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West Cancer Center Receives IRB Approval to Commence IceCure's ChoICE Study for Breast Cancer Cryoablation

(Very Positive)
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IceCure Medical (NASDAQ: ICCM) reported that the Institutional Review Board of West Cancer Center & Research Institute in Germantown, Tennessee has approved the Company’s post-marketing ChoICE Study evaluating ProSense® cryoablation for the local treatment of low-risk breast cancer, enabling patient enrollment in the coming weeks.

ProSense® is the first and only device with U.S. FDA marketing authorization for local treatment of low-risk breast cancer with endocrine therapy in women aged 70 and above. Prior ICE3 trial results showed a 3.1% local recurrence rate and very high cosmetic satisfaction among patients and physicians, which supported this authorization.

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Positive

  • IRB approval for ChoICE Study enables patient enrollment at West Cancer Center
  • ICE3 trial showed 3.1% local recurrence in early-stage, low-risk breast cancer
  • ProSense® reported 99.1% patient and 97% physician cosmetic satisfaction in survey
  • ProSense® is the first and only FDA-authorized device for local treatment of low-risk breast cancer with endocrine therapy in women 70+

Negative

  • None.

Market Reaction – ICCM

+2.44% $2.58 605.9x vol
15m delay
+2.44% Vs previous close
+13.6% Peak Tracked
-12.0% Trough Tracked
$2.58 Last Price
$2.37 $3.60 Day Range
$8.85M Market Cap
605.9x Rel. Volume

Following this news, ICCM has gained 2.44%, reflecting a moderate positive market reaction. Argus tracked a peak move of +13.6% during the session. Argus tracked a trough of -12.0% from its starting point during tracking. Our momentum scanner has triggered 18 alerts so far, indicating notable trading interest and price volatility. The stock is currently trading at $2.58. Trading volume is exceptionally heavy at 605.9x the average, suggesting very strong buying interest.

Data tracked by StockTitan Argus (15 min delayed). Upgrade to Gold for real-time data.

Market Context

The active F-3 resale registration covers up to 5,500,002 ordinary shares, according to the platform...
Analysis

The active F-3 resale registration covers up to 5,500,002 ordinary shares, according to the platform. That financing context complements this study update; key watchpoints are enrollment execution and subsequent real-world evidence.

Key Figures

Patient age: 70 years and above Local recurrence: 3.1% Patient satisfaction: 99.1% +1 more
4 metrics
Patient age 70 years and above FDA-authorized low-risk breast cancer treatment population
Local recurrence 3.1% ICE3 clinical trial in early-stage, low-risk breast cancer
Patient satisfaction 99.1% Reported satisfaction with cosmetic outcomes
Physician satisfaction 97% Reported satisfaction with cosmetic outcomes

Historical Context

5 past events · Latest: Aug 13 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Aug 13 Clinical publications Positive -3.4% Peer-reviewed publications supported breast cancer cryoablation and cited five-year ICE3 outcomes.
Aug 12 First-half earnings Negative -11.5% Revenue growth accompanied by a wider net loss and increased operating expenses.
Aug 06 Study site approval Positive -4.0% Adventist Health Glendale became the first U.S. site able to enroll patients.
Aug 05 Earnings date notice Neutral +2.6% The company scheduled release of first-half financial and operating results.
Jul 29 Guideline petition Positive +3.2% SIO petitioned NCCN to add cryoablation as an option for selected patients.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent positive clinical and corporate news often preceded negative 24-hour reactions, while the July 29 regulatory-related update aligned with a positive reaction.

Key Terms

irb, post-marketing study, cryoablation, endocrine therapy
4 terms
irb regulatory
"approval from the Institutional Review Board of West Cancer Center"
An Institutional Review Board (IRB) is an independent committee that reviews and approves medical and behavioral research involving people to ensure safety, informed consent, and ethical treatment—think of it as a safety inspector for studies. For investors, IRB decisions matter because their approval or requests for changes can speed up, delay, or halt clinical trials and other studies, directly affecting timelines, costs, and the value of companies developing treatments.
post-marketing study regulatory
"has granted approval for the Company's post-marketing study"
A post-marketing study is research conducted after a drug or medical device is approved and sold to check how it performs in everyday use, tracking long-term safety, side effects, and effectiveness. For investors it matters because results can change sales forecasts, trigger label updates or warnings, lead to additional costs or legal exposure, or open new markets — like a car recall study revealing issues that affect a maker’s reputation and future earnings.
cryoablation medical
"ProSense® cryoablation in the local treatment of low-risk breast cancer"
A medical treatment that uses extreme cold to freeze and destroy unwanted tissue, such as small tumors or heart tissue causing irregular rhythms; think of it like applying a focused freezer to stop a problem spot without cutting it out. It matters to investors because devices, tools, and drugs tied to cryoablation, plus clinical results, approval status and insurance coverage, can drive sales, shape market adoption and affect the financial outlook of healthcare companies.
endocrine therapy medical
"low-risk breast cancer with endocrine therapy in women aged 70 and above"
Endocrine therapy is a medical treatment that reduces or blocks hormones that help certain tumors grow, for example by lowering production of the hormone or preventing it from attaching to cancer cells. Think of it as cutting off the fuel supply to slow or stop growth. Investors care because these therapies drive sales, long-term treatment demand, regulatory milestones and clinical trial outcomes that directly affect healthcare companies’ revenues and valuations.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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Patients are expected to enroll in the post-marketing study in the coming weeks, following approval from the Institutional Review Board of West Cancer Center & Research Institute in Germantown, TN

CAESAREA, Israel, Aug. 20, 2026 /PRNewswire/ -- IceCure Medical Ltd. (NASDAQ: ICCM) ("IceCure," "IceCure Medical" or the "Company"), developer of minimally-invasive cryoablation technology that destroys tumors by freezing as an option to surgical tumor removal, today announced that the Institutional Review Board (JHM-IRB) of West Cancer Center & Research Institute in Germantown, Tennessee, has granted approval for the Company's post-marketing study ("ChoICE Study") for ProSense® cryoablation in the local treatment of low-risk breast cancer.

IceCure Medical Logo

The approval advances the study and enables patient enrollment, which is expected in the coming weeks. ProSense® is the first and only medical device to be granted U.S. Food and Drug Administration ("FDA") marketing authorization for the local treatment of low-risk breast cancer with endocrine therapy in women aged 70 and above.

The successful results from the Company's ICE3 clinical trial demonstrated that ProSense® cryoablation followed by endocrine therapy achieved a 3.1% rate of local recurrence in women with early-stage, low-risk breast cancer. 99.1% of patients and 97% of physicians that responded to a survey reported high rates of satisfaction with the cosmetic outcomes. These results supported the FDA's marketing authorization for ProSense® in appropriately selected patients aged 70 years and above.

The ChoICE Study builds on the Company's clinical leadership in breast cancer cryoablation, demonstrating its ongoing commitment to advancing evidence-based care for leading cancer diagnosis in women globally.

The site will be led by Dr. Richard Gilmore, MD, MBA, DipABLM, a breast surgical oncologist at the Margaret West Comprehensive Breast Center, part of West Cancer Center & Research Institute.

About the ChoICE Study

The ChoICE Study will be evaluating ProSense® cryoablation with endocrine therapy for low-risk, early-stage breast cancer in patients aged 70 years and older.

ProSense® is cleared by the FDA for the local treatment of breast cancer in patients aged 70 years and older with biologically low-risk tumors ≤1.5 cm in size who are treated with adjuvant endocrine therapy, including patients who are not eligible for surgery. The ChoICE Study aims to generate additional real-world data regarding the use of ProSense® in this indication.

Under the approved study design, 30 participating sites will serve both as ChoICE Study centers and as active commercial sites, enabling them to enroll a total of 400 patients while also offering ProSense® cryoablation to appropriate patients who are not participating in the ChoICE Study. This dual pathway expands access to breast cancer cryoablation and reflects increasing interest from eligible patients seeking a minimally invasive alternative outside the trial setting.

About IceCure Medical

IceCure Medical (NASDAQ: ICCM) develops and markets advanced liquid-nitrogen-based cryoablation therapy systems for the destruction of tumors (benign and cancerous) by freezing, with the primary focus areas being breast, kidney, bone and lung cancer. Its minimally invasive technology is a safe and effective option to surgical tumor removal that is easily performed in a relatively short procedure. The Company's flagship ProSense® system is marketed and sold worldwide for the indications cleared and approved to date including in the U.S., Europe, and Asia.

About West Cancer Center & Research Institute

West Cancer Center & Research Institute has proudly served the Mid-South for 47 years and continues as the leader in adult cancer care. Recognized for their talented team of oncology specialists, state-of-the-art technology, robust clinical trial program and personalized approach to care, West is committed to achieving the most positive outcomes and preserving quality of life.

Investor Contact

Meir Peleg
investors@icecure-medical.com
+1-888-902-5716

Site Contact:

To see if you qualify for the ChoICE trial, please contact to schedule an appointment:

Margaret West Comprehensive Breast Center
+1-901-692-9600

Forward Looking Statements

This press release contains "forward-looking statements" within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, that are intended to be covered by the "safe harbor" created by those sections. Forward-looking statements, which are based on certain assumptions and describe our future plans, strategies and expectations, can generally be identified by the use of forward-looking terms such as "believe," "expect," "may," "should," "could," "seek," "intend," "plan," "goal," "estimate," "anticipate" or other comparable terms. For example, the Company is using forward-looking statements when it discusses: expected patient enrollment in the ChoICE Study in the coming weeks; the goals and aims of the ChoICE Study; the enrollment and treatment of patients across 30 participating sites; and that West Cancer Center & Research Institute is committed to achieving the most positive outcomes and preserving quality of life. Historical results of scientific research and clinical and preclinical trials do not guarantee that the conclusions of future research or trials will suggest identical or even similar conclusions. Important factors that could cause actual results, developments and business decisions to differ materially from those anticipated in these forward-looking statements include, among others: the Company's planned level of revenues and capital expenditures; the Company's available cash and its ability to obtain additional funding; the Company's ability to market and sell its products; legal and regulatory developments in the United States and other countries; the Company's ability to maintain its relationships with suppliers, distributors and other partners; the Company's ability to maintain or protect the validity of its patents and other intellectual property; the Company's ability to expose and educate medical professionals about its products; political, economic and military instability in the Middle East, specifically in Israel; as well as those factors set forth in the Risk Factors section of the Company's Annual Report on Form 20-F for the year ended December 31, 2025 filed with the SEC on March 17, 2026, and other documents filed with or furnished to the SEC which are available on the SEC's website, www.sec.gov. The Company undertakes no obligation to update these statements for revisions or changes after the date of this release, except as required by law.

 

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SOURCE IceCure Medical

FAQ

What did IceCure Medical (NASDAQ: ICCM) announce about the ChoICE Study at West Cancer Center?

IceCure Medical announced IRB approval at West Cancer Center to begin its ChoICE post-marketing study of ProSense® cryoablation. According to IceCure Medical, this approval allows patient enrollment at the Germantown, Tennessee site in the coming weeks for low-risk breast cancer treatment evaluation.

What are the key ICE3 clinical trial results supporting IceCure Medical’s ProSense® device (ICCM)?

ICE3 trial results showed ProSense® cryoablation followed by endocrine therapy achieved a 3.1% local recurrence rate in early-stage, low-risk breast cancer. According to IceCure Medical, 99.1% of patients and 97% of surveyed physicians reported high satisfaction with cosmetic outcomes, supporting FDA marketing authorization.

How is ProSense® by IceCure Medical (ICCM) authorized by the FDA for breast cancer treatment?

ProSense® holds U.S. FDA marketing authorization for local treatment of low-risk breast cancer with endocrine therapy in women aged 70 and above. According to IceCure Medical, ICE3 trial outcomes and high cosmetic satisfaction supported this authorization for appropriately selected older patients.

Who is leading IceCure Medical’s ChoICE Study site at West Cancer Center for ICCM’s ProSense®?

The ChoICE Study site at West Cancer Center will be led by Dr. Richard Gilmore, a breast surgical oncologist at the Margaret West Comprehensive Breast Center. According to IceCure Medical, this center is part of West Cancer Center & Research Institute in Germantown, Tennessee.

What does the ChoICE Study mean for the clinical adoption of IceCure Medical’s ProSense® (ICCM)?

The ChoICE Study is a post-marketing study designed to build on existing clinical data for ProSense® in low-risk breast cancer. According to IceCure Medical, it reflects an ongoing commitment to evidence-based care in breast cancer cryoablation, potentially informing broader clinical practice.