BICALUTAMIDE tablet, film coated

Bicalutamide by

Drug Labeling and Warnings

Bicalutamide by is a Prescription medication manufactured, distributed, or labeled by Golden State Medical Supply, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • 1. INDICATIONS AND USAGE

    Bicalutamide tablets 50 mg daily is indicated for use in combination therapy with a luteinizing hormone-releasing hormone (LHRH) analog for the treatment of Stage D 2 metastatic carcinoma of the prostate.

    Bicalutamide tablets 150 mg daily is not approved for use alone or with other treatments [see Clinical Studies (14.2)].

  • 2. DOSAGE AND ADMINISTRATION

    2.1. Recommended Dose and Schedule

    The recommended dose for bicalutamide tablets therapy in combination with an LHRH analog is one 50 mg tablet once daily (morning or evening), with or without food. It is recommended that bicalutamide tablets be taken at the same time each day. Treatment with bicalutamide tablets should be started at the same time as treatment with an LHRH analog. If a dose of bicalutamide is missed, take the next dose at the scheduled time. Do not take the missed dose and do not double the next dose.

    2.2. Dosage Adjustment in Renal Impairment

    No dosage adjustment is necessary for patients with renal impairment [see Use in Specific Populations (8.7)] .

    2.3. Dosage Adjustment in Hepatic Impairment

    No dosage adjustment is necessary for patients with mild to moderate hepatic impairment. In patients with severe liver impairment (n=4), although there was a 76% increase in the half-life (5.9 and 10.4 days for normal and impaired patients, respectively) of the active enantiomer of bicalutamide, no dosage adjustment is necessary [see Use in Specific Populations (8.6)] .

  • 3. DOSAGE FORMS AND STRENGTHS

    Bicalutamide tablets, USP 50 mg for oral administration are white to off-white, round, biconvex, film coated tablets, debossed ‘B 50’ on one side and plain on other side.

  • 4. CONTRAINDICATIONS

    Bicalutamide is contraindicated in:

    • Hypersensitivity

    Bicalutamide is contraindicated in any patient who has shown a hypersensitivity reaction to the drug or any of the tablet’s components. Hypersensitivity reactions including angioneurotic edema and urticaria have been reported.

    • Women

    Bicalutamide has no indication for women, and should not be used in this population.

    • Pregnancy

    Bicalutamide can cause fetal harm when administered to a pregnant woman [see Use in Specific Populations (8.1)].

  • 5. WARNINGS AND PRECAUTIONS

    5.1. Hepatitis

    Cases of death or hospitalization due to severe liver injury (hepatic failure) have been reported postmarketing in association with the use of bicalutamide. Hepatotoxicity in these reports generally occurred within the first three to four months of treatment. Hepatitis or marked increases in liver enzymes leading to drug discontinuation occurred in approximately 1% of bicalutamide patients in controlled clinical trials.

    Serum transaminase levels should be measured prior to starting treatment with bicalutamide, at regular intervals for the first four months of treatment, and periodically thereafter. If clinical symptoms or signs suggestive of liver dysfunction occur (e.g., nausea, vomiting, abdominal pain, fatigue, anorexia, “flu-like” symptoms, dark urine, jaundice, or right upper quadrant tenderness), the serum transaminases, in particular the serum ALT, should be measured immediately. If at any time a patient has jaundice, or their ALT rises above two times the upper limit of normal, bicalutamide should be immediately discontinued with close follow-up of liver function.

    5.2. Hemorrhage with Concomitant Use of Coumarin Anticoagulant

    In the postmarketing setting, there have been reports of excessive prolongation of the prothrombin time (PT) and International Normalized Ratio (INR) days to weeks after the introduction of bicalutamide in patients who were previously stable on coumarin anticoagulants. Some patients had serious bleeding including intracranial, retroperitoneal, and gastrointestinal requiring blood transfusion and/or administration of vitamin K. Closely monitor the PT/INR, and adjust the anticoagulant dose as needed [see Drug Interactions (7) and Adverse Reactions (6.2)].

    5.3. Gynecomastia and Breast Pain

    In clinical trials with bicalutamide 150 mg as a single agent for prostate cancer, gynecomastia and breast pain have been reported in up to 38% and 39% of patients, respectively.

    5.4. Glucose Tolerance

    A reduction in glucose tolerance has been observed in males receiving LHRH agonists. This may manifest as diabetes or loss of glycemic control in those with pre-existing diabetes. Consideration should therefore be given to monitoring blood glucose in patients receiving bicalutamide in combination with LHRH agonists.

    5.5. Laboratory Tests

    Regular assessments of serum Prostate Specific Antigen (PSA) may be helpful in monitoring the patient’s response. If PSA levels rise during bicalutamide therapy, the patient should be evaluated for clinical progression. For patients who have objective progression of disease together with an elevated PSA, a treatment-free period of antiandrogen, while continuing the LHRH analog, may be considered.

  • 6. ADVERSE REACTIONS

    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.

    6.1. Clinical Trials Experience

    In patients with advanced prostate cancer treated with bicalutamide in combination with an LHRH analog, the most frequent adverse reaction was hot flashes (53%).

    In the multi-center, double-blind, controlled clinical trial comparing bicalutamide 50 mg once daily with flutamide 250 mg three times a day, each in combination with an LHRH analog, the following adverse reactions with an incidence of 5% or greater, regardless of causality, have been reported.

    Table 1. Incidence of Adverse Reactions (≥ 5% in Either Treatment Group) Regardless of Causality
    Body System Adverse ReactionTreatment Group Number of Patients (%)
    Bicalutamide Plus LHRH Analog (n=401)Flutamide Plus LHRH Analog (n=407)
    Body as a Whole
    Pain (General) 142 (35) 127 (31)
    Back Pain 102 (25) 105 (26)
    Asthenia 89 (22) 87 (21)
    Pelvic Pain 85 (21) 70 (17)

    Infection

    71(18)

    57 (14)

    Abdominal Pain

    46 (11)

    46 (11)

    Chest Pain

    34 (8)

    34 (8)

    Headache

    29 (7)

    27 (7)

    Flu Syndrome

    28 (7)

    30 (7)

    Cardiovascular

    Hot Flashes

    211 (53)

    217 (53)

    Hypertension

    34 (8)

    29 (7)

    Digestive

    Constipation

    87 (22)

    69 (17)

    Nausea

    62 (15)

    58 (14)

    Diarrhea

    49 (12)

    107 (26)

    Increased Liver Enzyme Test

    30 (7)

    46 (11)

    Dyspepsia

    30 (7)

    23 (6)

    Flatulence

    26 (6)

    22 (5)

    Anorexia

    25 (6)

    29 (7)

    Vomiting

    24 (6)

    32 (8)

    Hemic and Lymphatic

    Anemia

    45 (11)

    53 (13)

    Metabolic and Nutritional

    Peripheral Edema

    53 (13)

    42 (10)

    Weight Loss

    30 (7)

    39 (10)

    Hyperglycemia

    26 (6)

    27 (7)

    Alkaline Phosphatase Increased

    22 (5)

    24 (6)

    Weight Gain

    22 (5)

    18 (4)

    Musculoskeletal

    Bone Pain

    37 (9)

    43 (11)

    Myasthenia

    27 (7)

    19 (5)

    Arthritis

    21 (5)

    29 (7)

    Pathological Fracture

    17 (4)

    32 (8)

    Nervous System

    Dizziness

    41 (10)

    35 (9)

    Paresthesia

    31 (8)

    40 (10)

    Insomnia

    27 (7)

    39 (10)

    Anxiety

    20 (5)

    9 (2)

    Depression

    16 (4)

    33 (8)

    Respiratory System

    Dyspnea

    51 (13)

    32 (8)

    Cough Increased

    33 (8)

    24 (6)

    Pharyngitis

    32 (8)

    23 (6)

    Bronchitis

    24 (6)

    22 (3)

    Pneumonia

    18 (4)

    19 (5)

    Rhinitis

    15 (4)

    22 (5)

    Skin and Appendages

    Rash

    35 (9)

    30 (7)

    Sweating

    25 (6)

    20 (5)

    Urogenital

    Nocturia

    49 (12)

    55 (14)

    Hematuria

    48 (12)

    26 (6)

    Urinary Tract Infection

    35 (9)

    36 (9)

    Gynecomastia

    36 (9)

    30 (7)

    Impotence

    27 (7)

    35 (9)

    Breast Pain

    23 (6)

    15 (4)

    Urinary Frequency

    23 (6)

    29 (7)

    Urinary Retention

    20 (5)

    14 (3)

    Urinary Impaired

    19 (5)

    15 (4)

    Urinary Incontinence

    15 (4)

    32 (8)

    Other adverse reactions (greater than or equal to 2%, but less than 5%) reported in the bicalutamide-LHRH analog treatment group are listed below by body system and are in order of decreasing frequency within each body system regardless of causality.

    Body as a Whole: Neoplasm; Neck Pain; Fever; Chills; Sepsis; Hernia; Cyst

    Cardiovascular: Angina Pectoris; Congestive Heart Failure; Myocardial Infarct; Heart Arrest; Coronary Artery Disorder; Syncope

    Digestive: Melena; Rectal Hemorrhage; Dry Mouth; Dysphagia; Gastrointestinal Disorder; Periodontal Abscess; Gastrointestinal Carcinoma

    Metabolic and Nutritional: Edema; BUN Increased; Creatinine Increased; Dehydration; Gout; Hypercholesteremia

    Musculoskeletal: Myalgia; Leg Cramps

    Nervous: Hypertonia; Confusion; Somnolence; Libido Decreased; Neuropathy; Nervousness

    Respiratory: Lung Disorder; Asthma; Epistaxis; Sinusitis

    Skin and Appendages: Dry Skin; Alopecia; Pruritus; Herpes Zoster; Skin Carcinoma; Skin Disorder

    Special Senses: Cataract Specified

    Urogenital: Dysuria; Urinary Urgency; Hydronephrosis; Urinary Tract Disorder

    Abnormal Laboratory Test Values:

    Laboratory abnormalities including: elevated AST, ALT, bilirubin, BUN, and creatinine; and decreased hemoglobin and white cell count, have been reported in both bicalutamide-LHRH analog treated and flutamide-LHRH analog treated patients.

    6.2. Postmarketing Experience

    The following adverse reactions have been identified during post-approval use of bicalutamide. 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.

    Respiratory disorders: Interstitial lung disease (some fatal) including interstitial pneumonitis and pulmonary fibrosis, most often at doses greater than 50 mg.

    Hemorrhage: Increased PT/INR due to interaction between coumarin anticoagulants and bicalutamide. Serious bleeding reported. [see Warnings and Precautions (5.2)]

    Skin and subcutaneous tissue disorders: Photosensitivity

  • 7. DRUG INTERACTIONS

    Clinical studies have not shown any drug interactions between bicalutamide and LHRH analogs (goserelin or leuprolide). There is no evidence that bicalutamide induces hepatic enzymes.

    In vitro studies have shown that R-bicalutamide is an inhibitor of CYP 3A4 with lesser inhibitory effects on CYP 2C9, 2C19 and 2D6 activity. Clinical studies have shown that with co-administration of bicalutamide, mean midazolam (a CYP 3A4 substrate) levels may be increased 1.5-fold (for C max) and 1.9-fold (for AUC). Hence, caution should be exercised when bicalutamide is co-administered with CYP 3A4 substrates.

    In vitro protein-binding studies have shown that bicalutamide can displace coumarin anticoagulants from binding sites. PT/INR should be closely monitored in patients concomitantly receiving coumarin anticoagulants and bicalutamide. Adjustment of the anticoagulant dose may be necessary. [see Warnings and Precautions (5.2) and Adverse reaction (6.2) ]

  • 8. USE IN SPECIFIC POPULATIONS

    8.1. Pregnancy

    Risk Summary

    Bicalutamide is contraindicated for use in pregnant women because it can cause fetal harm. Bicalutamide is not indicated for use in females. There are no human data on the use of bicalutamide in pregnant women. In animal reproduction studies, oral administration of bicalutamide to pregnant rats during organogenesis caused abnormal development of reproductive organs in male fetuses at exposures approximately 0.7 to 2 times the human exposure at the recommended dose (see Data).

    Data

    Animal Data

    In an embryo-fetal development study in pregnant rats dosed during the period of organogenesis from gestation days 6 to15, male fetuses had reduced anogenital distance at doses of 10 mg/kg/day and above (approximately 0.7 to 2 times the human exposure at the recommended dose).

    In a pre- and post-natal development study, female rats were dosed from gestation day 7 to 16 and allowed to litter and rear their offspring to weaning. Male offspring of rats receiving doses of 10 mg/kg/day (approximately 0.7 times the human exposure at the recommended dose) and above, were observed to have reduced anogenital distance.

    In a peri- and post-natal development study, female rats were dosed from gestation day 16 to lactation day 22 and allowed to litter and rear their offspring to weaning. Survival and weights of offspring during lactation were reduced for litters from maternal rats receiving doses of 250 mg/kg/day (approximately 2 times the human exposure at the recommended dose). Male offspring of rats receiving doses of 10 mg/kg/day (approximately 0.7 times the human exposure at the recommended dose) and above, were observed to have reduced anogenital distance, smaller secondary sex organs, cryptorchidism and hypospadias resulting in an inability to mate and impregnate their female partners. Female offspring of rats receiving doses of 10 mg/kg/day (approximately 0.7 times the human exposure at the recommended dose) and above had reduced pregnancy rates.

    8.2. Lactation

    Risk Summary

    Bicalutamide is not indicated for use in pregnant women. There is no information available on the presence of bicalutamide in human milk, or on the effects on the breastfed infant or on milk production. Bicalutamide has been detected in rat milk.

    8.3. Females and Males of Reproductive Potential

    Contraception

    Males

    Antiandrogen therapy may cause morphological changes in spermatozoa [see Nonclinical Toxicology (13.1)]. Based on findings in animal reproduction studies and its mechanism of action, advise male patients with female partners of reproductive potential to use effective contraception during treatment and for 130 days after the final dose of bicalutamide [see Use in Specific Populations (8.1) and Clinical Pharmacology (12.1)].

    Infertility

    Males

    Based on animal studies, bicalutamide can lead to inhibition of spermatogenesis and may impair fertility in males of reproductive potential. The long-term effects of bicalutamide tablets on male fertility have not been studied. [see Nonclinical Toxicology (13.1)] .

    8.4. Pediatric Use

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

    Bicalutamide orodispersible tablet was studied in combination with anastrozole orodispersible tablet in an open-label, non-comparative, multi-center study that assessed the efficacy and safety of this combination regimen over 12 months in the treatment of gonadotropin-independent precocious puberty in boys with familial male-limited precocious puberty, also known as testotoxicosis. Patients were enrolled in the study if they had a baseline age ≥ 2 years and a diagnosis of testotoxicosis based on clinical features of progressive precocious puberty, symmetrical testicular enlargement, advanced bone age, pubertal levels of serum testosterone, prepubertal pattern of gonadotropin secretion following a GnRH stimulation test, and absence of other clinical and biochemical causes of testosterone excess. Thirteen out of the 14 patients enrolled completed 12 months of combination treatment (one patient was lost to follow-up). If central precocious puberty (CPP) developed, an LHRH analog was to be added. Four patients were diagnosed with CPP during the 12-month study and received LHRH analog treatment and 2 additional patients were diagnosed at the end of the 12 months and received treatment subsequently. Mean ± SD characteristics at baseline were as follows: chronological age: 3.9±1.9 years; bone age 8.8±2.5; bone age/chronological age ratio: 2.06 ± 0.51; growth rate (cm/yr): 10.81 ± 4.22; growth rate standard deviation score (SDS): 0.41 ± 1.36.

    The starting bicalutamide dose was 12.5 mg. Bicalutamide was titrated in each patient until steady-state R-bicalutamide (the active isomer of bicalutamide) trough plasma concentration reached 5 to 15 mcg/mL, which is the range of therapeutic concentrations achieved in adults with prostate cancer following the administration of the currently approved bicalutamide dose of 50 mg. The starting daily dose of anastrozole was 0.5 mg. Anastrozole was independently titrated in each patient until it reached at steady-state a serum estradiol concentration of <10 pmol/L (2.7 pg/mL). The following ascending doses were used for bicalutamide: 12.5 mg, 25 mg, 50 mg, and 100 mg. For anastrozole there were two ascending doses: 0.5 mg and 1 mg. At the end of the titration phase, 1 patient was on 12.5 mg bicalutamide, 8 patients were on 50 mg bicalutamide, and 4 patients were on 100 mg bicalutamide; 10 patients were on 0.5 mg anastrozole and 3 patients were on 1 mg anastrozole. In the majority of patients, steady-state trough concentrations of R-bicalutamide appeared to be attained by Day 21 with once daily dosing. Steady-state trough plasma anastrozole concentrations appeared to be attained by Day 8.

    The primary efficacy analysis of the study was to assess the change in growth rate after 12 months of treatment, relative to the growth rate during the ≥6 months prior to entering the study. Pre-study growth rates were obtained retrospectively. There was no statistical evidence that the growth rate was reduced during treatment. During bicalutamide /anastrozole treatment the mean growth rate (cm/yr) decreased by 1.6 cm/year, 95% CI (-4.7 to 1.5) p=0.28; the mean growth rate SDS decreased by 0.1 SD, 95% CI (–1.2 to 1.0) p=0.88. Table 2 shows descriptive data for growth rates for the overall population and for subgroups defined by history of previous treatment for testotoxicosis with ketoconazole, spironolactone, anastrozole or other aromatase inhibitors.

    Table 2. Growth Rates
  • * Change compared to pre-study growth rate.
  • † PT = Previous treatment for testotoxicosis with ketoconazole, spironolactone, anastrozole or other aromatase inhibitors.
  • ‡ Median calculated as midpoint of 3rd and 4th ranked observations.
  • § NPT = no previous treatment for testotoxicosis with ketoconazole, spironolactone, anastrozole, or other aromatase inhibitors.
    		•

    Endpoint

    Analysis population

    Pre-study Mean

    Change from pre-study to 12 months

    		% patients with growth reduction *

    Mean

    Median

    (Min, Max)

    Growth rate (cm/yr)

    All treated (n=13)

    10.8

    -1.6

    -2.8

    (-7.4, 8.4)

    9/13 (69%)

    PT † (n=6)

    10.3

    -0.2

    -2.6 ‡

    (-7.2, 8.4)

    4/6 (67%)

    NPT § (n=7)

    11.2

    -2.8

    -2.8

    (-7.4, 1.1)

    5/7 (71%)

    Growth rate (SD units)

    All treated (n=13)

    0.4

    -0.1

    -0.4

    (-2.7, 3.5)

    9/13 (69%)

    PT † (n=6)

    -0.1

    +0.7

    -0.2 ‡

    (-1.6, 3.5)

    4/6 (67%)

    NPT § (n=7)

    0.8

    -0.7

    -0.4

    (-2.7, 0.5)

    5/7 (71%)

    Total testosterone concentrations increased by a mean of 5 mmol/L over the 12 months of treatment from a baseline mean of 10 mmol/L. Estradiol concentrations were at or below the level of quantification (9.81 pmol/L) for 11 of 12 patients after 12 months of treatment. Six of the 12 patients started treatment at an estradiol concentration below the level of quantification.

    There were no deaths, serious adverse events, or discontinuations due to adverse events during the study. Of the 14 patients exposed to study treatment, 13 (92.9%) experienced at least one adverse event. The most frequently reported (>3 patients) adverse events were gynecomastia (7/14, 50%), central precocious puberty (6/14, 43%), vomiting (5/14, 36%), headache (3/14, 21%), pyrexia (3/14, 21%), and upper respiratory tract infection (3/14, 21%). Adverse reactions considered possibly related to bicalutamide by investigators included gynecomastia (6/14, 43%), central precocious puberty (2/14, 14%), breast tenderness (2/14, 14%), breast pain (1/14, 7%), asthenia (1/14, 7%), increased alanine aminotransferase [ALT] (1/14, 7%), increased aspartate aminotransferase [AST] (1/14, 7%), and musculoskeletal chest pain (1/14, 7%). Headache was the only adverse reaction considered possibly related to anastrozole by investigators. For the patient who developed elevated ALT and AST, the elevation was <3X ULN, and returned to normal without stopping treatment; there was no concomitant elevation in total bilirubin.

    8.5. Geriatric Use

    In two studies in patients given 50 or 150 mg daily, no significant relationship between age and steady-state levels of total bicalutamide or the active R-enantiomer has been shown.

    8.6. Hepatic Impairment

    Bicalutamide should be used with caution in patients with moderate-to-severe hepatic impairment. Bicalutamide is extensively metabolized by the liver. Limited data in subjects with severe hepatic impairment suggest that excretion of bicalutamide may be delayed and could lead to further accumulation. Periodic liver function tests should be considered for hepatic-impaired patients on long-term therapy [see Warnings and Precautions (5.1)].

    No clinically significant difference in the pharmacokinetics of either enantiomer of bicalutamide was noted in patients with mild-to-moderate hepatic disease as compared to healthy controls. However, the half-life of the R-enantiomer was increased approximately 76% (5.9 and 10.4 days for normal and impaired patients, respectively) in patients with severe liver disease (n=4).

    8.7. Renal Impairment

    Renal impairment (as measured by creatinine clearance) had no significant effect on the elimination of total bicalutamide or the active R-enantiomer.

  • 10. OVERDOSAGE

    Long-term clinical trials have been conducted with dosages up to 200 mg of bicalutamide daily and these dosages have been well tolerated. A single dose of bicalutamide that results in symptoms of an overdose considered to be life threatening has not been established.

    There is no specific antidote; treatment of an overdose should be symptomatic.

    In the management of an overdose with bicalutamide, vomiting may be induced if the patient is alert. It should be remembered that, in this patient population, multiple drugs may have been taken. Dialysis is not likely to be helpful since bicalutamide is highly protein bound and is extensively metabolized. General supportive care, including frequent monitoring of vital signs and close observation of the patient, is indicated.

  • 11. DESCRIPTION

    Bicalutamide tablets, USP contain 50 mg of bicalutamide, a non-steroidal androgen receptor inhibitor with no other known endocrine activity. The chemical name is propanamide, N [4 cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)sulfonyl]-2-hydroxy-2-methyl-,(+-). The structural and empirical formulas are:

    chem

    Bicalutamide has a molecular weight of 430.37. The pKa is approximately 12. Bicalutamide is a fine white to off-white powder which is practically insoluble in water at 37°C (5 mg per 1000 mL), slightly soluble in chloroform and absolute ethanol, sparingly soluble in methanol, and soluble in acetone and tetrahydrofuran.

    Bicalutamide is a racemate with its antiandrogenic activity being almost exclusively exhibited by the R-enantiomer of bicalutamide; the S-enantiomer is essentially inactive.

    The inactive ingredients of bicalutamide tablets, USP are lactose monohydrate, magnesium stearate, hypromellose E5, polyethylene glycol 400, povidone K 30, sodium starch glycolate, and titanium dioxide.

    Bicalutamide tablets, USP 50 mg meets USP Dissolution Test 2.

  • 12. CLINICAL PHARMACOLOGY

    12.1. Mechanism of Action

    Bicalutamide is a non-steroidal androgen receptor inhibitor. It competitively inhibits the action of androgens by binding to cytosol androgen receptors in the target tissue. Prostatic carcinoma is known to be androgen sensitive and responds to treatment that counteracts the effect of androgen and/or removes the source of androgen.

    When bicalutamide is combined with LHRH analog therapy, the suppression of serum testosterone induced by the LHRH analog is not affected. However, in clinical trials with bicalutamide as a single agent for prostate cancer, rises in serum testosterone and estradiol have been noted.

    In a subset of patients who have been treated with bicalutamide and an LHRH agonist, and who discontinue bicalutamide therapy due to progressive advanced prostate cancer, a reduction in Prostate Specific Antigen (PSA) and/or clinical improvement (antiandrogen withdrawal phenomenon) may be observed.

    12.3. Pharmacokinetics

    Absorption

    Bicalutamide is well-absorbed following oral administration, although the absolute bioavailability is unknown. Co-administration of bicalutamide with food has no clinically significant effect on rate or extent of absorption.

    Distribution

    Bicalutamide is highly protein-bound (96%) [see Drug Interactions (7)] .

    Metabolism/Elimination

    Bicalutamide undergoes stereospecific metabolism. The S (inactive) isomer is metabolized primarily by glucuronidation. The R (active) isomer also undergoes glucuronidation but is predominantly oxidized to an inactive metabolite followed by glucuronidation. Both the parent and metabolite glucuronides are eliminated in the urine and feces. The S-enantiomer is rapidly cleared relative to the R-enantiomer, with the R-enantiomer accounting for about 99% of total steady-state plasma levels.

    Pharmacokinetics of the active enantiomer of bicalutamide in normal males and patients with prostate cancer are presented in Table 3.

    Table 3. Pharmacokinetics of Bicalutamide Active Enantiomer

    ParameterMeanStandard Deviation

    Normal Males (n=30)

    Apparent Oral Clearance (L/hr)

    0.320

    0.103

    Single Dose Peak Concentration (µg/mL)

    0.768

    0.178

    Single Dose Time to Peak Concentration (hours)

    31.3

    14.6

    Half-life (days)

    5.8

    2.29

    Patients with Prostate Cancer (n=40)

    C ss (µg/mL)

    8.939

    3.504

  • 13. NONCLINICAL TOXICOLOGY

    13.1. Carcinogenesis, Mutagenesis, Impairment of Fertility

    Two-year oral carcinogenicity studies were conducted in both male and female rats and mice at doses of 5, 15, or 75 mg/kg/day of bicalutamide. A variety of tumor target organ effects were identified and were attributed to the antiandrogenicity of bicalutamide, namely, testicular benign interstitial (Leydig) cell tumors in male rats at all dose levels (the steady-state plasma concentration with the 5 mg/kg/day dose is approximately 0.7 times the human exposure at the recommended dose) and uterine adenocarcinoma in female rats at 75 mg/kg/day (approximately 1.5 times the human exposure at the recommended dose). There is no evidence of Leydig cell hyperplasia in patients; uterine tumors are not relevant to the indicated patient population

    A small increase in the incidence of hepatocellular carcinoma in male mice given 75 mg/kg/day of bicalutamide (approximately 4 times the human exposure at the recommended dose) and an increased incidence of benign thyroid follicular cell adenomas in rats given 5 mg/kg/day (approximately 0.7 times the human exposure at the recommended dose) and above were recorded. These neoplastic changes were progressions of non-neoplastic changes related to hepatic enzyme induction observed in animal toxicity studies. Enzyme induction has not been observed following bicalutamide administration in man. There were no tumorigenic effects suggestive of genotoxic carcinogenesis.

    A comprehensive battery of both in vitro and in vivo genotoxicity tests (yeast gene conversion, Ames, E. coli, CHO/HGPRT, human lymphocyte cytogenetic, mouse micronucleus, and rat bone marrow cytogenetic tests) has demonstrated that bicalutamide does not have genotoxic activity.

    In repeat-dose toxicology studies, atrophy of seminiferous tubules of the testes has been observed for all species examined, which is a predicted class effect with antiandrogens. In the 6- and 12-month rat study, testicular atrophy was seen at approximately 2 times the human exposure at the recommended dose. In the 12- month dog study, the incidence of testicular atrophy was seen at approximately 7 times the human exposure at the recommended dose. In male rats administered 250 mg/kg/day (approximately 2 times human exposure at the recommended dose), the precoital interval and time to successful mating were increased in the first pairing, but no effects on fertility following successful mating were seen. These effects were reversed by 7 weeks after the end of an 11-week period of dosing.

    Female rats dosed at 1, 10 and 250 mg/kg/day (less than to 2 times the human exposure at the recommended dose) had increased estrous cycle irregularity but there was no effect on fertility.

    In a peri- and post-natal development study, female offspring of rats receiving doses of 10 mg/kg/day (approximately 0.7 times the human exposure at the recommended clinical dose) and above had reduced pregnancy rates. Administration of bicalutamide to pregnant females resulted in feminization of the male offspring leading to hypospadias at doses of 10 mg/kg/day (approximately 0.7 times the human exposure at the recommended dose) and above. Affected male offspring were also impotent.

  • 14. CLINICAL STUDIES

    14.1. Bicalutamide Tablets 50 mg Daily in Combination with an LHRH-A

    In a multi-center, double-blind, controlled clinical trial, 813 patients with previously untreated advanced prostate cancer were randomized to receive bicalutamide 50 mg once daily (404 patients) or flutamide 250 mg (409 patients) three times a day, each in combination with LHRH analogs (either goserelin acetate implant or leuprolide acetate depot).

    In an analysis conducted after a median follow-up of 160 weeks was reached, 213 (52.7%) patients treated with bicalutamide-LHRH analog therapy and 235 (57.5%) patients treated with flutamide-LHRH analog therapy had died. There was no significant difference in survival between treatment groups (see Figure 1). The hazard ratio for time to death (survival) was 0.87 (95% confidence interval 0.72 to 1.05).

    Figure 1 - The Kaplan-Meier probability of death for both antiandrogen treatment groups.

    fig_1

    There was no significant difference in time to objective tumor progression between treatment groups (see Figure 2). Objective tumor progression was defined as the appearance of any bone metastases or the worsening of any existing bone metastases on bone scan attributable to metastatic disease, or an increase by 25% or more of any existing measurable extraskeletal metastases. The hazard ratio for time to progression of bicalutamide plus LHRH analog to that of flutamide plus LHRH analog was 0.93 (95% confidence interval, 0.79 to 1.10).

    Figure 2 - Kaplan-Meier curve for time to progression for both antiandrogen treatment groups.

    fig_2

    Quality of life was assessed with self-administered patient questionnaires on pain, social functioning, emotional well-being, vitality, activity limitation, bed disability, overall health, physical capacity, general symptoms, and treatment related symptoms. Assessment of the Quality of Life questionnaires did not indicate consistent significant differences between the two treatment groups.

    14.2 Safety Data from Clinical Studies using Bicalutamide Tablets 150 mg

    Bicalutamide tablet 150 mg is not approved for use either alone or with other treatments.

    Two identical multi-center, randomized, open-label trials comparing bicalutamide 150 mg daily monotherapy to castration were conducted in patients that had locally advanced (T3-4, NX, M0) or metastatic (M1) prostate cancer.

    Monotherapy — M1 Group

    Bicalutamide 150 mg daily is not approved for use in patients with M1 cancer of the prostate. Based on an interim analysis of the two trials for survival, the Data Safety Monitoring Board recommended that bicalutamide treatment be discontinued in the M1 patients because the risk of death was 25% (HR 1.25, 95% CI 0.87 to 1.81) and 31% (HR 1.31, 95% CI 0.97 to 1.77) higher in the bicalutamide treated group compared to that in the castrated group, respectively.

    Locally Advanced (T 3-4, NX, M0) Group

    Bicalutamide 150 mg daily is not approved for use in patients with locally advanced (T 3-4, NX, M0) cancer of the prostate. Following discontinuation of all M1 patients, the trials continued with the T3-4, NX, M0 patients until study completion. In the larger trial (N=352), the risk of death was 25% (HR 1.25, 95% CI 0.92 to 1.71) higher in the bicalutamide group and in the smaller trial (N=140), the risk of death was 36% (HR 0.64, 95% CI, 0.39 to 1.03) lower in the bicalutamide group.

    In addition to the above two studies, there are three other ongoing clinical studies that provide additional safety information for bicalutamide 150 mg, a dose that is not approved for use. These are three multi-center, randomized, double-blind, parallel group trials comparing bicalutamide 150 mg daily monotherapy (adjuvant to previous therapy or under watchful waiting) with placebo, for death or time to disease progression, in a population of 8113 patients with localized or locally advanced prostate cancer.

    Bicalutamide 150 mg daily is not approved for use as therapy for patients with localized prostate cancer who are candidates for watchful waiting. Data from a planned subgroup analysis of two of these trials in 1627 patients with localized prostate cancer who were under watchful waiting, revealed a trend toward decreased survival in the bicalutamide arm after a median follow-up of 7.4 years. There were 294 (37.7%) deaths in the bicalutamide treated patients versus 279 (32.9%) deaths in the placebo-treated patients (localized watchful waiting group) for a hazard ratio of 1.16 (95% CI 0.99 to 1.37).

  • 16. HOW SUPPLIED/STORAGE AND HANDLING

    Bicalutamide tablets, USP 50 mg are white to off-white, round, biconvex, film-coated tablets debossed "B 50" on one side and plain on other side and supplied in bottles of 30 tablets (NDC: 60429-177-30) , 100 tablets (NDC: 60429-177-01) and 500 tablets (NDC: 60429-177-05).

    16.1. Storage and Handling

    “Store at 20° to 25°C (68 to 77°F). [See USP Controlled Room Temperature]”

  • 17. PATIENT COUNSELING INFORMATION

    Advise the patient to read the FDA-approved patient labeling (Patient Information).

    Dose and Schedule: Inform patients that therapy with bicalutamide and the LHRH analog should be started at the same time and that they should not interrupt or stop taking these medications without consulting their healthcare provider [see Dosage and Administration (2.1)].

    Hepatitis: Inform patients that bicalutamide can cause hepatitis, which may result in hepatic failure and death. Advise patients that liver function tests should be monitored regularly during treatment and to report signs and symptoms of hepatitis [see Warnings and Precautions (5.1)].

    Hemorrhage with Concomitant Use of Coumarin Anticoagulant: Inform patients that serious bleeding has occurred with reported increased anticoagulant effects while taking bicalutamide. Advise patients to notify their healthcare provider of any bleeding or spontaneous bruising while on bicalutamide and taking anticoagulants [see Warnings and Precautions (5.2) and Adverse reaction (6.2) ] .

    Glucose Tolerance: Inform patients that diabetes or loss of glycemic control in patients with pre-existing diabetes has been reported during treatment with LHRH agonists. Consideration should therefore be given to monitoring blood glucose in patients receiving bicalutamide in combination with LHRH agonists [see Warnings and Precautions (5.4)].

    Somnolence: During treatment with bicalutamide, somnolence has been reported. Advise patients who experience this symptom to observe caution when driving or operating machines [see Adverse Reactions (6.1)].

    Photosensitivity: Inform patients that cases of photosensitivity have been reported during treatment with bicalutamide and that they should avoid direct exposure to excessive sunlight or UV-light exposure. Consideration should be given to the use of sunscreen [see Adverse Reactions (6.2)].

    Contraception and fertility: Advise male patients with female partners of reproductive potential to use effective contraception during treatment and for 130 days after the last dose of bicalutamide therapy. Advise male patients that bicalutamide may impair fertility [see Use in Specific Populations (8.3)].

    Manufactured For:

    Accord Healthcare, Inc.,

    1009, Slater Road,

    Suite 210-B,

    Durham, NC 27703,

    USA.

    Manufactured By:

    Intas Pharmaceuticals Limited,

    Plot No. : 457, 458,

    Village - Matoda,

    Bavla Road, Ta.:Sanand,

    Dist.: Ahmedabad : 382 210.

    India.

    10 0857 3 691691

    Marketed/Packaged by:

    GSMS, Inc.

    Camarillo, CA USA 93012

    Issued January 2019

  • PATIENT PACKAGE INSERT

    PATIENT INFORMATION

    Bicalutamide Tablets

    [bye-kah-LEW-tuh-mide]

    What are bicalutamide tablets?

    Bicalutamide is a prescription medicine called an androgen receptor inhibitor, used in combination with luteinizing hormone-releasing hormone (LHRH) medicines to treat Stage D 2 metastatic prostate cancer.

    Bicalutamide tablets 150 mg daily is not approved for use alone or with other treatments.

    It is not known if bicalutamide tablets are safe and effective in children.

    Do not take bicalutamide tablets if you are:

    • allergic to bicalutamide or any of the ingredients in bicalutamide tablets. See the end of this Patient Information leaflet for a complete list of ingredients in bicalutamide tablets. Get medical help right away if you develop any of the following symptoms of an allergic reaction:
      • itching
      • hives(raised bumps)
      • swelling of the face, lips or tongue
      • trouble breathing or swallowing
    • female. Bicalutamide tablets is not for use by women
    • pregnant or may become pregnant. Bicalutamide tablets may harm your unborn baby.

    Before taking bicalutamide tablets, tell your healthcare provider about all your medical conditions, including if you:

    • have liver problems.
    • take a medicine to thin your blood. Ask your healthcare provider or pharmacist if you are not sure if your medicine is a blood thinner.
    • have diabetes.
    • have a female partner who can become pregnant. Males who have a female partner who can become pregnant should use effective birth control during treatment with bicalutamide tablets and for 130 days after the final dose. Talk to your healthcare provider if you have any questions about birth control.

    Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Bicalutamide tablets may affect the way other medicines work and other medicines may affect how bicalutamide tablets works, causing side effects.

    Know the medicines you take. Keep a list of your medicines with you to show your healthcare providers when you get a new medicine.

    How should I take bicalutamide tablets?

    • Take bicalutamide tablets exactly as your healthcare provider tells you to take it.
    • Do not stop taking bicalutamide tablets unless your healthcare provider tells you to.
    • Bicalutamide tablets can be taken either in the morning or in the evening, but you should take it at the same time every day.
    • Your treatment with bicalutamide tablets should start at the same time as your treatment with the LHRH medicine.
    • If you miss a bicalutamide tablets dose do not take the missed dose, take the next dose at your next scheduled time. Do not take 2 doses at the same time.
    • Bicalutamide tablets can be taken with or without food.
    • If you take too much bicalutamide tablets, call your healthcare provider or go to the nearest hospital emergency room right away

    What should I avoid during treatment with bicalutamide tablets?

    • Do not drive, operate machinery, or do other dangerous activities until you know how bicalutamide tablets affect you. Bicalutamide tablets can make you sleepy.
    • Avoid sunlight, sunlamps and tanning beds and consider using sunscreen during treatment with bicalutamide tablets. Some people have had skin sensitivity to sunlight during treatment with bicalutamide tablets.

    What are the possible side effects of bicalutamide tablets?

    Bicalutamide tablets may cause serious side effects, including.

    • Liver problems. Severe liver problems including liver failure that may need to be treated in a hospital or that may lead to death have happened in people who take bicalutamide tablets Your healthcare provider should do blood tests to check your liver function before and during treatment with bicalutamide tablets. Tell your healthcare provider right away if you develop any of these symptoms of liver problems during treatment:
      • yellowing of the skin and eyes (jaundice)
      • dark urine
      • right upper stomach pain
      • nausea
      • vomiting
      • tiredness
      • loss of appetite
      • chills
      • fever
    • Bleeding problems. Serious bleeding problems have happened in people who take bicalutamide tablets in combination with a blood thinner medicine (coumarin anticoagulants). Bleeding problems have happened days to weeks after starting bicalutamide tablets treatment. If you take a blood thinner medicine during treatment with bicalutamide tablets, tell your healthcare provider if you develop any bleeding or unexplained bruising.
    • Breast enlargement (gynecomastia) and breast pain.
    • Blood sugar problems. Poor blood sugar control can happen in people who take bicalutamide tablets in combination with LHRH medicines.

    Your healthcare provider may do blood tests during treatment with bicalutamide tablets to check for side effects.

    Your prostate cancer may get worse during treatment with bicalutamide tablets in combination with LHRH medicines. Regular monitoring of your prostate cancer with your healthcare provider is important to determine if your disease is worse.

    Tell your healthcare provider if you have trouble breathing with or without a cough or fever. Some people taking bicalutamide tablets get an inflammation in the lungs called interstitial lung disease.

    The most common side effects of bicalutamide tablets include:

    • hot flashes (short periods of feeling warm and sweating)
    • body pain (including back, pelvis, stomach)
    • feeling weak
    • constipation
    • infection
    • nausea
    • swelling in your arms, ankles, legs or feet
    • shortness of breath (dyspnea)
    • dizziness
    • diarrhea
    • blood in your urine
    • frequent urination at night
    • a decrease in red blood cells (anemia)

    Bicalutamide tablets may have an effect on male fertility which could be reversible. Talk to your healthcare provider if this is a concern for you.

    Tell your healthcare provider if you have any side effect that bothers you or that does not go away.

    These are not all the possible side effects of bicalutamide tablets. For more information, ask your healthcare provider or pharmacist.

    Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

    How should I store bicalutamide tablets?

    Store bicalutamide tablets at room temperature between 68°F to 77°F (20°C to 25°C).

    Keep bicalutamide tablets and all medicines out of the reach of children.

    General information about the safe and effective use of bicalutamide tablets.

    Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use bicalutamide tablets for a condition for which it was not prescribed. Do not give bicalutamide tablets to other people, even if they have the same symptoms that you have. It may harm them.

    This Patient Information leaflet summarizes the most important information about bicalutamide tablets. If you would like more information about bicalutamide tablets, talk with your healthcare provider. You can ask your healthcare provider or pharmacist for information about bicalutamide tablets that is written for health professionals.

    For more information, go to www.accordhealthcare.us or call Accord Healthcare at 1-866-941-7875.

    What are the ingredients in bicalutamide tablets?

    Active ingredient: bicalutamide.

    Inactive ingredients: lactose monohydrate, magnesium stearate, hypromellose E5, polyethylene glycol 400, povidone K30, sodium starch glycolate, and titanium dioxide.

    Manufactured For:



    Accord Healthcare Inc.

    1009, Slater Road

    Suite 210-B, Durham, NC 27703,

    USA

    Manufactured By:



    Intas Pharmaceuticals Limited

    Plot No.: 457,458,

    Village-Matoda,

    Bavla Road, Ta. - Sanand,

    Dist.-Ahmedabad 382 210,

    India.

    10 0857 3 691691

    Marketed/Packaged by:

    GSMS, Inc.

    Camarillo, CA USA 93012

    Issued January 2019

  • PRINCIPAL DISPLAY PANEL

    PRINCIPAL DISPLAY PANEL

    NDC: 60429-177-01

    Bicalutamide Tablets USP

    50 mg

    Rx Only

    Pharmacist:Dispense with a patient package insert.

    100 Tablets

    60429-177-01.jpg

  • INGREDIENTS AND APPEARANCE
    BICALUTAMIDE 
    bicalutamide tablet, film coated
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 60429-177(NDC:16729-023)
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BICALUTAMIDE (UNII: A0Z3NAU9DP) (BICALUTAMIDE - UNII:A0Z3NAU9DP) BICALUTAMIDE50 mg
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    POVIDONE K30 (UNII: U725QWY32X)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Colorwhite (WHITE TO OFF WHITE) Scoreno score
    ShapeROUNDSize7mm
    FlavorImprint Code B50
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 60429-177-3030 in 1 BOTTLE; Type 0: Not a Combination Product05/08/2014
    2NDC: 60429-177-01100 in 1 BOTTLE; Type 0: Not a Combination Product05/08/2014
    3NDC: 60429-177-05500 in 1 BOTTLE; Type 0: Not a Combination Product05/08/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07891707/06/2009
    Labeler - Golden State Medical Supply, Inc. (603184490)
    Establishment
    NameAddressID/FEIBusiness Operations
    Golden State Medical Supply, Inc.603184490relabel(60429-177) , repack(60429-177)
    • © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.