- Novartis AG's NVS Kymriah (tisagenlecleucel) CAR-T therapy failed to meet its primary endpoint of event-free survival in a Phase 3 study in aggressive B-cell non-Hodgkin lymphoma (NHL).
- The BELINDA study included patients after relapse or lack of response to first-line treatment.
- The safety profile was consistent with the established safety profile of Kymriah.
- Novartis will complete a full evaluation of the BELINDA study data.
- Price Action: NVS shares are down 1.05% at $92.77 during the premarket session on the last check Tuesday.
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