PLUVICTO® is now approved in combination with ARPI therapy for patients with PSMA+ metastatic hormone-sensitive prostate cancer (mHSPC)1
PLUVICTO is the first and only FDA-approved, PSMA-targeted therapy to significantly delay progression in mHSPC and mCRPC.1
In PSMA+ mHSPC and PSMA+ mCRPC,
Choose PLUVICTO at the earliest eligible opportunity
PLUVICTO: For your patients across the continuum of metastatic prostate cancer
*For patients considered appropriate to delay taxane-based chemotherapy.1
Choose PLUVICTO: Proven in three phase 3 clinical trials.† And ~30K patients treated since FDA approval.1-5,‡
ARPI, androgen receptor pathway inhibitor; mAPMN/S PC, metastatic androgen pathway modulation-naive or -sensitive prostate cancer; mAPMR PC, metastatic androgen pathway modulation-resistant prostate cancer; mCRPC, metastatic castration-resistant prostate cancer; PSMA, prostate-specific membrane antigen; PSMA+, PSMA positive.
†PLUVICTO was studied in 1 clinical trial of mHSPC and 2 clinical trials of mCRPC.1,3,4
‡Based on data from March 2026.5


