UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 6-K
REPORT OF FOREIGN PRIVATE ISSUER
PURSUANT TO SECTION 13A-16 OR 15D-16
UNDER THE SECURITIES EXCHANGE ACT OF 1934
For the month of May 2024
Commission File Number: 001-41316
Alpha Tau Medical Ltd.
(Exact Name of Registrant as Specified in Its
Charter)
Kiryat HaMada St. 5
Jerusalem, Israel 9777605
+972 (3) 577-4115
(Address of principal executive offices)
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 13, 2024, Alpha Tau Medical Ltd. (the “Company”)
issued a press release titled “Alpha Tau Announces Alpha DaRT Treatment of First Patient with Liver Metastases of Colorectal Cancer.”
A copy of this press release is attached to this Form 6-K as Exhibit 99.1.
The information in this Report on Form 6-K, including
in Exhibit 99.1 attached hereto is being furnished and shall not be deemed “filed” for the purposes of Section 18 of the Securities
Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that Section, nor shall
it be deemed incorporated by reference in any filing made by the Company under the Securities Act of 1933, as amended, or the Exchange
Act, except as otherwise set forth herein or as shall be expressly set forth by specific reference in such a filing.
EXHIBIT INDEX
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934,
as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
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Alpha Tau Medical Ltd. |
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Date: May 13, 2024 |
By: |
/s/ Uzi Sofer |
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Uzi Sofer |
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Chief Executive Officer |
3
Exhibit
99.1
Alpha
Tau Announces Alpha DaRT Treatment of First Patient with Liver Metastases of Colorectal Cancer
JERUSALEM,
May 13, 2024 (GLOBE NEWSWIRE) -- Alpha Tau Medical Ltd. (“Alpha Tau”, or the “Company”) (NASDAQ: DRTS, DRTSW),
the developer of the innovative alpha-radiation cancer therapy Alpha DaRT™, announced today that its first patient with
liver cancer metastases has been treated in a feasibility and safety study of Alpha DaRT at the McGill University Health Center
in Montreal, Canada.
The
trial seeks to recruit up to 10 patients who are eligible for a two-staged hepatectomy to resect liver metastases of colorectal cancer.
Specifically, in the first stage, as many metastatic tumors as possible will be surgically removed in a non-curative intervention, while
Alpha DaRT sources will be inserted into a separate tumor in the second liver lobe, and in the second stage, after allowing for the resected
liver to regenerate naturally, the portion of the liver with the Alpha DaRT sources will be surgically removed.
The
study primarily aims to examine the feasibility of delivering Alpha DaRT sources into the liver metastases, as well as the safety of
utilizing the Alpha DaRT sources in the liver by assessing the frequency and severity of related adverse events. The study also aims
to examine Alpha DaRT’s efficacy in terms of radiological response, assessed after insertion of the Alpha DaRT sources, and via
pathological response, assessed after the second stage of surgery. Additional information about the trial can be found at https://clinicaltrials.gov/study/NCT05829291.
Alpha
Tau CEO Uzi Sofer commented, “The start of this trial marks a big milestone towards addressing the urgent need for new therapeutic
options in treating patients with liver metastases. This trial is part of our overall strategy to showcase the broad use and potential
of the Alpha DaRT in other hard-to-treat indications such as cancers of the brain, lung, vulva and pancreas. We would like to thank Dr.
Peter Metrakos and his team at the McGill University Health Center for enrolling and treating the first patient in this highly significant
feasibility and safety trial.”
Peter
Metrakos, MD, CM, FACS, FRCSC, Professor of Surgery, Pathology and Anatomy and Cell Biology, Director of Hepato-Pancreato-Bilary Surgery
and Senior Scientist, McGill University Health Centre -Research Institute, Cancer Research Program, Department of Surgery at McGill University,
and the principal investigator of the trial, commented “Liver Metastases associated with colorectal cancer is of major concern
and a leading cause of patient mortality with limited effective treatment options. We are encouraged by the early results of Alpha DaRT
treatment in other tumor types and are hopeful that the Alpha DaRT treatment will offer better outcomes to these patients with such a
challenging disease.”
Robert
Den MD, Alpha Tau CMO commented, “While we continue to accrue patients with cutaneous recurrent SCC to the ongoing pivotal ReSTART
trial, we also look to expand the use of the Alpha DaRT technology to high unmet medical need indications in internal organs such as
liver metastases. This trial is particularly exciting for us in light of previous preclinical work that has demonstrated the ability
of Alpha DaRT to generate an observed systemic immune response when used to treat a colorectal tumor model, and we hope to better understand
the effect of Alpha DaRT on liver metastases and immune cell populations in human patients. We look forward to the preliminary results
of this trial, which we hope will further our goal of advancing the use of Alpha DaRT across a range of indications and helping patients
worldwide.”
This
clinical study is the next phase of a multi-year research collaboration program between the McGill University Research Center and the
Alpha Tau Medical research team. This collaboration started with translation experiments using orthotopic animal models that mimic human
liver colorectal metastatic disease, showing a reduction in tumor growth rate when using Alpha DaRT compared to control and changes in
the hepatic immune microenvironment.
About
Alpha DaRT™
Alpha
DaRT (Diffusing Alpha-emitters Radiation Therapy) is designed to enable highly potent and conformal alpha-irradiation of solid tumors
by intratumoral delivery of radium-224 impregnated sources. When the radium decays, its short-lived daughters are released from the sources
and disperse while emitting high-energy alpha particles with the goal of destroying the tumor. Since the alpha-emitting atoms diffuse
only a short distance, Alpha DaRT aims to mainly affect the tumor, and to spare the healthy tissue around it.
About
Alpha Tau Medical Ltd.
Founded
in 2016, Alpha Tau is an Israeli medical device company that focuses on research, development, and potential commercialization of the
Alpha DaRT for the treatment of solid tumors. The technology was initially developed by Prof. Itzhak Kelson and Prof. Yona Keisari from
Tel Aviv University.
Forward-Looking
Statements
This
press release includes “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995.
When used herein, words including “anticipate,” “being,” “will,” “plan,” “may,” “continue,”
and similar expressions are intended to identify forward-looking statements. In addition, any statements or information that refer to
expectations, beliefs, plans, projections, objectives, performance or other characterizations of future events or circumstances, including
any underlying assumptions, are forward-looking. All forward-looking statements are based upon Alpha Tau’s current expectations and various
assumptions. Alpha Tau believes there is a reasonable basis for its expectations and beliefs, but they are inherently uncertain. Alpha
Tau may not realize its expectations, and its beliefs may not prove correct. Actual results could differ materially from those described
or implied by such forward-looking statements as a result of various important factors, including, without limitation: (i) Alpha Tau’s
ability to receive regulatory approval for its Alpha DaRT technology or any future products or product candidates; (ii) Alpha Tau’s limited
operating history; (iii) Alpha Tau’s incurrence of significant losses to date; (iv) Alpha Tau’s need for additional funding and ability
to raise capital when needed; (v) Alpha Tau’s limited experience in medical device discovery and development; (vi) Alpha Tau’s dependence
on the success and commercialization of the Alpha DaRT technology; (vii) the failure of preliminary data from Alpha Tau’s clinical studies
to predict final study results; (viii) failure of Alpha Tau’s early clinical studies or preclinical studies to predict future clinical
studies; (ix) Alpha Tau’s ability to enroll patients in its clinical trials; (x) undesirable side effects caused by Alpha Tau’s Alpha
DaRT technology or any future products or product candidates; (xi) Alpha Tau’s exposure to patent infringement lawsuits; (xii) Alpha
Tau’s ability to comply with the extensive regulations applicable to it; (xiii) the ability to meet Nasdaq’s listing standards; (xiv)
costs related to being a public company; (xv) changes in applicable laws or regulations; and the other important factors discussed under
the caption “Risk Factors” in Alpha Tau’s annual report filed on form 20-F with the SEC on March 7, 2024, and other filings
that Alpha Tau may make with the United States Securities and Exchange Commission. These and other important factors could cause actual
results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking
statements represent management’s estimates as of the date of this press release. While Alpha Tau may elect to update such forward-looking
statements at some point in the future, except as required by law, it disclaims any obligation to do so, even if subsequent events cause
its views to change. These forward-looking statements should not be relied upon as representing Alpha Tau’s views as of any date subsequent
to the date of this press release.
Investor
Relations Contact
IR@alphatau.com
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