients.[6][11]
Interactions
Fremanezumab does not interact with other antimigraine drugs such as triptans, ergot alkaloids and analgesics. It is expected to generally have a low potential for interactions, because it is not metabolized by cytochrome P450 enzymes.[6]
Pharmacology
Mechanism of action
Fremanezumab is a fully humanized monoclonal antibody directed against calcitonin gene-related peptides (CGRP) alpha and beta.[12] It potently and selectively binds to CGRPs, which prevents binding to receptors.
Pharmacokinetics
After subcutaneous injection, fremanezumab has a bioavailability of 55–66%. Highest concentrations in the body are reached after five to seven days. Like other proteins, the substance is degraded by proteolysis to small peptides and amino acids, which are reused or excreted via the kidney. The elimination half-life is estimated to be 31 days.[11]
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Chemistry
Fremanezumab is a humanized monoclonal antibody.[13] It is produced using recombinant DNA in Chinese hamster ovary cells.[14]
History
Fremanezumab was discovered and developed by Rinat Neuroscience, was acquired by Pfizer in 2006, and was then licensed to Teva.[15] It was approved by the US Food and Drug Administration in September 2018.[16] In March 2019, fremanezumab was approved for marketing and use in the European Union.[7][17]
References
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