Palisade Bio Reports Year End 2022 Financial Results And Provides Corporate Update; As Of December 31, 2022, The Company Had Cash, Cash Equivalents And Restricted Cash Of $12.4M

Phase 2 topline data readout for prevention of post-surgical abdominal adhesions on track for Q2 2023 Strong balance sheet with sufficient cash expected to

Phase 2 topline data readout for prevention of post-surgical abdominal adhesions on track for Q2 2023

Strong balance sheet with sufficient cash expected to fund operations into mid-2024

Carlsbad, CA, March 23, 2023 (GLOBE NEWSWIRE) — Palisade Bio, Inc. (NASDAQ:PALI) (“Palisade” or the “Company”), a biopharmaceutical company advancing therapies for acute and chronic gastrointestinal (GI) complications, today reported its financial results for the full year 2022 and provided a corporate update.

“Our team has made great progress executing our operational plan to strengthen our financial profile, focus our pipeline and position the Company for important near-term data readouts. With the cash proceeds from our recently completed financings and exercises of warrants, we believe we are in a strong financial position to build on this momentum,” commented J.D. Finley, interim Chief Executive Officer. “We are focused and optimistic about our U.S. Phase 2 adhesions study with our lead drug, LB1148. We expect the topline data from this study in the second quarter of 2023, which we anticipate will provide valuable insight to determine the next phase of development for this program as we drive towards commercialization while also evaluating plans for additional pipeline indications. We believe that 2023 is poised to be an important year with a number of catalysts and opportunities to unlock significant shareholder value.”

Clinical Program Update for LB1148

U.S. Phase 2 Adhesions Study

LB1148 is currently being evaluated in a Phase 2 study for its effectiveness in reducing intra-abdominal adhesions, accelerating return of gastrointestinal function, and the prevention of post-operative ileus in patients undergoing elective bowel resection (PROFILE).

In December 2022, the Company voluntarily closed enrollment with a total of 35 of the planned 70 patients in its Phase 2 study. The Company expects to report topline data from these patients during the second quarter of 2023.

Dose Optimization Study

The Company is currently planning a dose optimization study for all indications to determine if a different dosing protocol would enhance the risk profile of LB1148 while simultaneously providing efficacy. It is anticipated that this study will generate pharmacokinetic and pharmacodynamic data across multiple doses in patients, with enrollment expected to commence in the second quarter of 2023.

Summary of Financial Results for the Year Ended December 31, 2022

As of December 31, 2022, the Company had cash, cash equivalents and restricted cash of $12.4 million. With the additional net cash proceeds of $4.7 million received in the first week of January ($2.1 million from the Company’s registered direct offering and private placement, which closed on January 4, 2023, plus $2.6 million related to warrant exercises) management believes it has sufficient cash to fund the Company’s operations into mid-2024.

Research and development expenses were $6.5 million for the year ended December 31, 2022, compared to $2.4 million for the year ended December 31, 2021, an increase of $4.1 million, or approximately 169%. The year-over-year increase is a result of the increased clinical activities from resuming patient enrollment in the Company’s U.S Phase 2 clinical study of the prevention of post-surgical abdominal adhesions and from the initiation of enrollment in its U.S. Phase 3 clinical study of the accelerated return of bowel function following gastrointestinal surgery. As previously disclosed, in the fourth quarter of 2022 the Company paused its U.S. Phase 3 study and is now directing its clinical focus to the continued advancement of its U.S. Phase 2 adhesions study.

General and administrative expenses decreased from $9.3 million for the year ended December 31, 2021 to $8.8 million for the year ended December 31, 2022. The decrease of $0.5 million was primarily attributable a year-over-year decrease in stock compensation expense of $0.6 million. The decrease in stock-based compensation expense in 2022 compared to 2021 was due to (i) approximately $0.4 million of incremental expense recognized in the fourth quarter of 2021 due to the modification of certain outstanding stock options and (ii) approximately $0.2 million of expense recognized in the second quarter of 2021 related to stock options granted to executive management as a result of the successful completion of its 2021 reverse merger; neither of which recurred in 2022.

The Company recognized restructuring costs of $0.4 million for the year ended December 31, 2022, consisting of severance and benefits payments pursuant to employment agreements and the execution of severance and release agreements with employees terminated under a September 2022 cost-reduction plan. As a result of the September 2022 cost-reduction plan as well as the executive officer terminations in October 2022, which were unrelated to the September 2022 cost-reduction plan, the Company began 2023 with a reduction in workforce of approximately 30%, which it believes aligns operational costs with its current operating plan and strategic initiatives.

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