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Insulin glargine

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

Overview

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

Research Report

Published: Jul 8, 2025

Acetylsalicylic Acid (Aspirin): A Comprehensive Pharmacological and Clinical Monograph

I. Drug Identification and Physicochemical Properties

Acetylsalicylic acid, universally known by its common name Aspirin, is a synthetic organic compound that has become one of the most widely used medications in modern history. Its identity is defined by a precise set of chemical, physical, and regulatory identifiers that are foundational to its study and clinical application.

Chemical Identity and Nomenclature

The compound is recognized by several names across scientific and clinical domains. Its formal chemical name is acetylsalicylic acid.[1] According to the International Union of Pure and Applied Chemistry (IUPAC) nomenclature, it is designated as 2-acetoxybenzoic acid.[1] A multitude of synonyms are used in literature and databases, including O-Acetylsalicylic acid and the common abbreviation ASA.[1] Other historical and brand names include Acetosal, Acylpyrin, Colfarit, Dispril, Ecotrin, and Polopirin, reflecting its long history and global reach.[2]

Key Registry Numbers and Identifiers

For unambiguous identification in scientific databases and regulatory filings, acetylsalicylic acid is assigned several unique numbers. The most common is its Chemical Abstracts Service (CAS) Number, 50-78-2.[1] While this number is widely used in resources like PubChem, it is important to note that PubChem is not an authoritative source for CAS numbers and may contain depositor-supplied data that has not been independently verified.[5] Other key identifiers include its DrugBank accession number (DB00945), European Community (EC) Number (200-064-1), and PubChem Substance ID (24278218).[1]

Molecular and Structural Formulae

Continue reading the full research report

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2025/07/22
Not Applicable
Recruiting
2025/03/18
Phase 3
Active, not recruiting
2025/03/12
Phase 3
Active, not recruiting
2024/11/14
Phase 2
Recruiting
2024/09/30
Phase 3
Recruiting
Loyola University
2024/04/17
Phase 4
Active, not recruiting
2024/04/02
Phase 3
Completed
2024/02/21
Phase 3
Completed
2023/12/21
Not Applicable
Completed
2023/11/13
Phase 4
Recruiting
Sun Yat-sen University

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Winthrop U.S.
0955-1729
SUBCUTANEOUS
100 [iU] in 1 mL
1/3/2024
Eli Lilly and Company
0002-7715
SUBCUTANEOUS
100 [iU] in 1 mL
11/29/2023
Winthrop U.S, a business of sanofi-aventis U.S. LLC
0955-3900
SUBCUTANEOUS
300 [iU] in 1 mL
12/7/2023
Sanofi-Aventis U.S. LLC
0024-5869
SUBCUTANEOUS
300 U in 1 mL
3/10/2023
Mylan Specialty L.P.
49502-250
SUBCUTANEOUS
100 [iU] in 1 mL
10/17/2022
Mylan Specialty L.P.
49502-393
SUBCUTANEOUS
100 [iU] in 1 mL
7/15/2021
Mylan Specialty L.P.
49502-394
SUBCUTANEOUS
100 [iU] in 1 mL
7/15/2021
Biocon Biologics Inc.
83257-015
SUBCUTANEOUS
100 [iU] in 1 mL
7/28/2023
A-S Medication Solutions
50090-2193
SUBCUTANEOUS
300 U in 1 mL
8/31/2022
A-S Medication Solutions
50090-6439
SUBCUTANEOUS
100 [iU] in 1 mL
12/17/2021

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
LANTUS
sanofi-aventis canada inc
02294338
Solution - Subcutaneous
100 UNIT / ML
9/24/2007
LANTUS
sanofi-aventis canada inc
02280418
Solution - Subcutaneous
100 UNIT / ML
N/A
SEMGLEE
biocon sdn.bhd
02526441
Solution - Subcutaneous
100 UNIT / ML
10/14/2022
LANTUS
sanofi-aventis canada inc
02251930
Solution - Subcutaneous
100 UNIT / ML
5/4/2006
TOUJEO DOUBLESTAR
sanofi-aventis canada inc
02493373
Solution - Subcutaneous
300 UNIT / ML
2/4/2020
BASAGLAR
eli lilly canada inc
02461528
Solution - Subcutaneous
100 UNIT / ML
8/18/2017
LANTUS
sanofi-aventis canada inc
02245689
Solution - Subcutaneous
100 UNIT / ML
7/24/2002
SOLIQUA
sanofi-aventis canada inc
02478293
Solution - Subcutaneous
100 UNIT / ML
9/12/2018
BASAGLAR
eli lilly canada inc
02444852
Solution - Subcutaneous
100 UNIT / ML
12/18/2015
BASAGLAR
eli lilly canada inc
02444844
Solution - Subcutaneous
100 UNIT / ML
12/18/2015

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
LANTUS 100 UNIDADES/ML SOLUCION INYECTABLE EN UN VIAL
00134004
SOLUCIÓN INYECTABLE
Medicamento Sujeto A Prescripción Médica. Tratamiento De Larga Duración
Not Commercialized
SULIQUA 100 UNIDADES/ML + 33 MICROGRAMOS/ML SOLUCION INYECTABLE EN PLUMA PRECARGADA
1161157004
SOLUCIÓN INYECTABLE EN JERINGA PRECARGADA
Medicamento Sujeto A Prescripción Médica. Tratamiento De Larga Duración
Not Commercialized
SULIQUA 100 UNIDADES/ML + 50 MICROGRAMOS/ML SOLUCION INYECTABLE EN PLUMA PRECARGADA
1161157002
SOLUCIÓN INYECTABLE EN JERINGA PRECARGADA
Medicamento Sujeto A Prescripción Médica. Tratamiento De Larga Duración
Not Commercialized
TOUJEO 300 UNIDADES/ML DOUBLESTAR SOLUCION INYECTABLE EN PLUMA PRECARGADA
1000133038
SOLUCIÓN INYECTABLE
Medicamento Sujeto A Prescripción Médica. Tratamiento De Larga Duración
Commercialized
SEMGLEE 100 UNIDADES/ML SOLUCION INYECTABLE EN PLUMA PRECARGADA
1181270003
SOLUCIÓN INYECTABLE
Medicamento Sujeto A Prescripción Médica. Tratamiento De Larga Duración
Commercialized
LANTUS SOLOSTAR 100 UNIDADES/ML SOLUCION INYECTABLE EN PLUMA PRECARGADA
00134033
SOLUCIÓN INYECTABLE EN PLUMA PRECARGADA
Medicamento Sujeto A Prescripción Médica. Tratamiento De Larga Duración
Commercialized
ABASAGLAR 100 UNIDADES/ML KWIKPEN SOLUCION INYECTABLE EN PLUMA PRECARGADA
114944012
SOLUCIÓN INYECTABLE EN PLUMA PRECARGADA
Medicamento Sujeto A Prescripción Médica. Tratamiento De Larga Duración
Commercialized
LANTUS 100 UNIDADES/ML SOLUCION INYECTABLE EN UN VIAL
00134002
SOLUCIÓN INYECTABLE
Medicamento Sujeto A Prescripción Médica. Tratamiento De Larga Duración
Not Commercialized
LANTUS 100 UNIDADES/ML SOLUCION INYECTABLE EN UN VIAL
00134012
SOLUCIÓN INYECTABLE
Medicamento Sujeto A Prescripción Médica. Tratamiento De Larga Duración
Commercialized
LANTUS 100 UNIDADES/ML SOLUCION INYECTABLE EN UN CARTUCHO
00134005
SOLUCIÓN INYECTABLE EN CARTUCHO
Medicamento Sujeto A Prescripción Médica. Tratamiento De Larga Duración
Not Commercialized

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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