FDA lifts hold on Corautus Genetics angina trial
The FDA notified the clinical stage biopharmaceutical company that it has satisfactorily addressed the majority of the issues raised in the March 29, 2006 clinical hold letter and
The European Commission (EC) has approved an extended use of Johnson & Johnson’s Tecvayli (teclistamab), along with daratumumab, to treat adult patients with relapsed or refractory multiple myeloma (r/r MM).