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, Celgene) for treating moderate-to-severe plaque psoriasis in patients who are considered candidates for systemic therapy or phototherapy.
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 approved by FDA for the treatment of active psoriatic arthritis in adult patients. Approximately 10% to 20% of patients suffering from plaque psoriasis also have active psoriatric arthritis.
Scott Smith, president of inflammation & immunology for Celgene, commented that the new drug “offers a valuable treatment option for a spectrum of plaque psoriasis patients-patients who are treatment naïve as well as patients who are treatment-experienced, including those previously treated with biologic agents or conventional systemic agents.”
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.
The National Psoriasis Foundation estimates that psoriasis is the most common autoimmune disease in the United States, affecting 7.5 million people. It is estimated that 125 million people have psoriasis worldwide.
Navitus to Offer Unbranded Stelara Biosimilar, Remove Stelara from Formulary
March 13th 2025Lumicera Health Services, Navitus’ specialty pharmacy, has made a deal with Teva to offer an unbranded biosimilar that they estimate will save $112,000 and $336,000 per patient per year. Navitus will remove Stelara from formulary on July 1, 2025.
Read More
FDA Approves Neffy 1 mg Nasal Spray for Pediatric Patients
March 6th 2025Neffy 1 mg is now approved by the FDA to treat pediatric patients who weigh 33 to 65 lbs. Neffy was first FDA-approved as a 2 mg dose in August 2024 for the emergency treatment of anaphylaxis in children and adults weighing at least 66 lbs.
Read More