PolyPid Provides Corporate Update and Reports Fourth Quarter and Full-Year 2025 Financial Results
MWN-AI** Summary
PolyPid Ltd. (Nasdaq: PYPD) provided a corporate update and reported its financial results for Q4 and the full year 2025 on February 11, 2026, highlighting significant strides in the advancement of its lead product, D-PLEX™. The biopharmaceutical company is in advanced discussions for a U.S. commercial partnership for D-PLEX™, which is designed to prevent surgical site infections in abdominal colorectal surgeries. Positive feedback from the FDA regarding a pre-New Drug Application (NDA) meeting supports a planned rolling NDA submission set to begin by the end of Q1 2026.
Dikla Czaczkes Akselbrad, the CEO of PolyPid, emphasized the company's transformative potential in 2026 as it transitions from late-stage development to commercial execution. The recent appointment of Ms. Brooke Story as Chairman of the Board adds significant leadership expertise from her tenure at BD and Medtronic.
Financially, PolyPid reported a Q4 net loss of $8.5 million, unchanged from the previous year but improved on a per-share basis. For 2025, the total net loss rose to $34.2 million, reflecting ongoing investment in R&D and commercialization efforts. R&D expenditures increased to $23.8 million for the year due to the completion of the SHIELD II Phase 3 trial and regulatory preparations.
As of December 31, 2025, PolyPid held $12.9 million in cash and equivalents. Subsequent to the quarter, the company raised $3.7 million from warrant exercises, further strengthening its balance sheet.
Moving forward, PolyPid aims to leverage its Kynatrix™ technology to broaden its pharmacological capabilities. A conference call is scheduled for today at 8:30 AM ET to discuss these developments further.
MWN-AI** Analysis
PolyPid Ltd. (Nasdaq: PYPD) has recently provided a compelling corporate update indicating significant potential for the company's future, particularly with the progress surrounding its lead product, D-PLEX™. The company has advanced in its discussions for a commercial partnership in the U.S. and received positive FDA feedback, which supports its plans to initiate a rolling New Drug Application (NDA) submission by the end of Q1 2026. This momentum indicates PolyPid could soon transition from a development stage to commercial operation, a significant step that should excite investors.
Financially, while the company reported a net loss of $34.2 million for 2025, this represents an increase in the loss per share compared to 2024. However, the reduction in R&D expenses in Q4 2025 and a sustained cash reserves of $12.9 million (with an additional $3.7 million generated from warrant exercises) are signs of operational efficiency and liquidity that will support upcoming initiatives. Investors should also consider the appointments made at the leadership level, such as the addition of Ms. Brooke Story as Chairman, which could enhance corporate governance and strategic direction.
Looking ahead, PolyPid's emphasis on enhancing its drug delivery technology through Kynatrix™ and its expansion into metabolic diseases add to its growth narrative. If D-PLEX™ continues to garner regulatory approval and commercial traction, 2026 could indeed be transformative for the company.
In conclusion, for investors with an appetite for risk in the biopharmaceutical sector, PolyPid presents a compelling opportunity. As discussions progress and the NDA submission approaches, shareholders might want to closely monitor the stock, leveraging any fluctuations for potential entry points into a stock poised for growth. Long-term prospects appear promising, particularly if operational efficiencies manifest in coming quarters and market adoption accelerates.
**MWN-AI Summary and Analysis is based on asking OpenAI to summarize and analyze this news release.
The Company is in Advanced Stages of Commercial U.S. Partnership Discussions for D-PLEX???
Positive FDA Pre-NDA Feedback Supports Rolling NDA Review; Submission Expected to Begin by the End of the First Quarter of 2026
Conference Call Scheduled for Today at 8:30 AM ET
PETACH TIKVA, Israel, Feb. 11, 2026 (GLOBE NEWSWIRE) -- PolyPid Ltd. (Nasdaq: PYPD) (“PolyPid” or the “Company”), an innovative biopharmaceutical company dedicated to improving patient outcomes by elevating treatment effectiveness, right where care begins, today provided a corporate update and reported financial results for the three months and full year ended December 31, 2025.
Recent Corporate Highlights:
- Advancing Toward Commercialization: The Company made significant progress towards finalizing a potential partnership in the United States for D-PLEX???, including moving into advanced stages of discussions.
- Regulatory Momentum: Received positive feedback from the U.S. Food and Drug Administration (“FDA”) following the pre-New Drug Application (“NDA”) meeting minutes for D-PLEX??? in the prevention of abdominal colorectal surgical site infections (“SSIs”) for a planned rolling NDA submission beginning by the end of the first quarter of 2026.
- Strengthened the Company’s governance and leadership: Appointed Ms. Brooke Story as Chairman of the Board of Directors, effective December 11, 2025. Ms. Story brings extensive leadership experience in medical technology and surgical solutions, including senior executive roles at BD (Becton, Dickinson and Company) and Medtronic PLC.
- Participated in a virtual Key Opinion Leader event during the quarter, featuring Dr. Steven D. Wexner, MD, PhD (Hon), FACS, FRCS (Eng, Ed), Hon FRCS (Glasg, Eng, Ire), MAMSE, Executive Director and System Chief of Colorectal Surgery for MedStar Health and a globally recognized leader in colorectal surgery, to discuss the significant clinical and economic burden of SSIs and the potential role of D-PLEX??? in improving surgical outcomes based on the positive results of the Phase 3 SHIELD II trial.
- Unveiling the Kynatrix™ Technology: Over the past years, PolyPid has significantly expanded its drug delivery capabilities beyond the original PLEX technology. These advancements include the ability to support new therapeutic areas and delivery approaches, with the first test case being the Company’s expansion into metabolic diseases through an ultra long-acting GLP-1 receptor agonist program. These advancements have generated additional intellectual property beyond PLEX and are now unified under the newly introduced Kynatrix™ technology.
“2025 was a pivotal year for PolyPid as we successfully completed the SHIELD II Phase 3 trial and advanced D-PLEX??? into the final stages of regulatory approval,” said Dikla Czaczkes Akselbrad, Chief Executive Officer of PolyPid. “Following our positive Phase 3 results and progress made in the past quarter, we have moved into advanced stage discussions for potential commercial partnership in the U.S., reflecting the growing recognition of D-PLEX???’s clinical and commercial value. At the same time, positive engagement with the FDA, including agreement on a rolling NDA review, further advanced our regulatory path as we work toward an NDA submission beginning by end of the first quarter of 2026. We believe 2026 has the potential to be a transformative year for PolyPid, marking our transition from late-stage development into full commercial execution, and we look forward to providing updates as these developments occur.”
Financial results for three months ended December 31, 2025
- Research and development (“R&D”) expenses for the three months ended December 31, 2025, were $6.2 million, compared to $7.0 million in the same three-month period of 2024. The decrease in R&D expenses was primarily driven by the completion of the SHIELD II Phase 3 trial and the Company’s transition toward regulatory submissions.
- General and administrative (“G&A”) expenses for the three months ended December 31, 2025, were $1.8 million, compared to $1.0 million for the same period of 2024.
- Marketing and business development expenses for the three months ended December 31, 2025, were $0.6 million, compared to $0.2 million in the same period of 2024.
- For the three months ended December 31, 2025, the Company had a net loss of $8.5 million, or ($0.41) per share, compared to a net loss of $8.5 million, or ($1.13) per share, in the three-month period ended December 31, 2024.
Financial results for the full year ended December 31, 2025
- R&D expenses for the twelve months ended December 31, 2025, were $23.8 million, compared to $22.8 million for the same twelve-month period of 2024. The increase was primarily driven by continued activities related to the completion of the SHIELD II Phase 3 trial, along with regulatory preparation efforts and advancement of the Company’s development programs.
- G&A expenses for the twelve months ended December 31, 2025, were $7.2 million, compared to $4.3 million for the same period of 2024. The increase was primarily due to non-cash expenses related to performance-based options (“PSUs”), following the successful SHIELD II Phase 3 trial, which triggered the vesting of the PSUs.
- Marketing and business development expenses for the twelve months ended December 31, 2025, were $2.0 million, compared to $0.9 million for the same period of 2024, primarily due to increased business development and commercial preparation efforts.
- For the twelve months ended December 31, 2025, the Company had a net loss of $34.2 million, or ($2.09) per share, compared to a net loss of $29.0 million, or ($4.91) per share, in the twelve-month period ended December 31, 2024.
Balance Sheet Highlights
- As of December 31, 2025, the Company had cash, cash equivalents, and short-term deposits of $12.9 million, compared to $15.6 million on December 31, 2024.
- Subsequent to the end of the quarter, several long-time shareholders exercised warrants ahead of the warrants’ expiration date at prices ranging between $3.61 per share (for the warrants with an expiration date of August 2026) and $4.50 per share (for the warrants with an expiration date of June 2027), generating $3.7 million in additional proceeds, further strengthening the Company’s balance sheet.
- The Company believes that its current cash balance will be sufficient to fund operations into the second half of 2026 and through several significant upcoming potential milestones.
Conference Call Dial-In & Webcast Information:
| Date: | Wednesday, February 11, 2026 |
| Time: | 8:30 AM Eastern Time |
| Conference Call: | https://register-conf.media-server.com/register/BI793c5305462d49cea4ba91529d2636bf |
| Webcast: | https://edge.media-server.com/mmc/p/izp7gdk6 |
About PolyPid
PolyPid Ltd. (Nasdaq: PYPD) is an innovative biopharmaceutical company dedicated to elevating treatment effectiveness, right where care begins. The Company develops long-acting, controlled-release drugs designed to deliver therapy precisely at the site of care, addressing critical unmet medical needs across a wide and diverse pipeline spanning surgical care, metabolic diseases, and beyond. PolyPid’s lead product, D-PLEX???, successfully met its primary and all key secondary endpoints in the landmark Phase 3 SHIELD II trial for the prevention of surgical site infections. Guided by a commitment to precision and innovation, PolyPid is redefining how therapies perform and raise the standard of patient care.
For additional Company information, please visit http://www.polypid.com and follow us on Twitter (X) and LinkedIn.
Forward-looking Statements
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act and other securities laws. Words such as “expects,” “anticipates,” “intends,” “plans,” “believes,” “seeks,” “estimates” and similar expressions or variations of such words are intended to identify forward-looking statements. For example, the Company is using forward-looking statements when it discusses its regulatory strategy and planned timing for the submission of an NDA for D-PLEX???, including the use of a rolling NDA review, advanced stages of commercial U.S. partnership discussions for D-PLEX???, the potential role of D-PLEX??? in improving surgical outcomes, the Company’s evolution toward commercialization, the growing recognition of D-PLEX???’s clinical and commercial value, its belief that 2026 has the potential to be a transformative year for the Company, marking its transition from late-stage development into full commercial execution, and its expectation that current cash resources will be sufficient to fund operations into the second half of 2026 and through several significant upcoming potential milestones. Forward-looking statements are not historical facts, and are based upon management’s current expectations, beliefs and projections, many of which, by their nature, are inherently uncertain. Such expectations, beliefs and projections are expressed in good faith. However, there can be no assurance that management’s expectations, beliefs and projections will be achieved, and actual results may differ materially from what is expressed in or indicated by the forward-looking statements. Forward-looking statements are subject to risks and uncertainties that could cause actual performance or results to differ materially from those expressed in the forward-looking statements. For a more detailed description of the risks and uncertainties affecting the Company, reference is made to the Company’s reports filed from time to time with the Securities and Exchange Commission, including, but not limited to, the risks detailed in the Company’s Annual Report on Form 20-F filed on February 26, 2025. Forward-looking statements speak only as of the date the statements are made. The Company assumes no obligation to update forward-looking statements to reflect actual results, subsequent events or circumstances, changes in assumptions or changes in other factors affecting forward-looking information except to the extent required by applicable securities laws. If the Company does update one or more forward-looking statements, no inference should be drawn that the Company will make additional updates with respect thereto or with respect to other forward-looking statements. References and links to websites have been provided as a convenience, and the information contained on such websites is not incorporated by reference into this press release. PolyPid is not responsible for the contents of third-party websites.
Company Contact:
PolyPid Ltd.
Ori Warshavsky
908-858-5995
IR@Polypid.com
Investor Relations Contact:
Arx Investor Relations
North American Equities Desk
polypid@arxhq.com
| CONSOLIDATED BALANCE SHEETS (UNAUDITED) | |||||
| U.S. dollars in thousands | |||||
| December 31, | |||||
| 2025 | 2024 | ||||
| ASSETS | |||||
| CURRENT ASSETS: | |||||
| Cash and cash equivalents | $ | 6,402 | $ | 15,641 | |
| Restricted deposits | 193 | 168 | |||
| Short-term deposits | 6,531 | - | |||
| Pre-launch inventories | 1,106 | - | |||
| Prepaid expenses and other current assets | 995 | 764 | |||
| Total current assets | 15,227 | 16,573 | |||
| LONG-TERM ASSETS: | |||||
| Property and equipment, net | 5,094 | 6,075 | |||
| Operating lease right-of-use assets | 1,675 | 2,295 | |||
| Other long-term assets | 311 | 277 | |||
| Total long-term assets | 7,080 | 8,647 | |||
| Total assets | $ | 22,307 | $ | 25,220 | |
| CONSOLIDATED BALANCE SHEETS (UNAUDITED) | |||||
| U.S. dollars in thousands (except share and per share data) | |||||
| December 31, | |||||
| 2025 | 2024 | ||||
| LIABILITIES AND SHAREHOLDERS' EQUITY | |||||
| CURRENT LIABILITIES: | |||||
| Trade payables | $ | 2,856 | $ | 2,409 | |
| Accrued expenses and other current liabilities | 2,734 | 2,566 | |||
| Current maturities of long-term debt | 988 | 6,787 | |||
| Current maturities of operating lease liabilities | 1,161 | 919 | |||
| Total current liabilities | 7,739 | 12,681 | |||
| LONG-TERM LIABILITIES: | |||||
| Long-term debt | - | 634 | |||
| Deferred revenues | 2,548 | 2,548 | |||
| Long-term operating lease liabilities | 647 | 1,277 | |||
| Other liabilities | 400 | 396 | |||
| Total long-term liabilities | 3,595 | 4,855 | |||
| COMMITMENTS AND CONTINGENT LIABILITIES | |||||
| SHAREHOLDERS' EQUITY: | |||||
| Ordinary shares, no par value - | - | - | |||
| Authorized: 107,800,000 shares at December 31, 2025 and 2024, respectively; Issued and outstanding: 18,204,002 and 10,190,904 shares at December 31, 2025 and 2024, respectively | |||||
| Additional paid-in capital | 312,473 | 275,015 | |||
| Accumulated deficit | (301,500) | (267,331) | |||
| Total shareholders' equity | 10,973 | 7,684 | |||
| Total liabilities and shareholders' equity | $ | 22,307 | $ | 25,220 | |
| CONSOLIDATED STATEMENTS OF OPERATIONS (UNAUDITED) | ||||||||
| U.S. dollars in thousands (except share and per share data) | ||||||||
| Year Ended December 31, | ||||||||
| 2025 | 2024 | 2023 | ||||||
| Operating expenses: | ||||||||
| Research and development | $ | 23,807 | $ | 22,811 | $ | 16,148 | ||
| Marketing and business development | 1,977 | 945 | 1,196 | |||||
| General and administrative | 7,183 | 4,273 | 5,523 | |||||
| Operating loss | 32,967 | 28,029 | 22,867 | |||||
| Loss on extinguishment of debt | 512 | - | - | |||||
| Financial expense, net | 685 | 951 | 929 | |||||
| Loss before income tax | 34,164 | 28,980 | 23,796 | |||||
| Income tax expense | 5 | 42 | 69 | |||||
| Net loss | $ | 34,169 | $ | 29,022 | $ | 23,865 | ||
| Loss per share: | ||||||||
| Basic | $ | 2.09 | $ | 4.91 | $ | 16.99 | ||
| Diluted | $ | 2.09 | $ | 4.91 | $ | 16.93 | ||
| Weighted-average Ordinary shares outstanding: | ||||||||
| Basic | 16,351,890 | 5,912,890 | 1,404,368 | |||||
| Diluted | 16,351,890 | 5,912,890 | 1,421,308 | |||||
| CONSOLIDATED STATEMENTS OF OPERATIONS (UNAUDITED) | |||||
| U.S. dollars in thousands (except share and per share data) | |||||
| Three Months Ended December 31, | |||||
| 2025 | 2024 | ||||
| Operating expenses: | |||||
| Research and development, | $ | 6,218 | $ | 7,027 | |
| Marketing and business development expenses | 556 | 198 | |||
| General and administrative | 1,756 | 996 | |||
| Operating loss | 8,530 | 8,221 | |||
| Financial expense, net | 24 | 286 | |||
| Loss before income tax | 8,554 | 8,507 | |||
| Income tax expense (income) | (81) | 13 | |||
| Net loss attributable to Ordinary shares | $ | 8,473 | $ | 8,520 | |
| Loss per share: | |||||
| Basic | $ | 0.41 | $ | 1.13 | |
| Diluted | $ | 0.41 | $ | 1.13 | |
| Weighted average number of Ordinary shares used in computing basic and diluted loss per share | 20,588,114 | 7,507,420 | |||
FAQ**
What are the key factors driving the advanced stages of commercial U.S. partnership discussions for PolyPid Ltd. PYPD's D-PLEX??? and how might this influence the company's market entry strategy?
How does the positive FDA pre-NDA feedback for PolyPid Ltd. PYPD's D-PLEX??? enhance the likelihood of a successful rolling NDA submission by the end of Q1 2026?
What specific benefits does Ms. Brooke Story bring to the leadership of PolyPid Ltd. PYPD, and how could her experience impact the company's commercialization efforts?
Given the company's net loss and current cash balance, what financial strategies will PolyPid Ltd. PYPD pursue to sustain operations during 2026 and support its upcoming milestones?
**MWN-AI FAQ is based on asking OpenAI questions about PolyPid Ltd. (NASDAQ: PYPD).
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