August 03, 2026
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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
August 03, 2026
2 min read
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It’s an important nod for Novartis, which has bet big on the radiopharmaceutical industry. The approval nearly doubles the…

FDA approves Novartis' Pluvicto for earlier-stage metastatic prostate cancer, nearly doubling eligible patients.

Novartis's Pluvicto was approved by the Food and Drug Administration for use in combination with an androgen receptor pathway…

Novartis India has launched Pluvicto, the nation's first approved radioligand therapy for eligible prostate cancer patients. This…

Novartis launches Pluvicto, India's first approved radioligand therapy for advanced prostate cancer, enhancing precision oncology…

Novartis launches Pluvicto, India's first approved radioligand therapy for advanced prostate cancer, enhancing precision oncology…