Commission Decision of 01/03/2013 declaring a concentration to be compatible with the common market (Case No COMP/M.6708 - BMS / ASTRAZENECA / AMYLIN BUSINESS) according to Council Regulation (EC) No 139/2004 (Only the English text is authentic)

• Published date: 01 March 2013
• Subject Matter: Competition,Concentrations between undertakings

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Commission Decision of 01/03/2013 declaring a concentration to be compatible with the common market (Case No COMP/M.6708 - BMS / ASTRAZENECA / AMYLIN BUSINESS) according to Council Regulation (EC) No 139/2004 (Only the English text is authentic)

|EUROPEAN COMMISSION |

Brussels, 01/03/2013

C(2013)1299

PUBLIC VERSION

SIMPLIFIED MERGER PROCEDURE

To the notifying parties: | |

Dear Madam(s) and/or Sir(s),

Subject: Case No COMP/ M.6708 BMS / ASTRAZENECA / AMYLIN BUSINESS Commission decision pursuant to Article 6(1)(b) of Council Regulation (EC) No 139/2004 [1]

1. On 28 January 2013, the European Commission received a notification of a proposed concentration pursuant to Article 4 of Council Regulation (EC) No 139/2004 ("Merger Regulation") by which the undertakings Bristol-Myers Squibb Company (“BMS”, USA) and AstraZeneca Pharmaceuticals LP (“AZ”, UK) acquire within the meaning of Article 3(1)(b) of the Merger Regulation joint control of Amylin Collaboration Business (“Amylin Business”, USA) by way of acquisition of certain governance rights. [2]

2. The business activities of the undertakings concerned are:

- AZ : primarily engaged in the discovery, development, manufacture and commercialization of prescription medicines for gastrointestinal, cardiovascular, neuroscience, respiratory and inflammation, oncology and infectious diseases;

- BMS : active in the development and commercialization of treatments in several areas, in particular cardiovascular, virology (including HIV infection), oncology, neuroscience, immunoscience, and metabolics treatments;

- Amylin Business : joint development and commercialization of four Amylin compounds, namely exenatide, pramlintide, metreleptin and AC165198.

3. After examination of the notification, the European Commission has concluded that the notified operation falls within the scope of the Merger Regulation and of paragraph 5(a) of the Commission Notice on a simplified procedure for treatment of certain concentrations under Council Regulation (EC) No 139/2004 [3] .

4. For the reasons set out in the Notice on a simplified procedure, the European Commission has decided not to oppose the notified operation and to declare it compatible with the internal market and with the EEA Agreement [4] . This decision is adopted in application of Article 6(1)(b) of the Merger Regulation.

(signed) For the Commission

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