A. Markham et Kl. Goa, KETOTIFEN - A REVIEW OF ITS THERAPEUTIC EFFICACY IN DERMATOLOGICAL DISORDERS, CLINICAL IMMUNOTHERAPEUTICS, 5(5), 1996, pp. 400-411
In addition to its antihistaminic properties, ketotifen modulates the
immune response to allergen challenge in vitro and attenuates dermatol
ogical manifestations of the allergic response in vivo. In small rando
mised double-blind trials, ketotifen was significantly more effective
than placebo in patients with cold urticaria, paediatric mastocytosis
(urticaria pigmentosa) or atopic dermatitis, and in prevention of asth
ma in infants and children with atopic dermatitis. Additional comparat
ive studies showed the drug to be as effective as cetirizine, loratadi
ne, astemizole and emedastine as treatment for chronic urticaria, at l
east as effective as clemastine as treatment for chronic urticaria and
atopic dermatitis but inferior to hydroxyzine as treatment for paedia
tric mastocytosis. Ketotifen has shown promise as a treatment for neur
ofibromatosis, where previously no pharmacological treatment option wa
s available. The most common adverse event in patients treated with ke
totifen is sedation; however, the prevalence of this adverse event app
ears to subside during continued administration (approximate to 14% in
cidence at 3 months reducing to approximate to 2% at endpoint in a 12-
month postmarketing study). Other adverse events include dizziness, dr
y mouth, nausea, headache and weight gain (incidence approximate to 1
to 2%) Thus ketotifen is a potential therapy for cutaneous mastocytosi
s and neurofibromatosis, and has been shown to be an effective treatme
nt for urticaria and, particularly, atopic dermatitis. The potential f
or the drug to prevent the development of asthma in infants and childr
en with the latter provides further rationale for its use.