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Document C2015/397/06
Prior notification of a concentration (Case M.7872 — Novartis/GSK (Ofatumumab Autoimmune Indications)) (Text with EEA relevance)
Prior notification of a concentration (Case M.7872 — Novartis/GSK (Ofatumumab Autoimmune Indications)) (Text with EEA relevance)
Prior notification of a concentration (Case M.7872 — Novartis/GSK (Ofatumumab Autoimmune Indications)) (Text with EEA relevance)
OJ C 397, 28.11.2015, p. 20–20
(BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)
28.11.2015 |
EN |
Official Journal of the European Union |
C 397/20 |
Prior notification of a concentration
(Case M.7872 — Novartis/GSK (Ofatumumab Autoimmune Indications))
(Text with EEA relevance)
(2015/C 397/06)
1. |
On 18 November 2015, the Commission received a notification of a proposed concentration pursuant to Article 4 of Council Regulation (EC) No 139/2004 (1) by which Novartis AG (‘Novartis’, Switzerland) acquires from GlaxoSmithKline plc (‘GSK’, United Kingdom), within the meaning of Article 3(1)(b) of the Merger Regulation, sole control of the rights to the autoimmune indications with respect to the pharmaceutical Ofatumumab, by way of purchase of assets. |
2. |
The business activities of the undertakings concerned are:
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3. |
On preliminary examination, the Commission finds that the notified transaction could fall within the scope of the Merger Regulation. However, the final decision on this point is reserved. |
4. |
The Commission invites interested third parties to submit their possible observations on the proposed operation to the Commission. Observations must reach the Commission not later than 10 days following the date of this publication. Observations can be sent to the Commission by fax (+32 22964301), by email to COMP-MERGER-REGISTRY@ec.europa.eu or by post, under reference number M.7872 — Novartis/GSK (Ofatumumab Autoimmune Indications), to the following address:
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(1) OJ L 24, 29.1.2004, p. 1 (the ‘Merger Regulation’).