The European Commission (EC) has granted approval for Bristol Myers Squibb’s (BMS) Opdivo (nivolumab) in combination with the ...
The EC approves BMY's combination of Opdivo and Yervoy for the first-line treatment of adult patients with unresectable or ...
The FDA’s Oncologic Drugs Advisory Committee recently voted to narrow the label for checkpoint inhibitors Keytruda and Opdivo ...
European Commission approves Bristol Myers Squibb’s Opdivo plus Yervoy for first-line treatment of adult patients with unresectable or advanced HCC: Princeton, New Jersey Monday ...
CheckMate-816 is a randomized, open-label, multi-center trial which is evaluating the efficacy of Opdivo in combination with chemotherapy versus chemotherapy alone as a neoadjuvant treatment for ...
Replacing transplant and chemo with CI-based therapy and ISRT maintains survival, reduces side effects in younger patients ...
Bristol-Myers Squibb Company (NYSE:BMY) 45th Annual TD Cowen Health Care Conference March 4, 2025 2:30 PM ETCompany ParticipantsAdam Lenkowsky - ...
It covers all indications on the current Opdivo label for adults with solid tumours, including as monotherapy, for maintenance following completion of the checkpoint inhibitor plus Yervoy ...