By Olivia Bugault 
 

Novartis AG said Tuesday that its Phase 3 Belinda study assessing the efficacy and safety of Kymriah cell therapy as a second-line treatment for lymphoma compared with another standard treatment failed to meet its primary endpoint.

The primary endpoint "of event-free survival for patients with aggressive B-cell non-Hodgkin lymphoma who had primary refractory disease or who relapsed within 12 months of first-line treatment" wasn't met, the Swiss pharma said.

 

Write to Olivia Bugault at olivia.bugault@wsj.com

 

(END) Dow Jones Newswires

August 24, 2021 01:46 ET (05:46 GMT)

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