UCB and sanofi-aventis announced today that the U.S. Food and Drug Administration (FDA) has approved XYZAL(R) (levocetirizine dihydrochloride), a new once-daily prescription antihistamine that delivers a rapid and long-lasting effect for the relief of symptoms associated with seasonal and perennial allergic rhinitis and uncomplicated skin manifestations of chronic idiopathic urticaria in adults and children six years of age and older. "With allergies on the rise and longer-lasting allergy seasons, patients desire a fast and long-acting treatment," said Michael S. Blaiss, MD, Clinical Professor of Pediatrics and Medicine at the University of Tennessee Health Science Center in Memphis, Tennessee. "XYZAL(R) is a new treatment option in today's more challenging allergy environment." UCB filed the new drug application (NDA) with FDA in July 2006 and has extensively researched XYZAL(R) in numerous clinical trials. Studies in allergic rhinitis patients demonstrated XYZAL(R) significantly reduced the symptoms of sneezing, itchy nose, runny nose, and itchy eyes. Studies in chronic idiopathic urticaria patients showed XYZAL(R) significantly reduced the severity of itching and the number and size of wheals. In September 2006, UCB and sanofi-aventis entered into an agreement to launch and co-market XYZAL(R) in the U.S. UCB and sanofi-aventis have a long history in the allergy treatment arena and are committed to advancing treatment for allergy sufferers and helping meet unmet medical needs for patients with chronic allergy symptoms. XYZAL(R) once-daily tablets are expected to be available during the 2007 fall allergy season. "I am very pleased to have sanofi-aventis as our partner in bringing XYZAL(R) to the U.S. market," said UCB's U.S. President, Fabrice Egros. "The approval of XYZAL(R) will offer an alternative for U.S. physicians seeking a new prescription option for patients and we are confident that the attributes of XYZAL(R), along with our dedicated selling efforts, will result in the successful launch of this drug in the U.S." "We are excited about the FDA approval of XYZAL(R) and our partnership with UCB," said Brent Ragans, Vice President, Specialty Markets, sanofi- aventis. "Building upon our long history in the allergy treatment arena, this opportunity allows us to continue our leadership position in this field and demonstrates our commitment to providing new treatments for the millions of allergy sufferers in the U.S." About Allergic Conditions Many people suffer from the symptoms associated with common allergic conditions. The immune system of allergy sufferers over-reacts to something in the environment, leading to symptoms that affect their respiratory system, eyes, or skin. Estimates from the American College of Allergy, Asthma & Immunology (ACAAI) suggest that allergies affect as many as 40 to 50 million people in the United States. Seasonal allergic rhinitis (SAR), commonly referred to as "hay fever" or "outdoor allergies," is the most common form of allergic rhinitis. By definition, SAR includes allergies to seasonal pollens like grass, trees, and weeds, as well as mold. Perennial Allergic Rhinitis (PAR) is sometimes referred to as "year round" or "indoor allergies" and is characterized by allergic symptoms that last longer than four weeks. House dust mites, animal dander, and mold most commonly trigger PAR. Chronic Idiopathic Urticaria (CIU) is most commonly known as "hives of unknown origin" and is defined as the occurrence of daily, or almost daily, wheals and itching for at least six weeks with no obvious causes. About XYZAL(R) Indications and Important Safety Information XYZAL is indicated for the relief of symptoms associated with allergic rhinitis (seasonal and perennial), and uncomplicated skin manifestations of chronic idiopathic urticaria in adults and children 6 years of age and older. In clinical trials, the most common adverse reactions in greater than or equal to 2% of adult and adolescent patients (12 years and older) taking XYZAL 5 mg were mild to moderate in intensity and included somnolence (6% vs. 2% placebo), nasopharyngitis (4% vs. 3% placebo), fatigue (4% vs. 2% placebo) and dry mouth (2% vs. 1% placebo). The most common adverse reactions in greater than or equal to 2% of pediatric patients (6-12 years of age) taking XYZAL 5 mg included pyrexia (4% vs. 2% placebo), cough (3% vs. <1% placebo), somnolence (3% vs. <1% placebo), and epistaxis (2% vs. The use of XYZAL is contraindicated in patients with end-stage renal disease (CLcr <10 mL/min) and in patients undergoing hemodialysis. XYZAL is also contraindicated in pediatric patients aged 6 to 11 years with impaired renal function. Patients should be cautioned against engaging in hazardous occupations requiring complete mental alertness, and motor coordination such as operating machinery or driving a motor vehicle after ingestion of XYZAL. Concurrent use of XYZAL with alcohol or other central nervous system depressants should be avoided because additional reductions in alertness and additional impairment of CNS performance may occur. XYZAL(R) was first launched in Europe in 2001 and is currently marketed in over 80 countries around the world. The FDA approval is based primarily upon the results of eight randomized, placebo-controlled clinical trials involving over 2,000 patients. Please visit