Dulaglutide Explained

Tradename:Trulicity, others[1]
Dailymedid:Dulaglutide
Pregnancy Au:B3
Pregnancy Au Comment:[2]
Routes Of Administration:Subcutaneous
Class:Incretin mimetics
Atc Prefix:A10
Atc Suffix:BJ05
Legal Au:S4
Legal Au Comment:[3]
Legal Ca:Rx-only
Legal Ca Comment:[4]
Legal Us:Rx-only
Legal Eu:Rx-only
Cas Number:923950-08-7
Iuphar Ligand:7638
Drugbank:DB09045
Unii:WTT295HSY5
Kegg:D09889
Chembl:2108027
C:2646
H:4044
N:704
O:836
S:18

Dulaglutide, sold under the brand name Trulicity among others, is a medication used for the treatment of type 2 diabetes in combination with diet and exercise.[5] [6] It is also approved in the United States for the reduction of major adverse cardiovascular events in adults with type 2 diabetes who have established cardiovascular disease or multiple cardiovascular risk factors.[7] It is a once-weekly injection.

The most common side effects are nausea, diarrhea, vomiting, abdominal pain, and decreased appetite.

It is a glucagon-like peptide-1 receptor agonist (GLP-1 agonist) consisting of GLP-1(7-37) covalently linked to an Fc fragment of human IgG4. GLP-1 is a hormone that is involved in normalizing the level of glucose in blood (glycemia). The Food and Drug Administration (FDA) approved dulaglutide for use in the United States in September 2014.[8] [9] It was approved for use in the European Union in November 2014.[10] In 2021, it was the 70th most commonly prescribed medication in the United States, with more than 9million prescriptions.[11] [12]

Medical uses

The compound is indicated for adults with type 2 diabetes as an adjunct to diet and exercise to improve glycemic control. Dulaglutide is not indicated in the treatment of subjects with type 1 diabetes or patients with diabetic ketoacidosis because these problems are the result of the islet cells being unable to produce insulin and one of the actions of dulaglutide is to stimulate functioning islet cells to produce more insulin. Dulaglutide can be used either stand-alone or in combination with other medicines for type 2 diabetes, in particular metformin, sulfonylureas, thiazolidinediones, and insulin taken concomitantly with meals.[13]

The medication's phase 3 clinical trial program demonstrated reductions in hemoglobin A1c of approximately 1% with the 0.75 mg and 1.5 mg doses of the medication, along with approximately 5 pounds of weight loss on average. The higher 3.0 mg and 4.5 mg doses that were approved in 2020 demonstrated hemoglobin A1c reductions closer to 1.5% and slightly more weight loss.

A 2017 meta-analysis did not support the suggestion that treatment with GLP-1 agonists or DPP-4 inhibitors increased all-cause mortality in type 2 diabetics.[14]

Side effects

The most common side effects include gastrointestinal disorders, such as dyspepsia, decreased appetite, nausea, vomiting, abdominal pain, diarrhea.[15] Some patients may experience serious adverse reactions: acute pancreatitis (symptoms include persistent severe abdominal pain, sometimes radiating to the back and accompanied by vomiting), hypoglycemia, renal impairment (which may sometimes require hemodialysis). The risk of hypoglycemia is increased if the drug is used in combination with sulfonylureas or insulin.[16] [17] There is also a potential risk of medullary thyroid carcinoma associated with the use of the drug.

Contraindications

The compound is contraindicated in subjects with hypersensitivity to the active ingredient or any of the product's components.

People with a personal or family history of medullary thyroid cancer (MTC) or affected by multiple endocrine neoplasia type 2 should not take dulaglutide, because it could increase the risk of these cancers.[18] [8]

Mechanism of action

Dulaglutide binds to glucagon-like peptide 1 receptors, slowing gastric emptying and increasing insulin secretion by pancreatic Beta cells. Simultaneously the compound reduces the elevated glucagon secretion by inhibiting alpha cells of the pancreas, as glucagon is known to be inappropriately elevated in diabetic patients. GLP-1 is normally secreted by L cells of the gastrointestinal mucosa in response to a meal.[19]

History

The safety and effectiveness of dulaglutide were evaluated in six clinical trials in which 3,342 subjects with type 2 diabetes received dulaglutide. Subjects receiving dulaglutide had an improvement in their blood sugar control as observed with reductions in HbA1c level (hemoglobin A1c is a measure of blood sugar control).[8]

The U.S. Food and Drug Administration (FDA) approved dulaglutide with a Risk Evaluation and Mitigation Strategy (REMS),[8] and granted the approval of Trulicity to Eli Lilly and Company.[8] The REMS consists of a number of steps that Eli Lilly will take to make physicians aware of the risk of pancreatitis and the potential risk of medullary thyroid carcinoma associated with the drug.[20]

In 2020, the FDA approved two higher doses of the medication, 3.0 mg and 4.5 mg, based on results of the AWARD-11 trial demonstrating improved glucose lowering and weight benefits.[21]

Further reading

Notes and References

  1. Web site: Dulaglutide international . Drugs.com . 3 January 2020 . 4 February 2020.
  2. Web site: Dulaglutide (Trulicity) Use During Pregnancy . Drugs.com . 15 July 2019 . 4 February 2020.
  3. Web site: Prescription medicines: registration of new chemical entities in Australia, 2015 . Therapeutic Goods Administration (TGA) . 21 June 2022 . 10 April 2023.
  4. Web site: Health Canada New Drug Authorizations: 2015 Highlights . . 4 May 2016 . 7 April 2024.
  5. Tibble CA, Cavaiola TS, Henry RR . Longer acting GLP-1 receptor agonists and the potential for improved cardiovascular outcomes: a review of current literature . Expert Review of Endocrinology & Metabolism . 8 . 3 . 247–259 . May 2013 . 30780817 . 10.1586/eem.13.20 . 73313508 .
  6. Lilly's Once-Weekly Dulaglutide Shows Non-Inferiority to Liraglutide in Head-to-Head Phase III Trial for Type 2 Diabetes . Eli Lilly . 25 February 2014.
  7. Trulicity (dulaglutide) is the first and only type 2 diabetes medicine approved to reduce cardiovascular events in adults with and without established cardiovascular disease . Eli Lilly and Company . 21 February 2020 . 23 February 2020.
  8. FDA approves Trulicity to treat type 2 diabetes . 18 September 2014 . U.S. Food and Drug Administration (FDA) . https://web.archive.org/web/20160420090034/https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm415180.htm . 20 April 2016 . dead . 4 February 2020.
  9. Web site: Drug Approval Package: Trulicity (dulaglutide) NDA #125469 . U.S. Food and Drug Administration (FDA) . 27 October 2014 . 4 February 2020.
  10. Web site: Trulicity EPAR . European Medicines Agency (EMA) . 17 September 2018 . 23 February 2020.
  11. Web site: The Top 300 of 2021 . ClinCalc . 14 January 2024.
  12. Web site: Dulaglutide – Drug Usage Statistics . ClinCalc . 14 January 2024.
  13. Terauchi Y, Satoi Y, Takeuchi M, Imaoka T . Monotherapy with the once weekly GLP-1 receptor agonist dulaglutide for 12 weeks in Japanese patients with type 2 diabetes: dose-dependent effects on glycaemic control in a randomised, double-blind, placebo-controlled study . Endocrine Journal . 61 . 10 . 949–959 . July 2014 . 25029955 . 10.1507/endocrj.ej14-0147 . free .
  14. Liu J, Li L, Deng K, Xu C, Busse JW, Vandvik PO, Li S, Guyatt GH, Sun X . 6 . Incretin based treatments and mortality in patients with type 2 diabetes: systematic review and meta-analysis . BMJ . 357 . j2499 . June 2017 . 28596247 . 5463186 . 10.1136/bmj.j2499 .
  15. Nauck M, Weinstock RS, Umpierrez GE, Guerci B, Skrivanek Z, Milicevic Z . Efficacy and safety of dulaglutide versus sitagliptin after 52 weeks in type 2 diabetes in a randomized controlled trial (AWARD-5) . Diabetes Care . 37 . 8 . 2149–2158 . August 2014 . 24742660 . 4113177 . 10.2337/dc13-2761 .
  16. Amblee A . Dulaglutide for the treatment of type 2 diabetes . Drugs of Today . 50 . 4 . 277–289 . April 2014 . 24918645 . 10.1358/dot.2014.50.4.2132740 .
  17. Monami M, Dicembrini I, Nardini C, Fiordelli I, Mannucci E . Glucagon-like peptide-1 receptor agonists and pancreatitis: a meta-analysis of randomized clinical trials . Diabetes Research and Clinical Practice . 103 . 2 . 269–275 . February 2014 . 24485345 . 10.1016/j.diabres.2014.01.010 . 33922845 .
  18. Samson SL, Garber A . GLP-1R agonist therapy for diabetes: benefits and potential risks . Current Opinion in Endocrinology, Diabetes, and Obesity . 20 . 2 . 87–97 . April 2013 . 23403741 . 10.1097/MED.0b013e32835edb32 . 6933973 .
  19. Nadkarni P, Chepurny OG, Holz GG . Regulation of glucose homeostasis by GLP-1 . Progress in Molecular Biology and Translational Science . 121 . 23–65 . 2014 . 24373234 . 4159612 . 10.1016/B978-0-12-800101-1.00002-8 . 978-0-12-800101-1 .
  20. Web site: Risk Evaluation and Mitigation Strategy (REMS) . United States Food and Drug Administration . 24 March 2020 . September 2014.
  21. Frias JP, Bonora E, Nevarez Ruiz L, Li YG, Yu Z, Milicevic Z, Malik R, Bethel MA, Cox DA . 6 . Efficacy and Safety of Dulaglutide 3.0 mg and 4.5 mg Versus Dulaglutide 1.5 mg in Metformin-Treated Patients With Type 2 Diabetes in a Randomized Controlled Trial (AWARD-11) . Diabetes Care . 44 . 3 . 765–773 . March 2021 . 33397768 . 7896253 . 10.2337/dc20-1473 .