MedPath

Insulin glargine

Generic Name
Insulin glargine
Brand Names
Basaglar, Lantus, Rezvoglar, Semglee, Soliqua, Toujeo, Toujeo (previously Optisulin), Abasaglar (previously Abasria)
Drug Type
Biotech
Chemical Formula
-
CAS Number
160337-95-1
Unique Ingredient Identifier
2ZM8CX04RZ
Background

Insulin glargine is a long-acting form of insulin used for the treatment of hyperglycemia caused by Type 1 and Type 2 Diabetes. Insulin is typically prescribed for the management of diabetes mellitus to mimic the activity of endogenously produced human insulin, a peptide hormone produced by beta cells of the pancreas that promotes glucose metabolism. Insulin is released from the pancreas following a meal to promote the uptake of glucose from the blood into internal organs and tissues such as the liver, fat cells, and skeletal muscle. Absorption of glucose into cells allows for its transformation into glycogen or fat for storage. Insulin also inhibits hepatic glucose production, enhances protein synthesis, and inhibits lipolysis and proteolysis.

Insulin is an important treatment in the management of Type 1 Diabetes (T1D), which is caused by an autoimmune reaction that destroys the beta cells of the pancreas, resulting in the body not being able to produce or synthesize the insulin needed to manage circulating blood sugar levels. As a result, people with T1D rely primarily on exogenous forms of insulin, such as insulin glargine, to lower glucose levels in the blood. Insulin is also used in the treatment of Type 2 Diabetes (T2D), another form of diabetes mellitus that is a slowly progressing metabolic disorder caused by a combination of genetic and lifestyle factors that promote chronically elevated blood sugar levels. Without treatment or improvement in non-pharmacological measures such as diet and exercise to lower blood glucose, high blood sugar eventually causes cellular resistance to endogenous insulin, and in the long term, damage to pancreatic islet cells. Insulin is typically prescribed later in the course of T2D, after several oral medications such as Metformin, Gliclazide, or Sitagliptin have been tried, when sufficient damage has been caused to pancreatic cells that the body is no longer able to produce insulin on its own.

Available as the brand name product Lantus, insulin glargine has a duration of action up to 24 hours allowing for once-daily dosing, typically at bedtime. Due to its duration of action, Lantus is considered "basal insulin" as it provides low concentrations of background insulin that can keep blood sugar stable between meals or overnight. Basal insulin is often combined with short-acting "bolus insulin" such as Insulin lispro, Insulin glulisine, and Insulin aspart to provide higher doses of insulin that are required following meals. Use of basal and bolus insulin together is intended to mimic the pancreas' production of endogenous insulin, with a goal of avoiding any periods of hypoglycemia.

Insulin glargine is also available as the biosimilar, or "follow-on" product, Basaglar in the US and as Abasaglar in the EU. As of 2015, insulin glargine was reformulated by Sanofi as the product Toujeo in an extra-concentrated form containing 300IU/mL (compared to 100IU/mL contained in Lantus). Use of the higher concentrated Toujeo as compared to Lantus results in slightly different pharmacokinetics, with a later onset (up to 6 hours) and duration of action (up to 30 hours). In 2021, another biosimilar, Semglee (insulin glargine-yfgn), became the first interchangeable (with Lantus) biosimilar insulin to receive FDA approval.

Insulin glargine is produced by recombinant DNA technology using a non-pathogenic laboratory strain of Escherichia coli (K12) as the production organism. Insulin glargine differs from endogenous human insulin by the replacement of an asparagine residue at position A21 of the A-chain with glycine and addition of two arginines to the C-terminus (positions B31 and 32) of the B-chain. The resulting protein is soluble at pH 4 and forms microprecipitates at physiological pH 7.4 allowing for the slow release of small amounts of insulin glargine, giving the drug a long duration of action and no pronounced peak concentration.

Without an adequate supply of insulin to promote absorption of glucose from the bloodstream, blood sugar levels can climb to dangerously high levels and can result in symptoms such as fatigue, headache, blurred vision, and increased thirst. If left untreated, the body starts to break down fat, instead of glucose, for energy which results in a build-up of ketone acids in the blood and a syndrome called ketoacidosis, which is a life-threatening medical emergency. In the long term, elevated blood sugar levels increase the risk of heart attack, stroke, and diabetic neuropathy.

Indication

Insulin glargine is indicated to improve glycemic control in adults and pediatric patients with type 1 diabetes mellitus and in adults with type 2 diabetes mellitus.

Associated Conditions
Diabetes Mellitus, Type 1 Diabetes Mellitus, Type 2 Diabetes Mellitus
Associated Therapies
-

Comparison of NN1250 With Insulin Glargine in Type 2 Diabetes

Phase 3
Completed
Conditions
Diabetes Mellitus, Type 2
Diabetes
Interventions
First Posted Date
2009-11-01
Last Posted Date
2017-02-09
Lead Sponsor
Novo Nordisk A/S
Target Recruit Count
687
Registration Number
NCT01006291
Locations
🇬🇧

Novo Nordisk Investigational Site, Swansea, United Kingdom

Comparison of Hypoglycaemic Response Between NN1250 and Insulin Glargine in Type 1 Diabetics

Phase 1
Completed
Conditions
Diabetes Mellitus, Type 1
Diabetes
Interventions
First Posted Date
2009-10-27
Last Posted Date
2017-01-20
Lead Sponsor
Novo Nordisk A/S
Target Recruit Count
28
Registration Number
NCT01002768
Locations
🇦🇹

Novo Nordisk Investigational Site, Graz, Austria

Comparison of NN1250 Versus Insulin Glargine in Subjects With Type 2 Diabetes

Phase 3
Completed
Conditions
Diabetes
Diabetes Mellitus, Type 2
Interventions
First Posted Date
2009-09-23
Last Posted Date
2017-02-09
Lead Sponsor
Novo Nordisk A/S
Target Recruit Count
1030
Registration Number
NCT00982644
Locations
🇪🇸

Novo Nordisk Investigational Site, Valencia, Spain

Comparison of NN1250 Plus Insulin Aspart With Insulin Glargine Plus Insulin Aspart in Type 1 Diabetes

Phase 3
Completed
Conditions
Diabetes
Diabetes Mellitus, Type 1
Interventions
First Posted Date
2009-09-23
Last Posted Date
2017-04-06
Lead Sponsor
Novo Nordisk A/S
Target Recruit Count
629
Registration Number
NCT00982228
Locations
🇬🇧

Novo Nordisk Investigational Site, Sheffield, United Kingdom

24-week Treatment With Lixisenatide in Type 2 Diabetes Insufficiently Controlled With Metformin and Insulin Glargine

Phase 3
Completed
Conditions
Type 2 Diabetes Mellitus
Interventions
First Posted Date
2009-09-11
Last Posted Date
2016-10-11
Lead Sponsor
Sanofi
Target Recruit Count
446
Registration Number
NCT00975286
Locations
🇺🇸

Sanofi-Aventis Investigational Site Number 840210, Dallas, Texas, United States

🇺🇸

Sanofi-Aventis Investigational Site Number 840211, Baton Rouge, Louisiana, United States

🇺🇸

Sanofi-Aventis Investigational Site Number 840230, Hyattsville, Maryland, United States

and more 137 locations

Comparison of NN1250 With Insulin Glargine Plus Insulin Aspart With/Without Metformin and With/Without Pioglitazone in Type 2 Diabetes

Phase 3
Completed
Conditions
Diabetes
Diabetes Mellitus, Type 2
Interventions
First Posted Date
2009-09-04
Last Posted Date
2017-04-06
Lead Sponsor
Novo Nordisk A/S
Target Recruit Count
1006
Registration Number
NCT00972283
Locations
🇹🇷

Novo Nordisk Investigational Site, Mersin, Turkey

Test of the Efficacy and Safety of Insulin Glulisine Injected Subcutaneously in Patients With Type 1 Diabetes Mellitus

Phase 4
Completed
Conditions
Diabetes Mellitus, Type 1
Interventions
Drug: INSULIN GLULISINE (HMR1964)
Drug: INSULIN GLARGINE
First Posted Date
2009-08-25
Last Posted Date
2012-07-17
Lead Sponsor
Sanofi
Target Recruit Count
68
Registration Number
NCT00964574
Locations
🇧🇾

Sanofi-Aventis Administrative Office, Minsk, Belarus

A Trial Investigating the Effect of NN1250 in Young and Elderly Subjects With Type 1 Diabetes

Phase 1
Completed
Conditions
Diabetes
Diabetes Mellitus, Type 1
Interventions
First Posted Date
2009-08-25
Last Posted Date
2017-01-20
Lead Sponsor
Novo Nordisk A/S
Target Recruit Count
27
Registration Number
NCT00964418
Locations
🇦🇹

Novo Nordisk Investigational Site, Graz, Austria

A Trial Investigating the Within-subject Variability of NN1250 in Subjects With Type 1 Diabetes

Phase 1
Completed
Conditions
Diabetes Mellitus, Type 1
Diabetes
Interventions
First Posted Date
2009-08-18
Last Posted Date
2017-10-09
Lead Sponsor
Novo Nordisk A/S
Target Recruit Count
54
Registration Number
NCT00961324
Locations
🇩🇪

Novo Nordisk Investigational Site, Neuss, Germany

Study to Evaluate the Efficacy and Safety of Exenatide Once-Weekly Injection Compared to Once-Daily Insulin in Type 2 Diabetes Mellitus

Phase 3
Completed
Conditions
Type 2 Diabetes Mellitus
Interventions
First Posted Date
2009-07-09
Last Posted Date
2015-06-15
Lead Sponsor
AstraZeneca
Target Recruit Count
427
Registration Number
NCT00935532
Locations
🇯🇵

Research Site, Toyama, Japan

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