CLOBETASOL PROPIONATE FOAM 0.05%
-
clobetasol propionate aerosol, foam
DPT Laboratories, Ltd.
----------
Clobetasol Propionate Foam, 0.05%
Rx Only
For Dermatologic Use Only
Not for Ophthalmic Use
DESCRIPTION
Clobetasol propionate foam, 0.05% contains clobetasol propionate, USP, a synthetic corticosteroid, for topical dermatologic use. Clobetasol, an analog of prednisolone, has a high degree of glucocorticoid activity and a slight degree of mineralocorticoid activity.
Clobelasol propionate is is pregna-1,4-diene-3,20-dione,
21-chloro-9-fluoro-11-hydroxy-16-methyl-17-(1-oxopropoxy)-, (11β,16β)-, with the
empirical formula C
25H
32CIF0
5, a molecular weight of 466.97.
The following is the chemical structure:
Clobetasol propionate is a white or almost white, odorless, crystalline powder and is insoluble in water.
Clobetasol propionate foam, 0.05% contains 0.5 mg clobetasol propionate, USP, per gram in a thermolabile hydroethanolic foam vehicle consisting of cetyl alcohol, citric acid, ethanol (60%), polysorbate 60, potassium citrate, propylene glycol, purified water, and stearyl alcohol pressurized with a hydrocarbon (propane/butane) propellant.
CLINICAL PHARMACOLOGY
Like other topical corticosteroids, clobetasol propionate foam has
anti-inflammatory, antipruritic, and vasoconstrictive properties. The precise
mechanism of the anti-inflammatory activity of topical steroids in the treatment
of steroid-responsive dermatoses, in general, is uncertain. However,
corticosteroids are thought to act by the induction of phospholipase
A
2 inhibitory proteins, collectively called lipocortins. It is
postulated that these proteins control the biosynthesis of potent mediators of
inflammation such as prostaglandins and leukotrienes by inhibiting the release
of their common precursor arachidonic acid. Arachidonic acid is released from
membrane phospholipids by phospholipase A
2.
Pharmacokinetics
Topical corticosteroids can be absorbed from intact healthy skin. The extent of
percutaneous absorption of topical corticosteroids is determined by many
factors, including the vehicle and the integrity of the epidermal barrier.
Occlusion, inflammation and/or other disease processes in the skin may also
increase percutaneous absorption.
Once absorbed through the skin, topical corticosteroids are handled through
pharmacokinetic pathways similar to systemically administered corticosteroids.
Due to the fact that circulating levels are well below the level of detection,
the use of pharmacodynamic endpoints for assessing the systemic exposure of
topical corticosteroids is necessary. They are metabolized, primarily in the
liver, and are then excreted by the kidneys. In addition, some corticosteroids
and their metabolites are also excreted in the bile.
CLINICAL STUDIES
A well-controlled clinical study evaluated 188 subjects with moderate to severe scalp psoriasis. Subjects were treated twice daily for 2 weeks with one of four treatments: Clobetasol propionate foam, 0.05%, Vehicle foam, a commercially available clobetasol propionate solution, or Vehicle solution. The efficacy of clobetasol propionale foam, 0.05% in treating scalp psoriasis at the end of the 2 weeks' treatment was superior to that of Vehicle (foam and solution), and was comparable to that of the commercially available Scalp Application. See Table 1 below.
Table 1: Efficacy results from a controlled clinical trial in scalp psoriasis
| Clobetasol Propionate Foam, 0.05% n (%) | Vehicle Foam n (%) |
Total number of subjects | 62 | 31 |
Subjects with Treatment Success* | 39 (63) | 1 (3) |
Subjects with Parameter Clear at Endpoint (Scalp
Psoriasis) |
|
|
Scaling - Clear at Endpoint | 42 (68) | 3 (10) |
Erythema - Clear at Endpoint | 27 (44) | 2 (6) |
Plaque Thickness - Clear at
Endpoint | 41 (66) | 3 (10) |
*Defined as a composite of an Investigator's Global Assessment of "completely clear" or "almost clear," a plaque thickness score of 0, an erythema score of 0 or 1, and a scaling score of 0 or 1 at Endpoint, scored on a severity scale of 0-4.
Another well-controlled clinical study evaluated 279 subjects with mild to moderate plaque-type psoriasis (mean Body Surface Area at baseline was 6.7% with a range from 1 % to 20%) of non-scalp regions. Subjects were treated twice daily for 2 weeks with clobetasol propionate foam, 0.05% or Vehicle foam. The face and intertriginous areas were excluded from treatment. The efficacy of clobetasol propionate foam , 0.05% in treating non-scalp psoriasis at the end of 2 weeks' treatment was superior to that of Vehicle foam. See Table 2 below.
Table 2: Efficacy results from a controlled clinical trial in non-scalp psoriasis
| Clobetasol Propionate Foam, 0.05% n (%) | Vehicle Foam n (%) |
Total number of subjects | 139 | 140 |
Subjects with Treatment Success* | 39 (28) | 4 (3) |
Physician's Static Global Assessment - Clear or Almost
Clear at Endpoint | 94 (68) | 30 (21) |
Scaling - Clear or Almost Clear at Endpoint | 101 (73) | 42 (30) |
Erythema - Clear or Almost Clear at Endpoint | 88 (63) | 35 (25) |
Plaque Thickness - Clear at
Endpoint | 44 (32) | 5 (4) |
*Defined as a composite of a Physician's Static Global Assessment score of 0 or 1, scaling score of 0 or 1, an erythema score of 0 or 1 and a plaque thickness score of 0, based on a severity scale of 0-5 at Endpoint.
INDICATIONS AND USAGE
Clobetasol propionate foam, 0.05% is a super-potent topical corticosteroid indicated for short-term topical treatment of the inflammatory and pruritic manifestations of moderate to severe corticosteroid responsive dermatoses of the scalp, and for short-term topical treatment of mild to moderate plaque-type psoriasis of non-scalp regions excluding the face and intertriginous areas.
Treatment beyond 2 consecutive weeks is not recommended and the total dosage should not exceed 50 g per week because of the potential for the drug to suppress the hypothalamic-pituitary-adrenal (HPA) axis. In a controlled pharmacokinetic study, some subjects experienced reversible suppression of the adrenals following 14 days of clobetasol propionate foam, 0.05% therapy (See ADVERSE REACTIONS).
Use in children under 12 years of age is not recommended.
CONTRAINDICATIONS
Clobetasol propionate foam, 0.05% is contraindicated in patients who are hypersensitive 10 clobetasol propionate, to other corticosteroids, or 10 any ingredient in this preparation.
PRECAUTIONS
General: Clobetasol propionate is a super-potent topical corticosteroid that has been shown to suppress the ad renaIs at 7.0 g of clobetasol propionate foam, 0.05% per day. Lesser amounts of clobetasol propionate foam, 0.05% were not studied. Systemic absorption of topical corticosteroids has caused reversible adrenal suppression with Ihe potential for glucocorticosteroid insufficiency after withdrawal of treatment. Manifestations of Cushing's syndrome, hyperglycemia, and glucosuria can also be produced in some patients by systemic absorption of topical corticosteroids while on treatment.
Conditions which augment systemic absorption include the application of more potent steroids, use over large surface areas, prolonged use, and the addition of occlusive dressings.
Patients applying a topical steroid to a large surface area or to areas under occlusion should be evaluated periodically for evidence of adrenal suppression. If adrenal suppression is noted, an attempt should be made 10 withdraw the drug, to reduce the frequency of application, or to substitute a less potent steroid.
Recovery of HPA axis function is generally prompt upon discontinuation of topical corticosteroids. Infrequently, signs and symptoms of glucocorticosteroid insufficiency may occur requiring supplemental systemic corticosteroids. For information on systemic supplementation, see prescribing information for those products.
Pediatric patients may be more susceptible to systemic toxicity from equivalent doses due to their larger skin surface to body mass ratios. See PRECAUTIONS Pediatric Use.
If irritation develops, clobetasol propionate foam, 0.05% should be discontinued and appropriate therapy instituted. Allergic contact dermatitis with corticosteroids is usually diagnosed by observing a failure to heal rather than by noting a clinical exacerbation, as with most topical products not containing corticosteroids. Such an observation should be corroborated with appropriate diagnostic patch testing.
In the presence of dermatological infections, the use of an appropriate antifungal or antibacterial agent should be instituted. If a favorable response does not occur promptly, use of clobetasol propionate foam, 0.05% should be discontinued until the infection has been adequately controlled.
Information for Patients
Patients using topical corticosteroids should receive the following information
and instructions:
- This medication is to be used as directed by the physician and should not be
used longer than the prescribed time period. It is for external use only. Avoid
contact with the eyes.
- This medication should not be used for any disorder other than that for
which it was prescribed.
- The treated area should not be bandaged or otherwise covered or wrapped so
as to be occlusive unless directed by the physician.
- Patients should report to their physician any signs of local adverse
reactions.
Laboratory Tests
The following tests may be helpful in evaluating patients for adrenal
suppression:
ACTH stimulation test
A.M. plasma cortisol test
Urinary free cortisol test
Carcinogenesis, Mutagenesis, Impairment of Fertility
Long-term animal studies have not been performed to evaluate the carcinogenic
potential of clobetasol propionate.
Clobetasol propionate was non-mutagenic in three different test systems: the
Ames test, the Saccharomyces cerevisiae gene conversion assay, and the E.coli
B WP2 fluctuation test.
Studies in the rat following subcutaneous administration of clobetasol
propionate at dosage levels up to 0.05 mg/kg per day revealed that the females
exhibited an increase in the number of resorbed embryos and a decrease in the
number of living fetuses at the highest dose.
Pregnancy
Teratogenic effects
Pregnancy category C
Corticosteroids have been shown to be teratogenic in laboratory
animals when administered systemically at relatively low dosage levels. Some
corticosteroids have been shown to be teratogenic after dermal application to
laboratory animals.
Clobetasol propionate has not been tested for teratogenicity by the topical
route; however, it is absorbed percutaneously, and when administered
subcutaneously, it was a significant teratogen in both the rabbit and the mouse.
Clobetasol propionate has greater teratogenic potential than steroids that are
less potent.
Teratogenicity studies in mice using the subcutaneous route resulted in
fetotoxicity at the highest dose tested (1 mg/kg) and teratogenicity at all dose
levels tested down to 0.03 mg/kg. These doses are approximately 1.4 and 0.04
times, respectively, the human topical dose of clobetasol propionate based on body surface area
comparisons. Abnormalities seen included cleft palate and skeletal
abnormalities.
In rabbits, clobetasol propionate was teratogenic at doses of 0.003 and 0.01
mg/kg. These doses are approximately 0.02 and 0.05 times, respectively, the
human topical dose of clobetasol propionate based on body surface area comparisons. Abnormalities
seen included cleft palate, cranioschisis, and other skeletal abnormalities.
There are no adequate and well-controlled studies of the teratogenic
potential of clobetasol propionate in pregnant women. Clobetasol propionate foam should be used
during pregnancy only if the potential benefit justifies the potential risk to
the fetus.
Drugs of this class should not be used
extensively on pregnant patients, in large amounts, or for prolonged periods of
time.
Nursing Mothers
Systemically administered corticosteroids appear in human milk and could
suppress growth, interfere with endogenous corticosteroid production, or cause
other untoward effects. It is not known whether topical administration of
corticosteroids could result in sufficient systemic absorption to produce
detectable quantities in breast milk. Because many drugs are excreted in human
milk, caution should be exercised when clobetasol propionate foam is administered to a nursing
woman.
Pediatric Use
Safety and effectiveness of clobetasol propionate foam in pediatric patients have
not been established; therefore, use in children under 12 years of age is not
recommended. Because of a higher ratio of skin surface area to body mass,
pediatric patients are at a greater risk than adults of adrenal suppression and
Cushing’s syndrome when they are treated with topical corticosteroids. Pediatric
patients are therefore at greater risk of adrenal insufficiency during and/or
after withdrawal of treatment. Adverse effects including striae have been
reported with inappropriate use of topical corticosteroids in infants and
children.
Adrenal suppression, Cushing’s syndrome, linear growth retardation, delayed
weight gain, and intracranial hypertension have been reported in children
receiving topical corticosteroids. Manifestations of adrenal suppression in
children include low plasma cortisol levels and an absence of response to ACTH
stimulation. Manifestations of intracranial hypertension include bulging
fontanelles, headaches, and bilateral papilledema.
Geriatric Use
Clinical studies of clobetasol propionate foam did not include sufficient numbers of subjects
aged 65 and over to determine whether they respond differently from younger
subjects. Other reported clinical experience has not identified differences in
responses between the elderly and younger patients. In general, dose selection
for an elderly patient should be cautious, usually starting at the low end of
the dosing range, reflecting the greater frequency of decreased hepatic, renal,
or cardiac function, and of concomitant disease or other drug therapy.
ADVERSE REACTIONS
In a controlled pharmacokinetic study, 5 of 13 subjects experienced reversible suppression of the adrenals at any time during the 14 days of clobetasol propionate foam, 0.05% therapy to at least 20% of the body surface area. Of the 13 subjects studied, 1 of 9 with psoriasis were suppressed after 14 days and all 4 of the subjects with atopic dermatitis had abnormal cortisol levels indicative of adrenal suppression at some time after starting therapy with clobetasol propionate foam, 0.05%. (See Table 3 below.)
Table 3: Subjects with reversible HPA axis suppression at any time during treatment
Dermatosis | Clobetasol Propionate Foam, 0.05% |
Psoriasis | 1 of 9 |
Atopic Dermatatitis* | 4 of 4 |
*Clobetasol propionate foam, 0.05% is not indicated for non-scalp atopic dermatitis, as the safety and efficacy of clobetasol propionate foam, 0.05% in non-scalp atopic dermatitis has not been established. Use in children under 12 years of age is not recommended.
Systemic absorption of topical corticosteroids has produced reversible adrenal suppression, manifestations of Cushing's syndrome, hyperglycemia, and glucosuria in some patients (see PRECAUTIONS).
In a controlled clinical trial (188 subjects) with clobetasol propionate foam, 0.05% in subjects with psoriasis of the scalp, there were no localized scalp adverse reactions reported in the clobetasol propionate foam, 0.05% treated subjects. In two controlled clinical trials (360 subjects) with clobetasol propionate foam, 0.05% in subjects with psoriasis of non-scalp regions, localized adverse events that occurred in the clobetasol propionate foam, 0.05% treated subjects included application site burning (10%), application site dryness (less than 1%), and other application site reactions (4%).
In larger controlled trials with other clobetasol propionate formulations, the most frequently reported local adverse reactions have included burning, stinging, irritation, pruritus, erythema, folliculitis, cracking and fissuring of the skin, numbness of the fingers, skin atrophy, and telangiectasia (all less than 2%).
The following additional local adverse reactions have been reported with topical corticosteroids, bul they may occur more frequently wilh the use of occlusive dressings and higher potency corticosteroids such as clobetasol propionate foam, 0.05%. These reactions are listed in an approximate decreasing order of occurrence: dryness, hypertrichosis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, maceration of the skin, secondary infection, striae, and miliaria.
OVERDOSAGE
Topically applied clobetasol propionate foam, 0.05% can be absorbed in sufficient amounts 10 produce systemic effects. See PRECAUTIONS.
DOSAGE AND ADMINISTRATION
Note: For proper dispensing of foam, hold the can upside down and
depress the actuator.
Clobetasol propionate foam, 0.05% should be applied to the affected area twice daily, once in the
morning and once at night. Invert the can and dispense a small amount of clobetasol propionate foam, 0.05% (up to a maximum of a golf-ball-size dollop or one and a half capfuls) into
the cap of the can, onto a saucer or other cool surface, or to the lesion,
taking care to avoid contact with the eyes. Dispensing directly onto hands is
not recommended (unless the hands are the affected area), as the foam will begin
to melt immediately upon contact with warm skin. When applying clobetasol propionate foam, 0.05% to a
hair-bearing area, move the hair away from the affected area so that the foam
can be applied to each affected area. Pick up small amounts with fingertips and
gently massage into affected area until the foam disappears. Repeat until entire
affected area is treated.
Apply the smallest amount possible that sufficiently covers the affected
area(s). No more than one and a half capfuls of foam should be used at each
application. Do not apply to face or intertriginous areas.
Clobetasol propionate foam, 0.05% is a super-high-potency topical corticosteroid; therefore,
treatment should be limited to 2 consecutive weeks and amounts greater than 50
g/week should not be used. Use in pediatric patients under 12 years of age is
not recommended.
Unless directed by a physician, clobetasol propionate foam, 0.05% should not be used with occlusive
dressings.
Instructions for applying clobetasol propionate foam, 0.05%
Apply clobetasol propionate foam, 0.05% twice a day, once in the morning and once at night. Apply only enough to cover the affected areas. Clobetasol propionate foam, 0.05% should not be applied to the groin, armpits, or other skin fold areas.
To use clobetasol propionate foam, 0.05%:
- Before applying clobetasol propionate foam ,0.05% for the first time, break the tiny plastic piece at the base of the can's rim by gently pushing back (away from the piece)on the nozzle.
- Turn the can upside down. Push the button to squirt a small amount of clobetasol propionate foam, 0.05% into the cap of the can, onto a saucer or other cool surface,or your affected skin area. This amount should be no more than 1 1/2 capfuls, about the size of a golf ball. Do not squirt clobetasol propionate foam, 0.05% directly onto your hands (unless your hands are the affected areas), because the foam will begin to melt right away on contact with your warm skin. If your fingers are warm, rinse them in cold water first. (Be sure to dry them thoroughly before handling the foam.) If the can seems warm or the foam seems runny, run the can under cold water.
- Using your fingertips, gently massage clobetasol propionate foam, 0.05% into the affected areas until the foam disappears. If you are treating areas with hair such as the scalp, move any hair away so that the foam can be applied directly to the affected areas.Repeat the process until the affected areas are treated. Keep the foam away from your eyes, as it will sting and may cause eye problems if there is frequent contact with your eyes. If the foam gets in your eyes, rinse them well with cold water right away. If the stinging continues, contact your doctor right away.
- Wash your hands after applying clobetasol propionate foam, 0.05%. Throwaway any of the unused medicine that you squirted out of the can.
HOW SUPPLIED
Clobetasol propionate foam, 0.05% is supplied in 50 g (NDC 59366-2110-5) and 100 g (NDC 59366-2110-1) aluminum cans.
Store at controlled room temperature 68-77
oF (20-25
oC).
WARNING
FLAMMABLE. AVOID FIRE, FLAME OR SMOKING DURING AND IMMEDIATELY FOLLOWING APPLICATION. Keep out of reach of children. Contents under pressure. Do not puncture or incinerate container. Do not expose to heat or store at temperatures above 120
oF (49
oC).
Manufactured for
Glades Pharmaceuticals, LLC
Duluth, GA 30096
USA
AW No: AW-0788
P/N: 128831-1207
U.S. Patent No. 6,126,920
© 2007 Glades Pharmaceuticals. LLC
"G" and Design is a trademark of Stiefel Laboratories. Inc.
GLADES is a registered trademark of Stiefel Laboratories. Inc
Printed in: US
December 2007
Principal Display Panel
NDC 59366-2110-5
Clobetasol
Propionate
Foam 0.05%
Rx only
Glades
NET WT 50 g
NDC 59366-2110-1
Clobetasol
Propionate
Foam 0.05%
Rx only
Glades
NET WT 100 g
CLOBETASOL PROPIONATE
FOAM 0.05%
clobetasol propionate
aerosol, foam |
|
|
|
|
|
Revised: 08/2009DPT Laboratories, Ltd.