The European Union's Committee for Proprietary Medicinal Products hasrecommended granting marketing authorization for Roche Pharmaceuticals' anticancer drug, MabThera (rituxumab), in combination with standard chemotherapy (the CHOP regimen; (cyclophosphamide, vincristine, doxorubicin and prednisone) for the treatment of aggressive non-Hodgkin's lymphoma.
The recommendation is based on interim results from a pivotal study which demonstrated that MabThera plus CHOP caused a complete remission rate of 71%, compared to 59% for standard chemotherapy alone. Results from this study will be presented at the American Society of Hematology meeting in Orlando, USA, in December.
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