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New Data on Bristol-Myers Squibb’s Opdivo (nivolumab) Indicate Benefit in Heavily Pre-Treated Classical Hodgkin Lymphoma Patients in Phase 2, Single-Arm Pivotal Trial

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BMY

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Additional Relevant Details
Opdivo demonstrated objective response rate of 66.3% in classical Hodgkin lymphoma patients who had relapsed or progressed after auto-HSCT and subsequent brentuximab vedotin, as assessed by an independent radiologic review committee
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Catalyst Date
Occurred on:
Jun 10, 2016
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Related Keywords Nivolumab, Opdivo, Hodgkin Lymphoma, Brentuximab Vedotin