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US FDA Grants Pediatric Exclusivity for UCB's Keppra(R)
Date:6/6/2008

was nasopharyngitis.

The adverse events that result from Keppra(R) injection use for primary generalized tonic-clonic seizures in adults with idiopathic generalized epilepsy, myoclonic seizures in adults with juvenile myoclonic epilepsy and partial onset seizures in adults with epilepsy include all of those associated with Keppra(R) tablets and oral solution.

US prescribing information is available at http://www.keppra.com or by calling 1-866-822-0068.

Further information

Andrea Levin, Public Relations Manager, CNS, UCB, Inc.

Office: 770.970.8352 / Mobile: 404.483.7329/

Email: andrea.levin@ucb-group.com

About UCB

UCB, Brussels, Belgium (http://www.ucb-group.com) is a global leader in the biopharmaceutical industry dedicated to the research, development and commercialisation of innovative pharmaceutical and biotechnology products in the fields of central nervous system disorders, allergy/respiratory diseases, immune and inflammatory disorders and oncology. UCB focuses on securing a leading position in severe disease categories. Employing more than 10,000 people in over 40 countries, UCB achieved revenue of EURO 3.6 billion in 2007 on a pro forma basis. UCB S.A. is listed on the Euronext Brussels Exchange.

Forward looking statement

This press release contains forward-looking statements based on current plans, estimates and beliefs of management. Such statements are subject to risks and uncertainties that may cause actual results to be materially different from those that may be implied by such forward-looking statements contained in this press release. Important factors that could result in such differences include: changes in general economic, business and competitive conditions, effects of future judicial decisions, changes in regulation, exchange rate fluctuations and hiring and retention of
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