Dupilumab
Monoclonal antibody | |
---|---|
Type | Whole antibody |
Source | Human |
Target | IL4 receptor alpha |
Clinical data | |
Trade names | Dupixent |
Routes of administration | Injection |
ATC code | |
Legal status | |
Legal status |
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Identifiers | |
CAS Number | |
DrugBank | |
ChemSpider |
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KEGG | |
Chemical and physical data | |
Formula | C6512H10066N1730O2052S46 |
Molar mass | 146.9 kg/mol g·mol−1 |
Dupilumab, sold under the trade name Dupixent, is a monoclonal antibody designed for the treatment of allergic diseases such as eczema.[1][2] Side effects include allergic reactions, cold sores, and inflammation of the cornea.[2]
It was developed by Regeneron Pharmaceuticals and Sanofi Genzyme.[3][4] It received FDA approval in 2017.[2] As of 2017 it costs about 37,000 USD per year.[5]
Medical uses
It appears to be useful for moderate to severe atopic dermatitis for which it is approved in the United States.[6][7] There is also some evidence of benefit in asthma.[7]
Side effects
Dupilumab has the ability to cause several side effects including: allergic reactions, conjunctivitis, and keratitis.[2]
Pharmacology
Mechanism of action
It binds to the alpha subunit of the interleukin-4 receptor (IL-4Rα), making it a receptor antagonist.[8] Through blockade of IL-4Rα, dupilumab modulates signaling of both the interleukin 4 and interleukin 13 pathway. In clinical trials, patients saw decreased levels of Th2 bio-markers.[9]
Pharmacokinetics
Dupilumab shows a non-linear rate in regard to the target.[9] Dupilumab is also reported to have a bioavailability of 64%, with the average concentration occurring 1 week post injection.[9]
Development
Development of dupilumab was a joint effort by Regeneron and Sanofi. The latter of which provided 130 Million dollars to Regeneron for research and development towards monoclonal antibodies.[10]
The US FDA granted it priority review status.[11][12] On March 28, 2017, the U.S. Food and Drug Administration approved dupilumab injection to treat adults with moderate-to-severe eczema.[2]
As per the FDA, dupilumab was manufactured in accordance with current GMP.[13] In October 2016, Regeneron posted a phase III CHRONOS trial, contrasting dupilumab with topical corticosteroids. The study showed that in conjunction with topical corticosteroids, people had a larger decrease in symptoms than steroids alone.[14]
Phase III SOLO 1 and SOLO 2 trials were also performed, which evaluated the efficacy of dupilumab in combination with topical corticosteroids. In these trials 38% and 36% of patients respectively, met the primary efficacy goal of the trial.[9]
Phase II trials for asthma treatment showed increased lung function for patients, showing increased levels of forced expiratory volume.[9]
References
- ^ Statement On A Nonproprietary Name Adopted By The USAN Council - Dupilumab, American Medical Association.[dead link]
- ^ a b c d e "FDA approves new eczema drug Dupixent". FDA.
- ^ "Sanofi - Commercial collaboration". Sanofi. Retrieved 2017-03-09.
- ^ "Pipeline | A powerful research and development engine". www.regeneron.com. Retrieved 2017-03-09.
- ^ Thomas, Katie (28 March 2017). "Severe Eczema Drug Is Approved by F.D.A.; Price Tag Is $37,000 a Year". The New York Times. Retrieved 30 March 2017.
- ^ Kraft, M; Worm, M (April 2017). "Dupilumab in the treatment of moderate-to-severe atopic dermatitis". Expert review of clinical immunology. 13 (4): 301–310. doi:10.1080/1744666X.2017.1292134. PMID 28165826.
- ^ a b Humbert, M; Busse, W; Hanania, NA (20 October 2017). "Controversies and opportunities in severe asthma". Current Opinion in Pulmonary Medicine. doi:10.1097/MCP.0000000000000438. PMID 29059087.
- ^ [ Dupilumab in Persistent Asthma with Elevated Eosinophil Levels - Sally Wenzel, M.D., Linda Ford, M.D., David Pearlman, M.D., Sheldon Spector, M.D., Lawrence Sher, M.D., Franck Skobieranda, M.D., Lin Wang, Ph.D., Stephane Kirkesseli, M.D., Ross Rocklin, M.D., Brian Bock, D.O., Jennifer Hamilton, Ph.D., Jeffrey E. Ming, M.D., Ph.D., Allen Radin, M.D., Neil Stahl, Ph.D., George D. Yancopoulos, M.D., Ph.D., Neil Graham, M.D., and Gianluca Pirozzi, M.D., Ph.D.], NEJM.
- ^ a b c d e Shirley, Matt (2017-07-01). "Dupilumab: First Global Approval". Drugs. 77 (10): 1115–1121. doi:10.1007/s40265-017-0768-3. ISSN 0012-6667.
- ^ "SEC 10-Q Filing of Regeneron". SEC.gov. 2017-06-30. Retrieved 2017-10-20.
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(help) - ^ "Novel Biologic Dupilumab Improves Eczema Symptoms". Retrieved 30 October 2017.
- ^ Walker, Joseph (2016-05-30). "New Eczema Treatments Could Be Available Soon". Wall Street Journal. ISSN 0099-9660. Retrieved 2016-05-31.
- ^ "FDA Active Division Director Summary Review" (PDF). FDA. Retrieved 2017-10-25.
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(help) - ^ Hamilton, Jennifer D.; Ungar, Benjamin; Guttman-Yassky, Emma (2015). "Drug evaluation review: dupilumab in atopic dermatitisjournal=Immunotherapy". 7 (10): 1043–1058. doi:10.2217/imt.15.69. ISSN 1750-7448. PMID 26598956.
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