Open menu Close menu Open Search Close search

Hexalen Capsules (MGI)

  • Warnings
  • Description
  • Chemical Structure
  • Clinical Pharmacology
  • Indications and Usage
  • Contraindications
  • Warnings (2)
  • Precautions
  • Drug Interactions
  • Adverse Reactions
  • Overdosage
  • Dosage and Administration
  • How Supplied
  • References
  • How Supplied (2)

    - Drugs index
    - Manufacturers
    - Feedback


    1. HEXALEN® should only be given under the supervision of a physician experienced in the use of antineoplastic agents.
    2. Peripheral blood counts should be monitored at least monthly, prior to the initiation of each course of HEXALEN, and as clinically indicated (see Adverse Reactions ).
    3. Because of the possibility of HEXALEN-related neurotoxicity, neurologic examination should be performed regularly during HEXALEN administration (see Adverse Reactions ).


    HEXALEN (altretamine), is a synthetic cytotoxic antineoplastic s-triazine derivative. HEXALEN capsules contain 50 mg of altretamine for oral administration. Inert ingredients include lactose, anhydrous and calcium stearate. Altretamine, known chemically as N , N , N ', N ", N ", N "-hexamethyl-1,3,5-triazine-2,4,6-triamine, has the following structural formula:

    Its empirical formula is C 9 H 18 N 6 with a molecular weight of 210.28. Altretamine is a white crystalline powder, melting at 172° ± 1°C. Altretamine is practically insoluble in water but is increasingly soluble at pH 3 and below.


    The precise mechanism by which HEXALEN exerts its cytotoxic effect is unknown, although a number of theoretical possibilities have been studied. Structurally, HEXALEN resembles the alkylating agent triethylenemelamine, yet in vitro tests for alkylating activity of HEXALEN and its metabolites have been negative. HEXALEN has been demonstrated to be efficacious for certain ovarian tumors resistant to classical alkylating agents. Metabolism of altretamine is a requirement for cytotoxicity. Synthetic monohydroxymethylmelamines, and products of altretamine metabolism, in vitro and in vivo , can form covalent adducts with tissue macromolecules including DNA, but the relevance of these reactions to antitumor activity is unknown.

    HEXALEN is well-absorbed following oral administration in humans, but undergoes rapid and extensive demethylation in the liver, producing variation in altretamine plasma levels. The principal metabolites are pentamethylmelamine and tetramethylmelamine.

    Pharmacokinetic studies were performed in a limited number of patients and should be considered preliminary. After oral administration of HEXALEN to 11 patients with advanced ovarian cancer in doses of 120-300 mg/m 2 , peak plasma levels (as measured by gas-chromatographic assay) were reached between 0.5 and 3 hours, varying from 0.2 to 20.8 mg/l. Half-life of the (beta)-phase of elimination ranged from 4.7 to 10.2 hours. Altretamine and metabolites show binding to plasma proteins. The free fractions of altretamine, pentamethylmelamine and tetramethylmelamine are 6%, 25% and 50%, respectively.

    Following oral administration of 14 C-ring-labeled altretamine (4 mg/kg), urinary recovery of radioactivity was 61% at 24 hours and 90% at 72 hours. Human urinary metabolites were N-demethylated homologues of altretamine with <1% unmetabolized altretamine excreted at 24 hours.

    After intraperitoneal administration of 14 C-ring-labeled altretamine to mice, tissue distribution was rapid in all organs, reaching a maximum at 30 minutes. The excretory organs (liver and kidney) and the small intestine showed high concentrations of radioactivity, whereas relatively low concentrations were found in other organs, including the brain.

    There have been no formal pharmacokinetic studies in patients with compromised hepatic and/or renal function, though HEXALEN has been administered both concurrently and following nephrotoxic drugs such as cisplatin.

    HEXALEN (altretamine) has been administered in 4 divided doses, with meals and at bedtime, though there is no pharmacokinetic data on this schedule nor information from formal interaction studies about the effect of food on its bioavailability or pharmacokinetics.

    In two studies in patients with persistent or recurrent ovarian cancer following first-line treatment with cisplatin and/or alkylating agent-based combinations, HEXALEN was administered as a single agent for 14 or 21 days of a 28 day cycle. In the 51 patients with measurable or evaluable disease, there were 6 clinical complete responses, 1 pathologic complete response, and 2 partial responses for an overall response rate of 18%. The duration of these responses ranged from 2 months in a patient with a palpable pelvic mass to 36 months in a patient who achieved a pathologic complete response. In some patients, tumor regression was associated with improvement in symptoms and performance status.


    HEXALEN is indicated for use as a single agent in the palliative treatment of patients with persistent or recurrent ovarian cancer following first-line therapy with a cisplatin and/or alkylating agent-based combination.


    HEXALEN is contraindicated in patients who have shown hypersensitivity to it. HEXALEN should not be employed in patients with preexisting severe bone marrow depression or severe neurologic toxicity. HEXALEN has been administered safely, however, to patients heavily pretreated with cisplatin and/or akylating agents, including patients with preexisting cisplatin neuropathies. Careful monitoring of neurologic function in these patients is essential.


    See boxed Warnings .

    Concurrent administration of HEXALEN and antidepressants of the monoamine oxidase (MAO) inhibitor class may cause severe orthostatic hypotension. Four patients, all over 60 years of age, were reported to have experienced symptomatic hypotension after 4 to 7 days of concomitant therapy with HEXALEN and MAO inhibitors.

    HEXALEN causes mild to moderate myelosuppression and neurotoxicity. Blood counts and a neurologic examination should be performed prior to the initiation of each course of therapy and the dose of HEXALEN adjusted as clinically indicated (see Dosage and Administration ).

    Pregnancy: Category D

    HEXALEN has been shown to be embryotoxic and teratogenic in rats and rabbits when given at doses 2 and 10 times the human dose. HEXALEN may cause fetal damage when administered to a pregnant woman. If HEXALEN is used during pregnancy, or if the patient becomes pregnant while taking the drug, the patient should be apprised of the potential hazard to the fetus. Women of childbearing potential should be advised to avoid becoming pregnant.



    Neurologic examination should be performed regularly (see Adverse Reactions ).

    Laboratory Tests

    Peripheral blood counts should be monitored at least monthly, prior to the initiation of each course of HEXALEN, and as clinically indicated (see Adverse Reactions ).

    Drug Interactions

    Concurrent administration of HEXALEN and antidepressants of the MAO inhibitor class may cause severe orthostatic hypotension (see Warnings section). Cimetidine, an inhibitor of microsomal drug metabolism, increased altretamine's half-life and toxicity in a rat model.

    Data from a randomized trial of HEXALEN and cisplatin plus or minus pyridoxine in ovarian cancer indicated that pyridoxine significantly reduced neurotoxicity; however, it adversely affected response duration suggesting that pyridoxine should not be administered with HEXALEN and/or cisplatin (1).

    Carcinogenesis, Mutagenesis and Impairment of Fertility

    The carcinogenic potential of HEXALEN has not been studied in animals, but drugs with similar mechanisms of action have been shown to be carcinogenic. HEXALEN was weakly mutagenic when tested in strain TA100 of Salmonella typhimurium . HEXALEN administered to female rats 14 days prior to breeding through the gestation period had no adverse effect on fertility, but decreased postnatal survival at 120 mg/m 2 /day and was embryocidal at 240 m/m 2 /day. Administration of 120 mg/m 2 /day HEXALEN to male rats for 60 days prior to mating resulted in testicular atrophy, reduced fertility and a possible dominant lethal mutagenic effect. Male rats treated with HEXALEN at 450 mg/m 2 /day for 10 days had decreased spermatogenesis, atrophy of testes, seminal vesicles and ventral prostate.


    Pregnancy Category D: see Warnings section.

    Nursing Mothers

    It is not known whether altretamine is excreted in human milk. Because there is a possibility of toxicity in nursing infants secondary to HEXALEN treatment of the mother, it is recommended that breast feeding be discontinued if the mother is treated with HEXALEN.

    Pediatric Use

    The safety and effectiveness of HEXALEN in children have not been established.



    With continuous high-dose daily HEXALEN, nausea and vomiting of gradual onset occur frequently. Although in most instances these symptoms are controllable with anti-emetics, at times the severity requires HEXALEN dose reduction or, rarely, discontinuation of HEXALEN therapy. In some instances, a tolerance of these symptoms develops after several weeks of therapy. The incidence and severity of nausea and vomiting are reduced with moderate-dose administration of HEXALEN. In 2 clinical studies of single-agent HEXALEN utilizing a moderate, intermittent dose and schedule, only 1 patient (1%) discontinued HEXALEN due to severe nausea and vomiting.


    Peripheral neuropathy and central nervous system symptoms (mood disorders, disorders of consciousness, ataxia, dizziness, vertigo) have been reported. They are more likely to occur in patients receiving continuous high-dose daily HEXALEN (altretamine) than moderate-dose HEXALEN administered on an intermittent schedule. Neurologic toxicity has been reported to be reversible when therapy is discontinued. Data from a randomized trial of HEXALEN and cisplatin plus or minus pyridoxine in ovarian cancer indicated that pyridoxine significantly reduced neurotoxicity; however, it adversely affected response duration suggesting that pyridoxine should not be administered with HEXALEN and/or cisplatin (1).


    HEXALEN causes mild to moderate dose-related myelosuppression. Leukopenia below 3000 WBC/mm 3 occurred in <15% of patients on a variety of intermittent or continuous dose regimens. Less than 1% had leukopenia below 1000 WBC/mm 3 . Thrombocytopenia below 50,000 platelets/mm 3 was seen in <10% of patients. When given in doses of 8-12 mg/kg/day over a 21 day course, nadirs of leukocyte and platelet counts were reached by 3-4 weeks, and normal counts were regained by 6 weeks. With continuous administration at doses of 6-8 mg/kg/day, nadirs are reached in 6-8 weeks (median).

    Data in the following table are based on the experience of 76 patients with ovarian cancer previously treated with a cisplatin-based combination regimen who received single-agent HEXALEN. In one study, HEXALEN, 260 mg/m 2 /day, was administered for 14 days of a 28 day cycle. In another study, HEXALEN, 6-8 mg/kg/day, was administered for 21 days of a 28 day cycle.

    Adverse Experiences
    % Patients
        Nausea and Vomiting
           Mild to Moderate
        Increased Alkaline Phosphatase
        Peripheral Sensory Neuropathy
           Moderate to Severe
        Anorexia and Fatigue
           WBC 2000-2999/mm 3
           WBC <2000/mm 3
           Platelets 75,000-99,000/mm 3
           Platelets <75,000/mm 3
           Moderate to Severe
        Serum Creatinine 1.6-3.75 mg/dl
           25-40 mg%
           41-60 mg%
          >60 mg%

    Additional adverse reaction information is available from 13 single-agent altretamine studies (total of 1014 patients) conducted under the auspices of the National Cancer Institute. The treated patients had a variety of tumors and many were heavily pretreated with other chemotherapies; most of these trials utilized high, continuous daily doses of altretamine (6-12 mg/kg/day). In general, adverse reaction experiences were similar in the two trials described above. Additional toxicities, not reported in the above table, included hepatic toxicity, skin rash, pruritus and alopecia, each occurring in <1% of patients.


    No case of acute overdosage in humans has been described. The oral LD50 dose in rats was 1050 mg/kg and 437 mg/kg in mice.


    HEXALEN (altretamine) is administered orally. Doses are calculated on the basis of body surface area.

    HEXALEN may be administered either for 14 or 21 consecutive days in a 28 day cycle at a dose of 260 mg/m 2 /day. The total daily dose should be given as 4 divided oral doses after meals and at bedtime. There is no pharmacokinetic information supporting this dosing regimen and the effect of food on HEXALEN bioavailability or pharmacokinetics has not been evaluated.

    HEXALEN should be temporarily discontinued (for 14 days or longer) and subsequently restarted at 200 mg/m 2 /day for any of the following situations:

    1. Gastrointestinal intolerance unresponsive to symptomatic measures;
    2. White blood count <2000/mm 3 or granulocyte count <1000/mm 3 ;
    3. Platelet count <75,000/mm 3 ;
    4. Progressive neurotoxicity.

    If neurologic symptoms fail to stabilize on the reduced dose schedule, HEXALEN should be discontinued indefinitely.

    Procedures to proper handling and disposal of anticancer drugs should be considered. Several guidelines on this subject have been published (2-8). There is no general agreement that all of the procedures recommended in the guidelines are necessary or appropriate.


    HEXALEN is available in 50 mg clear, hard gelatin capsules imprinted with the following inscription: USB 001.

    Bottles of 100 capsules (NDC 58063-0001-70)

    Store at controlled room temperature 15° to 30°C (59° to 86°F).


    1. Wiernik PH, et al. Hexamethylmelamine and Low or Moderate Dose Cisplatin With or Without Pyridoxine for Treatment of Advanced Ovarian Carcinoma: A Study of the Eastern Cooperative Oncology Group. Cancer Investigation 10(1): 1-9, 1992.
    2. ONS Clinical Practice Committee. Cancer Chemotherapy Guidelines and Recommendations for Practice. Pittsburgh, Pa: Oncology Nursing Society; 1999:32-41.
    3. Recommendations for the Safe Handling of Cytotoxic Drugs. NIH Publication 92-2621. NIH: Division of Safety, Clinical Center Pharmacy Department and Cancer Nursing Service, 1992. U.S. Department of Health and Human Services, Public Health Service, National Institutes of Health.
    4. AMA Council on Scientific Affairs. Guidelines for Handling Parenteral Antineoplastics. Journal of the American Medical Association 1985;253:1590-1591.
    5. National Study Commission on Cytotoxic Exposure. Recommendations for Handling Cytotoxic Agents, 1987. Available from Louis P. Jeffrey, Chairman, National Study Commission on Cytotoxic Exposure. Massachusetts College of Pharmacy and Allied Health Sciences, 179 Longwood Avenue, Boston, MA 02115.
    6. Clinical Oncological Society of Australia. Guidelines and Recommendations for Safe Handling of Antineoplastic Agents. Medical Journal of Australia 1983;1:426-428.
    7. Jones RB, Frank R, Mass T. Safe Handling of Chemotherapeutic Agents: A Report from the Mount Sinai Medical Center. --A Cancer Journal for Clinicians 1983;33:258-263.
    8. American Society of Hospital Pharmacists. ASHP Technical Assistance Bulletin on Handling Cytotoxic and Hazardous Drugs. Am J of Hosp Pharm_ 1990;47:1033-1049.
    9. Controlling Occupational Exposure to Hazardous Drugs. (OSHA Work Practice Guidelines). Am J of Health Syst Pharm. 1996;53:1669-1685.

    Revised SEPTEMBER 2001

    Manufactured for:



    Mgi Pharma, INC.

    Bloomington, MN 55437

    - To bookmark this page (add it to your favorites), please click the image to the left.
    - If you wish to link to this page, you can do so by referring to the URL address below this line.

    This page was last modified 30-JUN-07
    Copyright © 1995-2021 ITA all rights reserved.