April 18, 2018 / 8:22 PM / a month ago

BRIEF-U.S. FDA Accepts Supplemental Biologics License Application For Opdivo In Previously Treated Patients With Small Cell Lung Cancer

April 18 (Reuters) - Bristol-Myers Squibb Co:

* U.S. FOOD AND DRUG ADMINISTRATION ACCEPTS SUPPLEMENTAL BIOLOGICS LICENSE APPLICATION FOR OPDIVO (NIVOLUMAB) IN PREVIOUSLY TREATED PATIENTS WITH SMALL CELL LUNG CANCER AND GRANTS PRIORITY REVIEW

* BRISTOL-MYERS SQUIBB - OPDIVO SUBMISSION BASED ON SAFETY AND EFFICACY DATA FROM SCLC COHORT OF PHASE 1/2 CHECKMATE -032 TRIAL Source text for Eikon: Further company coverage:

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