European Commission Approves Opdivo Regimen for Treatment of High-Risk Non-Small Cell Lung Cancer, Announce ONO Pharmaceutical and Bristol Myers Squibb

Reuters
19 May
European Commission Approves Opdivo Regimen for Treatment of High-Risk Non-Small Cell Lung Cancer, Announce ONO Pharmaceutical and Bristol Myers Squibb

ONO Pharmaceutical Co. Ltd., in partnership with Bristol Myers Squibb, has received approval from the European Commission for a new perioperative regimen involving the use of Opdivo® (nivolumab) in combination with chemotherapy, followed by adjuvant Opdivo for the treatment of resectable, high-risk non-small cell lung cancer with PD-L1 expression levels of 1% or more. This approval marks a significant advancement in the treatment options available for patients with this type of lung cancer, supporting ONO Pharmaceutical and Bristol Myers Squibb's ongoing efforts to improve cancer care.

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