Indaptus Therapeutics Chief Scientific Officer Dr. Michael Newman to Present at the Donor Selection & Cell Source Summit

Rhea-AI Summary

Indaptus Therapeutics (Nasdaq: INDP) announced that Founder and Chief Scientific Officer Dr. Michael Newman will present at the 3rd Donor Selection & Cell Source Summit in San Diego on November 19–20, 2025.

Dr. Newman will present preclinical research titled “Creating Super Donor Cells Post-Donation – Using Attenuated and Killed Bacteria to Induce, Polarize, and Activate Human Innate and Adaptive Immune Cells In Vitro,” describing how the company’s Decoy bacterial platform and lead candidate Decoy20 may reduce donor cell variability and enhance potency and consistency of allogeneic immune cell products.

NEW YORK, Nov. 17, 2025 (GLOBE NEWSWIRE) -- Indaptus Therapeutics, Inc. (Nasdaq: INDP) (“Indaptus” or the “Company”), a clinical stage biotechnology company dedicated to pioneering innovative cancer and viral infection treatments, today announced that Michael Newman, Ph.D., Founder and Chief Scientific Officer, will present at the 3rd Donor Selection & Cell Source Summit, taking place November 19–20, 2025, in San Diego, California.

Dr. Newman’s presentation, titled, “Creating Super Donor Cells Post-Donation – Using Attenuated and Killed Bacteria to Induce, Polarize, and Activate Human Innate and Adaptive Immune Cells In Vitro,” will highlight new research demonstrating how the Company’s Decoy bacterial platform may help address one of the biggest challenges in allogeneic immune cell cancer therapy: donor cell variability.

The presentation will describe how Decoy20, Indaptus’ lead candidate, harnesses the power of killed, multi-immune agonist bacteria to trigger a broad, coordinated immune response that can be applied both as a direct cancer therapy and potentially as a cell manufacturing enhancer to improve the quality and consistency of allogeneic immune cell products.

Dr. Newman stated, “Allogeneic therapies, which rely on donor-derived immune cells to create ‘off-the-shelf’ cancer treatments, face a major hurdle when it comes to achieving consistent potency across donor sources. Our preclinical data show that Decoy bacteria can activate or induce the production of key immune cell types—such as NK cells, gamma-delta T cells, and M1 macrophages—that are also central to the success of allogeneic immunotherapies. This suggests that Decoy bacteria may have potential as an enabling tool to enhance the potency and reproducibility of donor-derived cell therapies.”

The Donor Selection & Cell Source Summit, hosted by Hanson Wade, brings together leaders from industry and academia to address critical bottlenecks in donor screening, cell sourcing, and process standardization across the expanding allogeneic cell therapy landscape.

For more information about the conference, please visit: www.donor-selection-cell-source-summit.com

About Indaptus Therapeutics

Indaptus Therapeutics has evolved from more than a century of immunotherapy advances. The Company’s novel approach is based on the hypothesis that efficient activation of both innate and adaptive immune cells and pathways and associated anti-tumor and anti-viral immune responses will require a multi-targeted package of immune system-activating signals that can be administered safely intravenously (i.v.). Indaptus’ patented technology is composed of single strains of attenuated and killed, non-pathogenic, Gram-negative bacteria producing a multiple Toll-like receptor (TLR), Nucleotide oligomerization domain (NOD)-like receptor (NLR) and Stimulator of interferon genes (STING) agonist Decoy platform. The product candidates are designed to have reduced i.v. toxicity, but largely uncompromised ability to prime or activate many of the cells and pathways of innate and adaptive immunity. Decoy product candidates represent an antigen-agnostic technology that have produced single-agent activity against metastatic pancreatic and orthotopic colorectal carcinomas, single agent eradication of established antigen-expressing breast carcinoma, as well as combination-mediated eradication of established hepatocellular carcinomas and non-Hodgkin’s lymphomas in standard pre-clinical models, including syngeneic mouse tumors and human tumor xenografts. In pre-clinical studies tumor eradication was observed with Decoy product candidates in combination with anti-PD-1 checkpoint therapy, low-dose chemotherapy, a non-steroidal anti-inflammatory drug, or an approved, targeted antibody. Combination-based tumor eradication in pre-clinical models produced innate and adaptive immunological memory, involved activation of both innate and adaptive immune cells, and was associated with induction of innate and adaptive immune pathways in tumors after only one i.v. dose of Decoy product candidate, with associated “cold” to “hot” tumor inflammation signature transition. The Decoy platform has also been shown to induce activation, polarization or maturation of human macrophages, dendritic, NK, NKT, CD4 T and CD8 T cells in vitro. IND-enabling, nonclinical toxicology studies demonstrated i.v. administration without sustained induction of hallmark biomarkers of cytokine release syndromes, possibly due to passive targeting to liver, spleen, and tumor, followed by rapid elimination of the product candidate. Indaptus’ Decoy product candidates have also produced single agent activity against chronic hepatitis B virus (HBV) and chronic human immunodeficiency virus (HIV) infections in pre-clinical in vivo models.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act. These include statements regarding management’s expectations, beliefs and intentions regarding, among other things, the sufficiency of our cash and cash equivalents to fund our ongoing activities and our expectations and plans regarding our Phase 1 clinical trial of Decoy20 and our combination study and the anticipated effects of our product candidates, including Decoy20. Forward-looking statements can be identified by the use of forward-looking words such as “believe”, “expect”, “intend”, “plan”, “may”, “should”, “could”, “might”, “seek”, “target”, “will”, “project”, “forecast”, “continue” or “anticipate” or their negatives or variations of these words or other comparable words or by the fact that these statements do not relate strictly to historical matters. Because forward-looking statements relate to matters that have not yet occurred, these statements are inherently subject to risks and uncertainties that could cause our actual results to differ materially from any future results expressed or implied by the forward-looking statements. Many factors could cause actual activities or results to differ materially from the activities and results anticipated in forward-looking statements, including, but not limited to the following: our limited operating history; conditions and events that raise substantial doubt regarding our ability to continue as going concern; the need for, and our ability to raise, additional capital given our lack of current cash flow; our clinical and preclinical development, which involves a lengthy and expensive process with an uncertain outcome; our incurrence of significant research and development expenses and other operating expenses, which may make it difficult for us to attain profitability; our pursuit of a limited number of research programs, product candidates and specific indications and failure to capitalize on product candidates or indications that may be more profitable or have a greater likelihood of success; our ability to obtain and maintain regulatory approval of any product candidate; the market acceptance of our product candidates; our reliance on third parties to conduct our preclinical studies and clinical trials and perform other tasks; our reliance on third parties for the manufacture of our product candidates during clinical development; our ability to successfully commercialize Decoy20 or any future product candidates; our ability to obtain or maintain coverage and adequate reimbursement for our products; the impact of legislation and healthcare reform measures on our ability to obtain marketing approval for and commercialize Decoy20 and any future product candidates; product candidates of our competitors that may be approved faster, marketed more effectively, and better tolerated than our product candidates; our ability to adequately protect our proprietary or licensed technology in the marketplace; the impact of, and costs of complying with healthcare laws and regulations, and our failure to comply with such laws and regulations; information technology system failures, cyberattacks or deficiencies in our cybersecurity; and unfavorable global economic conditions. These and other important factors discussed under the caption “Risk Factors” included in our most recent Annual Report on Form 10-K filed with the SEC on March 13, 2025, and our other filings with the SEC, could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. All forward-looking statements speak only as of the date of this press release and are expressly qualified in their entirety by the cautionary statements included in this press release. We undertake no obligation to update or revise forward-looking statements to reflect events or circumstances that arise after the date made or to reflect the occurrence of unanticipated events, except as required by applicable law.

Contact: investors@indaptusrx.com

FAQ

When will Indaptus (INDP) present at the Donor Selection & Cell Source Summit?

Dr. Michael Newman will present on November 19–20, 2025 at the summit in San Diego.

What is the title of the Indaptus (INDP) presentation at the summit?

The presentation is titled “Creating Super Donor Cells Post-Donation – Using Attenuated and Killed Bacteria to Induce, Polarize, and Activate Human Innate and Adaptive Immune Cells In Vitro.”

What is Decoy20 and how will Indaptus (INDP) describe it at the conference?

Decoy20 is the company’s lead candidate; the talk will describe preclinical data showing killed multi-agonist bacteria may trigger broad immune activation to improve donor cell potency.

How might Indaptus’ (INDP) Decoy platform address donor variability in allogeneic cell therapy?

The company says Decoy bacteria can activate NK cells, gamma-delta T cells, and M1 macrophages to potentially enhance consistency and potency across donor sources.

Will Indaptus (INDP) present clinical data for Decoy20 at the summit?

The announcement references preclinical research; no clinical trial readouts or clinical results are indicated.

How can investors or attendees find more information about the Donor Selection & Cell Source Summit?

Additional conference details are available on the summit website at www.donor-selection-cell-source-summit.com.