Lantheus wins final FDA approval for BRAVNETSA radiopharmaceutical in GEP-NETs
LNTH•Final FDA approval for BRAVNETSA
Lantheus won final FDA clearance for BRAVNETSA (lutetium Lu 177 dotatate) to treat adult somatostatin receptor-positive GEP-NETs.
LNTH•Lantheus won final FDA clearance for BRAVNETSA (lutetium Lu 177 dotatate) to treat adult somatostatin receptor-positive GEP-NETs.
FDA deemed BRAVNETSA bioequivalent and therapeutically equivalent to Novartis’ LUTATHERA, enabling substitution under the ANDA pathway.