US pharmaceutical group Eli Lilly's cancer drug Alimta (permetrexed for injection) has been recommended for marketing by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMEA) in combination with cisplatin for the first-line treatment of patients with locally-advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology.
The Indianapolis-headquartered firm said that this novel use of histology opens the door for a more tailored approach to treating the world's most common cause of cancer deaths.
The CHMP recommendation was based on Phase III data from 1,752 patients which found that the approved Alimta regimen was non-inferior to the same background regimen plus Gemzar (gemcitabine for injection) in the first-line NSCLC setting.
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