Novartis Kymriah
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Phase III BELINDA study did not meet 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
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Kymriah demonstrated strong response rates and a remarkable safety profile in relapsed or refractory follicular lymphoma, with regulatory filings on track for second half of 2021