Generic Name: Nateglinide
Class: Meglitinides
VA Class: HS502
Chemical Name: (–)-N-[(trans-4-Isopropyl-cyclohexyl)carbonyl]-d-phenylalanine
Molecular Formula: C19H27NO3
CAS Number: 105816-04-4
Introduction
Nateglinide, a meglitinide derivative, is a short-acting, insulinotropic antidiabetic agent.
Uses for Starlix
Diabetes Mellitus
Used as monotherapy as an adjunct to diet and exercise for the management of type 2 (noninsulin-dependent) diabetes mellitus in patients whose hyperglycemia cannot be controlled by diet and exercise alone and who have not been treated chronically with other oral antidiabetic agents.1 5
May be used in combination with metformin as an adjunct to diet and exercise for the management of type 2 diabetes mellitus in patients who do not achieve adequate glycemic control with metformin monotherapy.1 Should be added to, not substituted for, metformin therapy in such patients.1
Should not be added to or substituted for other insulin secretagogues (e.g., sulfonylureas) in patients not controlled adequately with such drugs.1 5
Not indicated for type 1 diabetes mellitus or ketoacidosis.1
Starlix Dosage and Administration
Administration
Oral Administration
Administer 3 times daily 1–30 minutes before meals to reduce the risk of hypoglycemia.1
If a meal is skipped, the dose of nateglinide should be omitted.1
Dosage
Adults
Diabetes Mellitus
Oral
120 mg 3 times daily before meals.1 For patients who are near their goal glycosylated hemoglobin (HbA1c) when nateglinide therapy is initiated, 60 mg 3 times daily before meals.1 5
Special Populations
Hepatic Impairment
No dosage adjustment necessary in patients with mild impairment.1 Use with caution in patients with moderate or severe impairment.1
Renal Impairment
No dosage adjustment necessary.1
Geriatric Patients
No dosage adjustment necessary.1
Cautions for Starlix
Contraindications
Known hypersensitivity to nateglinide or any ingredient in the formulation.1
Type 1 (insulin-dependent) diabetes mellitus or diabetic ketoacidosis.1
Warnings/Precautions
General Precautions
Hypoglycemia
Potential for hypoglycemia.1 3 4 Malnourished or geriatric patients and patients with adrenal or pituitary insufficiency may be particularly susceptible.1 Strenuous exercise, alcohol ingestion, insufficient caloric intake acutely or chronically, or use in combination with other antidiabetic agents may increase risk.1 Hypoglycemia may be difficult to recognize in patients with autonomic neuropathy or in those receiving β-adrenergic blocking agents.1
Loss of Glycemic Control
Possible loss of glycemic control during periods of stress (e.g., fever, trauma, infection, surgery).1 Temporary discontinuance of nateglinide and administration of insulin may be required.1
Efficacy of nateglinide may decrease over time.1
Specific Populations
Pregnancy
Category C.1
Lactation
Distributed into milk in rats; use not recommended.1
Pediatric Use
Safety and efficacy not established.1
Geriatric Use
No substantial differences in safety, efficacy, or pharmacokinetics relative to younger adults, but increased sensitivity cannot be ruled out.1
Hepatic Impairment
Use with caution in patients with moderate to severe hepatic impairment.1
Common Adverse Effects
Upper respiratory tract infection, back pain, flu symptoms, dizziness, arthropathy, diarrhea, accidental trauma, bronchitis, cough, hypoglycemia.1
Interactions for Starlix
Extensively metabolized by CYP2C9 and, to a lesser extent, CYP3A4.1 3 Based on in vitro data, the drug is a potential inhibitor of CYP2C9 in vivo.1 (See Specific Drugs under Interactions.)
Drugs Affecting Hepatic Microsomal Enzymes
Potential pharmacokinetic interaction (altered metabolism of nateglinide) when administered concomitantly with inhibitors or inducers of CYP2C9 or CYP3A4.1
Drugs That May Increase Hypoglycemic Effects
Pharmacodynamic interaction with such drugs as MAO inhibitors, nonselective β-adrenergic-blocking agents, and NSAIAs (e.g., salicylates).1 Observe patient closely for altered glycemic control when these drugs are initiated or withdrawn in patients receiving nateglinide.1
Drugs That May Antagonize Hypoglycemic Effects
Pharmacodynamic interaction with such drugs as corticosteroids, sympathomimetic agents, thiazide diuretics, and thyroid hormones.1 Observe patient closely for altered glycemic control when these drugs are initiated or withdrawn in patients receiving nateglinide.1
Protein-bound Drugs
Potential pharmacokinetic interaction, but no important effects on nateglinide protein binding observed in vitro with highly protein-bound drugs such as furosemide, propranolol, captopril, nicardipine, pravastatin, glyburide, warfarin, phenytoin, aspirin, tolbutamide, and metformin.1 In addition, nateglinide had no influence in vitro on protein binding of propranolol, glyburide, nicardipine, warfarin, phenytoin, aspirin, or tolbutamide.1
Specific Drugs
Drug | Interaction |
---|---|
Diclofenac | No clinically important pharmacokinetic interaction observed with single dose of diclofenac1 |
Digoxin | No clinically important pharmacokinetic interaction observed with single dose of digoxin1 |
Glyburide | No clinically important pharmacokinetic interaction observed with single dose of glyburide1 |
Metformin | No clinically important pharmacokinetic interaction observed1 |
Tolbutamide | In vitro inhibition of tolbutamide metabolisma |
Warfarin | No clinically important pharmacokinetic interaction observed with single dose of warfarin1 |
Starlix Pharmacokinetics
Absorption
Bioavailability
Approximately 73% (absolute),1 b c indicating a modest first-pass effect.b c
Onset
Stimulates pancreatic insulin secretion within 20 minutes following oral administration.1
Duration
Peak insulin concentrations occur approximately 1 hour after dose and return to baseline by 4 hours.1
Food
When administered with or after meals, food delays absorption, as evidenced by a decrease in peak plasma concentration and prolongation of the time to peak plasma concentration; however, extent of absorption is not affected.1 When nateglinide is administered 10 minutes prior to a liquid meal, peak plasma drug concentrations are reduced appreciably.a Pharmacokinetics are not affected by the composition of a meal (e.g., high protein, fat, carbohydrate).a
Distribution
Extent
Distributed into milk in animals; not known whether the drug distributes into milk or crosses the placenta in humans.1
Plasma Protein Binding
98%.1
Elimination
Metabolism
Predominantly metabolized by CYP2C9 (70%) and CYP3A4 (30%).1 The major metabolites are less potent than the parent drug.1 The isoprene minor metabolite is as potent as the parent compound.1
Elimination Route
In urine, principally as unchanged drug and metabolites.1 b
Half-life
Approximately 1.5 hours.1 2
Special Populations
Mild hepatic insufficiency increases the peak and total exposure of nateglinide by 30%.1
Stability
Storage
Oral
Tablets
Tight containers at 25°C; may be exposed to 15–30°C.a
ActionsActions
Insulinotropic antidiabetic agent (a d-phenylalanine derivative).1 2 3 4 5 8 c
Requires functioning pancreatic β-cells for hypoglycemic activity.1 2 3 4 8 Lowers blood glucose concentrations principally by augmenting endogenous insulin secretion from the pancreas in response to a meal.1 2 3 4 8
Advice to Patients
Importance of patient managing hypoglycemia and hyperglycemia appropriately.1
Importance of patient taking medication 1–30 minutes before each meal and of skipping scheduled dose of nateglinide if a meal is skipped.1
Importance of patient adhering to diet and exercise regimen.1
Importance of regular monitoring of blood glucose (preferably self-monitoring) and glycosylated hemoglobin (HbA1c).1
Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.1
Importance of patient informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs.1
Importance of informing patients of other important precautionary information. (See Cautions.)
Preparations
Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.
Routes | Dosage Forms | Strengths | Brand Names | Manufacturer |
---|---|---|---|---|
Oral | Tablets | 60 mg | Starlix | Novartis |
120 mg | Starlix | Novartis |
Comparative Pricing
This pricing information is subject to change at the sole discretion of DS Pharmacy. This pricing information was updated 03/2011. Actual costs to patients will vary depending on the use of specific retail or mail-order locations and health insurance copays.
Starlix 120MG Tablets (NOVARTIS): 30/$71.99 or 90/$179.96
Starlix 60MG Tablets (NOVARTIS): 30/$66.99 or 90/$176.98
Disclaimer
This report on medications is for your information only, and is not considered individual patient advice. Because of the changing nature of drug information, please consult your physician or pharmacist about specific clinical use.
The American Society of Health-System Pharmacists, Inc. and Drugs.com represent that the information provided hereunder was formulated with a reasonable standard of care, and in conformity with professional standards in the field. The American Society of Health-System Pharmacists, Inc. and Drugs.com make no representations or warranties, express or implied, including, but not limited to, any implied warranty of merchantability and/or fitness for a particular purpose, with respect to such information and specifically disclaims all such warranties. Users are advised that decisions regarding drug therapy are complex medical decisions requiring the independent, informed decision of an appropriate health care professional, and the information is provided for informational purposes only. The entire monograph for a drug should be reviewed for a thorough understanding of the drug's actions, uses and side effects. The American Society of Health-System Pharmacists, Inc. and Drugs.com do not endorse or recommend the use of any drug. The information is not a substitute for medical care.
AHFS Drug Information. © Copyright, 1959-2011, Selected Revisions May 2010. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.
References
1. Novartis. Starlix (nateglinide) tablets prescribing information. East Hanover, NJ; 2001 Jan.
2. Landgraf R. Meglitinide analogues in the treatment of type 2 diabetes mellitus. Drugs Aging. 2000; 17:411-25. [PubMed 11190420]
3. Dunn CJ, Faulds D. Nateglinide. Drugs. 2000; 60:607-15. [PubMed 11030470]
4. Horton ES, Foley J, Clinkingbeard C et al. Nateglinide alone and in combination with metformin improves glycemic control by reducing mealtime glucose levels in type 2 diabetes. Diabetes Care. 2000; 23:1660-65. [IDIS 455201] [PubMed 11092289]
5. Novartis, East Hanover, NJ: Personal communication.
6. Hollander PA, Schwartz SL, Gatlin MR et al. Nateglinide, but not glyburide, selectively enhances early insulin release and more effectively controls post-meal glucose excursions with less total insulin exposure. Diabetes. 2000; 49(Suppl 1):A111.
7. Marre M, Whatmough I, Pongowski M et al. Nateglinide added to metformin offers safe and effective treatment for type 2 diabetes. Diabetes. 2000; 49(Suppl 1):A361.
8. Anon. Nateglinide for type 2 diabetes. Med Lett Drugs Ther. 2001; 43:29-30. [PubMed 11283474]
a. Novartis. Starlix (nateglinide) tablets prescribing information. East Hanover, NJ; 2002 Nov.
b. Weaver ML, Orwig BA, Rodriguez LC et al. Pharmacokinetics and metabolism of nateglinide in humans. Drug Metab Dispos. 2001; 29:415-21. [PubMed 11259325]
c. Halas CJ. Nateglinide. Am J Health Syst Pharm. 2001; 58:1200-5. [PubMed 11449877]
More Starlix resources
- Starlix Side Effects (in more detail)
- Starlix Dosage
- Starlix Use in Pregnancy & Breastfeeding
- Drug Images
- Starlix Drug Interactions
- Starlix Support Group
- 0 Reviews for Starlix - Add your own review/rating
- Starlix Prescribing Information (FDA)
- Starlix Consumer Overview
- Starlix Advanced Consumer (Micromedex) - Includes Dosage Information
- Starlix MedFacts Consumer Leaflet (Wolters Kluwer)
- Nateglinide Prescribing Information (FDA)
- Nateglinide Professional Patient Advice (Wolters Kluwer)
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