Megestrol Acetate Oral Suspension, USP 40 mg/mL

Megestrol Acetate Oral Suspension, USP contains megestrol acetate, a synthetic derivative of the steroid hormone, progesterone. Megestrol acetate is a white, crystalline solid chemically designated as 17-Hydroxy-6-methylpregna-4,6-diene-3,20-dione acetate. Solubility at 37°C in water is 2 µg per mL, solubility in plasma is 24 µg per mL. Its molecular weight is 384.52. The empirical formula is C ₂₄H ₃₂O ₄ and the structural formula is represented as follows:

Megestrol-01

Megestrol Acetate Oral Suspension, USP is supplied as an oral suspension containing 40 mg of micronized megestrol acetate per mL.

Megestrol Acetate Oral Suspension, USP contains the following inactive ingredients: alcohol (max. 0.34% v/v from flavor), citric acid anhydrous, lemon-lime flavor, poloxamer 124, propylene glycol, purified water, sodium benzoate, sodium citrate dihydrate, sucrose and xanthan gum. It may contain 10% citric acid solution or 10% sodium citrate solution for pH adjustment. The pH range is between 3.0 and 4.7.

The precise mechanism by which megestrol acetate produces effects in anorexia and cachexia is unknown at the present time.

There are several analytical methods used to estimate megestrol acetate plasma concentrations, including gas chromatography-mass fragmentography (GC-MF), high pressure liquid chromatography (HPLC) and radioimmunoassay (RIA). The GC-MF and HPLC methods are specific for megestrol acetate and yield equivalent concentrations. The RIA method reacts to megestrol acetate metabolites and is, therefore, non-specific and indicates higher concentrations than the GC-MF and HPLC methods. Plasma concentrations are dependent, not only on the method used, but also on intestinal and hepatic inactivation of the drug, which may be affected by factors such as intestinal tract motility, intestinal bacteria, antibiotics administered, body weight, diet, and liver function.

The major route of drug elimination in humans is urine. When radiolabeled megestrol acetate was administered to humans in doses of 4 to 90 mg, the urinary excretion within 10 days ranged from 56.5% to 78.4% (mean 66.4%) and fecal excretion ranged from 7.7% to 30.3% (mean 19.8%). The total recovered radioactivity varied between 83.1% and 94.7% (mean 86.2%). Megestrol acetate metabolites which were identified in urine constituted 5% to 8% of the dose administered. Respiratory excretion as labeled carbon dioxide and fat storage may have accounted for at least part of the readioactivity not found in urine and feces.

Plasma steady-state pharmacokinetics of megestrol acetate were evaluated in 10 adult, cachectic male patients with acquired immunodeficiency syndrome (AIDS) and an involuntary weight loss greater than 10% of baseline. Patients received single oral doses of 800 mg/day of Megestrol Acetate Oral Suspension, USP for 21 days. Plasma concentration data obtained on day 21 were evaluated for up to 48 hours past the last dose.

Mean (±1SD) peak plasma concentration (C _max) of megestrol acetate was 753 (±539) ng/mL. Mean area under the concentration time-curve (AUC) was 10476 (±7788) ng × hr/mL. Median T _max value was five hours. Seven of 10 patients gained weight in three weeks.

Additionally, 24 adult, asymptomatic HIV seropositive male subjects were dosed once daily with 750 mg of Megestrol Acetate Oral Suspension, USP. The treatment was administered for 14 days. Mean C _max and AUC values were 490 (±238) ng/mL and 6779 (±3048) ng × hr/mL, respectively. The median T _max value was three hours. The mean C _min value was 202 (±101) ng/mL. The mean percent of fluctuation value was 107 (±40).

The effect of food on the bioavailability of Megestrol Acetate Oral Suspension, USP has not been evaluated.

The clinical efficacy of Megestrol Acetate Oral Suspension, USP was assessed in two clinical trials. One was a multicenter, randomized, double-blind, placebo-controlled study comparing megestrol acetate (MA) at doses of 100 mg, 400 mg, and 800 mg per day versus placebo in AIDS patients with anorexia/cachexia and significant weight loss. Of the 270 patients entered on study, 195 met all inclusion/exclusion criteria, had at least two additional post baseline weight measurements over a 12-week period, or had one post baseline weight measurement but dropped out for therapeutic failure. The percent of patients gaining five or more pounds at maximum weight gain in 12 study weeks was statistically significantly greater for the 800 mg (64%) and 400 mg (57%) MA-treated groups than for the placebo group (24%). Mean weight increased from baseline to last evaluation in 12 study weeks in the 800 mg MA-treated group by 7.8 pounds, the 400 mg MA group by 4.2 pounds, the 100 mg MA group by 1.9 pounds, and decreased in the placebo group by 1.6 pounds. Mean weight changes at 4, 8, and 12 weeks for patients evaluable for efficacy in the two clinical trials are shown graphically. Changes in body composition during the 12 study weeks as measured by bioelectrical impedance analysis showed increases in non-water body weight in the MA-treated groups (see clinical studies table). In addition, edema developed or worsened in only 3 patients.

Greater percentages of MA-treated patients in the 800 mg group (89%), the 400 mg group (68%), and the 100 mg group (72%), than in the placebo group (50%), showed an improvement in appetite at last evaluation during the 12 study weeks. A statistically significant difference was observed between the 800 mg MA-treated group and the placebo group in the change in caloric intake from baseline to time of maximum weight change. Patients were asked to assess weight change, appetite, appearance, and overall perception of well-being in a 9-question survey. At maximum weight change, only the 800 mg MA-treated group gave responses that were statistically significantly more favorable to all questions when compared to the placebo-treated group. A dose response was noted in the survey with positive responses correlating with higher dose for all questions.

The second trial was a multicenter, randomized, double-blind, placebo-controlled study comparing megestrol acetate 800 mg/day versus placebo in AIDS patients with anorexia/cachexia and significant weight loss. Of the 100 patients entered on study, 65 met all inclusion/exclusion criteria, had at least two additional post baseline weight measurements over a 12-week period or had one post baseline weight measurement but dropped out for therapeutic failure. Patients in the 800 mg MA-treated group had a statistically significantly larger increase in mean maximum weight change than patients in the placebo group. From baseline to study week 12, mean weight increased by 11.2 pounds in the MA-treated group and decreased 2.1 pounds in the placebo group. Changes in body composition as measured by bioelectrical impedance analysis showed increases in non-water weight in the MA-treated group (see clinical studies table). No edema was reported in the MA-treated group. A greater percentage of MA-treated patients (67%) than placebo-treated patients (38%) showed an improvement in appetite at last evaluation during the 12 study weeks; this difference was statistically significant. There were no statistically significant differences between treatment groups in mean caloric change or in daily caloric intake at time to maximum weight change. In the same 9-question survey referenced in the first trial, patients' assessments of weight change, appetite, appearance, and overall perception of well-being showed increases in mean scores in MA-treated patients as compared to the placebo group.

In both trials, no statistically significant differences were seen between the treatment groups with regard to laboratory abnormalities, new opportunistic infections, lymphocyte counts, T ₄ counts, T ₈ counts, or skin reactivity tests (see ADVERSE REACTIONS).

Presented below are the results of mean weight changes for patients evaluable for efficacy in Trials 1 and 2.

Megestrol-02

Megestrol Acetate Oral Suspension, USP is indicated for the treatment of anorexia, cachexia, or an unexplained, significant weight loss in patients with a diagnosis of acquired immunodeficiency syndrome (AIDS).

History of hypersensitivity to megestrol acetate or any component of the formulation. Known or suspected pregnancy.

Megestrol acetate may cause fetal harm when administered to a pregnant woman. For animal data on fetal effects, see PRECAUTIONS: Carcinogenesis, Mutagenesis, Impairment of Fertility: Impairment of Fertility. There are no adequate and well-controlled studies in pregnant women. If this drug is used during pregnancy, or if the patient becomes pregnant while taking (receiving) this drug, the patient should be apprised of the potential hazard to the fetus. Women of childbearing potential should be advised to avoid becoming pregnant.

Megestrol acetate is not intended for prophylactic use to avoid weight loss.

(See also PRECAUTIONS: Carcinogenesis, Mutagenesis, Impairment of Fertility.)

The glucocorticoid activity of Megestrol Acetate Oral Suspension, USP has not been fully evaluated. Clinical cases of new onset diabetes mellitus, exacerbation of pre-existing diabetes mellitus, and overt Cushing's syndrome have been reported in association with the chronic use of Megestrol Acetate Oral Suspension, USP. In addition, clinical cases of adrenal insufficiency have been observed in patients receiving or being withdrawn from chronic Megestrol Acetate Oral Suspension, USP therapy in the stressed and non-stressed state. Furthermore, adrenocorticotropin (ACTH) stimulation testing has revealed the frequent occurrence of asymptomatic pituitary-adrenal suppression in patients treated with chronic Megestrol Acetate Oral Suspension, USP therapy. Therefore, the possibility of adrenal insufficiency should be considered in any patient receiving or being withdrawn from chronic Megestrol Acetate Oral Suspension, USP therapy who presents with symptoms and/or signs suggestive of hypoadrenalism (eg., hypotension, nausea, vomiting, dizziness, or weakness) in either the stressed or non-stressed state. Laboratory evaluation for adrenal insufficiency and consideration of replacement or stress doses of a rapidly acting glucocorticoid are strongly recommended in such patients. Failure to recognize inhibition of the hypothalamic-pituitary-adrenal axis may result in death. Finally, in patients who are receiving or being withdrawn from chronic Megestrol Acetate Oral Suspension, USP therapy, consideration should be given to the use of empiric therapy with stress doses of a rapidly acting glucocorticoid in conditions of stress or serious intercurrent illness (eg., surgery, infection).

General
Therapy with Megestrol Acetate Oral Suspension, USP for weight loss should only be
instituted after treatable causes of weight loss are sought and addressed. These
treatable causes include possible malignancies, systemic infections, gastrointestinal
disorders affecting absorption, endocrine disease, and renal or psychiatric diseases.
Effects on HIV viral replication have not been determined.
Use with caution in patients with a history of thromboembolic disease.
Use in Diabetics
Exacerbation of pre-existing diabetes with increased insulin requirements has been
reported in association with the use of Megestrol Acetate Oral Suspension, USP.
Information for Patients
Patients using megestrol acetate should receive the following instructions:
1. This medication is to be used as directed by the physician.
2. Report any adverse reaction experiences while taking this medication.
3. Use contraception while taking this medication if you are a woman capable of
becoming pregnant.
4. Notify your physician if you become pregnant while taking this medication.
Drug Interactions
Pharmacokinetic studies show that there are no significant alterations in
pharmacokinetic parameters of zidovudine or rifabutin to warrant dosage adjustment
when megestrol acetate is administered with these drugs. The effects of zidovudine
or rifabutin on the pharmacokinetics of megestrol acetate were not studied.
Megestrol acetate may interact with warfarin and increase International Normalized
Ratio (INR). Closely monitor INR in patients taking Megestrol Acetate Oral Suspension,
USP and warfarin.

Animal Toxicology
Long-term treatment with Megestrol Acetate Oral Suspension, USP may increase
the risk of respiratory infections. A trend toward increased frequency of respiratory
infections, decreased lymphocyte counts, and increased neutrophil counts was
observed in a 2-year chronic toxicity/carcinogenicity study of megestrol acetate
conducted in rats.
Carcinogenesis, Mutagenesis, Impairment of Fertility
Carcinogenesis
Data on carcinogenesis were obtained from studies conducted in dogs, monkeys,
and rats treated with megestrol acetate at doses 53.2, 26.6, and 1.3 times lower
than the proposed dose (13.3 mg/kg/day) for humans. No males were used in the
dog and monkey studies. In female beagles, megestrol acetate (0.01, 0.1, or
0.25 mg/kg/day) administered for up to 7 years induced both benign and malignant
tumors of the breast. In female monkeys, no tumors were found following 10 years
of treatment with 0.01, 0.1, or 0.5 mg/kg/day megestrol acetate. Pituitary tumors
were observed in female rats treated with 3.9 or 10 mg/kg/day of megestrol acetate
for 2 years. The relationship of these tumors in rats and dogs to humans is unknown
but should be considered in assessing the risk-to-benefit ratio when prescribing
Megestrol Acetate Oral Suspension, USP and in surveillance of patients on therapy.
(See WARNINGS.)
Mutagenesis
No mutagenesis data are currently available.

Impairment of Fertility
Perinatal/postnatal (segment III) toxicity studies were performed in rats at doses
(0.05-12.5 mg/kg) less than that indicated for humans (13.3 mg/kg); in these low
dose studies, the reproductive capability of male offspring of megestrol
acetate-treated females was impaired. Similar results were obtained in dogs.
Pregnant rats treated with megestrol acetate showed a reduction in fetal weight and
number of live births, and feminization of male fetuses. No toxicity data are currently
available on male reproduction (spermatogenesis).

Clinical Adverse Events
Adverse events which occurred in at least 5% of patients in any arm of the two
clinical efficacy trials and the open trial are listed below by treatment group. All
patients listed had at least one post baseline visit during the 12 study weeks. These
adverse events should be considered by the physician when prescribing Megestrol
Acetate Oral Suspension, USP.

Table

Table

Adverse events which occurred in 1% to 3% of all patients enrolled in the two clinical
efficacy trials with at least one follow-up visit during the first 12 weeks of the study
are listed below by body system. Adverse events occurring less than 1% are not
included. There were no significant differences between incidence of these events in
patients treated with megestrol acetate and patients treated with placebo.
Body as a Whole: abdominal pain, chest pain, infection, moniliasis and sarcoma
Cardiovascular System: cardiomyopathy and palpitation
Digestive System: constipation, dry mouth, hepatomegaly, increased salivation and
oral moniliasis
Hemic and Lymphatic System: leukopenia
Metabolic and Nutritional: LDH increased, edema and peripheral edema
Nervous System: paresthesia, confusion, convulsion, depression, neuropathy,
hypesthesia and abnormal thinking
Respiratory System: dyspnea, cough, pharyngitis and lung disorder
Skin and Appendages: alopecia, herpes, pruritus, vesiculobullous rash, sweating
and skin disorder
Special Senses: amblyopia
Urogenital System: albuminuria, urinary incontinence, urinary tract infection and
gynecomastia
Postmarketing
Postmarketing reports associated with Megestrol Acetate Oral Suspension, USP
include thromboembolic phenomena including thrombophlebitis and pulmonary
embolism, and glucose intolerance (see WARNINGS and PRECAUTIONS).
To report SUSPECTED ADVERSE REACTIONS, contact Xttrium Laboratories, Inc.
at 1-800-587-3721 or FDA at 1-800-FDA-1088.

No serious unexpected side effects have resulted from studies involving Megestrol Acetate Oral Suspension, USP administered in dosages as high as 1200 mg/day. In post-marketing experience, limited reports of overdose have been received. Signs and symptoms reported in the context of overdose included diarrhea, nausea, abdominal pain, shortness of breath, cough, unsteady gait, listlessness, and chest pain. There is no specific antidote for overdose with Megestrol Acetate Oral Suspension, USP. In case of overdose, appropriate supportive measures should be taken. Megestrol acetate has not been tested for dialyzability; however, due to its low solubility, it is postulated that dialysis would not be an effective means of treating overdose.

The recommended adult initial dosage of Megestrol Acetate Oral Suspension, USP is 800 mg/day (20 mL/day). Shake container well before using.

In clinical trials evaluating different dose schedules, daily doses of 400 and 800 mg/day were found to be clinically effective.

Megestrol Acetate Oral Suspension, USP 40 mg/mL is available as a creamy-white, lemon-lime flavored oral suspension, for oral administration, containing 40 mg of micronized megestrol acetate per mL.

NDC 0116-4011-08 Bottles of 8 fl oz (237 mL)

NDC 0116-4011-16 Bottles of 16 fl oz (473 mL)

NDC 0116-4011-10 10 mL unit dose cups in trays of 10

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

Dispense in a tight, light-resistant container with child-resistant closure.

Protect from heat.

Health Hazard Data

There is no threshold limit value established by OSHA, NIOSH, or ACGIH.

Exposure or "overdose" at levels approaching recommended dosing levels could result in side effects described above (see WARNINGSand ADVERSE REACTIONS). Woman at risk of pregnancy should avoid such exposure.

Rx Only

Manufactured by:

Xttrium Laboratories, Inc.

1200 E. Business Center Dr.

Mount Prospect, IL 60056

4011MEGINSTA REV. 06-25

NDC 0116-4011-08

MEGESTROL ACETATE ORAL SUSPENSION, USP 40 mg/mL

Each mL contains: 40 mg of micronized megestrol acetate in a lemon-lime flavored oral suspension.

Alcohol: max. 0.34% v/v.

Shake well immediately before dosing.

Rx Only

NET: 8 fl oz (237 mL)

Usual Dosage: See package insert for indications and dosage schedule.

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

Dispense in a tight, light-resistant container with child-resistant closure.

Protect from heat.

Manufactured by:

Xttrium Laboratories, Inc.

1200 E. Business Center Dr.

Mount Prospect, IL 60056

401108BTLLBLA

REV. 06-25

8 oz bottle

NDC 0116-4011-16

MEGESTROL ACETATE ORAL SUSPENSION, USP 40 mg/mL

Each mL contains: 40 mg of micronized megestrol acetate in a lemon-lime flavored oral suspension.

Alcohol: max. 0.34% v/v.

Shake well immediately before dosing.

Rx Only

NET: 1 Pint (473 mL)

Usual Dosage: See package insert for indications and dosage schedule.

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

Dispense in a tight, light-resistant container with child-resistant closure.

Protect from heat.

Manufactured by:

Xttrium Laboratories, Inc.

1200 E. Business Center Dr.

Mount Prospect, IL 60056

401116BTLLBLA

REV. 06-25

16 oz bottle

UNIT DOSE

Delivers 10 mL

NDC 0116-4011-10

Megestrol Acetate Oral Suspension, USP

400 mg per 10 mL

Shake well immediately before dosing

Institutional Use Only

Xttrium Laboratories, Inc.

Mount Prospect, IL

Rx Only

4011MEGLIDA

UD Cup Lid