Insulin glargine

Long-acting insulin From Wikipedia, the free encyclopedia

Insulin glargine sold, among others, under the brand name Lantus (manufactured and marketed by Sanofi) is a long-acting modified form of medical insulin, used in the management of type 1 and type 2 diabetes.[16] It is injected just under the skin.[16] Effects generally begin an hour after use.[16]

Trade namesLantus, others
Biosimilarsinsulin glargine-aglr,[1] insulin glargine-aldy,[2] insulin glargine-yfgn,[3] Abasaglar,[4] Langlara,[2] Ondibta,[5][6] Rezvoglar,[1] Semglee[7][3]
Quick facts Clinical data, Pronunciation ...
Insulin glargine
Toujeo branded insulin glargine
Clinical data
Pronunciation/ˌɪnsəlɪn ˈɡlɑːrn/
IN-sə-lin GLAR-jeen
Trade namesLantus, others
Biosimilarsinsulin glargine-aglr,[1] insulin glargine-aldy,[2] insulin glargine-yfgn,[3] Abasaglar,[4] Langlara,[2] Ondibta,[5][6] Rezvoglar,[1] Semglee[7][3]
AHFS/Drugs.comMonograph
MedlinePlusa600027
License data
Pregnancy
category
Routes of
administration
Subcutaneous
ATC code
Legal status
Legal status
Pharmacokinetic data
Onset of action~1 hour[16]
Duration of action24–36 hours[16]
Identifiers
  • Recombinant human insulin
CAS Number
IUPHAR/BPS
DrugBank
ChemSpider
  • none
UNII
KEGG
CompTox Dashboard (EPA)
ECHA InfoCard100.241.126 Edit this at Wikidata
Chemical and physical data
FormulaC267H404N72O78S6
Molar mass6062.96 g·mol−1
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Common side effects include low blood sugar, problems at the site of injection, itchiness, and weight gain.[16] Other serious side effects include low blood potassium.[16] NPH insulin rather than insulin glargine is generally preferred in pregnancy.[17] After injection, microcrystals slowly release insulin for about 24 hours.[16] This insulin causes body tissues to absorb glucose from the blood and decreases glucose production by the liver.[16]

Insulin glargine was patented, but the patent expired in most jurisdictions in 2014. It was approved for medical use in the United States in 2000.[16] It is on the World Health Organization's List of Essential Medicines.[18] In 2023, it was the 30th most commonly prescribed medication in the United States, with more than 18 million prescriptions.[19][20] In July 2021, the US Food and Drug Administration (FDA) approved an interchangeable biosimilar insulin product called Semglee (insulin glargine-yfgn) for the treatment of diabetes.[21]

Medical uses

The long-acting insulin class, which includes insulin glargine, do not appear much better than neutral protamine Hagedorn (NPH) insulin,[22] but do have a greater cost, making them, as of 2010, not cost effective for the treatment of type 2 diabetes.[23] In a previous review it was unclear if there is a difference in hypoglycemia, as there was not enough data to determine any differences with respect to long term outcomes,[24] however a more recent Cochrane systematic review did not find clinically significant difference when comparing insulin glargine to NPH insulin, insulin detemir or insulin degludec in the management of type 1 diabetes in either adults or children over periods of 6 months or longer.[22] It is not typically the recommended long-acting insulin in the United Kingdom.[17]

Semglee is indicated to improve glycemic control in adults and children with type 1 diabetes and in adults with type 2 diabetes.[21] Semglee is both biosimilar to, and interchangeable with, its reference product Lantus (insulin glargine), a long-acting insulin analog.[21]

Mixing with other insulins

The American Diabetes Association said in 2003 that, unlike some other longer-acting insulins, glargine should not be diluted or mixed with other insulin or solution in the same syringe, due to the low pH of its diluent.[25] However, a 2004 study found that mixing glargine with other insulins did not affect short-term glycemic profile.[26]

Adverse effects

Common side effects include low blood sugar, problems at the site of injection, itchiness, and weight gain.[16] Serious side effects include low blood potassium.[16]

As of 2012, tentative evidence shows no association between insulin glargine and cancer.[27] Previous studies had raised concerns.[28]

When comparing insulin glargine to NPH insulin, insulin detemir or insulin degludec, no significant adverse effects were found in the management of type 1 diabetes in either adults or children in periods of six months or longer.[22]

Pharmacology

Mechanism of action

Insulin glargine differs from human insulin by replacing asparagine with glycine in position 21 of the A-chain and by carboxy-terminal extension of B-chain by 2 arginine residues. The arginine amino acids shift the isoelectric point from a pH of 5.4 to 6.7, making the molecule more soluble at an acidic pH and less soluble at physiological pH. The isoelectric shift also allows for the subcutaneous injection of a clear solution. The glycine substitution prevents deamidation of the acid-sensitive asparagine at acidic pH. In the neutral subcutaneous space, higher-order aggregates form, resulting in a slow, peakless dissolution and absorption of insulin from the site of injection.[29]

History

In June 2000, the European Commission formally approved the launching of Lantus by Sanofi-Aventis Germany in the European Union.[30] The admission was prolonged on 9 June 2005.[31]

A three-fold more concentrated formulation, brand name Toujeo, was introduced after FDA approval in 2015.[32][33]

Biosimilars

Abasaglar was authorized for medical use in the European Union in September 2014.[4][34]

Lusduna was authorized for medical use in the European Union in January 2017.[35]

Semglee was authorized for medical use in the European Union in March 2018.[36]

Semglee (glargine-yfgn) was approved for medical use in the United States in July 2021.[3]

Rezvoglar (glargine-aglr) was approved for medical use in the United States in December 2021.[1]

In November 2025, the Committee for Medicinal Products for Human Use of the European Medicines Agency adopted a positive opinion, recommending the granting of a marketing authorization for the medicinal product Ondibta, intended for the treatment of diabetes.[5] The applicant for this medicinal product is Gan & Lee Pharmaceuticals Europe GmbH.[5] Ondibta is a biosimilar medicinal product that is highly similar to the reference product Lantus, which was authorized in the EU in June 2000.[5] Ondibta was authorized for medical use in the European Union in January 2026.[5][6]

Patent expiry

Patent protection for insulin glargine expired in the European Union and the United States in 2014.[37] Insulin glargine from competitor Eli Lilly became available in most countries during 2015, under the brand names Basaglar (as a follow-on in the US) and Abasaglar (as a biosimilar in the EU).[37]

Brand names

Insulin glargine is sold under various brand names including Basaglar,[12] Lantus,[11] and Toujeo.[13]

References

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