Under the European Union Merger Regulation, the European Commission has cleared the proposed creation of a joint venture to develop, manufacture and market a portfolio of biosimilar drugs (copies of compounds produced using biological processes), between drugmakers Lonza of Switzerland and Teva Pharmaceutical Industries of Israel (Marketletter January 26). The Commission concluded that the transaction would not significantly impede effective competition within the European Economic Area or any substantial part of it.
The Commission found that the proposed transaction would give rise to no overlaps between the activities of the parent companies and that no competition problems were likely to arise from overlaps between the JV and Teva in the finished dose pharmaceutical products sector, as Teva has reduced market shares in those where the JV will be active and a number of competitors are presents. It also ruled out any competition concerns due to vertical relationships between Lonza's contract manufacturing activities - in which it recognized that the Swiss firm is a relatively important player - and the JV's future downstream products.
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