Procept BioRobotics (PRCT) enrolled 280 patients in the WATER IV study evaluating its Aquablation therapy against radical prostatectomy for prostate cancer.
The company said Thursday it expects to present the primary endpoint results from the study at the American Urological Association annual meeting in spring 2027.
Procept also received Investigational Device Exemption approval from the US Food and Drug Administration for a second randomized protocol comparing Aquablation therapy with active surveillance in men with Grade Group 1 and 2 prostate cancer. The study will enroll up to 333 patients globally, the company said.
Both studies will follow patients for 10 years to assess disease control and quality-of-life outcomes, Procept said.
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