STOCK TITAN

Palisade Bio Reports Third Quarter 2023 Financial Results and Provides Business Outlook

Rhea-AI Impact
(Moderate)
Rhea-AI Sentiment
(Neutral)
Tags
Rhea-AI Summary
Palisade Bio, Inc. (Nasdaq: PALI) reported its financial results and business outlook, including a transformative transaction for the development of novel therapeutics for inflammatory bowel disease (IBD). The lead program, PALI-2108, an oral prodrug therapy for moderate-to-severe ulcerative colitis, is set to begin Phase 1 clinical study in 2024. The company has a strong financial position to achieve significant milestones into 2025.
Positive
  • Exclusive worldwide licensing agreement with Giiant Pharma, Inc. for multiple oral drug candidates targeting IBD
  • Appointment of GI clinical expert and biotech entrepreneur Mitch Jones, M.D., PhD as Chief Medical Officer
  • Bolstered cash runway with a $2 million, common-stock-only registered direct offering priced at market under Nasdaq rules
  • Anticipation of launching Phase 1 study for PALI-2108 in UC in 2024
  • Strong cash position to fund operations through value-driving milestones
  • Potential to gain significant market share in the IBD market
Negative
  • None.

– Transformational transaction jumpstarts development pipeline into high-value inflammatory bowel disease (IBD) market

– Lead program, PALI-2108, oral prodrug therapy for the treatment of moderate-to-severe ulcerative colitis (UC) is anticipated to commence Phase 1 clinical study in 2024

– Strong financial position with cash to execute on strategy and achieve significant milestones into 2025

Carlsbad, CA, Nov. 10, 2023 (GLOBE NEWSWIRE) -- Palisade Bio, Inc. (Nasdaq: PALI) (“Palisade”, “Palisade Bio” or the “Company”), a biopharmaceutical company focused on developing novel therapeutics for serious chronic gastrointestinal (GI) diseases, today reported its financial results for the third quarter 2023 and provided a business outlook.

Recent Corporate Developments

  • Entered into an exclusive worldwide licensing agreement with Giiant Pharma, Inc. for multiple oral drug candidates targeting IBD;
  • Appointed GI clinical expert and biotech entrepreneur Mitch Jones, M.D., PhD as Chief Medical Officer; and
  • Bolstered cash runway with a $2 million, common-stock-only registered direct offering priced at market under Nasdaq rules.

“The past quarter was marked by a transformative transaction for Palisade. The IBD market is large, well established, and expected to grow to $20 billion by 2031. We believe that novel therapeutics which demonstrate safety and efficacy have the potential to gain significant market share. Palisade has the only PDE4 inhibitor prodrug under development for the treatment of ulcerative colitis, our lead indication,” commented J.D. Finley, Chief Executive Officer. “We are committed to advancing the clinical development of PALI-2108 and expect to launch our Phase 1 study in UC in 2024. Importantly, we have a strong cash position to fund operations through value-driving milestones and believe we are positioned to build shareholder value in the near and long term.”

About PALI-2108

PALI-2108 is an orally administered, locally acting colon-specific phosphodiesterase-4B (PDE4B) inhibitor prodrug in development for patients affected by moderate-to-severely active ulcerative colitis (UC).

Key Program Highlights

  • Preferential enzymatic inhibition of PDE4B limiting the potential for off-target effects;
  • Isoenzyme inhibition profile superior to other PDE4 inhibitors and comparable to marketed anti-inflammatory and anti-fibrotic PDE4B selective inhibitors;
  • 20 times more potent at inhibiting lipopolysaccharide (LPS)-induced tumor necrosis factor-α (TNF-α) when compared to apremilast in human whole blood;
  • Demonstrated PDE4B target engagement comparable to apremilast in vivo;
  • Shown to be locally bioactivated within the colon in mouse studies and ex vivo in normal healthy subjects and in ulcerative colitis patient fecal samples;
  • Nonclinical data demonstrating prodrug significantly limits systemic drug exposure;
  • Nonclinical data demonstrating complete prevention of emesis, a well-known side effect limiting the use of PDE4 inhibitors in humans, at therapeutic doses of oral prodrug and compared with the active PDE4 moiety only; and
  • Shown to be effective and demonstrated a dose response across multiple nonclinical colitis studies.

Upcoming Milestones

  • Ongoing IND/CTA-enabling tox studies;
  • Complete nonclinical IND/CTA-enabling activities by the end of the third quarter of 2024;
  • Submit initial IND/CTA prior to the end of 2024; and
  • Initiate Phase 1a/b before the end of 2024.

Summary of Financial Results for the Third Quarter Ended September 30, 2023

As of September 30, 2023, the Company had cash and cash equivalents of $15.3 million. The Company believes it has sufficient cash to fund its currently planned operations into the first quarter of 2025.

Net loss was $3.6 million for the three months ended September 30, 2023, compared to $4.0 million for the same period in 2022.

Research and development expenses for the three months ended September 30, 2023, were $1.7 million, a decrease of approximately $0.2 million, or 10%, compared to $1.9 million for the same period last year. The decrease was primarily attributable to the Company concluding its U.S. Phase 2 PROFILE study of LB1148 in early third quarter of 2023 and its completion of enrollment in its dose-optimization study of LB1148 in the second quarter of 2023. The Company has subsequently concluded it will no longer pursue the development of LB1148 and has closed its PROFILE study. Comparatively, in the third quarter of 2022, the Company was actively enrolling its U.S. Phase 2 PROFILE study and incurring expenses while initiating its U.S. Phase 3 INTEGRITY study for the accelerated return of bowel function following GI surgery. Accordingly, drug-manufacturing related expenses decreased by approximately $0.5 million, investigator site fees decreased by approximately $0.2 million, and clinical trial consultants and contract labor decreased by approximately $0.1 million in the three months ended September 30, 2023, compared to the three months ended September 30, 2022. Also contributing to the year-over-year decrease was lower research and development salaries and benefits by approximately $0.1 million in the three months ended September 30, 2023, compared to the three months ended September 30, 2022, primarily due to a decrease in research and development employee headcount.

General and administrative expenses decreased by approximately $0.4 million, or 19%, from $2.1 million for the three months ended September 30, 2022, to $1.7 million for the three months ended September 30, 2023, primarily because of a $0.3 million decrease in salaries and benefits and a $0.1 million decrease in stock-based compensation expense.

In connection with the entering into the research collaboration and license agreement with Giiant Pharma, Inc., in the three months ended September 30, 2023, the Company recognized In-process research and development expenses in the amount of $0.4 million consisting of certain contingent consideration obligations incurred as well as direct transaction-related costs.

About Palisade Bio 
Palisade Bio is a biopharmaceutical company focused on developing novel therapeutics for serious chronic gastrointestinal 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 Statements
This 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; 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 the COVID-19 pandemic or 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, 2022, filed with the Securities and Exchange Commission (“SEC”) on March 22, 2023, as well as the Company’s Quarterly Report on Form 10-Q, for the three and nine months period ended September 30, 2023, filed with the SEC on November 9, 2023. 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, LLC
Jenene Thomas
833-475-8247
PALI@jtcir.com

Source: Palisade Bio

Palisade Bio, Inc.
Condensed Consolidated Balance Sheets (Unaudited)
(in thousands, except share and per share amounts)

  September 30, December 31,
   2023   2022 
     
     
ASSETS    
Current assets:    
Cash and cash equivalents $15,312  $12,383 
Prepaid expenses and other current assets  954   2,350 
Total current assets  16,266   14,733 
Restricted cash  26   26 
Property and equipment, net  10   10 
Right-of-use asset  224   300 
Other noncurrent assets  541   694 
Total assets $17,067  $15,763 
     
LIABILITIES AND STOCKHOLDERS' EQUITY    
Current liabilities:    
Accounts payable $950  $1,759 
Accrued liabilities  794   574 
Accrued compensation and benefits  529   486 
Current portion of lease liability  117   105 
Debt  259   88 
Total current liabilities  2,649   3,012 
Warrant liability  2   61 
Contingent consideration obligation  212    
Lease liability, net of current portion  122   211 
Total liabilities  2,985   3,284 
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 September 30, 2023 and December 31, 2022
  2   2 
Common stock, $0.01 par value; 280,000,000 shares authorized;
9,210,751 and 2,944,306 shares issued and outstanding
at September 30, 2023 and December 31, 2022, respectively
  92   30 
Additional paid-in capital  132,523   121,637 
Accumulated deficit  (118,535)  (109,190)
Total stockholders' equity  14,082   12,479 
Total liabilities and stockholders' equity $17,067  $15,763 


Palisade Bio, Inc.
Condensed Consolidated Statements of Operations (Unaudited)
(in thousands, except share and per share amounts)

  Three Months Ended September 30, Nine Months Ended September 30,
   2023   2022   2023   2022 
License revenue $  $  $250  $ 
Operating expenses:        
Research and development  1,742   1,928   5,160   4,204 
In-process research and development  362      362    
General and administrative  1,674   2,075   4,644   7,259 
Restructuring costs     410      410 
Total operating expenses  3,778   4,413   10,166   11,873 
Loss from operations  (3,778)  (4,413)  (9,916)  (11,873)
Other income (expense):        
Interest expense  (8)  (4)  (11)  (10)
Other income  190   426   598   2,453 
Loss on issuance of warrants           (1,110)
Total other income, net  182   422   587   1,333 
Net loss $(3,596) $(3,991) $(9,329) $(10,540)
Basic and diluted net loss per common share $(0.49) $(4.10) $(1.55) $(18.40)
Basic and diluted weighted average shares used in computing
basic and diluted net loss per common share
  7,344,351   974,197   6,031,099   572,684 


Palisade Bio, Inc.
Condensed Consolidated Statements of Cash Flows (Unaudited)
(in thousands)

  Nine Months Ended September 30,
   2023   2022 
   
Net loss $(9,329) $(10,540)
Adjustments to reconcile net loss to net cash used in operating activities:    
Depreciation and amortization  4   1 
Noncash lease expense  76   140 
Loss on issuance of warrants     1,110 
Fair value of contingent consideration obligation  212    
Change in fair value of warrant liabilities  (59)  (2,403)
Stock-based compensation and related charges  439   946 
Other  (108)  (213)
Changes in operating assets and liabilities:    
Prepaid and other assets and other noncurrent assets  596   744 
Accounts payable and accrued liabilities  (184)  706 
Accrued compensation  43   (418)
Operating lease liabilities  (77)  (127)
Net cash used in operating activities  (8,387)  (10,054)
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 debt  (290)  (524)
Proceeds from issuance of common stock and warrants  9,419   14,401 
Proceeds from the exercise of warrants  2,758    
Payment of equity issuance costs  (567)  (333)
Net cash provided by financing activities  11,320   13,544 
Net increase (decrease) in cash, cash equivalents and restricted cash  2,929   3,490 
Cash, cash equivalents and restricted cash, beginning of period  12,409   10,521 
Cash, cash equivalents and restricted cash, end of period $15,338  $14,011 
Reconciliation of cash, cash equivalents and restricted cash to the balance sheets:    
Cash and cash equivalents $15,312  $13,985 
Restricted cash  26   26 
Total cash, cash equivalents and restricted cash $15,338  $14,011 


FAQ

What is the ticker symbol for Palisade Bio, Inc.?

The ticker symbol for Palisade Bio, Inc. is PALI on the Nasdaq.

What is the lead program being developed by Palisade Bio, Inc.?

The lead program is PALI-2108, an oral prodrug therapy for the treatment of moderate-to-severe ulcerative colitis.

What is the financial outlook for Palisade Bio, Inc.?

Palisade Bio, Inc. has a strong financial position with cash to execute on strategy and achieve significant milestones into 2025.

Who was appointed as the Chief Medical Officer of Palisade Bio, Inc.?

GI clinical expert and biotech entrepreneur Mitch Jones, M.D., PhD was appointed as the Chief Medical Officer of Palisade Bio, Inc.

What recent agreement did Palisade Bio, Inc. enter into?

Palisade Bio, Inc. entered into an exclusive worldwide licensing agreement with Giiant Pharma, Inc. for multiple oral drug candidates targeting IBD.

Palisade Bio, Inc.

NASDAQ:PALI

PALI Rankings

PALI Latest News

PALI Stock Data

5.28M
1.31M
1.88%
3.58%
2.82%
Biotechnology
Biological Products, (no Disgnostic Substances)
Link
United States of America
CARLSBAD