XTANDI: the first and only androgen receptor inhibitor-based regimen to demonstrate overall survival benefit in non-metastatic hormone-sensitive prostate cancer (nmHSPC) with high-risk biochemical ...
The FDA approved updated labeling for Talzenna plus Xtandi for HRR gene-mutated metastatic castration-resistant prostate cancer, based on the TALAPRO-2 trial results. The TALAPRO-2 trial showed a ...
The probability of survival at 8 years was an unprecedented 78.9% with XTANDI plus leuprolide versus 69.5% with leuprolide, in men with non-metastatic hormone-sensitive prostate cancer with high-risk ...
At the 2026 American Society of Clinical Oncology (ASCO) annual congress, Pfizer presented top line data for the Phase III TALAPRO-3 clinical trial, which is evaluating the poly(ADP-ribose) polymerase ...
Xtandi, which was earlier approved for the treatment of patients with metastatic castration-resistant prostate cancer (:CRPC) who had previously received docetaxel (chemotherapy), can now be used in ...
Pfizer Inc. (NYSE: PFE) and Astellas Pharma U.S. Inc. (Head of Commercial: Mike Petroutsas, "Astellas") today announced final overall survival (OS) results from the Phase 3 EMBARK study evaluating ...
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