Plus, news about Enveric Biosciences and Kazia Therapeutics:
Johnson & Johnson’s bispecific gets a new dosing schedule: The FDA approved a reduced dosing regimen for J&J’s multiple myeloma bispecific antibody Tecvayli, the pharma company announced Tuesday evening. The reduced dosing approval comes as the drug’s side effects, such as cytokine release syndrome and serious infections, are substantial. The treatment is approved for multiple myeloma patients who have received four prior lines of therapy, but now those who have been in remission for at least six months can move down from a weekly to a biweekly dosing schedule. — Lei Lei Wu
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