KEYNOTE-189 tested chemo ± Keytruda is first-line non-squamous NSCLC for patients with any PD-L1 status. The hazard ratio for OS/PFS and other details will be presented at an unspecified medical conference (probably ASCO).
Success in KEYNIOTE-189 allows MRK to convert the accelerated approval from the small KEYNOTE-021G study (#msg-131249474) into a full FDA approval.
“The efficient-market hypothesis may be the foremost piece of B.S. ever promulgated in any area of human knowledge!”