Prostate Cancer

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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

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.

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

No dose-limiting toxicities or unexpected adverse effects occurred with carotuximab/apalutamide in metastatic castration-resistant prostate cancer.
Carotuximab/Apalutamide Shows Tolerability in Metastatic CRPC

July 16th 2025

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The Prostate Cancer Intervention Versus Observation Trial (PIVOT)

August 1st 1997

The Prostate Cancer Intervention Versus Observation Trial (PIVOT) is a randomized trial designed to determine whether radical prostatectomy or expectant management provides superior length and quality of life for men with clinically localized prostate cancer. Conducted at Department of Veterans Affairs and National Cancer Institute medical centers, PIVOT will enroll over 1,000 individuals less than 75 years of age. The primary study end point is all-cause mortality. Secondary outcomes include prostate cancer- and treatment-specific morbidity and mortality, health status, predictors of disease-specific outcomes, and cost-effectiveness. Within the first 3 years of enrollment, over 400 men have been randomized. Early analysis of participants' baseline characteristics indicate that enrollees are representative of men diagnosed with clinically localized prostate cancer throughout the United States. Therefore, results of PIVOT will be generalizable. These results are necessary in order to determine the preferred therapy for clinically localized prostate cancer. [ONCOLOGY 11(8):1133-1143, 1997]