19 On 5 January 2012, Teva Pharmaceuticals Europe BV (‘Teva Europe’) submitted an application on behalf of a company within the same group, namely Teva Pharma BV (‘Teva’), for authorisation to place on the market a generic version of medicinal product marketed under the commercial name Glivec, namely imatinib Ratiopharm, for therapeutic indications covering, first, the treatment of adult patients with newly diagnosed CML in chronic phase for whom bone marrow transplantation cannot be considered as a first line of treatment and adult patients with CML in chronic phase after failure of interferon-alpha therapy or in accelerated phase and, second, the treatment of the non-CML cancer indications for which the original orphan medicinal product had also been authorised.
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