Profound Medical Says Growing Body Of Clinical Evidence Points To The Potential Of TULSA Procedure Becoming A Mainstream Treatment Modality Across The Entire Prostate Disease Spectrum

— So far this year alone, 25 TULSA-related scientific research presentations have been delivered at major medical meetings around the world —

 

— Of those, eight (8) presentations were from leading urologists at AUA 2024 —

— Clinical evidence continues to highlight TULSA's ability to treat an unrivalled variety of patients with localized prostate cancer and/or BPH —

TORONTO, May 06, 2024 (GLOBE NEWSWIRE) -- Profound Medical Corp. (NASDAQ:PROF, TSX:PRN) ("Profound" or the "Company"), a commercial-stage medical device company that develops and markets customizable, incision-free therapies for the ablation of diseased tissue, is pleased to announce that a total of 25 paper, poster and podium presentations highlighting the Transurethral Ultrasound Ablation ("TULSA") procedure's ability to effectively, safely and efficiently treat an unrivaled variety of prostate cancer and/or benign prostatic hyperplasia ("BPH") patients have been made at major medical meetings already in 2024.

"The TACT 5-year clinical trial data, along with multiple real-world reports on the safety, efficacy and durability of TULSA from U.S. commercial centers, such as Mayo Clinic in Florida, Busch Center in Georgia, and UT Southwestern Medical Center in Texas, as well as international user sites, like Sapporo Hokuyu Hospital in Japan, ALTA Klinik in Germany, and Turku University Hospital in Finland, add to the growing body of evidence supporting the potential of TULSA as a mainstream treatment for prostate disease," said Arun Menawat, Profound's CEO and Chairman.

Of the 25 TULSA presentations delivered year-to-date, five were given at the European Congress of Radiology (ECR) (February 29-March 3; Vienna, Austria), one at the Annual Meeting of the Southeastern Section of the American Urological Association ("AUA") (March 20-23; Austin, TX), three at the Society of Interventional Radiology (SIR) Annual Scientific Meeting (March 23-28; Salt Lake City, UT), five at the Annual European Association of Urology (EAU) Congress (April 5-8; Paris, France), one at the Society of Abdominal Radiology (SAR) Annual Meeting (April 14-19; Hollywood, FL), one at the Japanese Urological Association (JUA) Annual Meeting (April 25-27; Kobe, Japan), one at the American Roentgen Ray Society (ARRS) Annual Meeting (May 5-9; Boston, MA), and eight at the AUA's Annual Meeting in San Antonio, TX, which just concluded today.

"The various presentations made at AUA and other major medical conferences have highlighted TULSA's clinical use across the entire prostate disease spectrum; ranging from low-, intermediate-, or high-risk prostate cancer; to hybrid patients suffering from both prostate cancer and BPH; to men with BPH only; and also, to patients requiring salvage therapy for radio-recurrent localized prostate cancer," added Dr. Menawat. "Importantly, real-world data from top institutions is also consistently demonstrating similar outcomes to the TACT FDA regulatory study. We would like to take this opportunity to thank the many esteemed researchers and clinicians who have contributed to the growing awareness of TULSA among urologists, both at home and abroad, and look forward to continuing to build on that positive momentum as the year progresses."