About Lialda
Lialda is part of a drug class called aminosalicylates, which contain 5-aminosalicyclic acid (5-ASA). 5-ASA is a well-established drug of choice and often a first-line treatment for UC. Lialda is indicated for the induction of remission in patients with active, mild to moderate UC. The safety and efficacy of Lialda have been established for up to eight weeks. Lialda is the first new formulation in this class to be approved since 2000. Lialda is the only ulcerative colitis treatment that utilizes MMX(R) Technology. Lialda with MMX Technology combines a pH dependent gastro-resistant coating, which delays the release of the medication to the colon (the site of the inflammation in ulcerative colitis), with a tablet core containing mesalamine with hydrophilic and lipophilic components.
Shire has licensed from Giuliani SpA the exclusive rights to develop
and commercialize Lialda in the US, Canada, Pacific Rim, and Europe
(excluding Italy). Lialda is known as MEZAVANT XL(TM) in the UK and
Ireland, and MEZAVANT(R) elsewhere outside of the US. Giuliani SpA retains
the development and commercialization rights in Italy. Cosmo
Pharmaceuticals SpA, Milan, developed the MMX technology.
For further information please contact:
Investor Relations Clea Rosenfeld (Rest of the World) +44 1256 894 160
Eric Rojas (North America) +1 484 595 8252
Media Blythe Bertolo (GolinHarris on behalf of Shire) +1 312 729 4463
Matthew Cabrey (North America) +1 484 595 8248
Jessica Mann (Rest of the World) +44 1256 894 280
Notes to editors
SHIRE LIMITED
Shire's strategic goal is to become the leading specialty
biopharmaceutical company that focuses on meeting the needs of the
specialist physician. Shire focuses its business on attention
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