EMCYT (ESTRAMUSTINE PHOSPHATE SODIUM) CAPSULE [PHARMACIA AND UPJOHN COMPANY LLC]

EMCYT (ESTRAMUSTINE PHOSPHATE SODIUM) CAPSULE [PHARMACIA AND UPJOHN COMPANY LLC]
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NDC 0013-0132-02
Set ID a9b01bc6-95ac-46f9-befa-d845a74d53c1
Category HUMAN PRESCRIPTION DRUG LABEL
Packager Pharmacia and Upjohn Company LLC
Generic Name
Product Class Alkylating Drug
Product Number
Application Number NDA018045
  • DESCRIPTION

    Estramustine phosphate sodium, an antineoplastic agent, is an off-white powder readily soluble in water. EMCYT Capsules are white and opaque, each containing estramustine phosphate sodium as the disodium salt monohydrate equivalent to 140 mg estramustine phosphate, for oral administration. Each capsule also contains magnesium stearate, silicon dioxide, sodium lauryl sulfate, and talc. Gelatin capsule shells contain the following pigment: titanium dioxide.

    Chemically, estramustine phosphate sodium is estra-1,3,5(10)-triene-3,17-diol(17β)-,3-[bis(2-chloroethyl)carbamate] 17-(dihydrogen phosphate), disodium salt, monohydrate. It is also referred to as estradiol 3-[bis(2-chloroethyl)carbamate] 17-(dihydrogen phosphate), disodium salt, monohydrate. Estramustine phosphate sodium has an empiric formula of C23H30Cl2NNa2O6P•H2O, a calculated molecular weight of 582.4, and the following structural formula:

    Chemical Structure
  • CLINICAL PHARMACOLOGY

    Estramustine phosphate (Figure 1) is a molecule combining estradiol and nornitrogen mustard by a carbamate link. The molecule is phosphorylated to make it water soluble.

    Chemical Structure

    Estramustine phosphate taken orally is readily dephosphorylated during absorption, and the major metabolites in plasma are estramustine (Figure 2), the estrone analog (Figure 3), estradiol, and estrone.

    Chemical Structure
    Chemical Structure

    Prolonged treatment with estramustine phosphate produces elevated total plasma concentrations of estradiol that fall within ranges similar to the elevated estradiol levels found in prostatic cancer patients given conventional estradiol therapy. Estrogenic effects, as demonstrated by changes in circulating levels of steroids and pituitary hormones, are similar in patients treated with either estramustine phosphate or conventional estradiol.

    The metabolic urinary patterns of the estradiol moiety of estramustine phosphate and estradiol itself are very similar, although the metabolites derived from estramustine phosphate are excreted at a slower rate.

  • INDICATIONS AND USAGE

    EMCYT Capsules are indicated in the palliative treatment of patients with metastatic and/or progressive carcinoma of the prostate.

  • CONTRAINDICATIONS

    EMCYT Capsules should not be used in patients with any of the following conditions:

    1)
    Known hypersensitivity to either estradiol or to nitrogen mustard.
    2)
    Active thrombophlebitis or thromboembolic disorders, except in those cases where the actual tumor mass is the cause of the thromboembolic phenomenon and the physician feels the benefits of therapy may outweigh the risks.
  • WARNINGS

    It has been shown that there is an increased risk of thrombosis, including fatal and nonfatal myocardial infarction, in men receiving estrogens for prostatic cancer. EMCYT Capsules should be used with caution in patients with a history of thrombophlebitis, thrombosis, or thromboembolic disorders, especially if they were associated with estrogen therapy. Caution should also be used in patients with cerebral vascular or coronary artery disease.

    Glucose Tolerance—Because glucose tolerance may be decreased, diabetic patients should be carefully observed while receiving EMCYT.

    Elevated Blood Pressure—Because hypertension may occur, blood pressure should be monitored periodically.

  • PRECAUTIONS

    General

    Fluid Retention. Exacerbation of preexisting or incipient peripheral edema or congestive heart disease has been seen in some patients receiving therapy with EMCYT Capsules. Other conditions which might be influenced by fluid retention, such as epilepsy, migraine, or renal dysfunction, require careful observation.

    EMCYT may be poorly metabolized in patients with impaired liver function and should be administered with caution in such patients.

    Because EMCYT may influence the metabolism of calcium and phosphorus, it should be used with caution in patients with metabolic bone diseases that are associated with hypercalcemia or in patients with renal insufficiency. Patients with prostate cancer and osteoblastic metastases are at risk for hypocalcemia and should have calcium levels closely monitored.

    Gynecomastia and impotence are known estrogenic effects.

    Allergic reactions and angioedema at times involving the airway have been reported.

    Information for the Patient

    Because of the possibility of mutagenic effects, patients should be advised to use contraceptive measures.

    Laboratory Tests

    Certain endocrine and liver function tests may be affected by estrogen-containing drugs. EMCYT may depress testosterone levels. Abnormalities of hepatic enzymes and of bilirubin have occurred in patients receiving EMCYT. Such tests should be done at appropriate intervals during therapy and repeated after the drug has been withdrawn for two months.

    Food/Drug Interaction

    Milk, milk products, and calcium-rich foods or drugs may impair the absorption of EMCYT.

    Carcinogenesis, Mutagenesis, Impairment of Fertility

    Long-term continuous administration of estrogens in certain animal species increases the frequency of carcinomas of the breast and liver. Compounds structurally similar to EMCYT are carcinogenic in mice. Carcinogenic studies of EMCYT have not been conducted in man. Although testing by the Ames method failed to demonstrate mutagenicity for estramustine phosphate sodium, it is known that both estradiol and nitrogen mustard are mutagenic. For this reason and because some patients who had been impotent while on estrogen therapy have regained potency while taking EMCYT, the patient should be advised to use contraceptive measures.

  • ADVERSE REACTIONS

    In a randomized, double-blind trial comparing therapy with EMCYT Capsules in 93 patients (11.5 to 15.9 mg/kg/day) or diethylstilbestrol (DES) in 93 patients (3.0 mg/day), the following adverse effects were reported:

    EMCYT
    n=93
    DES
    n=93
    CARDIOVASCULAR-RESPIRATORY
      Cardiac Arrest02
      Cerebrovascular Accident20
      Myocardial Infarction31
      Thrombophlebitis37
      Pulmonary Emboli25
      Congestive Heart Failure32
      Edema1917
      Dyspnea113
      Leg Cramps811
      Upper Respiratory Discharge11
      Hoarseness10
    GASTROINTESTINAL
      Nausea158
      Diarrhea1211
      Minor Gastrointestinal Upset116
      Anorexia43
      Flatulence20
      Vomiting11
      Gastrointestinal Bleeding10
      Burning Throat10
      Thirst10
    INTEGUMENTARY
      Rash14
      Pruritus22
      Dry Skin20
      Pigment Changes03
      Easy Bruising30
      Flushing10
      Night Sweats01
      Fingertip—Peeling Skin10
      Thinning Hair11
    BREAST CHANGES
      Tenderness6664
      Enlargement
        Mild6054
        Moderate1016
        Marked05
    MISCELLANEOUS
      Lethargy Alone43
      Depression02
      Emotional Lability20
      Insomnia30
      Headache11
      Anxiety10
      Chest Pain11
      Hot Flashes01
      Pain in Eyes01
      Tearing of Eyes11
      Tinnitus01
    LABORATORY ABNORMALITIES
      Hematologic
        Leukopenia42
        Thrombopenia12
      Hepatic
        Bilirubin Alone15
        Bilirubin and LDH01
        Bilirubin and SGOT21
        Bilirubin, LDH and SGOT20
        LDH and/or SGOT3128
      Miscellaneous
        Hypercalcemia—Transient01
  • OVERDOSAGE

    Although there has been no experience with overdosage to date, it is reasonable to expect that such episodes may produce pronounced manifestations of the known adverse reactions. In the event of overdosage, the gastric contents should be evacuated by gastric lavage and symptomatic therapy should be initiated. Hematologic and hepatic parameters should be monitored for at least 6 weeks after overdosage of EMCYT Capsules.

  • DOSAGE AND ADMINISTRATION

    The recommended daily dose is 14 mg per kg of body weight (ie, one 140 mg capsule for each 10 kg or 22 lb of body weight), given in 3 or 4 divided doses. Most patients in studies in the United States have been treated at a dosage range of 10 to 16 mg per kg per day.

    Patients should be instructed to take EMCYT Capsules at least 1 hour before or 2 hours after meals. EMCYT should be swallowed with water. Milk, milk products, and calcium-rich foods or drugs (such as calcium-containing antacids) must not be taken simultaneously with EMCYT.

    Patients should be treated for 30 to 90 days before the physician determines the possible benefits of continued therapy. Therapy should be continued as long as the favorable response lasts. Some patients have been maintained on therapy for more than 3 years at doses ranging from 10 to 16 mg per kg of body weight per day.

    Procedures for proper handling and disposal of anticancer drugs should be considered. Several guidelines on this subject have been published.1–8 There is no general agreement that all of the procedures recommended in the guidelines are necessary or appropriate.

  • HOW SUPPLIED

    White opaque capsules, each containing estramustine phosphate sodium as the disodium salt monohydrate equivalent to 140 mg estramustine phosphate—bottle of 100 (NDC 0013-0132-02).

    NOTE

    EMCYT Capsules should be stored in the refrigerator at 36° to 46°F (2° to 8°C).

  • REFERENCES

    1. Recommendations for the Safe Handling of Parenteral Antineoplastic Drugs. NIH Publication No. 83–2621. For sale by the Superintendent of Documents, U.S. Government Printing Office, Washington, DC, 20402.
    2. AMA Council Report, Guidelines for Handling Parenteral Antineoplastics, JAMA. 1985; 253 (11):1590–1592.
    3. National Study Commission on Cytotoxic Exposure-Recommendations for Handling Cytotoxic Agents. Available from Louis P. Jeffrey, Sc.D., Chairman, National Study Commission on Cytotoxic Exposure, Massachusetts College of Pharmacy and Allied Health Sciences, 179 Longwood Avenue, Boston, Massachusetts 02115.
    4. Clinical Oncological Society of Australia. Guidelines and Recommendations for Safe Handling of Antineoplastic Agents. Med J Australia. 1983; 1:426–428.
    5. Jones RB, et al. Safe Handling of Chemotherapeutic Agents: A Report from the Mount Sinai Medical Center. CA-A Cancer Journal for Clinicians. 1983; (Sept/Oct) 258–263.
    6. American Society of Hospital Pharmacists Technical Assistance Bulletin on Handling Cytotoxic and Hazardous Drugs. Am J Hosp Pharm. 1990; 47:1033–1049.
    7. OSHA Work-Practice Guidelines for Personnel Dealing with Cytotoxic (Antineoplastic) Drugs. Am J Hosp Pharm. 1986; 43:1193–1204.
    8. ONS Clinical Practice Committee. Cancer Chemotherapy Guidelines and Recommendations for Practice. Pittsburgh, Pa: Oncology Nursing Society; 1999:32–41.
  • SPL UNCLASSIFIED SECTION

    Rx only

    Logo

    LAB-0088-4.0
    June 2007

  • PRINCIPAL DISPLAY PANEL - 140 mg Capsule Bottle Label

    Pfizer

    NDC 0013-0132-02

    Emcyt®
    capsules

    140 mg*

    estramustine phosphate
    sodium capsules

    100 Capsules

    Rx only

    PRINCIPAL DISPLAY PANEL - 140 mg Capsule Bottle Label
  • PRINCIPAL DISPLAY PANEL - 140 mg Capsule Bottle Carton

    Pfizer

    NDC 0013-0132-02

    Emcyt®
    capsules

    140 mg*

    estramustine phosphate
    sodium capsules

    Store in refrigerator at 36° to 46°F
    (2° to 8°C).

    100 Capsules
    Rx only

    PRINCIPAL DISPLAY PANEL - 140 mg Capsule Bottle Carton
  • INGREDIENTS AND APPEARANCE
    EMCYT 
    estramustine phosphate sodium capsule
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0013-0132
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ESTRAMUSTINE PHOSPHATE SODIUM (UNII: 75F375MT2N) (ESTRAMUSTINE - UNII:35LT29625A) ESTRAMUSTINE PHOSPHATE140 mg
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorWHITE (opaque) Scoreno score
    ShapeCAPSULESize19mm
    FlavorImprint Code PHARMACIA;AND;UPJOHN;EMCYT;140MG
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0013-0132-021 in 1 CARTON01/01/1992
    1100 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA01804501/01/1992
    Labeler - Pharmacia and Upjohn Company LLC (618054084)
    Establishment
    NameAddressID/FEIBusiness Operations
    Valdepharm260128560API MANUFACTURE(0013-0132)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pfizer Italia S.r.l.458521908MANUFACTURE(0013-0132)
    Establishment
    NameAddressID/FEIBusiness Operations
    Excella GmbH & Co. KG329809800API MANUFACTURE(0013-0132)