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European Commission approves Opdivo as adjuvant treatment for esophageal or gastroesophageal junction cancer patients with residual pathologic disease following chemoradiotherapy.- BMS

Read time: 1 mins
Last updated:1st Aug 2021
Published:1st Aug 2021
Bristol Myers Squibb announced that the European Commission (EC) has approved Opdivo (nivolumab) for the adjuvant treatment of adult patients with esophageal or gastroesophageal junction (GEJ) cancer who have residual pathologic disease following prior neoadjuvant chemoradiotherapy (CRT).
Condition: Gastric /Junction/Esophageal Adenocarcinoma
Type: drug
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