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Medication From Wikipedia, the free encyclopedia
Exenatide, sold under the brand name Byetta among others, is a medication used to treat type 2 diabetes.[7] It is used together with diet, exercise, and potentially other antidiabetic medication.[7] It is a treatment option after metformin and sulfonylureas.[8] It is given by injection under the skin.[7]
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| Pronunciation | /ɛɡzˈɛnətaɪd/ |
| Trade names | Byetta, Bydureon, Bydureon BCise, others |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a605034 |
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| Routes of administration | Subcutaneous |
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| Pharmacokinetic data | |
| Bioavailability | N/A |
| Metabolism | proteolysis |
| Elimination half-life | 2.4 h |
| Excretion | Kidney |
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.212.123 |
| Chemical and physical data | |
| Formula | C184H282N50O60S |
| Molar mass | 4186.63 g·mol−1 |
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Common side effects include low blood sugar, nausea, dizziness, abdominal pain, and pain at the site of injection.[7] Other serious side effects may include medullary thyroid cancer, angioedema, pancreatitis, and kidney injury.[7] Use in pregnancy and breastfeeding is of unclear safety.[9] Exenatide is a glucagon-like peptide-1 receptor agonist (GLP-1 receptor agonist) also known as incretin mimetics.[7] It works by increasing insulin release from the pancreas and decreases excessive glucagon release.[7]
Exenatide was approved for medical use in the United States in 2005.[7] In 2019, it was the 312th most commonly prescribed medication in the United States, with more than 1 million prescriptions.[10]
Exenatide is used to treat type 2 diabetes as an add-on to metformin, a biguanide, or a combination of metformin and a sulfonylurea, or thiazolidinediones such as pioglitazone.[1][2]
A 2011 Cochrane review showed a HbA1c reduction of 0.20% more with Exenatide 2 mg compared to insulin glargine, exenatide 10 μg twice daily, sitagliptin and pioglitazone.[11] Exenatide, lead to greater weight loss than glucagon-like peptide analogues.[11] Due to shorter duration of studies, this review did not allow for long-term positive or negative effects to be assessed.[11]
The main side effects of exenatide use are gastrointestinal in nature, including acid or sour stomach, belching, diarrhea, heartburn, indigestion, nausea, and vomiting.[11] These tend to subside with time;[11] exenatide is therefore not meant for people with severe gastrointestinal disease. Other side effects include dizziness, headache, and feeling jittery.[12] Drug interactions listed on the package insert include delayed or reduced concentrations of lovastatin, paracetamol (acetaminophen), and digoxin, although this has not been proven to alter the effectiveness of these other medications.
In response to postmarketing reports of acute pancreatitis in patients using exenatide, the US Food and Drug Administration (FDA) added a boxed warning to the labeling of Byetta in 2007.[13][14] In August 2008, four additional deaths from pancreatitis in users of exenatide were reported to the FDA; while no definite relationship had been established, the FDA was reportedly considering additional changes to the drug's labeling.[15] Examination of the medical records of the millions of patients part of the United Healthcare Insurance plans did not show any greater rate of pancreatitis among Byetta users than among diabetic patients on other medications. However, diabetics do have a slightly greater incidence of pancreatitis than do non-diabetics.[16][17]
It also may increase risk of mild sulfonylurea-induced hypoglycemia.[18]
Additionally, the FDA has raised concerns over the lack of data to determine if the long-acting once-weekly version of exenatide (but not the twice-daily form of exenatide) may increase thyroid cancer risk. This concern comes out of observing a very small but nevertheless increased risk of thyroid cancer in rodents that was observed for another drug (liraglutide) that is in the same class as exenatide. The data available for exenatide showed less of a risk towards thyroid cancer than liraglutide, but to better quantify the risk the FDA has required Amylin to conduct additional rodent studies to better identify the thyroid issue. The approved form of the once weekly exenatide [Bydureon] has a black box warning discussing the thyroid issue. Eli Lilly has reported they have not seen a link in humans, but that it cannot be ruled out. Eli Lilly has stated the drug causes an increase in thyroid problems in rats given high doses.[19]
In March 2013, the FDA issued a Drug Safety Communication announcing investigations into incretin mimetics due to findings by academic researchers.[20] A few weeks later, the European Medicines Agency launched a similar investigation into GLP-1 agonists and DPP-4 inhibitors.[21]
Exenatide binds to the intact human Glucagon-like peptide-1 receptor (GLP-1R) in a similar way to the human peptide glucagon-like peptide-1 (GLP-1); exenatide bears a 50% amino acid homology to GLP-1 and it has a longer half-life in vivo.[22]
Exenatide is believed to facilitate glucose control in at least five ways:
Exenatide is a 39-amino-acid peptide; it is a synthetic version of exendin-4, a peptide found in the venom of the Gila monster.[27]
During the early 1980s, Jean-Pierre Raufman worked as a postdoctoral researcher at the National Institutes of Health for John Pisano, an "eccentric biochemist" who specialized in collecting venoms from various animals and looking for novel substances that could affect human physiology.[28] In the course of this work, Raufman focused on investigating the Gila monster because he was curious about how it only eats once or twice per year.[29] He discovered molecules in the monster's saliva "that caused inflammation of the pancreas in test animals".[29] He later recalled: "We got a tremendous response from Gila monster venom".[30]
When Raufman gave a lecture about his findings,[30] his research piqued the curiosity of John Eng, an endocrinologist at the Veterans Administration Medical Center in New York City.[28][29] Eng had trained under Rosalyn Sussman Yalow, who received a share of the 1977 Nobel Prize in Physiology or Medicine for development of the radioimmunoassay technique.[28][29]
In 1992, Eng used that technique to isolate a novel substance from Gila monster venom which he called exendin-4.[28][29][30] He tested exendin-4 on diabetic mice and discovered that it was not only effective for reducing blood glucose but was effective for several hours.[28][30] This was an enormously significant clinical finding, because it was GLP-1's extremely short half-life which had defeated earlier attempts to turn that substance into a drug.[28][30] Attempts to bypass that issue by infusing patients in clinical tests with very high doses of GLP-1—in order to overcome its rapid metabolism in the bloodstream—had produced extremely severe nausea, followed by immediate vomiting.[28][30]
Eng's employer, the U.S. Department of Veterans Affairs, turned out to have no interest in obtaining a drug patent on exendin-4, so Eng filed the patent application himself in 1993.[28] He then spent three years on fruitless efforts to persuade the pharmaceutical industry to develop exendin-4 into a drug.[28][30] Jens Juul Holst, a GLP-1 expert, later recalled seeing the skepticism which Eng encountered when he tried to present his work on a poster at industry conferences: "He was extremely frustrated ... Nobody was interested in his work. None of the important people. It was too strange for people to accept".[30]
At a 1996 American Diabetes Association conference in San Francisco, Eng finally caught the attention of scientist Andrew Young of Amylin Pharmaceuticals, who immediately recognized exendin-4's potential and arranged for his company to license Eng's patent.[28][29][30][31] Young was excited to see Eng's poster at the conference summarizing his findings, but then noticed an Eli Lilly and Company executive reading the same poster, and he became worried that Lilly might beat Amylin to a license.[30][31] When Eng arrived at Amylin's San Diego headquarters, he was astonished to discover how much Amylin scientists had already learned about exendin-4 in the brief period of time after Young saw his poster, which convinced him that Amylin was the right company to partner with.[31] Amylin went on to create exenatide, a synthetic version of exendin-4, and later formed an alliance with Lilly in 2002 to bring the drug to market.[28][29][32]
Exenatide was approved by the FDA in April 2005, for people whose diabetes is not well controlled on other oral medications.[33][34][35] This was a landmark event which proved that targeting the GLP-1 receptor was a viable strategy and inspired other pharmaceutical companies to focus their research and development on that receptor.[28][30]
In 2011, Lilly and Amylin dissolved their partnership, with Amylin keeping the rights to exenatide.[36] Meanwhile, Lilly had been awakened to the possibilities of this class of drugs and continued to develop newer drugs of the same class. By October 2024, the blockbuster drug tirzepatide had transformed Lilly into the most valuable drug company in the world.[37]
53 consolidated lawsuits against manufacturers of "GLP-1/DPP-4 products" were dismissed in 2015.[38]
In 2016, work published showing that it can reverse impaired calcium signalling in steatotic liver cells, which, in turn, might be associated with proper glucose control.[25]
It is being evaluated for use in the treatment of Parkinson's disease.[39] A phase 3 clinical trial, started in January 2020 has an Estimated Study Completion Date of 30 June 2024 (NCT04232969).[40]
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