Procept Biorobotics CorpFDA IDE approval for a second randomized study and completion of WATER IV enrollment are positive regulatory and clinical milestones.

PROCEPT BioRobotics received FDA approval for an Investigational Device Exemption for a second randomized study evaluating Aquablation therapy against active surveillance, and completed patient enrollment in the randomized WATER IV trial comparing Aquablation therapy with radical prostatectomy. The first randomized WATER IV trial, which included 280 intended patients, compared Aquablation treatment with radical prostatectomy, and the company expects to present primary endpoint data at the American Urological Association Annual Meeting in spring 2027. Both randomized WATER IV procedures will track patients for ten years to assess quality of life and disease control. Separately, Leerink downgraded the stock from Outperform to Market Perform with a $29 price target, implying over 33% upside potential.
Procept Biorobotics CorpFDA IDE approval for a second randomized study and completion of WATER IV enrollment are positive regulatory and clinical milestones.