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UNITED STATES
SECURITIES AND
EXCHANGE COMMISSION
WASHINGTON, D.C.
20549
FORM 8-K
CURRENT REPORT
PURSUANT TO SECTION 13 OR 15(d) OF THE
SECURITIES EXCHANGE ACT OF 1934
Date of Report (Date of earliest event reported): February
25, 2025
LIXTE BIOTECHNOLOGY
HOLDINGS, INC.
delaware |
001-39717 |
20-2903526 |
(State or other jurisdiction
of incorporation) |
(Commission
File Number) |
(IRS Employer
Identification No.) |
680 East Colorado Boulevard, Suite 180
Pasadena, California 91101
(Address of principal executive offices)
(631) 830-7092
(Registrant’s telephone number, including area
code)
Check the appropriate box below if the Form 8-K filing is intended to simultaneously
satisfy the filing obligation of the registrant under any of the following provisions (See General Instruction A.2. below):
☐ | Written communications pursuant to Rule 425 under the Securities Act of 1933 (17 CFR 230.425) |
| |
☐ | Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
| |
☐ | Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
| |
☐ | Pre-commencement communications pursuant to Rule 13e-4(e) under the Exchange Act (17 CFR 240.13e-4(c)) |
Securities registered pursuant to Section 12(b) of the Act:
Title of Each Class |
|
Trading Symbol(s) |
|
Name of each exchange on which registered |
Common Stock |
|
LIXT |
|
The Nasdaq Stock Market LLC |
Warrant to Purchase Common Stock |
|
LIXTW |
|
The Nasdaq Stock Market LLC |
Indicate by check mark whether the registrant is an emerging growth company
as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934
(§240.12b-2 of this chapter).
Emerging growth company ☐
If an emerging growth company,
indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised
financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Item 8.01 Other Events.
On February 25, 2025,
Lixte Biotechnology Holdings, Inc. (the “Company”) issued a press release announcing that it has it has added the Robert
H. Lurie Comprehensive Cancer Center (Lurie Cancer Center) of Northwestern University as a second site in a clinical trial combining
the Company’s proprietary compound LB-100 with GSK’s Dostarlimab to treat ovarian clear cell cancer. Patient recruitment
is underway, and the first patient has been dosed.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits
The Company is filing as part of this Report the exhibits
listed on the accompanying Index to Exhibits, which information is incorporated herein by reference.
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 hereunto duly authorized.
Date: February 25, 2025 |
LIXTE BIOTECHNOLOGY HOLDINGS, INC. |
|
(Registrant) |
|
|
|
|
By: |
/s/ BASTIAAN VAN DER BAAN |
|
|
Bastiaan van der Baan |
|
|
Chief Executive Officer |
INDEX TO EXHIBITS
Exhibit 99.1
LIXTE
Adds Northwestern University’s Lurie Cancer Center
as
Second Site in Ongoing Clinical Trial for Ovarian Clear Cell Cancer
--
Lurie Cancer Center Completes Dosing of First Patient with LIXTE’s LB-100
in
Combination with GSK’s Immunotherapy Dostarlimab --
PASADENA, CALIF., February 25, 2025 —
LIXTE Biotechnology Holdings, Inc. (“LIXTE” or the “Company”) (Nasdaq: LIXT and LIXTW), a clinical
stage pharmaceutical company, today announced it has added the Robert H. Lurie Comprehensive Cancer Center (Lurie Cancer Center) of Northwestern
University as a second site in a clinical trial combining the Company’s proprietary compound LB-100 with GSK’s Dostarlimab
to treat ovarian clear cell cancer.
Emily M. Hinchcliff, MD, MPH, will lead the clinical trial at Lurie Cancer
Center, a renown Chicago-based National Cancer Institute-designated Comprehensive Cancer Center, which is located at Northwestern
Memorial Hospital’s downtown medical campus. Patient recruitment is underway, and the first patient has been dosed.
“Clinical trials testing potentially effective therapies are essential
to move our field forward, with many recent great successes,” said Dr. Hinchcliff. “We are pleased to be participating in
this important clinical trial to assess whether adding LIXTE’s LB-100 to GSK’s Dostarlimab will enhance the effectiveness
of immunotherapy in the treatment of ovarian clear cell carcinoma, a disease of high unmet need.”
Bas van der Baan, LIXTE’s Chief Executive Officer, said, “The
addition of Lurie Cancer Center is a positive step in expanding the patient population and accelerating this clinical trial, which was
initiated in January 2024 at The University of Texas MD Anderson Cancer Center.
The trial is directed by lead clinical investigator Amir Jazaeri, MD, Professor of Gynecologic Oncology.”
About LIXTE Biotechnology Holdings, Inc.
LIXTE Biotechnology Holdings, Inc. is
a clinical-stage pharmaceutical company focused on new targets for cancer drug development and developing and commercializing cancer
therapies. LIXTE has demonstrated that its first-in-class lead clinical PP2A inhibitor, LB-100, is well-tolerated in cancer patients
at doses associated with anti-cancer activity. Based on extensive published preclinical data, LB-100 has the potential to significantly
improve outcomes for patients undergoing various chemotherapies or immunotherapies. LIXTE’s new approach has no known competitors
and is covered by a comprehensive patent portfolio. Proof-of-concept clinical trials are in progress. LB-100 is part of a
pioneering effort in an entirely new field of cancer biology – activation lethality – that is advancing a new treatment
paradigm. Additional information about LIXTE can be found at www.lixte.com.
Forward-Looking Statement Disclaimer
This announcement contains certain forward-looking statements within the
meaning of Section 27A of the Securities Act of 1933, and Section 21E of the Securities Exchange Act of 1934. For example, statements
regarding the Company’s financial position, business strategy and other plans and objectives for future operations, and assumptions and
predictions about future activities, including the continuing development of proprietary compounds, the planning, funding, coordination
and potential results of clinical trials, the patent and legal costs to protect and maintain the Company’s intellectual property worldwide,
and the Company’s ability to obtain and maintain compliance with Nasdaq’s continued listing requirements, are all forward-looking
statements. These statements are generally accompanied by words such as “intend,” anticipate,” “believe,” “estimate,”
“potential(ly),” “continue,” “forecast,” “predict,” “plan,” “may,” “will,”
“could,” “would,” “should,” “expect” or the negative of such terms or other comparable terminology.
The Company believes that the assumptions and expectations reflected in
such forward-looking statements are reasonable, based on information available to it on the date hereof, but the Company cannot provide
assurances that these assumptions and expectations will prove to have been correct or that the Company will take any action that the Company
may presently be planning. However, these forward-looking statements are inherently subject to known and unknown risks and uncertainties.
Actual results or experience may differ materially from those expected or anticipated in the forward-looking statements. Factors that
could cause or contribute to such differences include, but are not limited to, regulatory policies, available cash resources, research
results, competition from other similar businesses, and market and general economic factors.
Readers are urged to read the risk factors set forth in the Company’s
filings with the United States Securities and Exchange Commission at https://www.sec.gov. The Company disclaims any intention or
obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.
For more information about LIXTE, contact: info@lixte.com
General Phone: (631) 830-7092; Investor Phone: (888) 289-5533
or
PondelWilkinson Inc. Investor Relations
pwinvestor@pondel.com
Roger Pondel: (310) 279-5965; Laurie Berman: (310) 279-5962
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