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New data on Opdivo (nivolumab) indicate benefit in classical hodgkin lymphoma patients

  • Bristol-Myers Squibb Company (NYSE:BMY) announced results from CheckMate -205, a multi-cohort, non-comparative, single-arm, Phase 2 registrational trial evaluating Opdivo (nivolumab) in patients with classical Hodgkin lymphoma (cHL). These results, from cohort B of the trial, included patients who had relapsed or progressed after autologous hematopoietic stem cell transplantation (auto-HSCT) and post-transplantation brentuximab vedotin (n=80).
  • The primary endpoint of objective response rate (ORR) per an independent radiologic review committee (IRRC) was 66.3% (95% CI: 54.8-76.4). Median time to response was 2.1 months, and estimated median duration of remission was 7.8 months (95% CI: 6.6-NE). The majority of responses (62.3%) were ongoing at the time of analysis.
  • Source: Press Release

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