
Otezla approved for plaque psoriasis
FDA has approved Otezla (apremilast, Celgene) for treating moderate-to-severe plaque psoriasis in patients who are considered candidates for systemic therapy or phototherapy.
FDA has approved Otezla (apremilast,
Apremilast is an oral, selective inhibitor of phosphodiesterase 4 (PDE4). The drug is the first and only PDE4 inhibitor indicated for the treatment of plaque psoriasis, the most common manifestation of psoriasis. Psoriasis is a chronic inflammatory disease of the skin that stems from an uncontrolled immune response.
Previously, in March 2014, apremilast was
Scott Smith, president of inflammation & immunology for
FDA in large part based their decision to approve apremilast on findings from two phase 3, multicenter, double-blind, placebo-controlled clinical trials, ESTEEM 1 and ESTEEM 2. The Psoriasis Area and Severity Index was used to measure the effect of apremilast on plaque psoriasis among the roughly 1250 participating study subjects.
At week 16 of the studies, patients being treated with apremilast were observed to have a clinically meaningful, significant improvement in their condition. Also, on the static Physician’s Global Assessment, patients treated with the drug scored “clear” to “almost clear” of the raised red patches of skin covered with silvery white scales that characterize plaque psoriasis.
Before beginning a regimen of apremilast, patients should inform their physician if they have a history of depression or suicidal behavior. They should further inform their physician if these conditions or other mood changes develop or worsen while they are taking apremilast.
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