The FDA has told Regeneron to hit the brakes on its experimental blood cancer drug trial over safety concerns.
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.
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