The rate of metabolism and the leukopenic activity of Neoclomide reportedly are increased by chronic administration of high doses of phenobarbital. The physician should be alert for possible combined drug actions, desirable or undesirable, involving Neoclomide even though Neoclomide has been used successfully concurrently with other drugs, including other cytotoxic drugs. Neoclomide treatment, which causes a marked and persistent inhibition of cholinesterase activity, potentiates the effect of succinylcholine chloride. If a patient has been treated with Neoclomide within 10 days of general anesthesia, the anesthesiologist should be alerted.

Treatment of Malignant Diseases: Adults and Children When used as the only oncolytic drug therapy, the initial course of cyclophosphamide for patients with no hematologic deficiency usually consists of 40 to 50 mg/kg given intravenously in divided doses over a period of 2 to 5 days. Other intravenous regimens include 10 to 15 mg/kg given every 7 to 10 days or 3 to 5 mg/kg twice weekly. Oral cyclophosphamide dosing is usually in the range of 1 to 5 mg/kg/day for both initial and maintenance dosing.

Many other regimens of intravenous and oral cyclophosphamide have been reported. Dosages must be adjusted in accord with evidence of antitumor activity and/or leukopenia. The total leukocyte count is a good, objective guide for regulating dosage. Transient decreases in the total white blood cell count to 2000 cells/mm3 (following short courses) or more persistent reduction to 3000 cells/mm3 (with continuing therapy) are tolerated without serious risk of infection if there is no marked granulocytopenia.

When cyclophosphamide is included in combined cytotoxic regimens, it may be necessary to reduce the dose of cyclophosphamide as well as that of the other drugs. Cyclophosphamide and its metabolites are dialyzable although there are probably quantitative differences depending upon the dialysis system being used. Patients with compromised renal function may show some measurable changes in pharmacokinetic parameters of cyclophosphamide metabolism, but there is no consistent evidence indicating a need for cyclophosphamide dosage modification in patients with renal function impairment.

Treatment of Nonmalignant Diseases Biopsy Proven "Minimal Change" Nephrotic Syndrome in Children: An oral dose of 2.5 to 3 mg/kg daily for a period of 60 to 90 days is recommended. In males, the incidence of oligospermia and azoospermia increases if the duration of cyclophosphamide treatment exceeds 60 days. Treatment beyond 90 days increases the probability of sterility. Adrenocorticosteroid therapy may be tapered and discontinued during the course of cyclophosphamide therapy.

Continued use of cyclophosphamide is contraindicated in patients with severely depressed bone marrow function. Cyclophosphamide is contraindicated in patients who have demonstrated a previous hypersensitivity to it.

Information on adverse reactions associated with the use of Neoclomide is arranged according to body system affected or type of reaction. The adverse reactions are listed in order of decreasing incidence.

Digestive System: Nausea and vomiting commonly occur with Neoclomide therapy. Anorexia and, less frequently, abdominal discomfort or pain and diarrhea may occur. There are isolated reports of hemorrhagic colitis, oral mucosal ulceration and jaundice occurring during therapy. These adverse drug effects generally remit when Neoclomide treatment is stopped.

Skin and Its Structures: Alopecia occurs commonly in patients treated with Neoclomide. The hair can be expected to grow back after treatment with the drug or even during continued drug treatment, though it may be different in texture or color. Skin rash occurs occasionally in patients receiving the drug. Pigmentation of the skin and changes in nails can occur. Very rare reports of Stevens-Johnson syndrome and toxic epidermal necrolysis have been received during post-marketing surveillance; due to the nature of spontaneous adverse event reporting, a definitive causal relationship to cyclophospha- mide has not been established.

Hematopoietic System: Leukopenia occurs in patients treated with Neoclomide, is related to the dose of drug, and can be used as a dosage guide. Leukopenia of less than 2000 cells/mm 3 develops commonly in patients treated with an initial loading dose of the drug, and less frequently in patients maintained on smaller doses. The degree of neutropenia is particularly important because it correlates with a reduction in resistance to infections. Fever without documented infection has been reported in neutropenic patients. Thrombocytopenia or anemia develops occasionally in patients treated with Neoclomide. These hematologic effects usually can be reversed by reducing the drug dose or by interrupting treatment. Recovery from leukopenia usually begins in 7 to 10 days after cessation of therapy.

Urinary System: Hemorrhagic ureteritis and renal tubular necrosis have been reported to occur in patients treated with Neoclomide. Such lesions usually resolve following cessation of therapy.

Respiratory System: Interstitial pneumonitis has been reported as part of the postmarketing experience. Interstitial pulmonary fibrosis has been reported in patients receiving high doses of Neoclomide over a prolonged period. Other Anaphylactic reactions have been reported; death has also been reported in association with this event. Possible cross-sensitivity with other alkylating agents has been reported. SIADH (syndrome of inappropriate ADH secretion) has been reported with the use of Neoclomide. Malaise and asthenia have been reported as part of the postmarketing experience.

Pregnancy Category D. Cyclophosphamide is excreted in breast milk. Because of the potential for serious adverse reactions and the potential for tumorigenicity shown for cyclophosphamide in humans, 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.

Special attention to the possible development of toxicity should be exercised in patients being treated with Neoclomide if any of the following conditions are present.

Leukopenia

Thrombocytopenia

Tumor cell infiltration of bone marrow

Previous X-ray therapy

Previous therapy with other cytotoxic agents

Impaired hepatic function

Impaired renal function

Use in Special Populations

Pediatric use: The safety profile of Neoclomide in pediatric patients is similar to that of the adult population.

Geriatric use: Insufficient data from clinical studies of Neoclomide for malignant lymphoma, multiple myeloma, leukemia, mycosis fungoides, neuroblastoma, retinoblastoma, and breast carcinoma are available for patients 65 years of age and older to determine whether they respond differently than younger patients. In two clinical trials in which Neoclomide was compared with paclitaxel, each in combination with cisplatin, for the treatment of advanced ovarian carcinoma, 154 (28%) of 552 patients who received Neoclomide plus cisplatin were 65 years or older. Subset analyses (65 years) from these trials, published reports of clinical trials of Neoclomide containing regimens in breast cancer and non-Hodgkin’s lymphoma, and post marketing experience suggest that elderly patients may be more susceptible to Neoclomide toxicities. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range and adjusting as necessary based on patient response.

No specific antidote for Neoclomide is known. Overdosage should be managed with supportive measures, including appropriate treatment for any concurrent infection, myelosuppression, or cardiac toxicity should it occur.

Store at a temperature not exceeding 25°C in a dry place. Protect from light and moisture. Do not freeze.