Press Release

Jerini receives european commission approval for FIRAZYR® (Icatibant) in HAE treatment

Tuesday, July 15 2008

Shire Limited, the global specialty biopharmaceutical company, notes that Jerini AG has announced today that the European Commission has granted the company marketing authorization for its lead compound FIRAZYR® (Icatibant) in the treatment of acute attacks of hereditary angioedema (HAE).

HAE is a debilitating and potentially life-threatening genetic disease characterized by spontaneous and recurring attacks of edema.

As announced by Shire on 3 July, 2008, Maia Elfte Vermögensverwaltungs-GmbH, to be renamed "Shire Deutschland Investments GmbH", a German indirect subsidiary of Shire Limited, has launched a voluntary public takeover offer for all shares in Jerini AG.

Jerini's Supervisory and Management Boards unanimously support the transaction and are recommending acceptance of the offer to its shareholders. Subject to completion of certain sale and purchase agreements and registration of the newly issued shares, Shire will have rights to approximately 75% of Jerini’s share capital before the receipt of any takeover offer acceptances.

It is anticipated that the offer will be open for acceptance by the remaining shareholders until the end of Q3 2008 and is contingent upon the fulfilment of certain customary terms and conditions, including approval by relevant merger control authorities.

The European Commission’s approval allows Jerini to market FIRAZYR in the European Union’s 27 member states, making it the first product to be approved in all EU countries for the treatment of HAE.

Sylvie Gregoire, President of Shire Human Genetic Therapies (HGT) business commented, "We are very pleased that European approval has been granted to Jerini today. This is an important step in bringing this first in class orphan treatment to patients who suffer from HAE attacks.

"We look forward to the completion of our transaction with Jerini which will enable us to work together and ultimately build FIRAZYR into a global gold standard treatment."

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