- On 26 February 2015, the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion recommending a variation to the terms of the marketing authorisation for the medicinal product panitumumab (Vectibix). Read more here.
Thursday 5 March 2015
European Medicines Agency recommends a variation to the terms of the marketing authorisation for panitumumab
The change concerns first-line combination treatment with FOLIFIRI.
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