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Ibrutinib Cost was approved on the basis of phase 2 studies, and biotech analysts were pleased to note that FDA greenlighted the drug just four months after the NDA submission was filed – a two-month improvement over the standard six-month accelerated approval period – ostensibly thanks to Ibrutinib Cost’s Breakthrough status.Roughly 150 sales reps (half Janssen, half Pharmacyclics) will market Ibrutinib Cost, targeting around 7,000 of the 8,000 hematologist/oncologists practicing in the US. The drug was made available on the day it was approved, company executives said on the call.
