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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
-

Chronic Reduction of Fasting Glycaemia With Insulin Glargine Improves First and Second Phase Insulin Secretion in Patients With Type 2 Diabetes

Phase 4
Completed
Conditions
Type 2 Diabetes
Interventions
First Posted Date
2010-11-30
Last Posted Date
2010-11-30
Lead Sponsor
Ruhr University of Bochum
Target Recruit Count
14
Registration Number
NCT01249677
Locations
🇩🇪

Department of Medicine I; University Hospital St. Josef Hospital, Bochum, Germany

Patient Preference and Satisfaction With Insulin Glargine (Lantus) Solostar Pen vs Conventional Vial-Syringe Method of Lantus Injection Therapy in Patients With Type 2 Diabetes Mellitus

Phase 4
Completed
Conditions
Diabetes Mellitus, Type 2
Interventions
First Posted Date
2010-10-21
Last Posted Date
2013-08-12
Lead Sponsor
Sanofi
Target Recruit Count
405
Registration Number
NCT01226043
Locations
🇺🇸

Sanofi-Aventis Administrative Office, Bridgewater, New Jersey, United States

Comparison of Insulin Glargine/Insulin Glulisine Regimen to Insulin Aspart/Insulin Aspart Protamine 30/70 in Type 2 Diabetes Mellitus Patients (T2DM)

Phase 4
Completed
Conditions
Diabetes Mellitus, Type 2
Interventions
First Posted Date
2010-10-01
Last Posted Date
2013-07-08
Lead Sponsor
Sanofi
Target Recruit Count
161
Registration Number
NCT01212913
Locations
🇰🇷

Administrative Office, Seoul, Korea, Republic of

baSal BoluS Therapy in patIenTs With TypE 1 Diabetes Mellitus

Phase 4
Completed
Conditions
Diabetes Mellitus, Type 1
Interventions
First Posted Date
2010-09-17
Last Posted Date
2014-03-17
Lead Sponsor
Sanofi
Target Recruit Count
206
Registration Number
NCT01204593
Locations
🇩🇿

Investigational Site Number 01202, Algiers, Algeria

🇦🇷

Investigational Site Number 03201, Caba, Argentina

🇿🇦

Investigational Site Number 12468, Benoni, South Africa

and more 40 locations

Intensive Insulin Glulisine Therapy in Patients With Type 2 Diabetes Inadequately Controlled With Basal Insulin and Oral Glucose-lowering Drugs

Phase 4
Completed
Conditions
Diabetes Mellitus, Type 2
Interventions
First Posted Date
2010-09-16
Last Posted Date
2012-08-30
Lead Sponsor
Sanofi
Target Recruit Count
207
Registration Number
NCT01203111
Locations
🇻🇪

Administrative office, Caracas, Venezuela

Apidra Children & Adolescents Study

Phase 4
Completed
Conditions
Diabetes Mellitus, Type 1
Interventions
First Posted Date
2010-09-15
Last Posted Date
2012-12-18
Lead Sponsor
Sanofi
Target Recruit Count
100
Registration Number
NCT01202474
Locations
🇷🇺

Administrative office, Moscow, Russian Federation

Clinical Trial Evaluating the Efficacy and Safety of Technosphere® Inhalation Insulin (TI) Inhalation Powder Using the Gen2 Inhaler

Phase 3
Terminated
Conditions
Type 2 Diabetes
Interventions
Drug: Technosphere® Insulin Inhalation Powder
Drug: Insulin Aspart
Drug: Insulin Glargine
First Posted Date
2010-09-08
Last Posted Date
2014-10-30
Lead Sponsor
Mannkind Corporation
Target Recruit Count
39
Registration Number
NCT01196104
Locations
🇺🇸

Billings Clinic Research Center, Billings, Montana, United States

🇺🇸

Diabetes Research Center -Fletcher Allen Health Care, South Burlington, Vermont, United States

🇺🇸

Coastal Clinical Research Inc, Mobile, Alabama, United States

and more 26 locations

Safety/Efficacy Study of Subcutaneously Injected Prandial Insulins Compared to Insulin Lispro Alone in Patients With Type 2 Diabetes Mellitus

First Posted Date
2010-09-02
Last Posted Date
2014-08-20
Lead Sponsor
Halozyme Therapeutics
Target Recruit Count
132
Registration Number
NCT01194258
Locations
🇺🇸

Mercury Street Medical, Butte, Montana, United States

🇺🇸

UT Southwestern Medical Center at Dallas, Dallas, Texas, United States

🇺🇸

John Muir Physician Network Clinical Research Center, Concord, California, United States

and more 19 locations

Safety/Efficacy Study of Subcutaneously Injected Prandial Insulins Compared to Insulin Lispro Alone in Participants With Type 1 Diabetes Mellitus

First Posted Date
2010-09-02
Last Posted Date
2019-02-26
Lead Sponsor
Halozyme Therapeutics
Target Recruit Count
135
Registration Number
NCT01194245
Locations
🇺🇸

Mercury Street Medical, Butte, Montana, United States

🇺🇸

Mid-America Diabetes Associates, Wichita, Kansas, United States

🇺🇸

Rocky Mountain Diabetes and Osteoporosis Center, Idaho Falls, Idaho, United States

and more 16 locations

A Study in Participants With Type 2 Diabetes Mellitus (AWARD-4)

Phase 3
Completed
Conditions
Diabetes Mellitus, Type 2
Interventions
First Posted Date
2010-08-30
Last Posted Date
2014-10-08
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
884
Registration Number
NCT01191268
Locations
🇨🇳

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Yong Kang City, Taiwan

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