Tuesday, December 15, 2020 9:53:04 AM
The U.S. regulator has slapped a partial clinical hold on odronextamab, a CD20xCD3 bispecific antibody in tests for B-cell non-Hodgkin lymphoma (B-NHL), after the FDA said the company has to “further reduce the incidence of Grade 3 cytokine release syndrome (CRS),” a not uncommon safety issue in certain blood cancer trials but one that can be fatal.
This will see Regeneron pause new enrollment in the trial, allow treatment to continue for enrolled patients if they re-consent and send off a new protocol amendment to FDA, with the “goal of resuming patient enrollment in the first quarter of 2021.”
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