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FDA OKs Leuprolide Mesylate 3-Month Formulation in Advanced Prostate Cancer
FDA OKs Leuprolide Mesylate 3-Month Formulation in Advanced Prostate Cancer

August 29th 2025

Results from a phase 3 trial led to the approval of leuprolide mesylate as a 3-month formulation for patients with advanced prostate cancer.

Developers are enrolling those with metastatic castration-resistant prostate cancer on a phase 1/2 trial to assess the safety and tolerability of HLD-0915.
HLD-0915 Earns FDA Fast Track Designation in Metastatic CRPC

August 14th 2025

The FDA has accepted a new drug application for the prostate-specific membrane antigen PET imaging agent.
FDA Accepts NDA for New Formulation of PSMA PET Injection in Prostate Cancer

August 7th 2025

Developers plan to initiate a phase 2b trial in patients with less severe prostate cancer variants to better assess INKmune’s antitumor effects.
INKmune Exhibits Favorable Safety in Metastatic CRPC

August 4th 2025

Findings from the phase 3 TALAPRO-2 trial showed that the safety profile of talazoparib was consistent with its known profile in metastatic CRPC.
Talazoparib Combo Significantly Improves Overall Survival in Metastatic CRPC

August 1st 2025

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