IceCure Medical gets IRB approval for ProSense breast cancer study
IceCure Medical Ltd. secured Institutional Review Board approval from West Cancer Center & Research Institute for its ChoICE Study. The post-marketing study evaluates ProSense cryoablation for low-risk breast cancer in women aged 70 and above. Patient enrollment is scheduled to begin shortly following the regulatory clearance.

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IceCure Medical Ltd. (NASDAQ: ICCM) announced on Aug. 20, 2026, that the Institutional Review Board (JHM-IRB) of West Cancer Center & Research Institute in Germantown, Tennessee, has granted approval for its post-marketing study for ProSense cryoablation.
The approval enables patient enrollment for the ChoICE Study, which is expected to commence in the coming weeks. The study focuses on the local treatment of low-risk breast cancer using the company's minimally-invasive cryoablation technology.
ProSense is the first and only medical device to receive U.S. Food and Drug Administration marketing authorization for the local treatment of low-risk breast cancer with endocrine therapy in women aged 70 and above.
Study Details
The ChoICE Study aims to evaluate ProSense cryoablation as an alternative to surgical tumor removal. The technology destroys tumors by freezing them.
| Detail | Information |
|---|---|
| Study Name | ChoICE Study |
| Location | West Cancer Center & Research Institute, Germantown, TN |
| Approval Body | JHM-IRB |
| Device | ProSense cryoablation |
| Indication | Local treatment of low-risk breast cancer |
How might the successful enrollment and results of the ChoICE Study influence insurance coverage policies for cryoablation in low-risk breast cancer cases?
What is the projected timeline for IceCure Medical to expand the ChoICE Study to additional clinical sites beyond West Cancer Center?
Could the adoption of ProSense cryoablation as a standard alternative to surgery significantly reduce healthcare costs associated with breast cancer treatment?































