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Insulin degludec

Generic Name
Insulin degludec
Brand Names
Ryzodeg, Tresiba, Xultophy
Drug Type
Biotech
CAS Number
844439-96-9
Unique Ingredient Identifier
54Q18076QB
Background

Insulin degludec is an ultra-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 among many other functions.

Insulin is an essential 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 degludec, 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.

Marketed as the brand name product Tresiba, insulin degludec has a duration of action up to 42 hours allowing for once-daily dosing, typically at bedtime. Due to its duration of action, Tresiba 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, or Insulin aspart to provide higher doses of insulin required following meals. Use of basal and bolus insulin together is intended to mimic the pancreas' production of endogenous insulin, with the goal of avoiding any periods of hypoglycemia.

Compared to endogenous insulin, insulin degludec has an added hexadecanedioic acid on lysine at the B29 position, allowing for the formation of multi-hexamers. When injected subcutaneously, these multi-hexamers form a drug depot store from which monomers are slowly and continuously absorbed into circulation. As a result, Insulin Degludec has a protracted time action profile due to the delayed absorption from subcutaneous tissue depots into the systemic circulation. Compared to available long-acting analogs such as Insulin glargine and Insulin detemir, which have a duration of action of 20-24 hours, insulin degludec provides a consistent level of basal insulin over 42 hours with a low peak: trough ratio. Limitations of shorter-acting analogs include more frequent dosing and less stable pharmacokinetics, which may negatively impact patient adherence and glucose control, particularly nocturnal control.

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.

Insulin Degludec was approved by the FDA in September 2015 as the product Tresiba, for use in providing glycemic control to adults with diabetes mellitus.

Indication

Insulin degludec is indicated to improve glycemic control in patients 1 year of age and older with diabetes mellitus.

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

Investigation of Pharmacodynamic Characteristics of Explorative Formulation of Insulin Degludec in Male Subjects With Type 1 Diabetes

Phase 1
Completed
Conditions
Diabetes
Diabetes Mellitus, Type 1
Interventions
First Posted Date
2013-05-30
Last Posted Date
2015-10-22
Lead Sponsor
Novo Nordisk A/S
Target Recruit Count
36
Registration Number
NCT01865318

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Explorative Formulation of Insulin Degludec

Phase 1
Completed
Conditions
Diabetes
Diabetes Mellitus, Type 1
Diabetes Mellitus, Type 2
Interventions
Drug: placebo
Drug: isophane human insulin
First Posted Date
2013-05-30
Last Posted Date
2015-10-23
Lead Sponsor
Novo Nordisk A/S
Target Recruit Count
64
Registration Number
NCT01865279

Safety, Tolerability and Pharmacokinetic and Pharmacodynamic Characteristics of Explorative Formulations of Insulin Degludec and IDegAsp 50 in Healthy Japanese Subjects

Phase 1
Completed
Conditions
Diabetes
Healthy
Interventions
Drug: placebo
Drug: insulin degludec/insulin aspart 50
First Posted Date
2013-05-30
Last Posted Date
2016-01-15
Lead Sponsor
Novo Nordisk A/S
Target Recruit Count
32
Registration Number
NCT01865331

Comparison of Explorative Formulation of Insulin Degludec and Insulin Aspart Co-formulation Versus Explorative Formulation of Insulin Degludec and Insulin Aspart Separately Compared With Biphasic Insulin Aspart 30 in Male Subjects With Diabetes

Phase 1
Completed
Conditions
Diabetes
Diabetes Mellitus, Type 2
Diabetes Mellitus, Type 1
Interventions
Drug: insulin degludec/insulin aspart 40
Drug: insulin degludec/insulin aspart 30
Drug: insulin degludec/insulin aspart 50
First Posted Date
2013-05-30
Last Posted Date
2015-10-23
Lead Sponsor
Novo Nordisk A/S
Target Recruit Count
59
Registration Number
NCT01865305

A Trial Comparing Efficacy and Safety of Insulin Degludec and Insulin Glargine in Insulin naïve Subjects With Type 2 Diabetes

Phase 3
Completed
Conditions
Diabetes
Diabetes Mellitus, Type 2
Interventions
First Posted Date
2013-05-08
Last Posted Date
2017-04-07
Lead Sponsor
Novo Nordisk A/S
Target Recruit Count
833
Registration Number
NCT01849289
Locations
🇺🇦

Novo Nordisk Investigational Site, Vinnitsa, Ukraine

A Trial Investigating the Pharmacodynamic and Pharmacokinetic Properties of Insulin Degludec/Insulin Aspart 15 in Subjects With Type 1 Diabetes

Phase 1
Completed
Conditions
Diabetes Mellitus, Type 1
Diabetes
Interventions
First Posted Date
2013-01-23
Last Posted Date
2015-03-05
Lead Sponsor
Novo Nordisk A/S
Target Recruit Count
33
Registration Number
NCT01773798

A 26-week Trial Comparing Efficacy and Safety of Insulin Degludec/Insulin Aspart BID and Insulin Degludec OD Plus Insulin Aspart in Subjects With Type 2 Diabetes Mellitus Treated With Basal Insulin in Need of Treatment Intensification With Mealtime Insulin

Phase 3
Completed
Conditions
Diabetes Mellitus, Type 2
Diabetes
Interventions
First Posted Date
2012-10-24
Last Posted Date
2018-04-02
Lead Sponsor
Novo Nordisk A/S
Target Recruit Count
274
Registration Number
NCT01713530
Locations
🇳🇴

Novo Nordisk Investigational Site, Stavanger, Norway

A Trial Comparing the Effect of Exercise on Blood Glucose in Subjects With Type 1 Diabetes, Who Are Treated With Either Insulin Degludec or Insulin Glargine

Phase 1
Completed
Conditions
Diabetes
Diabetes Mellitus, Type 1
Interventions
First Posted Date
2012-10-11
Last Posted Date
2016-12-16
Lead Sponsor
Novo Nordisk A/S
Target Recruit Count
40
Registration Number
NCT01704417
Locations
🇩🇪

Novo Nordisk Investigational Site, Neuss, Germany

The Effect of Insulin Degludec in Combination With Liraglutide and Metformin in Subjects With Type 2 Diabetes Qualifying for Treatment Intensification

Phase 3
Completed
Conditions
Diabetes
Diabetes Mellitus, Type 2
Interventions
First Posted Date
2012-08-14
Last Posted Date
2017-09-25
Lead Sponsor
Novo Nordisk A/S
Target Recruit Count
346
Registration Number
NCT01664247
Locations
🇬🇧

Novo Nordisk Investigational Site, Stevenage, United Kingdom

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