– Continued progress toward commencement of Phase 1 human clinical study of lead product candidate, PALI-2108, for the treatment of Ulcerative Colitis (UC) before year end – Company continues to establish growing body of preclinical data for PALI-2108 and global patent estate – Sufficient cash on hand to execute on current business plan and reach clinical and regulatory milestones through first quarter of 2025 Carlsbad, CA, Aug. 13, 2024 (GLOBE NEWSWIRE) -- Palisade Bio, Inc. (Nasdaq: PALI) (“Palisade”, “Palisade Bio”, or the “Company”), a biopharmaceutical company focused on developing and advancing novel therapeutics for patients living with autoimmune, inflammatory, and fibrotic diseases, reported its financial results for the second quarter of 2024 and provided a business update. Recent Highlights Completed microbiome study confirming bacterial enzymes for local bioactivation of lead product candidate, PALI-2108, in development for Crohn’s disease and UC;Completed nonclinical IND/CTA-enabling studies;Expanded global intellectual property portfolio for PALI-2108 and PALI-1908 with a notice to grant patent from the European Patent Office;Completed the first Good Manufacturing Practice (GMP) batch of drug substance PALI-2108, an orally administered, locally acting colon-specific phosphodiesterase-4 (PDE4) inhibitor prodrug in development for patients affected by UC;Progressed on previously announced strategic collaboration with Strand Life Sciences including identification of promising PDE4-related biomarkers associated with UC pathology, providing valuable insights for targeted therapeutic interventions;Received notice of allowance for Canadian patent covering the proprietary composition of PALI-2108 titled, “Gut Microbiota Bioactivated PDE4 Inhibitor Precursors”; andPresented positive preclinical data from PALI-2018 demonstrating it to be safe, effective and well tolerated in mouse models at Digestive Disease Week (DDW) 2024. “Our team has made great progress this past quarter. Our growing body of encouraging data coupled with the successful completion of our first GMP batch for PALI-2108 has positioned us for some exciting momentum as we prepare for the initiation of our Phase 1 clinical trial. Based on the preclinical data demonstrated to date, we believe PALI-2108 has the potential to be the first approved PDE4 inhibitor for UC and importantly, provide a much-needed solution for patients,” commented J.D. Finley, Chief Executive Officer. PALI-2108 Development Program The Company continues to advance its lead program, PALI-2108, for the treatment of moderate-to-severe UC toward a Phase 1 clinical study. PALI-2108 is an orally administered, locally acting colon-specific PDE4 inhibitor prodrug in development for patients affected by UC. Upcoming Target Milestones
Complete analysis of ongoing IND/CTA-enabling tox studies by the end of the third quarter 2024;Submit initial IND/CTA prior to the end of the third quarter of 2024; andInitiate Phase 1a with UC patient cohort prior to the end of 2024. Precision Medicine Approach Additionally, the Company is in the process of developing a genetic- or biomarker-based patient selection approach that, if developed, will aid clinicians in identifying patients who may respond to therapy with a locally acting PDE4-inhibitor such as PALI-2108. The Company is working with a strategic collaborator on development and has completed the curation of a pipeline including over 1,600 UC patients’ clinical and biomarker data and is in ongoing discussions with potential partners with access to additional patient data to support development of an FDA-approved test. The Company plans to leverage this expertise and infrastructure to fuel a growing pipeline of validated and high-priority autoimmune, inflammatory, and fibrotic disease product candidates. Summary of Financial Results for the Quarter Ended June 30, 2024 As of June 30, 2024, the Company had cash and cash equivalents of $11.4 million. The Company believes it has sufficient cash to fund its currently planned operations through the first quarter of 2025. Net loss was $4.1 million for the three months ended June 30, 2024, up $0.7 million from a net loss of $3.4 million for the three months ended June 30, 2023. Research and development expenses for the three months ended June 30, 2024 were $2.6 million, a 21% increase compared to $2.2 million for the three months ended June 30, 2023. The increase is attributable to higher expenses recognized for the three months ended June 30, 2024 that were directly related to the development of the Company’s lead asset, PALI-2108, and higher share-based compensation expense, partially offset by a decrease in costs directly related to our development of LB1148, which Palisade ceased in August of 2023, and lower other employee-related costs. General and administrative expenses increased by $0.2 million, or 11%, from $1.4 million for the three months ended June 30, 2023 to $1.6 million for the three months ended June 30, 2024. About Palisade Bio Palisade Bio is a biopharmaceutical company focused on developing and advancing novel therapeutics for patients living with autoimmune, inflammatory, and fibrotic diseases. The Company believes that by using a targeted approach with its novel therapeutics it will transform the treatment landscape. For more information, please go to www.palisadebio.com. Forward Looking StatementsThis communication contains “forward-looking” statements for purposes of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include statements regarding the Company’s intentions, beliefs, projections, outlook, analyses or current expectations concerning, among other things: the extent of our cash runway; our ability to successfully develop our licensed technologies; the timing and outcome of our current and anticipated applications and studies related to our product candidates; estimates about the size and growth potential of the markets for our product candidates, and our ability to serve those markets, including any potential revenue generated; future regulatory, judicial, and legislative changes or developments in the United States (U.S.) and foreign countries and the impact of these changes; our ability to maintain the Nasdaq listing of our securities; our ability to build a commercial infrastructure in the U.S. and other markets; our ability to compete effectively in a competitive industry; our ability to identify and qualify manufacturers to provide API and manufacture drug product; our ability to enter into commercial supply agreements; the success of competing technologies that are or may become available; our ability to attract and retain key scientific or management personnel; the accuracy of our estimates regarding expenses, future revenues, capital requirements and needs for additional financing; our ability to obtain funding for our operations; our ability to attract collaborators and strategic partnerships; and the impact of any global event on our business, and operations, and supply. Any statements contained in this communication that are not statements of historical fact may be deemed to be forward-looking statements. These forward-looking statements are based upon the Company’s current expectations. Forward-looking statements involve risks and uncertainties. The Company’s actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of these risks and uncertainties, which include, without limitation, the Company’s ability to advance its nonclinical and clinical programs, the uncertain and time-consuming regulatory approval process; and the Company’s ability to secure additional financing to fund future operations and development of its product candidates. Additional risks and uncertainties can be found in the Company’s Annual Report on Form 10-K for the fiscal year ended December 31, 2023, filed with the Securities and Exchange Commission (“SEC”) on March 26, 2024, Form 10-Q for the three months ended June 30, 2024, filed with the SEC on August 12, 2024. These forward-looking statements speak only as of the date hereof and the Company expressly disclaims any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in the Company’s expectations with regard thereto or any change in events, conditions or circumstances on which any such statements are based. Investor Relations Contact JTC Team, LLCJenene Thomas 833-475-8247PALI@jtcir.com Palisade Bio, Inc.Condensed Consolidated Balance Sheets (Unaudited)(in thousands, except share and per share amounts) June 30, December 31, 2024 2023
ASSETS
Current assets:
Cash and cash equivalents $11,353 $12,432 Prepaid expenses and other current assets 959 896 Total current assets 12,312 13,328 Restricted cash 26 26 Property and equipment, net 4 10 Operating lease right-of-use asset 142 198 Other noncurrent assets 387 490 Total assets $12,871 $14,052
LIABILITIES AND STOCKHOLDERS' EQUITY
Current liabilities:
Accounts payable $514 $698 Accrued liabilities 1,555 831 Accrued compensation and benefits 288 778 Current portion of operating lease liability 130 121 Insurance financing debt 349 158 Total current liabilities 2,836 2,586 Warrant liability 2 2 Contingent consideration obligation 60 61 Operating lease liability, net of current portion 24 90 Total liabilities 2,922 2,739 Commitments and contingencies
Stockholders' equity:
Series A Convertible Preferred Stock, $0.01 par value, 7,000,000 shares authorized; 200,000 issued and outstanding at June 30, 2024 and December 31, 2023 2 2 Common stock, $0.01 par value; 280,000,000 shares authorized;966,345 and 618,056 shares issued and outstanding at June 30, 2024 and December 31, 2023, respectively 9 6 Additional paid-in capital 139,051 132,811 Accumulated deficit (129,113) (121,506)Total stockholders' equity 9,949 11,313 Total liabilities and stockholders' equity $12,871 $14,052 Palisade Bio, Inc.Condensed Consolidated Statements of Operations (Unaudited)(in thousands, except share and per share amounts) Three Months Ended June 30, Six Months Ended June 30, 2024 2023 2024 2023 License revenue $— $— $— $250 Operating expenses:
Research and development 2,628 2,177 4,842 3,418 General and administrative 1,583 1,432 3,042 2,970 Total operating expenses 4,211 3,609 7,884 6,388 Loss from operations (4,211) (3,609) (7,884) (6,138)Other (expense) income:
Interest expense (2) (3) (3) (3)Other income, net 133 219 280 408 Total other income, net 131 216 277 405 Net loss $(4,080) $(3,393) $(7,607) $(5,733)
Basic and diluted weighted average shares used in computing basic and diluted net loss per common share* 1,228,453 427,862 1,000,367 357,572 Basic and diluted net loss per common share* $(3.32) $(7.93) $(7.60) $(16.03) (*) Basic and diluted loss per common share and basic and diluted weighted average share used in computing basic and diluted loss per common share for the three and six months ended June 30, 2023 has been adjusted to reflect the 1-for-15 reverse stock split effected on April 5, 2024. Palisade Bio, Inc.Condensed Consolidated Statements of Cash Flows (Unaudited)(in thousands, except share and per share amounts) Six Months Ended June 30, 2024 2023
Net loss $(7,607) $(5,733)Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation 2 3 Non-cash operating lease expense 56 50 Recurring fair value measurements of liabilities 5 (59)Issuance of common stock to vendors 73 — Loss on disposal of property and equipment 4 — Stock-based compensation and related charges 480 237 Other — (108)Changes in operating assets and liabilities:
Prepaid and other current assets and other noncurrent assets 349 497 Accounts payable and accrued liabilities 506 (367)Accrued compensation and benefits (490) (195)Operating lease liabilities (57) (50)Net cash used in operating activities (6,679) (5,725)Cash flows from investing activities:
Purchases of property and equipment — (4)Net cash used in investing activities — (4)Cash flows from financing activities:
Payments on insurance financing debt (158) (138)Proceeds from issuance of common stock and warrants 4,000 7,681 Proceeds from the exercise of warrants 2,503 2,758 Payment of warrant inducement issuance costs (343) — Payment of equity issuance costs (388) (552)Proceeds from issuance of common stock under Employee Stock Purchase Plan 11 — Shares withheld for payment of employee withholding tax liability (25) — Net cash provided by financing activities 5,600 9,749 Net (decrease) increase in cash, cash equivalents and restricted cash (1,079) 4,020 Cash, cash equivalents and restricted cash, beginning of year 12,458 12,409 Cash, cash equivalents and restricted cash, end of period $11,379 $16,429 Reconciliation of cash, cash equivalents and restricted cash to the balance sheets:
Cash and cash equivalents $11,353 $16,403 Restricted cash 26 26 Total cash, cash equivalents and restricted cash $11,379 $16,429
