NATEGLINIDE tablet, coated

Nateglinide by

Drug Labeling and Warnings

Nateglinide by is a Prescription medication manufactured, distributed, or labeled by Par Pharmaceutical, Inc., Par Pharmaceutical Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • 1 INDICATIONS AND USAGE

    Nateglinide is indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.

    Limitations of Use:

    Nateglinide should not be used in patients with type 1 diabetes mellitus or for the treatment of diabetic ketoacidosis.

  • 2 DOSAGE AND ADMINISTRATION

    The recommended dose of nateglinide is 120 mg orally three times daily before meals.

    The recommended dose of nateglinide is 60 mg orally three times daily before meals in patients who are near glycemic goal when treatment is initiated.

    Instruct patients to take nateglinide 1 to 30 minutes before meals.

    In patients who skip meals, instruct patients to skip the scheduled dose of nateglinide to reduce the risk of hypoglycemia [see Warnings and Precautions (5.1)].

  • 3 DOSAGE FORMS AND STRENGTHS

    • 60 mg tablets: Pink color coated, round biconvex, beveled edge tablet debossed with “P 984” on one side and plain on the other side

    • 120 mg tablets: Orange color coated, oval shaped biconvex, tablet debossed with “P 985” on one side and plain on the other side

  • 4 CONTRAINDICATIONS

    Nateglinide tablets are contraindicated in patients with a history of hypersensitivity to nateglinide or its inactive ingredients.

  • 5 WARNINGS AND PRECAUTIONS

    5.1 Hypoglycemia

    All glinides, including nateglinide, can cause hypoglycemia [see Adverse Reactions (6.1)]. Severe hypoglycemia can cause seizures, may be life-threatening, or cause death. Hypoglycemia can impair concentration ability and reaction time; this may place an individual and others at risk in situations where these abilities are important (e.g., driving or operating other machinery).

    Hypoglycemia can happen suddenly and symptoms may differ in each individual and change over time in the same individual. Symptomatic awareness of hypoglycemia may be less pronounced in patients with longstanding diabetes, in patients with diabetic neuropathy (nerve disease), in patients using medications that block the sympathetic nervous system (e.g., beta-blockers) [see Drug Interactions (7)], or in patients who experience recurrent hypoglycemia.

    Factors which may increase the risk of hypoglycemia include changes in meal pattern (e.g., macronutrient content), changes in level of physical activity, changes to coadministered medication [see Drug Interactions (7)], and concomitant use with other antidiabetic agents. Patients with renal or hepatic impairment may be at higher risk of hypoglycemia [seeUse in Specific Populations (8.6, 8.7)], Clinical Pharmacology (12.3)]

    Patients should take nateglinide before meals and be instructed to skip the dose of nateglinide if a meal is skipped [see Dosage and Administration (2)]. Patients and caregivers must be educated to recognize and manage hypoglycemia. Self-monitoringof blood glucose plays an essential role in the prevention and management of hypoglycemia. In patients athigher risk for hypoglycemia and patients who have reduced symptomatic awareness of hypoglycemia, increasedfrequency of blood glucose monitoring is recommended.

    5.2 Macrovascular Outcomes

    There have been no clinical studies establishing conclusive evidence of macrovascular risk reduction with nateglinide.

  • 6 ADVERSE REACTIONS

    The following serious adverse reaction is also described elsewhere in the labeling:

          Hypoglycemia [see Warnings and Precautions (5.1)]

    6.1 Clinical Trials Experience

    Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

    In clinical trials, approximately 2,600 patients with type 2 diabetes mellitus were treated with nateglinide. Of these, approximately 1,335 patients were treated for 6 months or longer and approximately 190 patients for one year or longer. Table 1 shows the most common adverse reactions associated with nateglinide.

    Table 1. Adverse Reactions other than Hypoglycemia (%) occurring Greater than or Equal to 2% in Nateglinide-Treated Patients from Pool of 12 to 64 week Placebo Controlled Trials

    Placebo

    N=458

    Nateglinide

    N=1441

    Preferred Term

    Upper Respiratory Infection

    8.1

    10.5

    Back Pain

    3.7

    4.0

    Flu Symptoms

    2.6

    3.6

    Dizziness

    2.2

    3.6

    Arthropathy

    2.2

    3.3

    Diarrhea

    3.1

    3.2

    Accidental Trauma

    1.7

    2.9

    Bronchitis

    2.6

    2.7

    Coughing

    2.2

    2.4

    Hypoglycemia

    Episodes of severe hypoglycemia (plasma glucose less than 36 mg/dL) were reported in two patients treated with nateglinide. Non-severe hypoglycemia occurred in 2.4 % of nateglinide treated patients and 0.4 % of placebo treated patients [see Warnings and Precautions (5.1)].

    Weight Gain

    Patients treated with nateglinide had statistically significant mean increases in weight compared to placebo. In clinical trials, the mean weight increases with nateglinide 60 mg (3 times daily) and nateglinide 120 mg (3 times daily) compared to placebo were 1.0 kg and 1.6 kg respectively.

    Laboratory Test

    Increases in Uric Acid: There were increases in mean uric acid levels for patients treated with nateglinide alone, nateglinide in combination with metformin, metformin alone, and glyburide alone. The respective differences from placebo were 0.29 mg/dL, 0.45 mg/dL, 0.28 mg/dL, and 0.19 mg/dL.


    6.2 Postmarketing Experience

    The following adverse reactions have been identified during post-approval use of nateglinide. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

    • Hypersensitivity reactions: Rash, itching, and urticaria
    • Hepatobiliary Disorders: Jaundice, cholestatic hepatitis, and elevated liver enzymes
  • 7 DRUG INTERACTIONS

    Table 2 includes a list of drugs with clinically important drug interactions when concomitantly administered or withdrawn with nateglinide and instructions for managing or preventing them.

    Table 2. Clinically Significant Drug Interactions with Nteglinide

    Drugs That May Increase the Blood-Glucose-Lowering Effect of Nateglinide and

    Susceptibility to Hypoglycemia

    Drugs:

    Nonsteroidal anti-inflammatory drugs (NSAIDs), salicylates, monoamine oxidase inhibitors, non-selective beta-adrenergic-blocking agents, anabolic hormones (e.g. methandrostenolone), guanethidine, gymnema sylvestre, glucomannan, thioctic acid, and inhibitors of CYP2C9 (e.g. amiodarone, fluconazole, voriconazole, sulfinpyrazone),or in patients known to be poor metabolizers of CYP2C9 substrates, alcohol.

    Intervention:

    Dose reductions and increased frequency of glucose monitoring may be required when nateglinide is coadministered with these drugs.

    Drugs and Herbals That May Reduce the Blood-Glucose-Lowering Effect of Nateglinide and Increase Susceptibility to Hyperglycemia

    Drugs:

    Thiazides, corticosteroids, thyroid products, sympathomimetics, somatropin, somatostatin analogues (e.g. lanreotide, octreotide), and CYP inducers (e.g. rifampin, phenytoin and St John’s Wort).

    Intervention:

    Dose increases and increased frequency of glucose monitoring may be required when nateglinide is coadministered with these drugs.

    Drugs That May Blunt Signs and Symptoms of Hypoglycemia

    Drugs:

    beta-blockers, clonidine, guanethidine, and reserpine

    Intervention:

    Increased frequency of glucose monitoring may be required when nateglinide is coadministered with these drugs.

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Pregnancy Category C

    There are no adequate and well-controlled studies of nateglinide in pregnant women. It is unknown whether nateglinide can cause fetal harm when administered to a pregnant woman. Nateglinide should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

    In the rabbit, embryonic development was adversely affected and the incidence of gall bladder agenesis or small gallbladder was increased at a dose of 500 mg/kg (approximately 27 times the human therapeutic exposure of 120 mg three times daily, based on body surface area). Nateglinide was not teratogenic in rats at doses up to 1,000 mg/kg (approximately 27 times the human therapeutic exposure based on body surface area).

    8.3 Nursing Mothers

    It is not known whether nateglinide is excreted in human milk. Nateglinide is excreted in rat milk. Offspring of rats exposed to 1,000 mg/kg nateglinide (approximately 27 times the human therapeutic exposure of 120 mg three times daily, based on body surface area) had lower body weight. Because the potential for hypoglycemia in nursing infants may exist, a decision should be made as to whether nateglinide should be discontinued in nursing mothers, or if mothers should discontinue nursing.

    8.4 Pediatric Use

    The safety and effectiveness of nateglinide have not been established in pediatric patients.

    8.5 Geriatric Use

    436 patients 65 years and older, and 80 patients 75 years and older were exposed to nateglinide in clinical studies. No differences were observed in safety or efficacy of nateglinide between patients age 65 and over, and those under age 65. However, greater sensitivity of some older individuals to nateglinide therapy cannot be ruled out.

    8.6 Renal Impairment

    No dosage adjustment is recommended in patients with mild to severe renal impairment [see Clinical Pharmacology (12.3)].

    8.7 Hepatic Impairment

    No dose adjustment is recommended for patients with mild hepatic impairment. Use of nateglinide in patients with moderate-to-severe hepatic impairment has not been studied and therefore, should be used with caution in these patients [see Clinical Pharmacology (12.3)].

  • 10 OVERDOSAGE

    There have been no instances of overdose with nateglinide in clinical trials. However, an overdose may result in an exaggerated glucose-lowering effect with the development of hypoglycemic symptoms. Hypoglycemic symptoms without loss of consciousness or neurological findings should be treated with oral glucose and adjustments in dosage and/or meal patterns. Severe hypoglycemic reactions with coma, seizure, or other neurological symptoms should be treated with intravenous glucose. As nateglinide is highly protein bound, dialysis is not an efficient means of removing it from the blood.

  • 11 DESCRIPTION

    Nateglinide Tablets, USP are an oral blood glucose-lowering drug of the glinide class. Nateglinide, (-)-N-[(trans-4-isopropylcyclohexane)carbonyl]-D-phenylalanine, is structurally unrelated to the oral sulfonylurea insulin secretagogues.

    The structural formula is as shown:

    structure

    Nateglinide is a white powder with a molecular weight of 317.43. It is freely soluble in methanol, ethanol, and chloroform, soluble in ether, sparingly soluble in acetonitrile and octanol, and practically insoluble in water. Nateglinide biconvex tablets contain 60 mg, or 120 mg, of nateglinide for oral administration.

    Inactive Ingredients: colloidal silicon dioxide, croscarmellose sodium, lactose monohydrate, magnesium stearate, microcrystalline cellulose, povidone, pregelatinized starch (starch 1500®).  Starch 1500® is partially pregelatinized maize starch. The 60 mg also contains iron oxide red, polyethylene glycol, polyvinyl alcohol, talc, and titanium dioxide.  In addition, the 120 mg contains FD&C Yellow #6/Sunset Yellow Aluminum Lake, iron oxide yellow.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Nateglinide lowers blood glucose levels by stimulating insulin secretion from the pancreas. This action is dependent upon functioning beta-cells in the pancreatic islets. Nateglinide interacts with the ATP-sensitive potassium (K+ATP) channel on pancreatic beta-cells. The subsequent depolarization of the beta cell opens the calcium channel, producing calcium influx and insulin secretion. The extent of insulin release is glucose dependent and diminishes at low glucose levels. Nateglinide is highly tissue selective with low affinity for heart and skeletal muscle.

    12.2 Pharmacodynamics

    Nateglinide stimulates pancreatic insulin secretion within 20 minutes of oral administration. When nateglinide is dosed before meals, the peak rise in plasma insulin occurs approximately 1 hour after dosing and falls to baseline by 4 hours after dosing.

    12.3 Pharmacokinetics

    In patients with Type 2 diabetes, multiple dose administration of nateglinide over the dosage range of 60 mg to 240 mg shows linear pharmacokinetics for both AUC and Cmax. In patients with Type 2 diabetes, there is no apparent accumulation of nateglinide upon multiple dosing of up to 240 mg three times daily for 7 days.

    Absorption

    Absolute bioavailability of nateglinide is approximately 73%. Plasma profiles are characterized by multiple plasma concentration peaks when nateglinide is administered under fasting conditions. This effect is diminished when nateglinide is taken prior to a meal. Following oral administration immediately prior to a meal, the mean peak plasma nateglinide concentrations (Cmax) generally occur within 1 hour (Tmax) after dosing. Tmax is independent of dose.

    The pharmacokinetics of nateglinide are not affected by the composition of a meal (high protein, fat, or carbohydrate). However, peak plasma levels are significantly reduced when nateglinide is administered 10 minutes prior to a liquid meal as compared to solid meal. When given with or after meals, the extent of nateglinide absorption (AUC) remains unaffected. However, there is a delay in the rate of absorption characterized by a decrease in Cmax and a delay in time to peak plasma concentration (Tmax).

    Nateglinide did not have any effect on gastric emptying in healthy subjects as assessed by acetaminophen testing.

    Distribution

    Following intravenous (IV) administration of nateglinide, the steady-state volume of distribution of nateglinide is estimated to be approximately 10 L in healthy subjects. Nateglinide is extensively bound (98%) to serum proteins, primarily serum albumin, and to a lesser extent α1 acid glycoprotein. The extent of serum protein binding is independent of drug concentration over the test range of 0.1 to 10 mcg/mL.

    Elimination

    In healthy volunteers and patients with type 2 diabetes mellitus, nateglinide plasma concentrations declined with an average elimination half-life of approximately 1.5 hours.

    Metabolism

    In vitro drug metabolism studies indicate that nateglinide is predominantly metabolized by the cytochrome P450 isozyme CYP2C9 (70%) and to a lesser extent CYP3A4 (30%).

    The major routes of metabolism are hydroxylation followed by glucuronide conjugation. The major metabolites are less potent antidiabetic agents than nateglinide. The isoprene minor metabolite possesses potency similar to that of the parent compound nateglinide.

    Excretion

    Nateglinide and its metabolites are rapidly and completely eliminated following oral administration. Eighty-three percent of the 14C-nateglinide was excreted in the urine with an additional 10% eliminated in the feces. Approximately 16% of the 14C-nateglinide was excreted in the urine as parent compound.

    Specific Populations

    Renal Impairment

    No pharmacokinetic data are available in subjects with mild renal impairment (CrCl 60 to 89 mL/min). Compared to healthy matched subjects, patients with type 2 diabetes mellitus and moderate and severe renal impairment (CrCl 15-50 mL/min) not on dialysis displayed similar apparent clearance, AUC, and Cmax. Patients with type 2 diabetes and renal failure on dialysis exhibited reduced overall drug exposure (Cmax decreased by 49%; not statistically significant). However, hemodialysis patients also experienced reductions in plasma protein binding compared to the matched healthy volunteers.

    In a cohort of 8 patients with type 2 diabetes and end-stage renal disease (ESRD) (eGFR < 15 mL/min/1.73m2) M1 metabolite accumulation up to 1.2 ng/mL occurred with a dosage of 90 mg once daily for 1 to 3 months. In another cohort of 8 patients with type 2 diabetes on hemodialysis, M1 concentration decreased after a single session of hemodialysis. Although the hypoglycemic activity of the M1 metabolite is approximately 5 times lower than nateglinide, metabolite accumulation may increase the hypoglycemic effect of the administered dose.

    Hepatic Impairment

    In patients with mild hepatic impairment, the mean increase in Cmax and AUC of nateglinide were 37% and 30 % respectively, as compared to healthy matched control subjects. There is no data on pharmacokinetics of nateglinide in patients with moderate-to-severe hepatic impairment.

    Gender

    No clinically significant differences in nateglinide pharmacokinetics were observed between men and women.

    Race

    Results of a population pharmacokinetic analysis including subjects of Caucasian, Black, and other ethnic origins suggest that race has little influence on the pharmacokinetics of nateglinide.

    Age

    Age does not influence the pharmacokinetic properties of nateglinide.

    Drug Interactions:

    In vitroassessment of drug interactions

    Nateglinide is a potential inhibitor of the CYP2C9 isoenzyme in vivo as indicated by its ability to inhibit the in vitro metabolism of tolbutamide. Inhibition of CYP3A4 metabolic reactions was not detected in in vitro experiments.

    In vitro displacement studies with highly protein-bound drugs such as furosemide, propranolol, captopril, nicardipine, pravastatin, glyburide, warfarin, phenytoin, acetylsalicylic acid, tolbutamide, and metformin showed no influence on the extent of nateglinide protein binding. Similarly, nateglinide had no influence on the serum protein binding of propranolol, glyburide, nicardipine, warfarin, phenytoin, acetylsalicylic acid, and tolbutamide in vitro. However, prudent evaluation of individual cases is warranted in the clinical setting.

    In vivoassessment of drug interactions

    The effect of coadministered drugs on the pharmacokinetics of nateglinide and the effect of nateglinide on pharmacokinetics of coadministered drugs are shown in Tables 3 and 4. No clinically relevant change in pharmacokinetic parameters of either agent was reported when nateglinide was coadministered with glyburide, metformin, digoxin, warfarin, and diclofenac.

    Table 3. Effect of Coadministered drugs on Pharmacokinetics of Nateglinide

    Coadministered Drug

    Dosing regimen of coadministered drug

    Dosing regimen of nateglinide

    Change in Cmax

    Change in AUC

    Glyburide

    10 mg once daily for 3 weeks

    120 mg three times a day, single dose

    8.78% ↓

    3.53% ↓

    Metformin

    500 mg three times a day for 3 weeks

    120 mg three times a day, single dose

    AM: 7.14% ↑

    PM: 11.4% ↓

    AM: 1.51% ↑

    PM: 5.97% ↑

    Digoxin

    1 mg, single dose

    120 mg three times a day, single dose

    AM: 2.17% ↓

    PM: 3.19% ↑

    AM: 7.62% ↑

    PM: 2.22% ↑

    Warfarin

    30 mg, single dose

    120 mg three times a day for 4 days

    2.65% ↑

    3.72% ↓

    Diclofenac

    75 mg, single dose

    120 mg twice daily, single dose

    AM: 13.23% ↓

    *PM: 3.76% ↑

    AM: 2.2% ↓

    *PM: 7.5% ↑

    AM: after morning dose; PM: after evening dose; * after second dose; ↑: increase in the parameter; ↓: decrease in the parameter


    Table 4. Effect of Nateglinide on Pharmacokinetics of Coadministered Drugs

    Coadministered Drug

    Dosing regimen of coadministered drug

    Dosing regimen of nateglinide

    Change in Cmax

    Change in AUC

    Glyburide

    10 mg once daily for 3 weeks

    120 mg three times a day, single dose

    3.18% ↓

    7.34% ↓

    Metformin

    500 mg three times a day for 3 weeks

    120 mg three times a day, single dose

    AM: 10.7% ↑

    PM: 0.40% ↑

    AM: 13.3% ↑

    PM: 2.27% ↓

    Digoxin

    1 mg, single dose

    120 mg three times a day, single dose

    5.41% ↓

    6.58% ↑

    Warfarin

    30 mg, single dose

    120 mg three times a day for 4 days

    R-warfarin: 1.03% ↓

    S-warfarin: 0.85% ↓

    R-warfarin: 0.74% ↑

    S-warfarin: 7.23% ↑

    Diclofenac

    75 mg, single dose

    120 mg twice daily, single dose

    2.19% ↑

    7.97% ↑

    AM: after morning dose; PM: after evening dose; SD: single dose; ↑: increase in the parameter; ↓: decrease in the parameter

     

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis and Mutagenesis and Impairment of Fertility

    Carcinogenicity: Nateglinide did not increase tumors in two year carcinogenicity studies conducted in mice and rats. Oral doses of Nateglinide up to 900 mg/kg in rats and 400 mg/kg in mice were tested, which produced exposures in rats approximately 30 to 40 times and in mice 10 to 30 times the human therapeutic exposure of nateglinide at a dose of 120 mg three times daily, based on AUC.

    Mutagenesis: Nateglinide was not genotoxic in the in vitro Ames test, mouse lymphoma assay, chromosome aberration assay or in the in vivo mouse micronucleus test.

    Impairment of Fertility: Fertility was unaffected by administration of nateglinide to rats at doses up to 600 mg/kg (approximately 16 times the human therapeutic exposure with a recommended nateglinide dose of 120 mg three times daily before meals).

  • 14 CLINICAL STUDIES

    14.1 Monotherapy

    In a 24-week, double-blind, placebo-controlled study, patients with type 2 diabetes were randomized to receive either nateglinide (60 mg or 120 mg three times daily before meals) or placebo. Patients previously treated with antidiabetic medications were required to discontinue that medication for at least 2 months before randomization.

    At Week 24, treatment with nateglinide before meals resulted in statistically significant reductions in mean HbA1C and mean fasting plasma glucose (FPG) compared to placebo (see Table 5). The reductions in HbA1C and FPG were similar for patients naïve to, and those previously exposed to, antidiabetic medications.

    Table 5. Endpoint results for a 24-week, fixed dose study of nateglinide monotherapy

    HbA1c (%)

    Placebo

     


     N=168

    Nateglinide

    60 mg

    three times daily before meals

    N=167

    Nateglinide

    120 mg

    three times daily before meals

    N=168

    Baseline (mean)

    Change from baseline (mean)

    Difference from placebo (mean)

    FPG (mg/dL)

    8.0

    +0.2


    N=172

    7.9

    -0.3

    -0.5a

    N=171

    8.1

    -0.5

    -0.7a

    N=169

    Baseline (mean)

    Change from baseline (mean)

    Difference from placebo (mean)

    167.9

    +9.1

    161.0

    +0.4

    -8.7a

    166.5

    -4.5

    -13.6a

    a p-value ≤ 0.004


    14.2 Monotherapy Compared to Glyburide

    In a 24-week, double-blind, active-controlled trial, patients with type 2 diabetes who had been on a sulfonylurea for 3 or more months and who had a baseline HbA1C greater than or equal to 6.5% were randomized to receive nateglinide (60 mg or 120 mg three times daily before meals) or glyburide 10 mg once daily. Patients randomized to nateglinide had statistically significant increases in mean HbA1C and mean FPG at endpoint compared to patients randomized to glyburide.

    Table 6. Endpoint Results for a 24-week Study of Nateglinide Monotherapy Compared to Glyburide

    Glyburide

    10 mg

    Once daily

    Nateglinide

    60 mg

    three times daily

    before meal

    Nateglinide

    120 mg

    three times daily

    before meals

    HbA1c (%)

    N=183

    N=178

    N=179

    Baseline (mean)

    7.8

    8.0

    7.9

    Change from baseline (mean)

    0.3

    1.3

    1.1

    Difference from glyburide

    1.0a

    0.9a

    FPG (mmol/L)

    N=184

    N=182

    N=180

    Baseline (mean)

    9.44

    9.67

    9.61

    Change from baseline (mean)

    0.19

    3.06

    2.84

    Difference from glyburide

    2.87a

    2.66a

    a p-Value < 0.001

    14.3 Monotherapy and In Combination With Metformin

    In a 24-week, double-blind, active- and placebo-controlled study, patients with type 2 diabetes were randomized to receive either nateglinide alone (120 mg three times daily before meals), metformin alone (500 mg three times daily), a combination of nateglinide 120 mg (three times daily before meals) and metformin (500 mg three times daily), or placebo. Fifty-seven percent of patients were previously untreated with oral antidiabetic therapy. Patients previously treated with antidiabetic medications were required to discontinue medication for at least 2 months before randomization.

    At Week 24, statistically significant reductions in mean HbA1C and FPG were observed with metformin monotherapy compared to nateglinide monotherapy, and the combination of nateglinide and metformin compared to either nateglinide or metformin monotherapy (see Table 7).

    Compared to placebo, nateglinide monotherapy was associated with a statistically significant increase in mean body weight, while no significant change in body weight was observed with metformin monotherapy or combination of nateglinide and metformin therapy (see Table 7). Among the subset of patients previously treated with other antidiabetic agents, primarily glyburide, HbA1C in the nateglinide monotherapy group increased slightly from baseline, whereas HbA1C was reduced in the metformin monotherapy group (see Table 7).

    Table 7. Endpoint Results for a 24-week Study of Nateglinide Monotherapy and Combination with Metformin

    HbA1c (%)

    All

    Placebo

    N=160

    Nateglinide

    120 mg

    three times

    daily before

    meals

    N=171

    Metformin

    500 mg

    three times

    daily

    N=172

    Nateglinide

    120 mg

    before meals plus

    Metformin*

    N=162

    Baseline (mean)

    Change from baseline (mean)

    Difference from placebo

    Naïve

    8.3

    +0.4

    N=98

    8.3

    -0.4bc

    -0.8a

    N=99

    8.4

    -0.8c

    -1.2a

    N=98

    8.4

    -1.5

    -1.9a

    N=81

    Baseline (mean)

    Change from baseline (mean)

    Difference from placebo

    Non-Naïve

    8.2

    +0.3

    N=62

    8.1

    -0.7c

    -1.0a

    N=72

    8.3

    -0.8c

    -1.1a

    N=74

    8.2

    -1.6

    -1.9a

    N=81

    Baseline (mean)

    Change from baseline (mean)

    Difference from placebo

    FPG (mg/dL)

    All

    8.3

    +0.6

    N=166

    8.5

    +0.004bc

    -0.6a

    N=173

    8.7

    -0.8c

    -1.4a

    N=174

    8.7

    -1.4

    -2.0a

    N=167

    Baseline (mean)

    Change from baseline (mean)

    Difference from placebo

    194.0

    +8.0

    196.5

    -13.1bc

    -21.1a

    196.0

    -30.0c

    -38.0a

    197.7

    -44.9

    -52.9a

    a  p-value ≤0.05 vs. placebo

    b p-value ≤0.03 vs. metformin

    c p-value ≤0.05 vs. combination

    * Metformin was administered three times daily

    In another 24-week, double-blind, placebo-controlled trial, patients with type 2 diabetes with HbA1C greater than or equal to 6.8% after treatment with metformin (greater than or equal to 1500 mg daily for at least 1 month) were first entered into a four week run-in period of metformin monotherapy (2000 mg daily) and then randomized to receive either nateglinide (60 mg or 120 mg three times daily before meals) or placebo as add-on to metformin. At the end of treatment, nateglinide 60 mg and 120 mg three times daily resulted in a statistically significantly greater reductions in HbA1C compared to placebo when added to metformin (-0.4% and -0.6% for nateglinide 60 mg and nateglinide 120 mg plus metformin, respectively).

    Table 8. Endpoint Results for a 24-week Study of Nateglinide Monotherapy as Add-on to Metformin

    HbA1c (%)

    Placebo

    + metformin

    N=150

    Nateglinide

    60 mg

    +

    metformin

    N=152

    Nateglinide

    120 mg

    +

    metformin

    N=154

    Baseline (mean)

    Change from baseline (mean)

    Difference from metformin

    8.2

    0.01

    8.0

    -0.4

    -0.4a

    8.2

    -0.6

    -0.6b

    a p-value 0.003 vs. metformin

    b p-value < 0.001 vs. metformin

    All nateglinide/placebo taken three times daily before meals; all metformin 1000mg twice daily.

     

    14.4 Add-On Combination Therapy With Rosiglitazone

    A 24-week, double blind, multicenter, placebo-controlled trial was performed in patients with type 2 diabetes not adequately controlled on rosiglitazone 8 mg daily. The addition of nateglinide (120 mg three times per day with meals) was associated with statistically significantly greater reductions in HbA1C compared to placebo as add-on to rosiglitazone. The mean change in weight from baseline was +3 kg for patients treated with nateglinide compared to +1 kg for patients treated with placebo when added to rosiglitazone.

    Table 9. Endpoint Results for a 24-week Study of the Effect of Adding Nateglinide or Placebo to Rosiglitazone

    HbA1c (%)

    Placebo

    + rosiglitazone 8 mg once daily

    N=191

    Nateglinide

    120 mg before meals

    +

    rosiglitazone 8 mg once daily

    N=194

    Baseline (mean)

    Change from baseline (mean)

    Difference from rosiglitazone (mean)

    8.4

    0.03

    8.3

    -0.7

    -0.7a

    a p-value < 0.0001

    14.5 Add-On Combination Therapy With Glyburide

    In a 12-week study of patients with type 2 diabetes inadequately controlled on glyburide 10 mg once daily, the addition of nateglinide (60 mg or 120 mg three times daily before meals) did not produce any additional benefit.

    Table 10. Endpoint Results for a 12-week Study of the Effect of Adding Nateglinide or Placebo to Glyburide

    HbA1c (%)

    Placebo + glyburide 10 mg once daily

    N=58

    Nateglinide

    60 mg before meals +

    glyburide 10 mg once daily

    N=55

    Nateglinide

    120 mg before meals +

    glyburide 10 mg once daily

    N=54

    Baseline (mean)

    Change from baseline (mean)

    Difference from glyburide (mean)

    8.7

    0.3

    8.7

    0.2

    -0.1a

    8.7

    -0.02

    -0.3b

    Placebo or nateglinide given 10 minutes prior to breakfast, lunch, and dinner; glyburide given with the breakfast dose of nateglinide or placebo.

    a p-value 0.6959

    b p-value 0.1246

  • 16 HOW SUPPLIED

    How Supplied

    Nateglinide Tablets, USP are supplied in the following package and dose strength forms:

    60 mg

    Pink color coated, round biconvex, beveled edge tablet debossed with “P 984” on one side and plain on the other side.

                Bottles of 100……………NDC: 49884-984-01

    120 mg

    Orange color coated, oval shaped biconvex, tablet debossed with “P 985” on one side and plain on the other side.

                Bottles of 100……………NDC: 49884-985-01

    Storage and Handling

    Store at 25°C (77°F); excursions permitted to 15°C to 30°C (59°F to 86°F). [See USP Controlled Room Temperature]

    Dispense in a tight, light resistant container.

  • 17 PATIENT COUNSELING INFORMATION

    Administration

    Instruct patients to take nateglinide 1 to 30 minutes before meals. Instruct patients that skip meals to skip their dose of nateglinide [see Dosage and Administration (2)].

    Hypoglycemia

    Inform patients that nateglinide can cause hypoglycemia and instruct patients and their caregivers on self-management procedures including glucose monitoring and management of hypoglycemia. Inform patients that their ability to concentrate and react may be impaired as a result of hypoglycemia. In patients at higher risk for hypoglycemia and patients who have reduced symptomatic awareness of hypoglycemia, increased frequency of blood glucose monitoring is recommended [see Warnings and Precautions (5.1)].

    Drug Interactions

    Discuss potential drug interactions with patients and inform them of potential drug-drug interactions with nateglinide.

    Manufactured by:

    Par Pharmaceutical

    Chestnut Ridge, NY 10977

    Rev. 01/2019

    OS 984-01-1-09

  • PRINCIPAL DISPLAY PANEL - NATEGLINIDE TABLETS USP, 60 MG - 100 COUNTS

    60mg-100s
  • PRINCIPAL DISPLAY PANEL - NATEGLINIDE TABLETS USP, 120 MG - 100 COUNTS

    120 mg-100s
  • INGREDIENTS AND APPEARANCE
    NATEGLINIDE 
    nateglinide tablet, coated
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 49884-984
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NATEGLINIDE (UNII: 41X3PWK4O2) (NATEGLINIDE - UNII:41X3PWK4O2) NATEGLINIDE60 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POVIDONE (UNII: FZ989GH94E)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    Product Characteristics
    ColorPINKScoreno score
    ShapeROUNDSize1mm
    FlavorImprint Code P;984
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 49884-984-01100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/08/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07746309/08/2009
    NATEGLINIDE 
    nateglinide tablet, coated
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 49884-985
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NATEGLINIDE (UNII: 41X3PWK4O2) (NATEGLINIDE - UNII:41X3PWK4O2) NATEGLINIDE120 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POVIDONE (UNII: FZ989GH94E)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Product Characteristics
    ColorORANGEScoreno score
    ShapeOVALSize6mm
    FlavorImprint Code P;985
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 49884-985-01100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/08/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07746309/08/2009
    Labeler - Par Pharmaceutical, Inc. (092733690)
    Registrant - Par Pharmaceutical Inc. (092733690)
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