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: May 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 May 7, 2024, IceCure Medical
Ltd. (the “Company”) issued a press release titled “Independent Study Results in Japan Demonstrate Zero (0%) Breast
Cancer Local Recurrence 5 Years Following Treatment with IceCure’s ProSense®, Adding to Continued Positive Data Published Globally”,
a copy of which is furnished as Exhibit 99.1 with this Report of Foreign Private Issuer on Form 6-K.
The first, second, third and
sixth paragraphs and the section titled “Forward Looking Statements” in the press release furnished herewith 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 and 333-262620), 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a part thereof from the date on which this Report of Foreign Private Issuer on Form 6-K is submitted, to the extent not superseded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: May 7, 2024 |
By: |
/s/ Eyal Shamir |
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Name |
Eyal Shamir |
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Title: |
Chief Executive Officer |
Exhibit 99.1
Independent Study
Results in Japan Demonstrate Zero (0%) Breast Cancer Local Recurrence 5 Years Following Treatment with IceCure’s
ProSense®, Adding to Continued Positive Data Published Globally
| ● | Study
published in the peer reviewed journal Breast Cancer |
| ● | Excellent
cosmetic outcomes, high degree of patient satisfaction, and improved quality of life post-cryoablation |
| ● | Strategic
distribution partner of ProSense® in Japan, Terumo Corporation, expects to submit an application for regulatory clearance for breast
cancer in the second half of 2024 |
CAESAREA, Israel, May 7, 2024 – IceCure
Medical Ltd. (Nasdaq: ICCM) (“IceCure” or the “Company”), developer of the ProSense® System, a minimally-invasive
cryoablation technology that destroys tumors by freezing as an alternative to surgical tumor removal, announced today that positive data
from an independent study (the “Study”) performed in Japan was published in an article titled “Percutaneous ultrasound-guided
cryoablation for early-stage primary breast cancer: a follow-up study in Japan,” in the journal Breast Cancer on April 27,
2024. The Study, which focused on the local control of cancer, safety, patient quality of life, patient satisfaction, and cosmetic outcomes
of cryoablation for patients with early-stage breast cancer, is the continuation of a prior pilot study that demonstrated percutaneous
cryoablation treated with ProSense® is a potential standard treatment for early-stage breast cancer patients, given compliance to
pre-defined patient selection criteria.
The Study was led by Dr. Hisanori Kawamoto, M.D.,
Ph.D. from the Department of Breast Surgery, Breast and Imaging Center at St. Marianna University School of Medicine in Japan. Eighteen
early-stage breast cancer patients, with a mean age of 59.0 [±9.0 years], with a mean tumor size of 9.8 ±2.3 mm, who underwent
treatment with ProSense® were followed for a mean of 44.3 months. No patients had local recurrence or distant metastasis in the 5-year
follow-up. No serious adverse events were reported. Cosmetic outcomes were excellent and the overall patient satisfaction level and patient
quality of life improved post-cryoablation.
The article states that minimally invasive non-surgical
techniques, including cryoablation, aim for curative outcomes while also acknowledging the importance of preserving or enhancing the quality
of life and cosmetic appearance following the procedure. The authors of the Study refer to recent trials, including IceCure’s ICE3
trial, for evidence that cryoablation results in local cancer control rates comparable to lumpectomies in early-stage breast cancer patients.
Dr. Kawamoto commented, “This is a very
important study in Japan, where we are experiencing an upward trend in breast cancer cases, especially among women in their late 40s to
early 60s. These are women who often are at very active stages of their life and therefore there is a growing demand for treatment options
that minimize the chance of or avoid hospitalization, in addition to resulting in favorable clinical and cosmetic outcomes. We are very
pleased with these results and are hopeful that ProSense® may become a favored option in Japan upon regulatory approval for early-stage
breast cancer.”
“We thank Dr. Kawamoto and his colleagues
for conducting this independent study, which adds to the growing body of efficacy and safety data for ProSense® as a minimally-invasive
option for early-stage breast cancer,” stated IceCure CEO, Eyal Shamir. “We anticipate that our in-country distribution partner,
Terumo Corporation, will file for regulatory clearance of ProSense® for breast cancer in Japan later this year, which may soon lead
to the approval and commercialization for it in a market where there is high demand for a minimally-invasive option.”
Terumo Corporation owns the exclusive distribution
rights for ProSense® in Japan for a 5-year term following regulatory approval. In exchange for exclusive distribution rights, IceCure
is expected to receive a total of $13.2 million in proceeds from Terumo during this initial term, of which it has received $4 million
to date, with an additional $8.2 million expected upon the completion of orders, as well as $1 million expected for milestone-based payments.
About ProSense®
The ProSense® Cryoablation System provides
a minimally invasive treatment option to destroy tumors by freezing them. The system uniquely harnesses the power of liquid nitrogen to
create large lethal zones for maximum efficacy in tumor destruction in benign and cancerous lesions, including breast, kidney, lung, and
liver.
ProSense® enhances patient and provider value
by accelerating recovery, reducing pain, surgical risks, and complications. With its easy, transportable design and liquid nitrogen utilization,
ProSense® opens that door to fast and convenient office-based procedure for breast tumors.
About IceCure Medical
IceCure Medical (Nasdaq: ICCM) develops and markets
ProSense®, an advanced liquid-nitrogen-based cryoablation therapy 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 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,” “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: that percutaneous cryoablation
treated with ProSense® is a potential standard treatment for early-stage breast cancer patients, the growing demand for minimally
invasive treatment options, the hope that ProSense® may become a favored option in Japan upon regulatory approval for early-stage
breast cancer, the expectation that Terumo Corporation will file for regulatory clearance in the second half of 2024, and the expected
proceeds of IceCure in connection with its exclusive distribution rights agreement with Terumo. 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 U.S. Securities
and Exchange Commission (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
IceCure Medical (NASDAQ:ICCM)
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