Bristol-Myers' Opdivo-Yervoy NSCLC Application In EU Withdrawn

 | Feb 03, 2020 05:42AM ET

Bristol-Myers Squibb Company (NYSE:BMY) announced the withdrawal of its application in the European Union (EU) for the combination of anti-PD-1 antibody Opdivo (nivolumab) and Yervoy (ipilimumab) for the treatment of advanced non-small cell lung cancer (NSCLC) based on data from the CheckMate-227 study. The application was initially filed in 2018 for patients with first-line NSCLC, who have tumor mutational burden.

However, the application was later amended to include the statistically significant overall survival data, a co-primary endpoint, from CheckMate-227 Part 1a, evaluating Opdivo plus Yervoy versus chemotherapy in patients whose tumors expressed PD-L1 ≥1%

Per the company, Europe's Committee for Medicinal Products for Human Use (CHMP) stated that it was not possible to assess the data provided by the company because of "multiple protocol changes" it made in the study.

Bristol-Myers has no intention of refiling the application anytime soon. In January 2020, the FDA granted a Priority Review for the combination of Opdivo and Yervoy for the treatment of first-line NSCLC based on data from Part 1 of the phase III CheckMate -227 study.

Shares of Bristol-Myers have rallied 24.7% in the past year, outperforming the industry’s growth of 10.2%.