UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 6-K
REPORT OF FOREIGN PRIVATE ISSUER
PURSUANT TO RULE 13a-16 OR 15d-16
UNDER THE SECURITIES EXCHANGE ACT OF 1934
For the Month of: October 2024
Commission File Number: 001-40753
ICECURE MEDICAL LTD.
(Translation of registrant’s name into
English)
7 Ha’Eshel St., PO Box 3163
Caesarea, 3079504 Israel
(Address of principal executive office)
Indicate by check mark whether the registrant files or will file annual
reports under cover of Form 20-F or Form 40-F:
☒ Form 20-F
☐ Form 40-F
CONTENTS
On October 7, 2024, IceCure
Medical Ltd. (the “Company”) issued a press release titled “IceCure’s ProSense® Featured in 6 Global Studies
on Cryoablation of Breast Tumors at the 2024 European Society of Breast Imaging Conference,” a copy of which is furnished as Exhibit
99.1 with this Report of Foreign Private Issuer on Form 6-K.
The first four paragraphs,
the section that summarizes the six abstracts featuring ProSense® presented at EUSOBI 2024 and the section titled “Forward Looking
Statements” in the press release attached herewith as Exhibit 99.1 are incorporated by reference into the Company’s Registration
Statements on Form F-3 (Registration Nos. 333-258660
and 333-267272) and Form S-8
(Registration Nos. 333-270982,
333-264578, 333-262620
and 333-281587), filed with
the Securities and Exchange Commission, to be a part thereof from the date on which this Report of Foreign Private Issuer on Form 6-K
is submitted, to the extent not superseded by documents or reports subsequently filed or furnished.
SIGNATURES
Pursuant to the requirements
of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto
duly authorized.
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ICECURE MEDICAL LTD. |
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Date: October 7, 2024 |
By: |
/s/ Eyal Shamir |
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Name: |
Eyal Shamir |
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Title: |
Chief Executive Officer |
Exhibit 99.1
IceCure’s
ProSense® Featured in 6 Global Studies on Cryoablation
of Breast Tumors at the 2024 European Society of Breast Imaging
Conference
| ● | ICE3
trial results presentation by Co-Principal Investigator Dr. Kenneth Tomkovich wins EUSOBI
2024 Abstract Award |
| ● | THERMAC
Trial on Treatment of Breast Cancer with Percutaneous Thermal Ablation (cryoablation, radiofrequency,
and microwave) wins EUSOBI Young Physician Scientist Competition – cryoablation demonstrates
94% complete rate of ablation |
| ● | IceCure
exhibited ProSense® and conducted hands-on demos and Q&A sessions with
breast cryoablation experts Dr. Lucía Graña-López and Dr. Federica Di
Naro |
CAESAREA,
Israel, October 7, 2024 – IceCure Medical Ltd. (Nasdaq: ICCM) (“IceCure”, “IceCure Medical” or the
“Company”), developer of minimally-invasive cryoablation technology that destroys tumors by freezing as an alternative to
surgical tumor removal, today announced that IceCure’s ICE3 trial and five additional studies featuring new data on ProSense’s®
use in breast cancer and fibroadenoma were presented at the 2024 European Society of Breast Imaging (EUSOBI) Scientific Meeting
and Annual Conference which took place in Lisbon, Portugal on October 3-5, 2024.
The
2024 EUSOBI Abstract Award was received by Dr. Kenneth Tomkovich, Co-Primary Investigator of the ICE3 trial, for his abstract “Image
Guided Cryoablation as a Primary Treatment for Low-Risk Breast Cancers: Results and Imaging Findings of the ICE3 Trial.” Dr. Tomkovich
remarked, “The significance of a U.S. study gaining such high recognition by a European medical society is a testament to the excellent
results—a 96.3% recurrence free rate for those treated with ProSense® and endocrine therapy—that demonstrates
cryoablation for small, low-risk breast cancer to be a safe and effective primary treatment option to surgical lumpectomy.”
The
THERMAC Trial on Treatment of Breast Cancer with Percutaneous Thermal Ablation from the Netherlands was awarded the EUSOBI Young Physician
Scientists Prize. The THERMAC trial compared the efficacy of treatment in terms of complete ablation with radiofrequency, microwave,
and cryoablation. Cryoablation demonstrated the highest complete rate of ablation at 94% with no adverse events, making it the safest
and most effective among the methods used in the trial. In comparison, for patients in the same study who underwent radiofrequency there
was a complete ablation rate of 33% and 50% experienced mild to moderate adverse events. For patients in the same study treated with
microwave, there was a complete ablation rate of 73% and 40% experienced mild to moderate adverse events.
An
estimated 1700+ professionals in attendance at EUSOBI had the opportunity to learn more about the ProSense® Cryoablation
System for the treatment of fibroadenoma and breast cancer, both of which are approved indications for ProSense® in Europe.
IceCure’s booth featured live demonstrations from expert users and the IceCure team, who were on hand to discuss the growing evidence
for breast cancer cryoablation and ProSense®’s advantages. On October 4, world-leading cryoablation experts, Dr.
Lucía Graña-López of Servizo Galego de Saúde, Spain, and Dr. Federica Di Naro of Azienda Ospedaliero-Universitaria
Careggi, Italy were at the booth for demonstrations and Q&A. Both Dr. Grana-Lopez and Dr. Di Naro have previously published studies
demonstrating ProSense® destroyed or reduced 100% of breast cancer tumors.
“The
fact that six major studies on ProSense® in the treatment of breast cancer were presented, and two won awards, in Europe’s
most prestigious breast imaging conference speaks volumes to the potential of ProSense® to treat more patients in Europe
and around the world,” stated IceCure CEO Eyal Shamir. “The growing body of evidence from independent, investigator initiated
studies supports our commercial activities globally. We had highly productive talks at the EUSOBI conference with hospitals, clinics,
and doctors interested in acquiring ProSense® systems so they can offer a safe and effective minimally invasive option to their patients.”
The
following is a summary of six abstracts featuring ProSense® Cryoablation, including IceCure’s ICE3 trial, presented
at EUSOBI 2024:
| ● | Study
Title: Image Guided Cryoablation as a Primary Treatment for Low-Risk Breast Cancers:
Results and Imaging Findings of the ICE3 Trial – Dr. Kenneth Tomkovich, USA |
Winner
of the EUSOBI 2024 Abstract Award; Received the highest score in the topic
Conclusion:
“The overall 5-year recurrence rate of 4.3% in the ICE3 trial is similar to reported recurrence rates for the current gold
standard surgical lumpectomy. Substantial benefits as compared to surgery include performance in an outpatient setting using local anesthesia,
only minor reported adverse events, and 100% satisfaction with cosmetic outcomes. Results of the ICE3 trial suggest that cryoablation
for small low-risk breast cancers is a safe and effective primary treatment option alternative to surgical lumpectomy. Additional trials
are encouraged.”
| ● | Study
Title: The Treatment of Breast Cancer with Percutaneous Thermal Ablation: Results of
the THERMAC trial – Dr. Sophie Wooldrik, the Netherlands |
Winner
of the EUSOBI Young Physician Scientist Competition; Rated among the top 5 abstracts
Conclusion:
In this study, cryoablation demonstrated the highest completed ablation rate (94%) with no adverse events, making it the most effective
and safest method compared to radiofrequency and microwave.
| ● | Study
Title: The Treatment of Breast Cancer with Percutaneous Thermal Ablation – Cosmetic
Outcome and Patient Satisfaction – Dr. Sophie Wooldrik, the Netherlands |
Conclusion:
Patients reported cosmetic outcomes to be more favorable following thermal ablation as compared to surgery. Patients appeared to
experience the least among of pain with cryoablation.
| ● | Study
Title: Assessment of pain level and quality of life (QoL) in breast cancer (BC) patients
treated with Ultrasound-guided Cryoablation – Dr. S.E Balidi Giorgi, D. Di Naro, et
al. |
Conclusion:
Ultrasound-guided cryoablation is a non-invasive and effective treatment in breast cancer patients ineligible for surgical excision.
It is associated with improvement of pain and QoL. No significant differences in QoL were found between patients treated with cryoablation
and hormone therapy compared to patients treated only with cryoablation, confirming that cryoablation maintains good QoL levels in all
breast cancer patients.
| ● | Study
Title: Single-center Experience with Percutaneous Cryoablation for benign and malignant
breast lesions in Romania: Tumor Reduction and Safety – Dr. Georgina Camen, Romania |
Conclusion:
Cryoablation with a LN2 based system was safe and effective for tumors 26 mm and smaller. Data collection continues with high expectations
for long-term outcomes.
| ● | Study
Title: Single Center Experience with Percutaneous Cryoablation of Fibroadenomas in
Hungary: Volume Reduction and Safety – Dr. Teodora Filipov |
Conclusion:
Liquid nitrogen-based cryoablation demonstrated both safety and efficacy for the treatment of fibroadenomas resulting in a 92.9%
reduction in volume one year post procedure.
About
IceCure Medical
IceCure
Medical (Nasdaq: ICCM) develops and markets advanced liquid-nitrogen-based cryoablation therapy systems for the treatment 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 alternative to hospital 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 China.
Forward
Looking Statements
This
press release contains forward-looking statements within the meaning of the “safe harbor” provisions of the Private Securities
Litigation Reform Act of 1995 and other Federal securities laws. Words such as “expects,” “anticipates,” “intends,”
“plans,” “believes,” “seeks,” “potential,” “estimates” and similar expressions
or variations of such words are intended to identify forward-looking statements. For example, IceCure is using forward looking statements
in this press release when it discusses the potential of ProSense to treat more patients in Europe and around the world. 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, 2023 filed with the SEC
on April 3, 2024, 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.
IR
Contact:
Email:
investors@icecure-medical.com
Michael
Polyviou
Phone:
732-232-6914
Todd
Kehrli
Phone:
310-625-4462
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