A different molecular design: See how once-daily Tresiba® works

Tresiba® was engineered to provide a steady rate of absorption, giving Tresiba® a 42+ hour duration of action that won’t taper off at the end of the day.1,2,a Adult patients who miss a dose of Tresiba® should inject their daily dose during waking hours upon discovering the missed dose, then continue with their regular dosing schedule. Ensure that at least 8 hours have elapsed between Tresiba® injections. If a pediatric patient misses a dose, they should contact their health care provider for guidance and monitor blood glucose levels more frequently until the next scheduled dose.1
View the animated video below to see the full MOP.

aAfter the last of 8 once-daily injections (0.4 units/kg).


Tresiba® mechanism of protraction

Blue Molecule

1. INJECTION

Prior to injection, Tresiba® exists as dihexamers inside the pen in the presence of zinc and phenol.3

Many Blue Molecules

2. ASSEMBLY

After injection, phenol diffuses and Tresiba® dihexamers assemble and form multihexamer chains, resulting in a subcutaneous insulin depot.3

Small Blue Molecules

3. ABSORPTION

Zinc diffuses and insulin monomers are released slowly from the ends of the chains and absorbed continuously from the depot into circulation.3


Tresiba® MOP

References

  1. Jonassen I, Havelund S, Hoeg-Jensen T, Steensgaard DB, Wahlund PO, Ribel U. Pharm Res. 2012;29(8):2104-2114.
  2. Haahr H, Heise T. Clin Pharmacokinet. 2014;53(9):787-800.
  3. Tresiba [package insert]. Plainsboro, NJ: Novo Nordisk Inc; September 2015.
  4. De Rycke A, Mathieu C. Eur Endocrinol. 2011;7(2):84-87. doi:http://doi.org/10.17925/EE.2011.07.02.84.
  5. Seested T, Havelund S, Jonassen IB, Hoeg-Jensen T, Pyke C, Nishimura E. Diabetes. 2012;61(suppl 1):A250 [abstract 980-P].


“When I prescribe a basal insulin, I take a close look at how it works and consider why it works the way it does."
-Dr James R. Gavin, III, former president, American Diabetes Association (ADA)

Dive deeper into Tresiba®



Once-daily Tresiba®: A basal insulin with a flat and stable profile1,2,4

See how Tresiba® compares with insulin glargine U-100

Selected Important Safety Information

Contraindications

  • Tresiba® is contraindicated during episodes of hypoglycemia and in patients with hypersensitivity to Tresiba® or one of its excipients

Warnings and Precautions

  • Never Share a Tresiba® FlexTouch® Pen Between Patients, even if the needle is changed. Sharing poses a risk for transmission of blood-borne pathogens
  • Monitor blood glucose in all patients treated with insulin. Changes in insulin may affect glycemic control. These changes should be made cautiously and under medical supervision. Adjustments in concomitant oral anti-diabetic treatment may be needed
  • Hypoglycemia is the most common adverse reaction of insulin, including Tresiba®, and may be life-threatening

Indications and Usage

Tresiba® (insulin degludec injection) is indicated to improve glycemic control in patients 1 year of age and older with diabetes mellitus.

Limitations of Use

Tresiba® is not recommended for treating diabetic ketoacidosis or for pediatric patients requiring less than 5 units of Tresiba®.

Important Safety Information

Contraindications

  • Tresiba® is contraindicated during episodes of hypoglycemia and in patients with hypersensitivity to Tresiba® or one of its excipients

Warnings and Precautions

  • Never Share a Tresiba® FlexTouch® Pen Between Patients, even if the needle is changed. Sharing poses a risk for transmission of blood-borne pathogens
  • Monitor blood glucose in all patients treated with insulin. Changes in insulin may affect glycemic control. These changes should be made cautiously and under medical supervision. Adjustments in concomitant oral anti-diabetic treatment may be needed
  • Hypoglycemia is the most common adverse reaction of insulin, including Tresiba®, and may be life-threatening. Increase monitoring with changes to: insulin dose, co-administered glucose lowering medications, meal pattern, physical activity; and in patients with hypoglycemia unawareness or renal or hepatic impairment
  • Accidental mix-ups between basal insulin products and other insulins, particularly rapid-acting insulins, have been reported. To avoid medication errors, always instruct patients to check the insulin label before each injection
  • Severe, life-threatening, generalized allergy, including anaphylaxis, can occur with insulin products, including Tresiba®
  • As with all insulins, Tresiba® use can lead to life-threatening hypokalemia, which then may cause respiratory paralysis, ventricular arrhythmia, and death. Closely monitor potassium levels in patients at risk of hypokalemia and treat if indicated
  • Fluid retention and heart failure can occur with concomitant use of thiazolidinediones (TZDs), which are PPAR-gamma agonists, and insulin, including Tresiba®. Patients should be observed for signs and symptoms of heart failure. If heart failure occurs, dosage reduction or discontinuation of the TZD must be considered

Adverse Reactions

  • Adverse reactions commonly associated with Tresiba® are hypoglycemia, allergic reactions, injection site reactions, lipodystrophy, pruritus, rash, edema, and weight gain

Drug Interactions

  • Certain drugs may affect glucose metabolism, requiring insulin dose adjustment and close monitoring of blood glucose. The signs and symptoms of hypoglycemia may be reduced or absent in patients taking anti-adrenergic drugs (e.g., beta-blockers, clonidine, guanethidine, and reserpine)

Please click here for Prescribing Information.

 

References:

  1. Tresiba [package insert]. Plainsboro, NJ: Novo Nordisk Inc; December 2016.
  2. Heise T, Korsatko S, Nosek L, et al. J Diabetes. 2016;8(1):132-138.
  3. Jonassen I, Havelund S, Hoeg-Jensen T, Steensgaard DB, Wahlund PO, Ribel U. Pharm Res. 2012;29(8):2104-2114.
  4. Heise T, Hermanski L, Nosek L, Feldman A, Rasmussen S, Haahr H. Diabetes Obes Metab. 2012;14(9):859-864.