EFTA00598930Set 9
2015-10-025p4,184w
ALERT
Today, the FDA approved Keytruda (PD-1) with a companion diagnostic Pharmaceuticals — Major &
(PD-L1 IHC 22C3 pharmDx test) for second-line PD-L1+ lung cancer Specialty
patients ... label, we expect the uptake to be skewed towards (1-212)622-1267
the PD-L1+ non-sq patients. For, BMY, today's Keytruda label further
reinforces our view that ... harboring MMR mutations. Dana Flanders, CFA
(1-212)622-1256
• Keytruda approved in 2L PD-L1+ NSCLC. The FDA approved
M. Morgan Securities LLC
Keytruda for use with a companion
https://www.justice.gov/epstein/files/DataSet%209/EFTA00598930.pdf