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
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
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 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
Authorised | 1/11/2017 | ||
Authorised | 9/9/2014 | ||
Authorised | 3/23/2018 | ||
Authorised | 6/9/2000 | ||
Authorised | 6/26/2000 | ||
Authorised | 6/26/2000 |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
BASALOG ONE® SOLUTION FOR INJECTION IN A PRE-FILLED PEN 100 IU/ML | SIN15954P | INJECTION, SOLUTION | 100 IU/ml | 6/12/2020 | |
SOLIQUA SOLUTION FOR INJECTION IN A PRE-FILLED PEN 100UNITS/ML + 33MCG/ML | SIN15542P | INJECTION, SOLUTION | 100 Units/ml | 9/20/2018 | |
LANTUS 100 Units/ml Solution for injection in a vial | SIN11934P | INJECTION | 100 iu/ml | 5/16/2002 | |
Toujeo SoloStar 300 units/ml solution for injection in a pre-filled pen | SIN15138P | INJECTION, SOLUTION | 300 Units/ml | 12/14/2016 | |
SEMGLEE™ SOLUTION FOR INJECTION IN A PREFILLED PEN 100U/ML | SIN16009P | INJECTION, SOLUTION | 3.64 mg/ml | 9/14/2020 | |
Lantus SoloStar 100 Units/ml Solution for injection in a pre-filled pen | SIN13426P | INJECTION, SOLUTION | 100 iu/ml | 3/18/2008 | |
SOLIQUA SOLUTION FOR INJECTION IN A PRE-FILLED PEN 100UNITS/ML + 50MCG/ML | SIN15540P | INJECTION, SOLUTION | 100 units/ml | 9/20/2018 |
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. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
BASAGLAR insulin glargine (rbe) 100 IU/mL solution for injection cartridge | 215551 | Medicine | A | 11/21/2014 | |
OPTISULIN SOLOSTAR 100IU/mL insulin glargine (rbe) 3mL solution for injection injector pen | 159302 | Medicine | A | 11/5/2009 | |
BASAGLAR KwikPen insulin glargine (rbe) 100 IU/mL solution for injection cartridge | 215552 | Medicine | A | 11/21/2014 | |
Lantus Vial | 396268 | Medicine | A | 9/21/2022 | |
Lantus SoloStar Injector Pen | 395453 | Medicine | A | 9/5/2022 | |
TOUJEO SOLOSTAR insulin glargine 300 units/mL solution for injection injector pen | 223457 | Medicine | A | 6/30/2015 | |
Lantus Cartridge | 407544 | Medicine | A | 4/12/2023 | |
SEMGLEE insulin glargine (rDNA) 100 IU/mL, 3 mL solution for injection injector pen | 286207 | Medicine | A | 3/28/2018 | |
OPTISULIN 100IU/mL insulin glargine (rbe) 3mL solution for injection cartridge | 159295 | Medicine | A | 11/5/2009 | |
TOUJEO MAX SOLOSTAR insulin glargine 300 units/mL solution for injection injector pen | 312220 | Medicine | A | 11/5/2019 |
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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