Leap Therapeutics Reports Third Quarter 2024 Financial Results
CAMBRIDGE, Mass., Nov. 13, 2024 /PRNewswire/ -- Leap Therapeutics, Inc. (Nasdaq:LPTX), a biotechnology company focused on developing targeted and immuno-oncology therapeutics, today reported financial results for the third quarter ended September 30, 2024.
Leap Highlights:
-- Completed enrollment in the expanded randomized controlled Part B of the
Phase 2 DeFianCe study evaluating DKN-01, Leap's anti-DKK1 monoclonal
antibody, in combination with standard of care bevacizumab and
chemotherapy in second-line patients with advanced colorectal cancer
(CRC); data expected in mid-2025
-- Patient follow-up continuing in the randomized controlled Part C of the
Phase 2 DisTinGuish study evaluating DKN-01 in combination with
tislelizumab and chemotherapy in first-line patients with advanced
gastroesophageal junction (GEJ) and gastric cancer; data expected in
late 2024 or early 2025
-- Initiated development of FL-501, Leap's anti-GDF-15 monoclonal antibody
"We have made significant progress advancing our pipeline this quarter, including the completion of enrollment in the expanded Part B of the Phase 2 DeFianCe study of DKN-01 in patients with advanced colorectal cancer," said Douglas E. Onsi, President and Chief Executive Officer of Leap. "We look forward to sharing initial randomized controlled data from the DisTinGuish study and the DeFianCe study in the coming months. In addition, based on positive preclinical data, we are enthusiastically moving FL-501 into development. With a strong cash position that is expected to fund operations into Q2 2026, Leap is well positioned for continued success and long-term growth to deliver personalized medicines to patients fighting against cancer."
DKN-01 Development Update
-- Enrollment completed in the expanded randomized controlled Part B of the
DeFianCe study evaluating DKN-01 in combination with standard of care
bevacizumab and chemotherapy as a second-line treatment for patients
with advanced CRC. Part B of the DeFianCe study (NCT05480306) is a Phase
2, randomized, controlled, open-label 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. Part B of the
study enrolled 188 patients. The Company expects to report initial data
in mid-2025.
-- Patient follow-up continuing in the randomized controlled Part C of the
DisTinGuish study evaluating DKN-01 in combination with tislelizumab and
chemotherapy in patients with GEJ and gastric cancer, with initial data
expected in late 2024 or early 2025. Part C of the DisTinGuish study
(NCT0436380) is a Phase 2, randomized, controlled, open-label study of
DKN-01 in combination with tislelizumab and chemotherapy in first-line,
HER-2 negative patients with GEJ and gastric cancer. Part C of the study
enrolled 170 patients. The Company expects to report initial data in
late 2024 or early 2025.
Pipeline Update:
-- Advancing FL-501 into development as a potential best-in-class
anti-GDF-15 antibody with promising preclinical data. FL-501 is a
potential best-in-class monoclonal antibody designed to neutralize
GDF-15 to treat patients with cachexia and other GDF-15-driven diseases.
FL-501 may also enhance the activity of the immune system in the tumor
micro-environment. FL-501 was engineered for higher target affinity and
a longer plasma half-life compared to competing therapies. In
preclinical cachexia models, FL-501 increased body weight and restored
muscle mass.
Selected Third Quarter 2024 Financial Results
Net Loss was $18.2 million for the third quarter 2024, compared to $13.7 million for the same period in 2023. The increase was primarily due to an increase in research and development expenses.
Research and development expenses were $14.9 million for the third quarter 2024, compared to $11.5 million for the same period in 2023. The increase of $3.4 million was primarily due to an increase of $1.7 million in manufacturing costs related to clinical trial material and manufacturing campaigns, and an increase of $0.8 million in clinical trial costs due to patient enrollment, the duration of patients on study, the enhancement of correlative studies, increase in site activity associated with Part C of the DisTinGuish study, and the expansion of the size of Part B of the DeFianCe study. There was also an increase of $0.5 million in consulting fees associated with research and development activities and an increase of $0.4 million in payroll and other related expenses due to an increase in headcount of our research and development full-time employees.
General and administrative expenses were $2.9 million for the third quarter 2024, compared to $3.3 million for the same period in 2023. The decrease of $0.4 million in general and administrative expenses during the three months ended September 30, 2024 as compared to the same period in 2023, was due to a $0.4 million decrease in professional fees.
Cash and cash equivalents totaled $62.8 million at September 30, 2024.
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, colorectal, and gynecological cancers. Leap's pipeline also includes FL-501, a humanized monoclonal antibody targeting the growth and differentiation factor 15 (GDF-15) protein, in preclinical development. 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 potential safety, efficacy, and regulatory and clinical progress of Leap's product candidates; the anticipated timing for initiation or completion of clinical trials and release of clinical trial data and the expectations surrounding the outcomes thereof; Leap's future clinical or preclinical product development plans for any of Leap's product candidates; Leap's estimations of projected cash runway; 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; (iii) Leap's ability to successfully enter into new strategic partnerships for DKN-01 or any of its other programs and to maintain its ongoing collaborations with BeiGene and Adimab; (iv) whether any Leap clinical trials and products will receive approval from the U.S. Food and Drug Administration or equivalent foreign regulatory agencies; and (v) exposure to inflation, currency rate and interest rate fluctuations, as well as fluctuations in the market price of Leap's traded securities. 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 a 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
Leap Therapeutics, Inc.
Condensed Consolidated Statements of
Operations
(in thousands, except share and per share
amounts)
(Unaudited)
(Unaudited)
Three Months Ended September 30, Nine Months Ended September 30,
2024 2023 2024 2023
Operating expenses:
Research and development $14,915 $11,503 $44,099 $61,549
General and administrative 2,940 3,330 9,833 10,672
Total operating expenses 17,855 14,833 53,932 72,221
Loss from operations (17,855) (14,833) (53,932) (72,221)
Interest income 894 1,084 2,534 3,089
Australian research and development incentives (499) 554 1,124
Foreign currency loss (8) (501) (18) (953)
Change in fair value of Series X preferred stock warrant liability 12
Loss before income taxes (17,468) (13,696) (51,416) (68,949)
Provision for income taxes (708) (708)
Net
loss (18,176) (13,696) (52,124) (68,949)
Dividend attributable to down round feature of warrants (234)
Net loss attributable to common stockholders $(18,176) $(13,696) $(52,358) $(68,949)
Net loss per share
Basic & diluted $(0.44) $(0.51) $(1.44) $(3.78)
Weighted average common shares outstanding
Basic & diluted 41,209,639 26,987,182 36,307,890 18,240,455
Leap Therapeutics, Inc.
Consolidated Balance Sheets
(in thousands, except share and per share amounts)
September 30, December 31,
2024 2023
Assets
Current assets:
Cash and cash equivalents $62,823 $70,643
Research and development incentive receivable 780 771
Prepaid expenses and other current assets 209 183
Total current assets 63,812 71,597
Property and equipment, net - 5
Right of use assets, net 370 257
Deposits 865 966
Total assets $65,047 $72,825
Liabilities and Stockholders' Equity
Current liabilities:
Accounts payable $5,946 $6,465
Accrued expenses 9,049 5,957
Income tax payable 722 -
Lease liability - current portion 376 262
Total current liabilities 16,093 12,684
Total liabilities 16,093 12,684
Stockholders' equity:
Preferred stock, $0.001 par value; 10,000,000 shares authorized; - -
0 shares issued and outstanding
Common stock, $0.001 par value; 240,000,000 shares authorized; 38,264,464 and
25,565,414 38 26
shares issued and outstanding as of September 30, 2024 and December 31, 2023,
respectively
Additional paid-in capital 500,850 459,591
Accumulated other comprehensive income 6 106
Accumulated deficit (451,940) (399,582)
Total stockholders' equity 48,954 60,141
Total liabilities and stockholders' equity $65,047 $72,825
Leap Therapeutics, Inc.
Condensed Consolidated Statements of Cash
Flows
(in thousands)
(Unaudited) (Unaudited)
Three Months Ended September 30 Nine Months Ended September 30
2024 2023 2024 2023
Cash used in operating activities $(15,600) $(10,488) $(44,787) $(33,373)
Cash provided by investing activities 48,969
Cash provided by (used in) financing activities (66) (1) 37,080 (30)
Effect of exchange rate changes on cash and cash equivalents 10 (183) (113) (323)
Net increase (decrease) in cash and cash equivalents (15,656) (10,672) (7,820) 15,243
Cash and cash equivalents at beginning of period 78,479 91,415 70,643 65,500
Cash and cash equivalents at end of period $62,823 $80,743 $62,823 $80,743
View original content to download multimedia:https://www.prnewswire.com/news-releases/leap-therapeutics-reports-third-quarter-2024-financial-results-302303295.html
SOURCE Leap Therapeutics, Inc.
