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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):
September 30, 2024
Leap Therapeutics, Inc.
(Exact name of registrant as specified in its charter)
Delaware |
|
001-37990 |
|
27-4412575 |
(State or other jurisdiction of incorporation) |
|
(Commission
File Number) |
|
(IRS Employer
Identification No.) |
47 Thorndike Street, Suite B1-1
Cambridge, MA |
02141 |
(Address of principal executive offices) |
(Zip Code) |
Registrant’s telephone
number, including area code: (617) 714-0360
N/A
(Former name or former address,
if changed since last report)
Check the appropriate box below if the Form
8-K is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
| ¨ | Written
communications pursuant to Rule 425 under the Securities Act (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(c) 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, par value $0.001 |
LPTX |
Nasdaq Capital Market |
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 September 30, 2024, Leap
Therapeutics, Inc. (the “Company”) issued a press release entitled “Leap Therapeutics Announces Completion of Enrollment
in Part B of the DeFianCe Study of DKN-01 for the Treatment of Colorectal Cancer Patients.”
The full text of the press release is filed as Exhibit 99.1 to
this Current Report on Form 8-K and incorporated herein by reference; provided, however that information on or connected to our website
referenced in the Company’s press release is expressly not incorporated by reference into or intended to be filed as a part of this
Current Report on Form 8-K.
| Item 9.01. | Financial Statements and Exhibits. |
(d) Exhibits.
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.
Dated: September 30, 2024 |
By: |
/s/ Douglas E. Onsi |
|
Name: |
Douglas E. Onsi |
|
Title: | Chief Executive Officer and President |
Exhibit 99.1
Leap Therapeutics Announces Completion of Enrollment
in Part B of the DeFianCe Study
of DKN-01 for the Treatment of Colorectal Cancer
Patients
Cambridge,
MA – September 30, 2024 – Leap Therapeutics, Inc. (Nasdaq:LPTX), a biotechnology company focused on developing
targeted and immuno-oncology therapeutics, today announced that enrollment of 188 patients has been completed in the randomized controlled
Part B of the DeFianCe study evaluating DKN-01, Leap's anti-Dickkopf-1 (DKK1) antibody, in combination with standard of care bevacizumab
and chemotherapy as a second-line treatment for patients with advanced colorectal cancer (CRC).
“The
completion of enrollment in Part B of the DeFianCe study marks a significant achievement and highlights the enthusiasm in the potential
of DKN-01 from both patients and healthcare providers,” said Cynthia Sirard, M.D., Chief Medical Officer of Leap. “The encouraging
data from Part A of the study which showed clinically meaningful response rates and durable tumor reductions, as well as a favorable
safety profile in advanced CRC patients, provides a strong foundation to the expanded Part B of the study. We look forward
to sharing initial data from Part B, including the subpopulation of patients with left-sided CRC, in mid 2025.”
The
DeFianCe study (NCT05480306) is a Phase 2, open-label, global study of DKN-01 in combination with standard of care bevacizumab
and chemotherapy in patients with advanced CRC who have received one prior systemic therapy for advanced disease. Part B of the
study expanded from a 130 to a 188-patient randomized controlled trial, with the primary endpoint being progression free survival (PFS).
An additional primary endpoint will measure PFS in the subpopulation of patients with left-sided CRC. Secondary objectives include objective
response rate, duration of response, and overall survival.
About Leap Therapeutics
Leap
Therapeutics (Nasdaq: LPTX) is focused on developing targeted and immuno-oncology therapeutics. Leap's most advanced clinical candidate,
DKN-01, is a humanized monoclonal antibody targeting the Dickkopf-1 (DKK1) protein. DKN-01 is being developed in patients with esophagogastric,
gynecologic, and colorectal cancers. For more information about Leap Therapeutics, visit http://www.leaptx.com or
view our public filings with the SEC that are available via EDGAR at http://www.sec.gov or via https://investors.leaptx.com/.
FORWARD-LOOKING STATEMENTS
This press release contains forward-looking statements
within the meaning of the federal securities laws. Such statements are based upon current plans, estimates and expectations of the management
of Leap that are subject to various risks and uncertainties that could cause actual results to differ materially from such statements.
The inclusion of forward-looking statements should not be regarded as a representation that such plans, estimates and expectations will
be achieved. Words such as “anticipate,” “expect,” “project,” “intend,” “believe,”
“may,” “will,” “should,” “plan,” “could,” “continue,” “target,”
“contemplate,” “estimate,” “forecast,” “guidance,” “predict,” “possible,”
“potential,” “pursue,” “likely,” and words and terms of similar substance used in connection with
any discussion of future plans, actions or events identify forward-looking statements.
All
statements, other than historical facts, including statements regarding the anticipated timing of the release of clinical data,
and any outcomes of such trials; the interpretation or signficiance of, or any conclusions or suggestions that can or should be drawn
from, the results of, and the clinical data generated from, any of our clinical trials; the potential safety, efficacy, and regulatory
and clinical progress of Leap’s product candidates; our future preclinical and clinical development plans in connection with our
programs; the ability to enter into a strategic partnership for DKN-01 or any of Leap’s other programs; and any assumptions underlying
any of the foregoing, are forward-looking statements. Important factors that could cause actual results to differ materially from Leap’s
plans, estimates or expectations could include, but are not limited to: (i) Leap’s ability to successfully execute its clinical
trials and the timing of enrollment in and cost of such clinical trials; (ii) the results of Leap’s clinical trials and pre-clinical
studies, including that subsequent or final results from Leap’s clinical trials or pre-clinical studies may supersede, qualify,
limit, or change the interpretation or significance of, preliminary or earlier results of Leap’s clinical trials or pre-clinical
studies; (iii) Leap’s ability to successfully enter into new strategic partnerships for DKN-01 or any of its other programs;
(iv) whether any Leap products will receive approval from the U.S. Food and Drug Administration or equivalent foreign regulatory
agencies; (v) exposure to inflation, currency rate and interest rate fluctuations, as well as fluctuations in the market price of
Leap’s traded securities; and (vi) that the initiation, conduct, and completion of clinical trials, laboratory operations,
manufacturing campaigns, and other studies may be delayed, adversely affected, or impacted by global conflict or supply chain related
issues. New risks and uncertainties may emerge from time to time, and it is not possible to predict all risks and uncertainties. No representations
or warranties (expressed or Implied) are made about the accuracy of any such forward-looking statements. Leap may not actually achieve
the forecasts disclosed in such forward-looking statements, and you should not place undue reliance on such forward-looking statements.
Such forward-looking statements are subject to a number of material risks and uncertainties including but not limited to those set forth
under the caption “Risk Factors” in Leap’s most recent Annual Report on Form 10-K filed with the SEC, as well as
discussions of potential risks, uncertainties, and other important factors in its subsequent filings with the SEC. Any forward-looking
statement speaks only as of the date on which it was made. Neither Leap, nor any of its affiliates, advisors or representatives, undertake
any obligation to publicly update or revise any forward-looking statement, whether as result of new information, future events or otherwise,
except as required by law. These forward-looking statements should not be relied upon as representing Leap’s views as of any date
subsequent to the date hereof.
CONTACT:
Douglas E. Onsi
President & Chief Executive Officer
Leap Therapeutics, Inc.
617-714-0360
donsi@leaptx.com
Matthew DeYoung
Investor Relations
Argot Partners
212-600-1902
leap@argotpartners.com
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