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Super-fast approval for Genentech's 2nd-line ALK inhibitor in NSCLC

By Jennifer Boggs
Managing Editor

Friday, December 11, 2015

Barely three months after accepting a new drug application for Genentech Inc's Alecensa, the FDA granted accelerated approval to the breakthrough therapy-designated drug for treating ALK-positive NSCLC patients who have progressed or are intolerant to Xalkori.

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