Prostate Ca assay appears similarly predictive of adverse pathology in African American, Caucasian patients

The Contouring Assistant now marks Profound Medical’s second FDA-cleared TULSA-AI module.

In this podcast episode, Adam B. Murphy, MD, MBA, MSCI, discusses the need to increase diversity in clinical trials, specifically focusing on studies in prostate cancer.

The FDA is set to have a decision regarding the subcutaneous nivolumab formulation on or by February 28, 2025.

Zeyad Schwen, MD, a urologic oncologist at Cleveland Clinic, discusses how patient factors and cancer characteristics are key to deciding between focal therapies and whole gland treatment for prostate cancer.

The test, which was launched in Canada in September 2023, is available through Nanostics’ accredited laboratory in Edmonton, Alberta.

All patients have been successfully dosed in the first cohort of patients, and the Safety Review Committee has granted approval for progression of the study to the second dose level of INKmune.