Alpha Tau Medical Ltd. has received FDA approval for an Investigational Device Exemption $(IDE)$ to initiate a pilot study of its Alpha DaRT technology for patients with locally recurrent prostate cancer. This marks the company's fifth active IDE in the United States. The clinical trial will enroll up to 12 U.S. patients to primarily evaluate the safety of the treatment, with secondary objectives assessing efficacy through biochemical and clinical measures of disease progression and overall survival. No funding or grant from other organizations was mentioned.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Alpha Tau Medical Ltd. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9594947-en) on December 02, 2025, and is solely responsible for the information contained therein.
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