The FDA has expanded approval for a radioligand therapy that nearly doubles the number of men with advanced prostate cancer eligible to receive the treatment, according to a Novartis press release.Men with prostate-specific membrane antigen (PSMA)-positive metastatic hormone-sensitive prostate cancer can now use lutetium Lu-177 vipivotide tetraxetan (Pluvicto, Novartis) in combination with an

The FDA has expanded approval for a radioligand therapy that nearly doubles the number of men with advanced prostate cancer eligible to receive the treatment, according to a…

Novartis’ blockbuster radioligand therapy Pluvicto has cleared a key milestone on its quest to hit $5 billion in peak sales, securing a U.S. | Novartis’ blockbuster radioligand…