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PolyPid's D-PLEX₁₀₀ Wins BioTech Breakthrough Award for "Therapeutics Solution of the Year"

Key Takeaway: PolyPid Ltd. announced that its lead candidate, D-PLEX™1800, has won the 'Therapeutics Solution of the Year' award from BioTech Breakthrough. This innovative product aims to prevent surgical site infections (SSIs) through localized antibiotic delivery. The recent Phase 3 SHIELD II trial showed a significant 58% reduction in SSIs, highlighting its potential impact on surgical care.
Price reaction · baseline $3.79 (2025-11-05 close) · hit pre-market · clean, no other PYPD news in the window
day 0 close · peak
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Market Sentiment Analysis

POSITIVE FACTORS

  • D-PLEX™1800 recognized as 'Therapeutics Solution of the Year'.
  • Demonstrated a 58% relative risk reduction in SSIs.
  • Potential to transform surgical care and improve patient outcomes.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+50%
120-day peak, hindsight
Typical move
4.8%
average across 4 past catalysts
Lead asset
D-PLEX
Phase 3 · Surgical Site Infection

Full Press Release Details

PETACH TIKVA, Israel, Nov. 06, 2025 (GLOBE NEWSWIRE) --PolyPid Ltd.(Nasdaq: PYPD) ("PolyPid" or the "Company"), a late-stage biopharma company focused on improving surgical outcomes, today announced that D-PLEX₁₀₀, the company’s lead candidate, has been named "Therapeutics Solution of the Year" byBioTech Breakthrough, a leading independent market intelligence organization which evaluates and recognizes standout life sciences and biotechnology companies, products and services around the globe.
D-PLEX₁₀₀, powered by PolyPid’s proprietary PLEX (Polymer-Lipid Encapsulation matriX) technology is designed to prevent surgical site infections (SSIs) with extended, localized antibiotic delivery directly at the surgical site. Administered during the surgery, D-PLEX₁₀₀ delivers continuous, targeted release of doxycycline for 30 days, protecting patients during the period of highest vulnerability to infection.
"PolyPid is setting a new standard for SSI prevention. These infections remain among the most common and costly post-operative complications, causing extended hospital stays and higher morbidity rates. Standard antibiotics often fail to reach surgical sites due to disrupted blood supply," said Bryan Vaughn, Managing Director, BioTech Breakthrough. "By addressing one of surgery's most persistent challenges, D-PLEX₁₀₀ delivers better patient outcomes while reducing provider burdens and generating healthcare savings. Congratulations on winning 'Therapeutics Solution of the Year!'"
"We are deeply honored by this recognition, which recognizes the importance of our mission to address one of healthcare's most persistent challenges," said Dikla Czaczkes Akselbrad, Chief Executive Officer of PolyPid. "With SSIs accounting for 20% to 31% of all hospital-acquired infections1, D-PLEX₁₀₀ represents a significant breakthrough. Our Phase 3 SHIELD II trial demonstrated a remarkable relative risk reduction of 58% (p< 0.005) in SSIs following abdominal colorectal surgery, addressing a critical gap where current approaches often fall short. At a time when hospitals face complex challenges in both preventing and reporting infections, D-PLEX₁₀₀ has the potential to transform surgical care by directly improving patient outcomes and hospital efficiency through meaningful infection reduction."
D-PLEX₁₀₀ has received Breakthrough Therapy Designation, three QIDP designations, and three Fast Track designations from the U.S. Food and Drug Administration. NDA submission is expected early 2026.
About D-PLEX₁₀₀D-PLEX₁₀₀, PolyPid’s lead product candidate, is designed to provide local prolonged and controlled anti-bacterial activity directly at the surgical site to prevent surgical site infections (“SSIs”). Following the administration of D-PLEX₁₀₀ into the surgical site, the PLEX (Polymer-Lipid Encapsulation matriX) technology pairs with Active Pharmaceutical Ingredients, enabling a prolonged and continuous release of the broad-spectrum antibiotic doxycycline, resulting in a high local concentration of the drug for a period of 30 days for the prevention of SSIs, with additional potential to prevent SSIs caused by antibiotic-resistant bacteria at the surgical site. D-PLEX₁₀₀ recently demonstrated positive results in the Phase 3 SHIELD II trial, achieving a statistically significant 58% (p< 0.005) relative risk reduction in SSI incidence following abdominal colorectal surgery with large incisions. D-PLEX₁₀₀ received Breakthrough Therapy designation from the U.S. Food and Drug Administration for the prevention of SSIs in patients undergoing elective colorectal surgery.
About PolyPidPolyPid Ltd. (Nasdaq:PYPD) is a late-stage biopharma company aiming to improve surgical outcomes. Through locally administered, controlled, prolonged-release therapeutics, PolyPid's proprietary PLEX (Polymer-Lipid Encapsulation matriX) technology pairs with Active Pharmaceutical Ingredients (APIs), enabling precise delivery of drugs at optimal release rates over durations ranging from several days to months. Following positive phase 3 results, New Drug Application (NDA) submission of D-PLEX₁₀₀, PolyPid's lead product candidate, for the prevention of abdominal colorectal surgical site infections, is expected in early 2026. In addition, the Company has an innovative pipeline in oncology, obesity and diabetes.For additional Company information, please visithttp://www.polypid.comand follow us onTwitter (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 D-PLEX₁₀₀ potential to transform surgical care by directly improving patient outcomes and hospital efficiency through meaningful infection reduction, the planned NDA submission for D-PLEX₁₀₀ and timing thereof. 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 Warshavsky908-858-5995IR@Polypid.com

Investor Relations Contact:Arx Investor RelationsNorth American Equities Deskpolypid@arxhq.com

1The Burden of Health Care Utilization, Cost, and Mortality Associated with Select Surgical Site Infections Shambhu, Sonali et al. Joint Commission Journal on Quality and Patient Safety, Volume 50, Issue 12, 857 - 866

Frequently Asked Questions

What is D-PLEX™1800?

D-PLEX™1800 is PolyPid's lead candidate designed to prevent surgical site infections through localized antibiotic delivery.

What award did D-PLEX™1800 win?

D-PLEX™1800 was awarded 'Therapeutics Solution of the Year' by BioTech Breakthrough.

What was the result of the Phase 3 trial?

The Phase 3 SHIELD II trial showed a 58% relative risk reduction in surgical site infections.

What technology powers D-PLEX™1800?

D-PLEX™1800 is powered by PolyPid's proprietary PLEX technology for controlled antibiotic release.

When is the NDA submission for D-PLEX™1800 expected?

The NDA submission for D-PLEX™1800 is expected in early 2026.

Last updated: Nov 6, 2025