If approved, JEMDEL will be the first high-potency topical steroid treatment for plaque psoriasis with dosing for as long as eight weeks.
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[14-February-2018] |
PDUFA Date Set for Oct. 5, 2018 JEMDEL Studied for Up to Eight Weeks of Use LAVAL, Quebec, Feb. 14, 2018 /PRNewswire/ -- Ortho Dermatologics, a division of Valeant Pharmaceuticals, today announced that the U.S. Food and Drug Administration (FDA) accepted the New Drug Application for JEMDEL™1 (halobetasol propionate 0.01%) (IDP-122) lotion with a PDUFA action date of Oct. 5, 2018. If approved, JEMDEL will be the first high-potency topical steroid treatment for plaque psoriasis with dosing for as long as eight weeks. In the clinical trials, the most common adverse event was upper respiratory tract infection. “The impact of psoriasis can be devastating for the millions of patients who live with the pain and stigma of this lifelong chronic condition,” said Joseph C. Papa, chairman and CEO, Valeant. “If approved, we believe JEMDEL will be an important option for patients with plaque psoriasis.” Psoriasis is a chronic, painful and frequently life-altering immune-mediated inflammatory skin disease associated with serious comorbidities and substantial impairment of physical and psychological quality of life. More than 75% of patients with moderate-to-severe plaque psoriasis experience significant itching, and greater than 55% report moderate or worse levels of pain.2 About Ortho Dermatologics About Valeant Forward-looking Statements © 2018 Valeant Pharmaceuticals North America LLC VNP.0060.USA.17
1 Provisional Name Contact Information: Media Contact: Arthur Shannon Lainie Keller arthur.shannon@valeant.com lainie.keller@valeant.com 514-856-3855 908-927-0617 877-281-6642 (toll free)
View original content with multimedia:http://www.prnewswire.com/news-releases/ortho-dermatologics-announces-us-fda-filing-acceptance-for-jemdel-plaque-psoriasis-treatment-300598372.html SOURCE Valeant Pharmaceuticals International, Inc. | ||
Company Codes: NYSE:VRX, Toronto:VRX |