STOCK TITAN

IceCure Medical Adds Adventist Health as U.S. Clinical Site for its Post-Marketing "ChoICE" Study for Low-Risk Breast Cancer Cryoablation Treatment

(Very High)
(Very Positive)
Tags

IceCure Medical (Nasdaq: ICCM) announced that Adventist Health Glendale in California has signed an agreement and received Institutional Review Board (IRB) approval to become the first U.S. clinical site able to enroll patients in the post-marketing ChoICE Study of ProSense® for local treatment of low-risk breast cancer, following FDA marketing authorization in October 2025.

According to IceCure Medical, the ChoICE Study is planned to enroll up to 400 patients across multiple U.S. sites to collect real-world data that may support clinical adoption and broader access. The Adventist Health Glendale site will be led by breast surgeon Dr. Dennis Holmes, MD, FACS, described as a recognized authority and leading researcher in breast cancer cryoablation, with a focus on minimally invasive options for carefully selected, typically older patients with low-risk, early-stage disease.

Loading...
Loading translation...

Positive

  • First U.S. ChoICE Study site activated with agreement and IRB approval at Adventist Health Glendale
  • Planned enrollment of up to 400 patients across multiple U.S. sites for real-world ProSense® data
  • Site led by Dr. Dennis Holmes, described as a recognized authority in breast cancer cryoablation

Negative

  • None.

Market reaction after post-marketing clinical data: ICCM -4.05% in the Aug 6 session

-4.05%
5 alerts
-4.05% Session close to close
-12.5% Trough in 7 hr 16 min
$11.63M Market Cap
0.9x Rel. Volume

In the Aug 6 session, ICCM declined 4.05%, reflecting a moderate negative market reaction. Argus tracked a trough of -12.5% from its starting point during tracking. Our momentum scanner triggered 5 alerts that day, indicating moderate trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

The prior ChoICE-site announcement, news_id 1087138, was followed by a -6.49% reaction, offering a d...
Analysis

The prior ChoICE-site announcement, news_id 1087138, was followed by a -6.49% reaction, offering a direct historical comparison for this enrollment expansion. The active F-3 resale registration and low short positioning are additional factors to monitor.

Key Figures

Planned enrollment: up to 400 patients FDA marketing authorization: October 2025
2 metrics
Planned enrollment up to 400 patients ChoICE Study across multiple U.S. sites
FDA marketing authorization October 2025 ProSense® for local treatment of low-risk breast cancer

Historical Context

5 past events · Latest: Jul 27 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Jul 27 Post-marketing study launch Positive -6.5% West Cancer Center agreement initiated first U.S. ChoICE Study clinical site
Jul 06 FDA authorization update Positive -14.0% Brazil adoption update followed prior FDA marketing authorization for low-risk breast cancer
Jun 25 Nasdaq compliance update Positive -24.5% Nasdaq confirmed 10 consecutive business days meeting minimum bid requirement
Jun 23 Clinical research publication Positive +3.2% Peer-reviewed article reported cryoablation advantages over radiofrequency ablation
Jun 17 Private placement Neutral +200.5% Private placement priced at $3.00 per share for $5.5 million gross proceeds

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

Pattern Detected

Positive corporate and clinical announcements in the record often coincided with negative reactions; one clinical-news event aligned positively.

Key Terms

institutional review board, post-marketing, cryoablation, endocrine therapy
4 terms
institutional review board regulatory
"received approval from the Institutional Review Board to become the first clinical site"
An institutional review board is an independent committee that reviews and approves research involving people to make sure studies are safe, ethical, and protect participants’ rights and privacy. For investors, IRB approval is a gatekeeper: it can determine whether a clinical trial can start or continue, affecting timelines, regulatory risk, cost and the credibility of trial results—similar to a safety inspector whose sign-off is required before work can proceed.
post-marketing regulatory
"become the first clinical site able to enroll patients for the Company's post-marketing"
Post-marketing describes the period after a drug, medical device, or other regulated product has been approved and is being sold to the public, during which companies and regulators monitor how it performs in real-world use. Like a car owner tracking performance and repairs after buying a new model, post-marketing activities — such as safety monitoring, additional studies, and reporting of side effects — matter to investors because they can reveal unexpected risks, trigger label changes, recalls, or costly follow-up studies that affect sales and valuation.
cryoablation medical
"developer of minimally-invasive cryoablation technology that destroys tumors by freezing"
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
"including follow-up assessment and adherence to endocrine therapy"
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.

See more from StockTitan in Google Search and AI answers. Adds StockTitan as a preferred source · opens Google
Add on Google

Adventist Health Glendale is the first site able to enroll patients in the ChoICE Study after signing both an agreement and receiving IRB approval

The site will be led by breast surgeon, Dr. Dennis Holmes, MD, FACS, a recognized leader in breast cancer cryoablation

CAESAREA, Israel, August 6, 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 Adventist Health Glendale in Glendale, California has signed an agreement and received approval from the Institutional Review Board to become the first clinical site able to enroll patients for the Company's post-marketing "ChoICE ," study (the "ChoICE Study"), for ProSense® in the local treatment of low-risk breast cancer following U.S Food and Drug Administration  ("FDA") marketing authorization in October 2025. The ChoICE Study will enroll up to 400 patients across multiple U.S. sites, gathering real-world data to support further clinical adoption and broader access for eligible patients.

IceCure Medical Logo

Adventist Health Glendale brings the ChoICE Study into an established hospital setting with breast cancer care expertise, supporting IceCure's goal of expanding real-world experience with ProSense® across leading U.S. clinical sites.

"We are pleased to welcome Dr. Dennis Holmes and Adventist Health Glendale to the ChoICE Study," said Eyal Shamir, Chief Executive Officer of IceCure Medical. "Adventist Health Glendale brings strong clinical infrastructure and breast care expertise, while Dr. Holmes brings deep leadership and research experience in breast cancer cryoablation. We believe this is an important milestone as we work with leading clinical teams across the U.S. to expand real-world experience with ProSense® and support broader access to minimally invasive cryoablation for eligible breast cancer patients."

"For some older patients with low-risk, early-stage breast cancer, treatment decisions must balance cancer control with quality of life, overall health, and personal goals," said Dr. Dennis Holmes, MD, FACS, breast surgeon at Adventist Health Glendale and leading researcher in the field of breast cancer cryoablation. "Cryoablation may offer a less invasive approach for carefully selected patients, and the ChoICE Study will help further evaluate its use in real-world clinical practice, including follow-up assessment and adherence to endocrine therapy. We are proud to help advance evidence that may expand appropriate treatment options for patients."

The ChoICE Trial builds on the Company's clinical leadership in breast cancer cryoablation, demonstrating its ongoing commitment to advancing evidence-based care for one of the most common cancer diagnoses among women globally. The Adventist Health Glendale site will be led by Dr. Dennis Holmes, MD, FACS, a breast surgeon and recognized authority in breast cancer cryoablation. Dr. Holmes has contributed extensively to the clinical evaluation of cryoablation for early-stage breast cancer. His research also includes published work on breast cancer cryoablation and its potential role in expanding minimally invasive local treatment options for appropriately selected patients.

About the ChoICE Study

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

ProSense® is cleared by the U.S. Food and Drug Administration ("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 sites and as active commercial sites, enabling them to enroll and treat 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 Adventist Health Glendale

 Adventist Health Glendale is a faith-based, nonprofit medical center that encompasses a 515-bed tertiary care hospital along with primary care and specialty care clinics. The hospital is nationally recognized for clinical excellence and patient safety. Award-winning services include oncology, cardiovascular medicine, neurosciences, pulmonology, gastroenterology, orthopedics, and more. For more than a century, Adventist Health Glendale has been committed to the well-being of the community with a focus on whole-person health.

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 Adventist Glendale Health serving as the first U.S. clinical site able to enroll patients for the ChoICE Study; the progress of the ChoICE Study; the enrollment and treatment of up to 400 patients across 30 U.S. clinical sites; the ability of participating sites to serve both as ChoICE Study centers and active commercial sites and to offer ProSense® cryoablation to eligible patients who are not participating in the ChoICE Study; the potential for the ChoICE Study and the resulting data to support clinical and commercial adoption of ProSense® and broader patient access; and the Company's efforts to expand real-world experience with ProSense® and access to minimally invasive cryoablation for eligible breast cancer patients. 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.

Investor Relations:

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

Logo - https://mma.prnewswire.com/media/2319310/IceCure_Medical_Logo.jpg

Cision View original content:https://www.prnewswire.com/news-releases/icecure-medical-adds-adventist-health-as-us-clinical-site-for-its-post-marketing-choice-study-for-low-risk-breast-cancer-cryoablation-treatment-302844865.html

SOURCE IceCure Medical

FAQ

What did IceCure Medical (ICCM) announce about the ChoICE Study on August 6, 2026?

IceCure Medical announced Adventist Health Glendale as the first U.S. site able to enroll patients in the post-marketing ChoICE Study. According to IceCure Medical, the study follows FDA marketing authorization of ProSense® in October 2025 and focuses on low-risk breast cancer cryoablation.

How many patients will IceCure Medical's ChoICE Study for ProSense® enroll in the U.S.?

The ChoICE Study is planned to enroll up to 400 patients across multiple U.S. sites. According to IceCure Medical, this real-world data is intended to support further clinical adoption of ProSense® and broader access for eligible low-risk breast cancer patients.

Who is leading the Adventist Health Glendale site in IceCure Medical's (ICCM) ChoICE Study?

The Adventist Health Glendale site will be led by breast surgeon Dr. Dennis Holmes, MD, FACS. According to IceCure Medical, Dr. Holmes is a recognized authority in breast cancer cryoablation with extensive research on minimally invasive treatment for early-stage breast cancer.

What is the focus of IceCure Medical’s ProSense® cryoablation in the ChoICE Study for ICCM shareholders?

The ProSense® cryoablation focus is local treatment of low-risk, early-stage breast cancer as a minimally invasive option. According to IceCure Medical, the ChoICE Study will evaluate real-world use, follow-up assessment, and adherence to endocrine therapy in carefully selected patients.

How does Adventist Health Glendale’s participation impact IceCure Medical’s ChoICE Study in the U.S.?

Adventist Health Glendale becomes the first U.S. site able to enroll ChoICE Study patients after agreement signature and IRB approval. According to IceCure Medical, the hospital adds established breast cancer care infrastructure and supports expanding real-world experience with ProSense®.

What type of breast cancer patients may be targeted in IceCure Medical’s (ICCM) ChoICE Study?

The ChoICE Study targets carefully selected patients with low-risk, early-stage breast cancer, often older individuals balancing treatment and quality of life. According to IceCure Medical and Dr. Holmes, cryoablation may offer a less invasive local treatment option for these patients.