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Medical Areas: Dermatology/Plastic Surgery
Drug Information
The following information is obtained from various newswires, published
medical journal articles, and medical conference presentations.
Company: Connetics
Approval Status: Approved September 2006
Treatment Area: atopic dermatitis
Verdeso (desonide) Foam is a petrolatum-based emulsion aerosol
foam containing the active ingredient desonide, a low-potency
topical corticosteroid. Desonide is a white powder or crystal that
is practically insoluble in water, sparingly soluble in ethanol and
in acetone, and soluble in chloroform.
Verdeso is specifically indicated for the treatment of mild to
moderate atopic dermatitis in patients 3 months of age and
older.
Verdeso is supplied in 100 g aluminum cans. The recommended
initial dose of the drug is a thin layer applied to the affected
area(s) twice daily. The smallest amount of foam necessary to
adequately cover the affected area(s) with a thin layer should be
used.
FDA Approval
FDA approval of Verdeso was based on results of one clinical trial.
This double-blind, randomized trial enrolled 581 subjects, ages 3
months to 17 years old, with mild to moderate atopic dermatitis,
who received Verdeso Foam applied twice daily for 4 weeks. Of the
subjects on the Verdeso treatment 39% achieved success, defined as
an Investigator's Static Global Assessment (ISGA) score of
clear or almost clear, a minimum improvement in the 5 point ISGA
score of 2 grades from baseline to week 4, and a score of absent or
minimal for both erythema and induration/papulation at week 4. Only
9% of the subjects on placebo achieved success.
Ongoing Study Commitments
- Connetics has agreed to commit to conducting a dermal
carcinogenicity study with Verdeso (desonide) Foam.
90-day dose range-finding study: By April 1, 2008
Study protocol submission: By October 1, 2008
Study start date: By June 1, 2009
Final report submission: By December 1, 2012
-
Connetics has agreed to commit to
conducting a study to determine the photoco-carcinogenic potential
of Verdeso (desonide) Foam.
90-day dose range-finding study: By April 1, 2008
Study protocol submission: By October 1, 2008
Study start date: By June 1, 2009
Final report submission: By December 1, 2011
Adverse events associated with the use of Verdeso may include,
but are not limited to , the following:
- Upper respiratory tract infection
- Cough
- Application site burning
- Application site reaction
- Viral infection
- Headache
- Irritability
- Asthma
In addition, in a clinical study Verdeso was shown to cause
adrenal suppression in 4% of the pediatric subjects after 4 weeks
of use. Systemic absorption of topical corticosteroids has produced
reversible HPA axis suppression, manifestations of Cushing’s
syndrome, hyperglycemia, and glucosuria in some patients. Verdeso
Foam is contraindicated in subjects who are hypersensitive to
desonide or to any ingredient in this preparation. Treatment should
not exceed four consecutive weeks.
Verdeso Foam is a topical corticosteroid which are thought to
act by the induction of phospholipase A2 inhibitory proteins,
collectively called lipocortins. These proteins are believed to
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 A2.
Wong VK, Fuchs B, Lebwohl M Overview on
desonide 0.05%: a clinical safety profile. Journal of Drugs in
Dermatology 2004 Jul-Aug;3(4):393-7
Lucky AW, Grote GD, Williams JL, Tuley MR, Czernielewski
JM, Dolak TM, Herndon JH, Baker MD Effect of desonide
ointment, 0.05%, on the hypothalamic-pituitary-adrenal axis of
children with atopic dermatitis. Cutis; cutaneous medicine for
the practitioner 1997 Mar;59(3):151-3.
Jorizzo J, Levy M, Lucky A, Shavin J, Goldberg G, Dunlap
F, Hinds A, Strelka L, Baker M, Tuley M, et al Multicenter
trial for long-term safety and efficacy comparison of 0.05%
desonide and 1% hydrocortisone ointments in the treatment of atopic
dermatitis in pediatric patients. Journal of the American
Academy of Dermatology 1995 Jul;33(1):74-7.
Tarayre JP, Aliaga M, Barbara M, Ballester R,
Tisne-Versailles J, Couzinier JP Comparison of the
cutaneous/systemic antiinflammatory activity ratios for desonide
and hydrocortisone in various experimental models.
Arzneimittelforschung1988 Apr;38(4):542-5.
For additional information regarding Verdeso or atopic
dermatitis, please vist the Connetics web page.