NIASPAN® niacin extended-release tablets

niaspan (niacintablet, extended release 
[Abbott Laboratories]

DESCRIPTION

NIASPAN® (niacin extended-release tablets), contains niacin, which at therapeutic doses is an antihyperlipidemic agent. Niacin (nicotinic acid, or 3-pyridinecarboxylic acid) is a white, crystalline powder, very soluble in water, with the following structural formula:

Image from Drug Label Content

NIASPAN® is an unscored, medium-orange, film-coated tablet for oral administration and is available in three tablet strengths containing 500, 750, and 1000 mg niacin. NIASPAN® tablets also contain the inactive ingredients hypromellose, povidone, stearic acid, and polyethylene glycol, and the following coloring agents: FD&C yellow #6/sunset yellow FCF Aluminum Lake, synthetic red and yellow iron oxides, and titanium dioxide.

CLINICAL PHARMACOLOGY

Niacin functions in the body after conversion to nicotinamide adenine dinucleotide (NAD) in the NAD coenzyme system. Niacin (but not nicotinamide) in gram doses reduces total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C) and triglycerides (TG), and increases high-density lipoprotein cholesterol (HDL-C). The magnitude of individual lipid and lipoprotein responses may be influenced by the severity and type of underlying lipid abnormality. The increase in total HDL-C is associated with an increase in apolipoprotein A-I (Apo A-I) and a shift in the distribution of HDL subfractions. These shifts include an increase in the HDL2:HDL3 ratio, and an elevation in lipoprotein A-I (Lp A-I, an HDL particle containing only Apo A-I). Niacin treatment also decreases serum levels of apolipoprotein B-100 (Apo B), the major protein component of the very low-density lipoprotein (VLDL) and LDL fractions, and of Lp(a), a variant form of LDL independently associated with coronary risk.1 In addition, preliminary reports suggest that niacin causes favorable LDL particle size transformations, although the clinical relevance of this effect requires further investigation. The effect of niacin-induced changes in lipids/lipoproteins on cardiovascular morbidity or mortality in individuals without pre-existing coronary disease has not been established.

A variety of clinical studies have demonstrated that elevated levels of TC, LDL-C, and Apo B promote human atherosclerosis. Similarly, decreased levels of HDL-C are associated with the development of atherosclerosis. Epidemiological investigations have established that cardiovascular morbidity and mortality vary directly with the level of TC and LDL-C, and inversely with the level of HDL-C.

Like LDL, cholesterol-enriched triglyceride-rich lipoproteins, including VLDL, intermediate-density lipoprotein (IDL), and their remnants, can also promote atherosclerosis. Elevated plasma TG are frequently found in a triad with low HDL-C levels and small LDL particles, as well as in association with non-lipid metabolic risk factors for coronary heart disease (CHD). As such, total plasma TG have not consistently been shown to be an independent risk factor for CHD. Furthermore, the independent effect of raising HDL-C or lowering TG on the risk of coronary and cardiovascular morbidity and mortality has not been determined.

Mechanism of Action

The mechanism by which niacin alters lipid profiles has not been well defined. It may involve several actions including partial inhibition of release of free fatty acids from adipose tissue, and increased lipoprotein lipase activity, which may increase the rate of chylomicron triglyceride removal from plasma. Niacin decreases the rate of hepatic synthesis of VLDL and LDL, and does not appear to affect fecal excretion of fats, sterols, or bile acids.

Pharmacokinetics/Metabolism

Absorption

Niacin is rapidly and extensively absorbed (at least 60 to 76% of dose) when administered orally. To maximize bioavailability and reduce the risk of gastrointestinal (GI) upset, administration of NIASPAN® with a low-fat meal or snack is recommended.

Single-dose bioavailability studies have demonstrated that the 500 mg and 1000 mg tablet strengths are dosage form equivalent but the 500 mg and 750 mg tablet strengths are not dosage form equivalent.

Distribution

Studies using radiolabeled niacin in mice show that niacin and its metabolites concentrate in the liver, kidney and adipose tissue.

Metabolism

The pharmacokinetic profile of niacin is complicated due to rapid and extensive first-pass metabolism, which is species and dose-rate specific. In humans, one pathway is through a simple conjugation step with glycine to form nicotinuric acid (NUA). NUA is then excreted in the urine, although there may be a small amount of reversible metabolism back to niacin. The other pathway results in the formation of nicotinamide adenine dinucleotide (NAD). It is unclear whether nicotinamide is formed as a precursor to, or following the synthesis of, NAD. Nicotinamide is further metabolized to at least N-methylnicotinamide (MNA) and nicotinamide-N-oxide (NNO). MNA is further metabolized to two other compounds, N-methyl-2-pyridone-5-carboxamide (2PY) and N-methyl-4-pyridone-5-carboxamide (4PY). The formation of 2PY appears to predominate over 4PY in humans. At the doses used to treat hyperlipidemia, these metabolic pathways are saturable, which explains the nonlinear relationship between niacin dose and plasma concentrations following multiple-dose NIASPAN® administration.

Nicotinamide does not have hypolipidemic activity; the activity of the other metabolites is unknown.

Elimination

Niacin and its metabolites are rapidly eliminated in the urine. Following single and multiple doses, approximately 60 to 76% of the niacin dose administered as NIASPAN® was recovered in urine as niacin and metabolites; up to 12% was recovered as unchanged niacin after multiple dosing. The ratio of metabolites recovered in the urine was dependent on the dose administered.

Special Populations

Hepatic

No studies have been performed. NIASPAN® should be used with caution in patients with a past history of liver disease, who consume substantial quantities of alcohol, or have unexplained transaminase elevations. NIASPAN® is contraindicated in patients with active liver disease (see WARNINGS, Liver Dysfunction).

Renal

There are no data in this population. NIASPAN® should be used with caution in patients with renal disease (see PRECAUTIONS).

Gender

Steady-state plasma concentrations of niacin and metabolites after administration of NIASPAN® are generally higher in women than in men, with the magnitude of the difference varying with dose and metabolite. Recovery of niacin and metabolites in urine, however, is generally similar for men and women, indicating that absorption is similar for both genders. The gender differences observed in plasma levels of niacin and its metabolites may be due to gender-specific differences in metabolic rate or volume of distribution. Data from the clinical trials suggest that women have a greater hypolipidemic response than men at equivalent doses of NIASPAN®.

Niacin Clinical Studies

The role of LDL-C in atherogenesis is supported by pathological observations, clinical studies, and many animal experiments. Observational epidemiological studies have clearly established that high TC or LDL-C and low HDL-C are risk factors for CHD. Additionally, elevated levels of Lp(a) have been shown to be independently associated with CHD risk.1 The efficacy of niacin in improving lipoprotein lipid profiles, either alone or in combination with other lipid-altering drugs, as an adjunct to diet therapy in the treatment of hyperlipoproteinemia has been well documented.

Niacin's ability to reduce mortality and the risk of definite, nonfatal myocardial infarction (MI) has also been assessed in long-term studies. The Coronary Drug Project,2 completed in 1975, was designed to assess the safety and efficacy of niacin and other lipid-altering drugs in men 30 to 64 years old with a history of MI. Over an observation period of 5 years, niacin treatment was associated with a statistically significant reduction in nonfatal, recurrent MI. The incidence of definite, nonfatal MI was 8.9% for the 1,119 patients randomized to nicotinic acid versus 12.2% for the 2,789 patients who received placebo (p < 0.004). Total mortality was similar in the two groups at 5 years (24.4% with nicotinic acid versus 25.4% with placebo; p = N.S.). At the time of a 15-year follow-up, there were 11% (69) fewer deaths in the niacin group compared to the placebo cohort (52.0% versus 58.2%; p = 0.0004).3 However, mortality at 15 years was not an original endpoint of the Coronary Drug Project. In addition, patients had not received niacin for approximately 9 years, and confounding variables such as concomitant medication use and medical or surgical treatments were not controlled.

The Cholesterol-Lowering Atherosclerosis Study (CLAS) was a randomized, placebo-controlled, angiographic trial testing combined colestipol and niacin therapy in 162 non-smoking males with previous coronary bypass surgery.4 The primary, per-subject cardiac endpoint was global coronary artery change score. After 2 years, 61% of patients in the placebo cohort showed disease progression by global change score (n = 82), compared with only 38.8% of drug-treated subjects (n = 80), when both native arteries and grafts were considered (p < 0.005); disease regression also occurred more frequently in the drug-treated group (16.2% versus 2.4%; p = 0.002). In a follow-up to this trial in a subgroup of 103 patients treated for 4 years, again, significantly fewer patients in the drug-treated group demonstrated progression than in the placebo cohort (48% versus 85%, respectively; p < 0.0001).5

The Familial Atherosclerosis Treatment Study (FATS) in 146 men ages 62 and younger with Apo B levels ≥ 125 mg/dL, established coronary artery disease, and family histories of vascular disease, assessed change in severity of disease in the proximal coronary arteries by quantitative arteriography.6 Patients were given dietary counseling and randomized to treatment with either conventional therapy with double placebo (or placebo plus colestipol if the LDL-C was elevated); lovastatin plus colestipol; or niacin plus colestipol. In the conventional therapy group, 46% of patients had disease progression (and no regression) in at least one of nine proximal coronary segments; regression was the only change in 11%. In contrast, progression (as the only change) was seen in only 25% in the niacin plus colestipol group, while regression was observed in 39%. Though not an original endpoint of the trial, clinical events (death, MI, or revascularization for worsening angina) occurred in 10 of 52 patients who received conventional therapy, compared with 2 of 48 who received niacin plus colestipol.

The Harvard Atherosclerosis Reversibility Project (HARP) was a randomized placebo-controlled, 2.5-year study of the effect of a stepped-care antihyperlipidemic drug regimen on 91 patients (80 men and 11 women) with CHD and average baseline TC levels less than 250 mg/dL and ratios of TC to HDL-C greater than 4.0.7 Drug treatment consisted of an HMG-CoA reductase inhibitor administered alone as initial therapy followed by addition of varying dosages of either a slow-release nicotinic acid, cholestyramine, or gemfibrozil. Addition of nicotinic acid to the HMG-CoA reductase inhibitor resulted in further statistically significant mean reductions in TC, LDL-C, and TG, as well as a further increase in HDL-C in a majority of patients (40 of 44 patients). The ratios of TC to HDL-C and LDL-C to HDL-C were also significantly reduced by this combination drug regimen (see WARNINGS, Skeletal Muscle).

NIASPAN® Clinical Studies

Placebo-Controlled Clinical Studies in Patients with Primary Hypercholesterolemia and Mixed Dyslipidemia: In two randomized, double-blind, parallel, multi-center, placebo-controlled trials, NIASPAN® dosed at 1000, 1500 or 2000 mg daily at bedtime with a low-fat snack for 16 weeks (including 4 weeks of dose escalation) favorably altered lipid profiles compared to placebo (Table 1). Women appeared to have a greater response than men at each NIASPAN® dose level (see Gender Effect, below).

Table 1. Lipid Response to NIASPAN® Therapy
Mean Percent Change from Baseline to Week 16*

n = number of patients at baseline;

* Mean percent change from baseline for all NIASPAN® doses was significantly different (p < 0.05) from placebo for all lipid parameters shown except Apo A-I at 2000 mg.

TreatmentnTC LDL-C HDL-C TC/HDL-C TG Lp(a) Apo B Apo A-I
NIASPAN® 1000 mg at bedtime 41 -3 -5 +18 -17 -21 -13 -6 +9
NIASPAN® 2000 mg at bedtime 41 -10 -14 +22 -25 -28 -27 -16 +8
Placebo 40 0 -1 +4 -3 0 0 +1 +3
NIASPAN® 1500 mg at bedtime 76 -8 -12 +20 -20 -13 -15 -12 +8
Placebo 73 +2 +1 +2 +1 +12 +2 +1 +2

In a double-blind, multi-center, forced dose-escalation study, monthly 500 mg increases in NIASPAN® dose resulted in incremental reductions of approximately 5% in LDL-C and Apo B levels in the daily dose range of 500 mg through 2000 mg (Table 2). Women again tended to have a greater response to NIASPAN® than men (see Gender Effect, below).

Table 2. Lipid Response in Dose-Escalation Study
Mean Percent Change from Baseline*

n = number of patients enrolled;

Placebo data shown are after 24 weeks of placebo treatment.

* For all NIASPAN® doses except 500 mg, mean percent change from baseline was significantly different (p < 0.05) from placebo for all lipid parameters shown except Lp(a) and Apo A-I which were significantly different from placebo starting with 1500 mg and 2000 mg, respectively.

TreatmentnTCLDL-CHDL-CTC/HDL-CTGLp(a)Apo BApo A-I
Placebo44-2-1+5-7-6-5-2+4
NIASPAN®87
   500 mg at bedtime -2-3+10-10-5-3-2+5
   1000 mg at bedtime -5-9+15-17-11-12-7+8
  1500 mg at bedtime -11-14+22-26-28-20-15+10
   2000 mg at bedtime -12-17+26-29-35-24-16+12

Pooled results for major lipids from these three placebo-controlled studies are shown below (Table 3).

Table 3. Selected Lipid Response to NIASPAN® in Placebo-Controlled Clinical Studies*
Mean Baseline and Median Percent Change from Baseline
(25th, 75th Percentiles)

* Represents pooled analyses of results; minimum duration on therapy at each dose was 4 weeks.

NIASPAN®
Dose
n LDL-C HDL-C TG
1000 mg at bedtime 104
   Baseline (mg/dL) 218 45 172
      Percent Change -7 (-15, 0) +14 (+7, +23) -16 (-34, +3)
1500 mg at bedtime 120
   Baseline (mg/dL) 212 46 171
      Percent Change -13 (-21, -4) +19 (+9, +31) -25 (-45, -2)
2000 mg at bedtime 85
   Baseline (mg/dL) 220 44 160
      Percent Change -16 (-26, -7) +22 (+15, +34) -38 (-52, -14)

Gender Effect: Combined data from the three placebo-controlled NIASPAN® studies in patients with primary hypercholesterolemia and mixed dyslipidemia suggest that, at each NIASPAN® dose level studied, changes in lipid concentrations are greater for women than for men (Table 4).

Table 4. Effect of Gender on NIASPAN® Dose Response
Mean Percent Change from Baseline

n = number of male/female patients enrolled.

* Percent change significantly different between genders(p < 0.05).

NiaspannLDL-CHDL-CTGApo B
Dose(M/F)MFMFMFMF
500 mg at bedtime50/37-2-5+11+8-3-9-1-5
1000 mg at bedtime76/52-6*-11*+14+20-10-20-5*-10*
1500 mg at bedtime104/59-12-16+19+24-17-28-13-15
2000 mg at bedtime75/53-15-18+23+26-30-36-16-16

Other Patient Populations: In a double-blind, multi-center, 19-week study the lipid-altering effects of NIASPAN® (forced titration to 2000 mg at bedtime) were compared to baseline in patients whose primary lipid abnormality was a low level of HDL-C (HDL-C ≤ 40 mg/dL, TG ≤ 400 mg/dL, and LDL-C ≤ 160, or < 130 mg/dL in the presence of CHD). Results are shown below (Table 5).

Table 5. Lipid Response to NIASPAN® in Patients with Low HDL-C
Mean Baseline and Mean Percent Change from Baseline*

n = number of patients

* Mean percent change from baseline was significantly different (p < 0.05) for all lipid parameters shown except LDL-C.

n = 72 at baseline and 69 at week 19.

†† n = 30 at baseline and week 19.

n TC LDL-C HDL-C TC/HDL-C TG Lp(a)Apo BApo A-ILp A-I††
Baseline
   (mg/dL)
88 190 120 31 6 194 8 106 105 32
Week 19
   (% Change)
71 -3 0 +26 -22 -30 -20 -9 +11 +20

At NIASPAN® 2000 mg/day, median changes from baseline (25th, 75th percentiles) for LDL-C, HDL-C, and TG were -3% (-14, +12%), +27% (+13, +38%), and -33% (-50, -19%), respectively.

Combination NIASPAN®and Lovastatin Study: In a multi-center, randomized, double-blind, parallel, 28-week study, a combination tablet of NIASPAN® and lovastatin was compared to each individual component in patients with Type IIa and IIb hyperlipidemia. Using a forced dose-escalation study design, patients received each dose for at least 4 weeks. Patients randomized to treatment with the combination tablet of NIASPAN® and lovastatin initially received 500 mg/20 mg (expressed as mg of niacin/mg of lovastatin) once daily before bedtime. The dose was increased by 500 mg at 4-week intervals (based on the NIASPAN® component) to a maximum dose of 1000 mg/20 mg in one-half of the patients and 2000 mg/40 mg in the other half. The NIASPAN® monotherapy group underwent a similar titration from 500 mg to 2000 mg. The patients randomized to lovastatin monotherapy received 20 mg for 12 weeks titrated to 40 mg for up to 16 weeks. Up to a third of the patients randomized to the combination tablet of NIASPAN® and lovastatin or NIASPAN® monotherapy discontinued prior to Week 28. Results from this study showed that combination therapy decreased LDL-C, TG and Lp(a), and increased HDL-C in a dose-dependent fashion (Tables 6, 7, 8, and 9). Results from this study for LDL-C mean percent change from baseline (the primary efficacy variable) showed that:

  1. LDL-lowering with the combination tablet of NIASPAN® and lovastatin was significantly greater than that achieved with lovastatin 40 mg only after 28 weeks of titration to a dose of 2000 mg/40 mg (p < 0.0001)
  2. The combination tablet of NIASPAN® and lovastatin at doses of 1000 mg/20 mg or higher achieved greater LDL-lowering than NIASPAN® (p < 0.0001)

The LDL-C results are summarized in Table 6.

Table 6. LDL-C mean percent change from baseline
WeekCombination tablet of
NIASPAN® and lovastatin
NIASPAN®Lovastatin
* n = number of patients remaining in trial at each time point
n*DoseLDLn*DoseLDLn*DoseLDL
(mg/mg)(mg)(mg)
Baseline57190.9 mg/dL61189.7 mg/dL61185.6 mg/dL
12471000/20-30%461000-3%5620-29%
16451000/40-36%441000-6%5640-31%
20421500/40-37%431500-12%5440-34%
28422000/40-42%412000-14%5340-32%

Combination therapy achieved significantly greater HDL-raising compared to lovastatin and NIASPAN® monotherapy at all doses (Table 7).

Table 7. HDL-C mean percent change from baseline
WeekCombination tablet of
NIASPAN® and lovastatin
NIASPAN®Lovastatin
* n = number of patients remaining in trial at each time point
n*DoseHDLn*DoseHDLn*DoseHDL
(mg/mg)(mg)(mg)
Baseline5745 mg/dL6147 mg/dL6143 mg/dL
12471000/20+20%461000+14%5620+3%
16451000/40+20%441000+15%5640+5%
20421500/40+27%431500+22%5440+6%
28422000/40+30%412000+24%5340+6%

In addition, combination therapy achieved significantly greater TG-lowering at doses of 1000 mg/20 mg or greater compared to lovastatin and NIASPAN® monotherapy (Table 8).

Table 8. TG median percent change from baseline
WeekCombination tablet of
NIASPAN® and lovastatin
NIASPAN®Lovastatin
* n = number of patients remaining in trial at each time point
n*DoseTGn*DoseTGn*DoseTG
(mg/mg)(mg)(mg)
Baseline57174 mg/dL61186 mg/dL61171 mg/dL
12471000/20-32%461000-22%5620-20%
16451000/40-39%441000-23%5640-17%
20421500/40-44%431500-31%5440-21%
28422000/40-44%412000-31%5340-20%

The Lp(a)-lowering effects of combination therapy and NIASPAN® monotherapy were similar, and both were superior to lovastatin (Table 9). The independent effect of lowering Lp(a) with NIASPAN® or combination therapy on the risk of coronary and cardiovascular morbidity and mortality has not been determined.

Table 9. Lp(a) median percent change from baseline
WeekCombination tablet of
NIASPAN® and lovastatin
NIASPAN®Lovastatin
* n = number of patients remaining in trial at each time point
n*DoseLp(a)n*DoseLp(a)n*DoseLp(a)
(mg/mg)(mg)(mg)
Baseline5734 mg/dL6141 mg/dL6042 mg/dL
12471000/20-9%461000-8%5520+8%
16451000/40-9%441000-12%5540+8%
20421500/40-17%431500-22%5340+6%
28422000/40-22%412000-32%52400%

INDICATIONS AND USAGE

Therapy with lipid-altering agents should be only one component of multiple risk factor intervention in individuals at significantly increased risk for atherosclerotic vascular disease due to hypercholesterolemia. Niacin therapy is indicated as an adjunct to diet when the response to a diet restricted in saturated fat and cholesterol and other nonpharmacologic measures alone has been inadequate (see also Table 10 and the NCEP treatment guidelines8). Prior to initiating therapy with niacin, secondary causes for hypercholesterolemia (e.g., poorly controlled diabetes mellitus, hypothyroidism, nephrotic syndrome, dysproteinemias, obstructive liver disease, other drug therapy, alcoholism) should be excluded, and a lipid profile obtained to measure TC, HDL-C, and TG.

  1. NIASPAN® is indicated as an adjunct to diet for reduction of elevated TC, LDL-C, Apo B and TG levels, and to increase HDL-C in patients with primary hypercholesterolemia (heterozygous familial and nonfamilial) and mixed dyslipidemia (Fredrickson Types IIa and IIb; Table 11), when the response to an appropriate diet has been inadequate.
  2. NIASPAN® in combination with lovastatin is indicated for the treatment of primary hypercholesterolemia (heterozygous familial and nonfamilial) and mixed dyslipidemia (Fredrickson Types IIa and IIb; Table 11) when treatment with both NIASPAN® and lovastatin is appropriate and as an adjunct to diet.
  3. In patients with a history of myocardial infarction and hypercholesterolemia, niacin is indicated to reduce the risk of recurrent nonfatal myocardial infarction.
  4. In patients with a history of coronary artery disease (CAD) and hypercholesterolemia, niacin, in combination with a bile acid binding resin, is indicated to slow progression or promote regression of atherosclerotic disease.
  5. NIASPAN® in combination with a bile acid binding resin is indicated as an adjunct to diet for reduction of elevated TC and LDL-C levels in adult patients with primary hypercholesterolemia (Type IIa; Table 11), when the response to an appropriate diet, or diet plus monotherapy, has been inadequate.
  6. Niacin is also indicated as adjunctive therapy for treatment of adult patients with very high serum triglyceride levels (Types IV and V hyperlipidemia; Table 11) who present a risk of pancreatitis and who do not respond adequately to a determined dietary effort to control them. Such patients typically have serum TG levels over 2000 mg/dL and have elevations of VLDL-C as well as fasting chylomicrons (Type V hyperlipidemia; Table 11). Patients who consistently have total serum or plasma TG below 1000 mg/dL are unlikely to develop pancreatitis. Therapy with niacin may be considered for those patients with TG elevations between 1000 and 2000 mg/dL who have a history of pancreatitis or of recurrent abdominal pain typical of pancreatitis. Some Type IV patients with TG under 1000 mg/dL may, through dietary or alcohol indiscretion, convert to a Type V pattern with massive TG elevations accompanying fasting chylomicronemia, but the influence of niacin therapy on risk of pancreatitis in such situations has not been adequately studied. Drug therapy is not indicated for patients with Type I hyperlipoproteinemia, who have elevations of chylomicrons and plasma TG, but who have normal levels of VLDL-C. Inspection of plasma refrigerated for 14 hours is helpful in distinguishing Types I, IV, and V hyperlipoproteinemia.9
Table 10. NCEP Treatment Guidelines: LDL-C Goals and Cutpoints for Therapeutic Lifestyle Changes and Drug Therapy in Different Risk Categories
Risk Category LDL Goal
(mg/dL)
LDL Level at Which
to Initiate Therapeutic
Lifestyle Changes
(mg/dL)
LDL Level at Which to
Consider Drug
Therapy (mg/dL)

CHD, coronary heart disease

†† Some authorities recommend use of LDL-lowering drugs in this category if an LDL-C level of < 100 mg/dL cannot be achieved by therapeutic lifestyle changes. Others prefer use of drugs that primarily modify triglycerides and HDL-C, e.g., nicotinic acid or fibrate. Clinical judgment also may call for deferring drug therapy in this subcategory.

††† Almost all people with 0-1 risk factor have 10-year risk < 10%; thus, 10-year risk assessment in people with 0-1 risk factor is not necessary.

CHD or CHD
risk equivalents
(10-year risk > 20%)

< 100 ≥ 100 ≥ 130
(100-129: drug optional) ††
2+ Risk factors 10-year risk 10%-20%: ≥ 130
(10-year risk ≤ 20%)

< 130 ≥ 130 10-year risk < 10%: ≥ 160
0-1 Risk factor†††< 160 ≥ 160 ≥ 190
(160-189: LDL-lowering drug optional)

After the LDL-C goal has been achieved, if the TG is still ≥ 200 mg/dL, non-HDL-C (TC minus HDL-C) becomes a secondary target of therapy. Non-HDL-C goals are set 30 mg/dL higher than LDL-C goals for each risk category.

Table 11. Classification of Hyperlipoproteinemias

TC = total cholesterol; TG = triglycerides; LDL = low-density lipoprotein;

VLDL = very low-density lipoprotein; IDL = intermediate-density lipoprotein

↑→ = increased or no change

TypeLipoproteins ElevatedLipid Elevations
MajorMinor
I (rare) chylomicrons TG ↑→TC
IIa LDL TC
IIb LDL, VLDL TC TG
III (rare) IDL TC/TG
IV VLDL TG ↑→TC
V (rare) chylomicrons, VLDL TG ↑→TC

CONTRAINDICATIONS

NIASPAN® is contraindicated in patients with a known hypersensitivity to niacin or any component of this medication, significant or unexplained hepatic dysfunction, active peptic ulcer disease, or arterial bleeding.

WARNINGS

NIASPAN® preparations should not be substituted for equivalent doses of immediate-release (crystalline) niacin. For patients switching from immediate-release niacin to NIASPAN®, therapy with NIASPAN® should be initiated with low doses (i.e., 500 mg at bedtime) and the NIASPAN® dose should then be titrated to the desired therapeutic response (see DOSAGE AND ADMINISTRATION).

Liver Dysfunction

Cases of severe hepatic toxicity, including fulminant hepatic necrosis, have occurred in patients who have substituted sustained-release (modified-release, timed-release) niacin products for immediate-release (crystalline) niacin at equivalent doses.

NIASPAN® should be used with caution in patients who consume substantial quantities of alcohol and/or have a past history of liver disease. Active liver diseases or unexplained transaminase elevations are contraindications to the use of NIASPAN®.

Niacin preparations, like some other lipid-lowering therapies, have been associated with abnormal liver tests. In three placebo-controlled clinical trials involving titration to final daily NIASPAN® doses ranging from 500 to 3000 mg, 245 patients received NIASPAN® for a mean duration of 17 weeks. No patient with normal serum transaminase levels (AST, ALT) at baseline experienced elevations to more than 3 times the upper limit of normal (ULN) during treatment with NIASPAN®. In these studies, fewer than 1% (2/245) of NIASPAN® patients discontinued due to transaminase elevations greater than 2 times the ULN.

In three safety and efficacy studies with a combination tablet of NIASPAN® and lovastatin involving titration to final daily doses (expressed as mg of niacin/ mg of lovastatin) 500 mg/10 mg to 2500 mg/40 mg, ten of 1028 patients (1.0%) experienced reversible elevations in AST/ALT to more than 3 times the upper limit of normal (ULN). Three of ten elevations occurred at doses outside the recommended dosing limit of 2000 mg/40 mg; no patient receiving 1000 mg/20 mg had 3-fold elevations in AST/ALT.

In the placebo-controlled clinical trials and the long-term extension study, elevations in transaminases did not appear to be related to treatment duration; elevations in AST levels did appear to be dose related. Transaminase elevations were reversible upon discontinuation of NIASPAN®.

Liver tests should be performed on all patients during therapy with NIASPAN®. Serum transaminase levels, including AST and ALT (SGOT and SGPT), should be monitored before treatment begins, every 6 to 12 weeks for the first year, and periodically thereafter (e.g., at approximately 6-month intervals). Special attention should be paid to patients who develop elevated serum transaminase levels, and in these patients, measurements should be repeated promptly and then performed more frequently. If the transaminase levels show evidence of progression, particularly if they rise to 3 times ULN and are persistent, or if they are associated with symptoms of nausea, fever, and/or malaise, the drug should be discontinued.

Skeletal Muscle

Rare cases of rhabdomyolysis have been associated with concomitant administration of lipid-altering doses (≥ 1 g/day) of niacin and HMG-CoA reductase inhibitors. In clinical studies with a combination tablet of NIASPAN® and lovastatin, no cases of rhabdomyolysis and one suspected case of myopathy have been reported in 1079 patients who were treated with doses up to 2000 mg of NIASPAN® and 40 mg of lovastatin daily for periods up to 2 years. Physicians contemplating combined therapy with HMG-CoA reductase inhibitors and NIASPAN® should carefully weigh the potential benefits and risks and should carefully monitor patients for any signs and symptoms of muscle pain, tenderness, or weakness, particularly during the initial months of therapy and during any periods of upward dosage titration of either drug. Periodic serum creatine phosphokinase (CPK) and potassium determinations should be considered in such situations, but there is no assurance that such monitoring will prevent the occurrence of severe myopathy.

PRECAUTIONS

General

Before instituting therapy with NIASPAN® an attempt should be made to control hyperlipidemia with appropriate diet, exercise, and weight reduction in obese patients, and to treat other underlying medical problems (see INDICATIONS AND USAGE).

Patients with a past history of jaundice, hepatobiliary disease, or peptic ulcer should be observed closely during NIASPAN® therapy. Frequent monitoring of liver function tests and blood glucose should be performed to ascertain that the drug is producing no adverse effects on these organ systems. Diabetic patients may experience a dose-related rise in glucose intolerance, the clinical significance of which is unclear. Diabetic or potentially diabetic patients should be observed closely. Adjustment of diet and/or hypoglycemic therapy may be necessary.

Caution should also be used when NIASPAN® is used in patients with unstable angina or in the acute phase of an MI, particularly when such patients are also receiving vasoactive drugs such as nitrates, calcium channel blockers, or adrenergic blocking agents.

Elevated uric acid levels have occurred with niacin therapy, therefore use with caution in patients predisposed to gout.

NIASPAN® has been associated with small but statistically significant dose-related reductions in platelet count (mean of -11% with 2000 mg). In addition, NIASPAN® has been associated with small but statistically significant increases in prothrombin time (mean of approximately +4%); accordingly, patients undergoing surgery should be carefully evaluated. Caution should be observed when NIASPAN® is administered concomitantly with anticoagulants; prothrombin time and platelet counts should be monitored closely in such patients.

In placebo-controlled trials, NIASPAN® has been associated with small but statistically significant, dose-related reductions in phosphorus levels (mean of -13% with 2000 mg). Although these reductions were transient, phosphorus levels should be monitored periodically in patients at risk for hypophosphatemia.

Niacin is rapidly metabolized by the liver, and excreted through the kidneys. NIASPAN® is contraindicated in patients with significant or unexplained hepatic dysfunction (see CONTRAINDICATIONS and WARNINGS) and should be used with caution in patients with renal dysfunction.

Information for Patients

Patients should be advised:

Drug Interactions

HMG-CoA Reductase Inhibitors: See WARNINGS, Skeletal Muscle.

Antihypertensive Therapy: Niacin may potentiate the effects of ganglionic blocking agents and vasoactive drugs resulting in postural hypotension.

Aspirin: Concomitant aspirin may decrease the metabolic clearance of nicotinic acid. The clinical relevance of this finding is unclear.

Bile Acid Sequestrants: An in vitro study was carried out investigating the niacin-binding capacity of colestipol and cholestyramine. About 98% of available niacin was bound to colestipol, with 10 to 30% binding to cholestyramine. These results suggest that 4 to 6 hours, or as great an interval as possible, should elapse between the ingestion of bile acid-binding resins and the administration of NIASPAN®.

Other: Concomitant alcohol or hot drinks may increase the side effects of flushing and pruritus and should be avoided around the time of NIASPAN® ingestion. Vitamins or other nutritional supplements containing large doses of niacin or related compounds such as nicotinamide may potentiate the adverse effects of NIASPAN®.

Drug/Laboratory Test Interactions

Niacin may produce false elevations in some fluorometric determinations of plasma or urinary catecholamines. Niacin may also give false-positive reactions with cupric sulfate solution (Benedict's reagent) in urine glucose tests.

Carcinogenesis, Mutagenesis, Impairment of Fertility

Niacin administered to mice for a lifetime as a 1% solution in drinking water was not carcinogenic. The mice in this study received approximately 6 to 8 times a human dose of 3000 mg/day as determined on a mg/m2 basis. Niacin was negative for mutagenicity in the Ames test. No studies on impairment of fertility have been performed. No studies have been conducted with NIASPAN® regarding carcinogenesis, mutagenesis, or impairment of fertility.

Pregnancy

Pregnancy Category C.

Animal reproduction studies have not been conducted with niacin or with NIASPAN®. It is also not known whether niacin at doses typically used for lipid disorders can cause fetal harm when administered to pregnant women or whether it can affect reproductive capacity. If a woman receiving niacin for primary hypercholesterolemia (Types IIa or IIb) becomes pregnant, the drug should be discontinued. If a woman being treated with niacin for hypertriglyceridemia (Types IV or V) conceives, the benefits and risks of continued therapy should be assessed on an individual basis.

Nursing Mothers

Niacin has been reported to be excreted in human milk. Because of the potential for serious adverse reactions in nursing infants from lipid-altering doses of nicotinic acid, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother. No studies have been conducted with NIASPAN® in nursing mothers.

Pediatric Use

Safety and effectiveness of niacin therapy in pediatric patients (≤ 16 years) have not been established. No studies in patients under 21 years of age have been conducted with NIASPAN®.

Geriatric Use

Of 979 patients in clinical studies of NIASPAN®, 21% of the patients were age 65 and over. No overall differences in safety and effectiveness were observed between these patients and younger patients, and other reported clinical experience has not identified differences in responses between the elderly and younger patients, but greater sensitivity of some older individuals cannot be ruled out.

ADVERSE REACTIONS

NIASPAN® is generally well tolerated; adverse reactions have been mild and transient. In the placebo-controlled clinical trials, flushing episodes (i.e., warmth, redness, itching and/or tingling) were the most common treatment-emergent adverse events (reported by as many as 88% of patients) for NIASPAN®. Spontaneous reports suggest that flushing may also be accompanied by symptoms of dizziness, tachycardia, palpitations, shortness of breath, sweating, chills, and/or edema, which in rare cases may lead to syncope. In pivotal studies, fewer than 6% (14/245) of NIASPAN® patients discontinued due to flushing. In comparisons of immediate-release (IR) niacin and NIASPAN®, although the proportion of patients who flushed was similar, fewer flushing episodes were reported by patients who received NIASPAN®. Following 4 weeks of maintenance therapy at daily doses of 1500 mg, the incidence of flushing over the 4-week period averaged 8.56 events per patient for IR niacin versus 1.88 following NIASPAN®.

Other adverse events occurring in 5% or greater of patients treated with NIASPAN®, at least remotely related to NIASPAN®, are shown in Table 12 below.

Table 12. Treatment-Emergent Adverse Events by Dose Level in ≥ 5% of Patients; Events Considered At Least Remotely Related to Study Medication
Placebo-Controlled Studies
NIASPAN® Treatment

Note: Percentages are calculated from the total number of patients in each column. AEs are reported at the lowest dose where they occurred.

Pooled results from placebo-controlled studies; for NIASPAN®, n = 245 and mean treatment duration = 17 weeks. Number of NIASPAN® patients (n) are not additive across doses.

The 500 mg, 2500 mg and 3000 mg/day doses are outside the recommended daily maintenance dosing range; see DOSAGE AND ADMINISTRATION.

* Significantly different from placebo at p ≤ 0.05; Chi-square test (cell sizes > 5), Fisher's Exact test (cell sizes ≤ 5).

Recommended Daily
Maintenance Doses
Greater Than Recommended
Daily Doses
Placebo 500 mg1000 mg 1500 mg 2000 mg 2500 mg3000 mg
(n = 157) (n = 87) (n = 110) (n = 136) (n = 95) (n = 49) (n = 46)
% % % % % % %
Headache 15 5* 9 11 8 4* 4
Pain 3 1 2 5 3 0 2
Pain, Abdominal 3 3 2 3 5 0 0
Diarrhea 8 6 7 6 8 10 11
Dyspepsia 8 2 4 5 5 6 0
Nausea 4 2 5 3 8 10 4
Vomiting 2 0 2 3 8* 8 2
Rhinitis 7 2 5 4 3 0 0
Pruritus 1 6 < 1 3 1 0 0
Rash < 1 5 5 4 0 0 0

In general, the incidence of adverse events was higher in women compared to men.

The following adverse events have also been reported with NIASPAN® or other niacin products, either during clinical trials or in routine patient management.

Body as a Whole:  generalized edema; face edema; peripheral edema; asthenia; chills

Cardiovascular:  atrial fibrillation and other cardiac arrhythmias; tachycardia; palpitations; orthostasis; syncope; hypotension

Eye:  toxic amblyopia; cystoid macular edema

Gastrointestinal:   activation of peptic ulcers and peptic ulceration; jaundice; eructation; flatulence

Metabolic:   decreased glucose tolerance; gout

Musculoskeletal:  myalgia; myasthenia

Nervous:  dizziness; insomnia; leg cramps; nervousness; paresthesia

Respiratory:   dyspnea

Skin:   hyper-pigmentation; acanthosis nigricans; maculopapular rash; urticaria; dry skin; sweating

Other:   migraine

Hypersensitivity reactions:  An apparent hypersensitivity reaction has been reported rarely that has included one or more of the following features: anaphylaxis, angioedema, urticaria, flushing, dyspnea, tongue edema, larynx edema, face edema, peripheral edema, laryngismus, and vesiculobullous rash.

Clinical Laboratory Abnormalities

Chemistry: Elevations in serum transaminases (see WARNINGS, Liver Dysfunction), LDH, fasting glucose, uric acid, total bilirubin, and amylase; reductions in phosphorus

Hematology: Slight reductions in platelet counts and prolongation in prothrombin time (see WARNINGS)

DRUG ABUSE AND DEPENDENCE

Niacin is a non-narcotic drug. It has no known addiction potential in humans.

OVERDOSAGE

Supportive measures should be undertaken in the event of an overdose.

DOSAGE AND ADMINISTRATION

NIASPAN® should be taken at bedtime, after a low-fat snack, and doses should be individualized according to patient response. Therapy with NIASPAN® must be initiated at 500 mg at bedtime in order to reduce the incidence and severity of side effects which may occur during early therapy. The recommended dose escalation is shown in Table 13 below.

Table 13. Recommended Dosing
Week(s) Daily dose NIASPAN® Dosage

* After Week 8, titrate to patient response and tolerance. If response to 1000 mg daily is inadequate, increase dose to 1500 mg daily; may subsequently increase dose to 2000 mg daily. Daily dose should not be increased more than 500 mg in a 4-week period, and doses above 2000 mg daily are not recommended. Women may respond at lower doses than men.

INITIAL
TITRATION
1 to 4 500 mg
1 NIASPAN® 500 mg tablet at bedtime
SCHEDULE 5 to 8 1000 mg
1 NIASPAN® 1000 mg tablet or
2 NIASPAN® 500 mg tablets at bedtime
* 1500 mg
2 NIASPAN® 750 mg tablets or
3 NIASPAN® 500 mg tablets at bedtime
* 2000 mg
2 NIASPAN® 1000 mg tablets or
4 NIASPAN® 500 mg tablets at bedtime

Maintenance Dose

The daily dosage of NIASPAN® should not be increased by more than 500 mg in any 4-week period. The recommended maintenance dose is 1000 mg (two 500 mg tablets or one 1000 mg tablet) to 2000 mg (two 1000 mg tablets or four 500 mg tablets) once daily at bedtime. Doses greater than 2000 mg daily are not recommended. Women may respond at lower NIASPAN® doses than men (see CLINICAL PHARMACOLOGY, Gender Effect).

Single-dose bioavailability studies have demonstrated that two of the 500 mg and one of the 1000 mg tablet strengths are interchangeable but three of the 500 mg and two of the 750 mg tablet strengths are not interchangeable.

If lipid response to NIASPAN® alone is insufficient (see NCEP treatment guidelines; Table 10), or if higher doses of NIASPAN® are not well tolerated, some patients may benefit from combination therapy with a bile acid binding resin or an HMG-CoA reductase inhibitor (see WARNINGS, PRECAUTIONS, Drug Interactions, Concomitant Therapy below, and CLINICAL PHARMACOLOGY, NIASPAN Clinical Studies).

Flushing of the skin (see ADVERSE REACTIONS) may be reduced in frequency or severity by pretreatment with aspirin (taken 30 minutes prior to NIASPAN® dose) or non-steroidal anti-inflammatory drugs. Tolerance to this flushing develops rapidly over the course of several weeks. Flushing, pruritus, and gastrointestinal distress are also greatly reduced by slowly increasing the dose of niacin and avoiding administration on an empty stomach.

Equivalent doses of NIASPAN® should not be substituted for sustained-release (modified-release, timed-release) niacin preparations or immediate-release (crystalline) niacin (see WARNINGS). Patients previously receiving other niacin products should be started with the recommended NIASPAN® titration schedule (see Table 13), and the dose should subsequently be individualized based on patient response.

If NIASPAN® therapy is discontinued for an extended period, reinstitution of therapy should include a titration phase (see Table 13).

NIASPAN® tablets should be taken whole and should not be broken, crushed or chewed before swallowing.

Concomitant Therapy

Concomitant Therapy with Lovastatin

Patients already receiving a stable dose of lovastatin who require further TG-lowering or HDL-raising (e.g., to achieve NCEP non-HDL-C goals), may receive concomitant dosage titration with NIASPAN® per NIASPAN® recommended initial titration schedule (see Table 13,DOSAGE AND ADMINISTRATION section). For patients already receiving a stable dose of NIASPAN® who require further LDL-lowering (e.g., to achieve NCEP LDL-C goals; Table 10), the usual recommended starting dose of lovastatin is 20 mg once a day. Dose adjustments should be made at intervals of 4 weeks or more. Combination therapy with NIASPAN® and lovastatin should not exceed doses of 2000 mg and 40 mg daily, respectively.

Dosage in Patients with Renal or Hepatic Insufficiency

Use of NIASPAN® in patients with renal or hepatic insufficiency has not been studied. NIASPAN® is contraindicated in patients with significant or unexplained hepatic dysfunction. NIASPAN® should be used with caution in patients with renal insufficiency (see WARNINGS, PRECAUTIONS).

HOW SUPPLIED

NIASPAN® tablets are supplied as unscored, medium-orange, film-coated, capsule-shaped tablets containing 500, 750 or 1000 mg of niacin in an extended-release formulation. Tablets are debossed KOS on one side and the tablet strength (500, 750 or 1000) on the other side. Tablets are supplied in bottles of 90 and 100 as shown below.

500 mg tablets:  bottles of 90 - NDC# 0074-3074-90
500 mg tablets: bottles of 100 - NDC# 0074-3074-11

750 mg tablets:  bottles of 90 - NDC# 0074-3079-90
750 mg tablets: bottles of 100 - NDC# 0074-3079-11

1000 mg tablets:  bottles of 90 - NDC# 0074-3080-90
1000 mg tablets:  bottles of 100 - NDC# 0074-3080-11

Store at room temperature (20 to 25°C or 68 to 77°F).

REFERENCES

  1. Bostom AG et al. JAMA 1996; 276:544-548.
  2. The Coronary Drug Project Research Group, JAMA 1975; 231:360-381.
  3. Canner PL et al. J Am Coll Cardiol 1986; 8(6):1245-1255.
  4. Blankenhorn DH et al. JAMA 1987; 257(23):3233-3240.
  5. Cashin-Hemphill L et al. JAMA 1990; 264(23):3013-3017.
  6. Brown G et al. N Engl J Med 1990; 323:1289-1298.
  7. Pasternak RC et al. Annals Int Med 1996; 125:529-540.
  8. Executive Summary of the Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III), JAMA 2001; 285:2486-2497.
  9. Nikkila EA, In: The Metabolic Basis of Inherited Disease, 5th ed., Chap. 30, 622-642. 1983.

Manufactured for:
Abbott Laboratories
North Chicago, IL 60064, U.S.A.

2007 Abbott Laboratories, North Chicago, IL 60064, U.S.A.

Printed in U.S.A.

U.S. Patent Nos. 6,080,428; 6,129,930; 6,406,715 B1; 6,676,967; 6,746,691; 6,818,229; 7,011,848; 6,469,035 and other patents pending.


Niaspan (niacin)
PRODUCT INFO
Product Code0074-3074Dosage FormTABLET, EXTENDED RELEASE
Route Of AdministrationORALDEA Schedule
INGREDIENTS
Name (Active Moiety)TypeStrength
Niacin (Niacin) Active500 MILLIGRAM  In 1 TABLET
hypromelloseInactive 
povidoneInactive 
stearic acidInactive 
polyethylene glycolInactive 
titanium dioxideInactive 
synthetic red and yellow iron oxidesInactive 
FD&C yellow #6/sunset yellow FCF Aluminum LakeInactive 
IMPRINT INFORMATION
CharacteristicAppearanceCharacteristicAppearance
ColorORANGE (MEDIUM-ORANGE) Score1
ShapeOVAL (OVAL) Symbolfalse
Imprint Code KOS;500 Coatingtrue
Size17mm
PACKAGING
#NDCPackage DescriptionMultilevel Packaging
10074-3074-9090 TABLET In 1 BOTTLENone
20074-3074-11100 TABLET In 1 BOTTLENone

Niaspan (niacin)
PRODUCT INFO
Product Code0074-3079Dosage FormTABLET, EXTENDED RELEASE
Route Of AdministrationORALDEA Schedule
INGREDIENTS
Name (Active Moiety)TypeStrength
niacin (Niacin) Active750 MILLIGRAM  In 1 TABLET
hypromelloseInactive 
povidoneInactive 
stearic acidInactive 
polyethylene glycolInactive 
titanium dioxideInactive 
synthetic red and yellow iron oxidesInactive 
FD&C yellow #6/sunset yellow FCF Aluminum LakeInactive 
IMPRINT INFORMATION
CharacteristicAppearanceCharacteristicAppearance
ColorORANGE (MEDIUM-ORANGE) Score1
ShapeOVAL (OVAL) Symbolfalse
Imprint Code KOS;750 Coatingtrue
Size19mm
PACKAGING
#NDCPackage DescriptionMultilevel Packaging
10074-3079-9090 TABLET In 1 BOTTLENone
20074-3079-11100 TABLET In 1 BOTTLENone

Niaspan (niacin)
PRODUCT INFO
Product Code0074-3080Dosage FormTABLET, EXTENDED RELEASE
Route Of AdministrationORALDEA Schedule
INGREDIENTS
Name (Active Moiety)TypeStrength
niacin (Niacin) Active1000 MILLIGRAM  In 1 TABLET
hypromelloseInactive 
povidoneInactive 
stearic acidInactive 
polyethylene glycolInactive 
titanium dioxideInactive 
synthetic red and yellow iron oxidesInactive 
FD&C yellow #6/sunset yellow FCF Aluminum LakeInactive 
IMPRINT INFORMATION
CharacteristicAppearanceCharacteristicAppearance
ColorORANGE (MEDIUM-ORANGE) Score1
ShapeOVAL (OVAL) Symbolfalse
Imprint Code KOS;1000 Coatingtrue
Size19mm
PACKAGING
#NDCPackage DescriptionMultilevel Packaging
10074-3080-9090 TABLET In 1 BOTTLENone
20074-3080-11100 TABLET In 1 BOTTLENone

Revised: 01/2008Abbott Laboratories