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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, DC 20549

 

FORM 8-K

 

CURRENT REPORT

Pursuant to Section 13 or 15(d)

of the Securities Exchange Act of 1934

 

Date of Report (Date of earliest event reported) November 12, 2024

 

INDAPTUS THERAPEUTICS, INC.

(Exact name of registrant as specified in its charter)

 

Delaware   001-40652   86-3158720

(State or other jurisdiction

of incorporation)

 

(Commission

File Number)

 

(IRS Employer

Identification No.)

 

3 Columbus Circle    
15th Floor    
New York, New York   10019
(Address of principal executive offices)   (Zip Code)

 

(646) 427-2727

(Registrant’s telephone number, including area code)

 

 

(Former name or former address, if changed since last report)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):

 

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
   
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
   
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
   
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

 

Securities registered pursuant to Section 12(b) of the Act:

 

Title of each class   Trading Symbol   Name of each exchange on which registered
Common Stock, $0.01 par value   INDP   Nasdaq Capital Market

 

Indicate by check mark whether the registrant is an emerging growth company as defined in as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).

 

Emerging growth company

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐

 

 

 

 
 

 

Item 2.02. Results of Operations and Financial Condition.

 

On November 12, 2024, Indaptus Therapeutics, Inc. (the “Company”) issued a press release announcing its financial results for the quarter ended September 30, 2024. The full text of the press release is furnished as Exhibit 99.1 to this Current Report on Form 8-K and is incorporated herein by reference.

 

The information in this Current Report on Form 8-K (including Exhibit 99.1) shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that Section, nor shall it be deemed to be incorporated by reference into any filing of the Company under the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth by specific reference in such filing.

 

Item 9.01. Financial Statements and Exhibits.

 

(d) Exhibits.

 

Exhibit No.   Description
     
99.1   Press Release of Indaptus Therapeutics, Inc., dated November 12, 2024.
     
104   Cover Page Interactive Data File (formatted as Inline XBRL document)

 

 
 

 

SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

Date: November 12, 2024

 

  INDAPTUS THERAPEUTICS, INC.
     
  By: /s/ Nir Sassi
  Name: Nir Sassi
  Title: Chief Financial Officer

 

 

 

 

Exhibit 99.1

 

 

Indaptus Therapeutics Reports Third Quarter 2024 Financial Results and Provides Corporate Update

 

NEW YORK (November 12, 2024) - 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 financial results for the third quarter ended September 30, 2024, and provided a corporate update.

 

Jeffrey Meckler, Indaptus Therapeutics’ Chief Executive Officer, commented, “The recent announcement highlighting our clinical supply agreement with BeiGene is an important milestone, representing a significant step forward in our clinical development as we plan the first clinical trial combining BeiGene’s anti-PD-1 antibody, tislelizumab, with Indaptus’ Decoy20 product candidate for cancer treatment. PD-1 inhibitors have proven meaningful in treating multiple cancer types, and we are optimistic that we can improve patient outcomes by broadly and safely stimulating the immune system to enhance the effectiveness of currently approved treatments. We have also progressed our Phase 1 clinical trial to now allow for unrestricted enrollment of patients in weekly administration at the lower Decoy20 dose, which will enable us to gather more safety and efficacy data, which is important for assessing the full potential of Decoy20. Those data will guide how we initiate the combination trial next year. To date, Decoy20 continues to be well tolerated and we are anxiously awaiting further outcomes, which we will report as the trial progresses. We continue to carefully manage our resources and will provide status updates as they develop.”

 

Key recent highlights:

 

Announced clinical supply agreement with BeiGene to evaluate novel cancer treatment combinations for the treatment of patients with advanced solid tumors

 

Initiated unrestricted enrollment of patients in Indaptus’ Phase 1 clinical trial of Decoy20 allowing for weekly dosing based on encouraging safety data

 

  Announced that Dr. Michael Newman, Founder and Chief Scientific Officer, has published his groundbreaking research in the peer-reviewed journal, Frontiers in Immunology. The article was titled, “Invention and Characterization of a Systemically Administered, Attenuated and Killed Bacteria-Based Multiple Immune Receptor Agonist for Antitumor Immunotherapy”

 

Completed a $3 million registered direct offering and concurrent private placement on August 8, 2024 (the “August 2024 Offering”), for net proceeds of approximately $2.5 million

 

Participated in Lumanity webinar regarding the future of innate immunity in cancer immunotherapy

 

Financial Highlights for the Third Quarter Ended September 30, 2024

 

Research and development expenses for the three months ended September 30, 2024, were approximately $1.5 million, a decrease of approximately $0.7 million compared with approximately $2.2 million in the three months ended September 30, 2023. The decrease for the three-month period was primarily due to the development of our manufacturing processes of Decoy20 that were conducted in the three months ended September 30, 2023. Research and development expenses for the nine months ended September 30, 2024, were approximately $4.8 million, a decrease of approximately $0.8 million compared with approximately $5.6 million in the nine months ended September 30, 2023. The decrease for the nine-month period was primarily due to a decrease of approximately $1.1 million in the development of our manufacturing processes of Decoy20 that were conducted in 2023 and was offset by an increase of approximately $0.3 million in our Phase 1 clinical trial and in payroll and related expenses.

 

General and administrative expenses for the three months ended September 30, 2024, were approximately $1.7 million, a decrease of approximately $0.3 million compared with approximately $2.0 million in the three months ended September 30, 2023. The decrease was primarily due to stock-based compensation, legal fees and recruitment costs. General and administrative expenses for the nine months ended September 30, 2024, were approximately $6.4 million, a decrease of approximately $0.2 million compared with approximately $6.6 million in the nine months ended September 30, 2023. The decrease for the nine-month period was primarily due to a decrease of approximately $0.7 million in legal fees, payroll and related expenses, recruitment costs and directors’ and officers’ insurance expenses, and was offset by an increase of approximately $0.5 million in investor relations and business development expenses.

 

Loss per share for the three months ended September 30, 2024, was approximately $0.32 compared with approximately $0.47 for the three months ended September 30, 2023. Loss per share for the nine months ended September 30, 2024, was approximately $1.23 compared with approximately $1.36 per share for the nine months ended September 30, 2023.

 

As of September 30, 2024, the Company had cash and cash equivalents of approximately $7.4 million. As of December 31, 2023, the Company had cash and cash equivalents of $13.4 million. The Company expects that its current cash and cash equivalents will support its ongoing operating activities into the first quarter of 2025. This cash runway guidance is based on the Company’s current operational plans and excludes any additional funding and any business development activities that may be undertaken. Indaptus continues to assess all financing options that would support its corporate strategy.

 

Net cash used in operating activities was approximately $8.9 million for the nine months ended September 30, 2024, compared with net cash used in operating activities of approximately $10.8 million for the nine months ended September 30, 2023. The decrease resulted primarily from a decrease in our research and development activities and general and administrative expenses and by net changes in operating asset and liability items.

 

 
 

 

There was no net cash provided by or used in investing activities in the nine months ended September 30, 2024. Net cash provided by investing activities was approximately $17.1 million for the nine months ended September 30, 2023, which was related to the maturity of $24.0 million in marketable securities, offset by net investment of approximately $6.9 million in marketable securities.

 

Net cash provided by financing activities for the nine months ended September 30, 2024, was approximately $2.9 million, which was provided by the issuance and sale of our common stock under the ATM Agreement and the issuance and sale of our common stock and warrants in the August 2024 Offering. There was no net cash provided by or used in financing activities in the nine months ended September 30, 2023.

 

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, pancreatic 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 meaningful single agent activity against chronic hepatitis B virus (HBV) and chronic human immunodeficiency virus (HIV) infections in pre-clinical 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: our expectations and plans regarding our clinical supply agreement with BeiGene; our plans to advance clinical evaluation of the combination of BeiGene’s anti-PD-1 antibody, tislelizumab, with Decoy20; our ability to gather more safety and efficacy data from our Phase 1 clinical trial; our plans to seek FDA approval and to initiate a combination trial, and the timing thereof; the anticipated effects of our product candidates, including Decoy20; the plans and objectives of management for future operations; our research and development activities and costs; the sufficiency of our cash and cash equivalents to fund our ongoing activities and our cash management strategy; and our assessment of financing options to support our corporate strategy. 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 Quarterly Report on Form 10-Q for the quarter ended September 30, 2024 to be filed with the SEC, our most recent Annual Report on Form 10-K filed with the SEC on March 13, 2024, 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

 

Investor Relations Contact:

 

CORE IR
Louie Toma
louie@coreir.com

 

Media Contact:

 

Cuttlefish Communications

Shira Derasmo

shira@cuttlefishpr.com

917-280-2497

 

 
 

 

INDAPTUS THERAPEUTICS, INC.

 

Unaudited Condensed Consolidated Balance Sheets

 

   September 30, 2024   December 31, 2023 
Assets          
Current assets:          
Cash and cash equivalents  $7,380,686   $13,362,053 
Prepaid expenses and other current assets   248,737    633,156 
           
Total current assets   7,629,423    13,995,209 
           
Non-current assets:          
Property and equipment, net   -    735 
Right-of-use asset   105,655    173,206 
Other assets   504,728    754,728 
           
Total non-current assets   610,383    928,669 
           
Total assets  $8,239,806   $14,923,878 
           
Liabilities and stockholders’ equity          
Current liabilities:          
Accounts payable and other current liabilities  $2,128,491   $2,672,327 
Operating lease liability, current portion   103,982    101,705 
           
Total current liabilities   2,232,473    2,774,032 
           
Non-current liabilities:          
Operating lease liability, net of current portion   4,007    73,348 
           
Total non-current liabilities   4,007    73,348 
           
Total liabilities   2,236,480    2,847,380 
           
Commitments and contingencies          
           
Stockholders’ equity:          
Common stock: $0.01 par value, 200,000,000 shares authorized as of September 30, 2024 and December 31, 2023; 10,196,884 shares issued and outstanding as of September 30, 2024 and 8,401,047 shares issued and outstanding as of December 31, 2023   101,969    84,011 
Additional paid in capital   62,209,493    57,409,643 
Accumulated deficit   (56,308,136)   (45,417,156)
           
Total stockholders’ equity   6,003,326    12,076,498 
           
Total liabilities and stockholders’ equity  $8,239,806   $14,923,878 

 

 
 

 

Unaudited Condensed Consolidated Statements of Operations and Comprehensive Loss

 

  

Three Months Ended

September 30,

  

Nine Months Ended

September 30,

 
   2024   2023   2024   2023 
Operating expenses:                    
Research and development  $1,466,037   $2,226,688   $4,771,152   $5,587,073 
General and administrative   1,676,020    2,021,724    6,423,029    6,611,767 
                     
Total operating expenses   3,142,057    4,248,412    11,194,181    12,198,840 
                     
Loss from operations   (3,142,057)   (4,248,412)   (11,194,181)   (12,198,840)
                     
Other income, net   73,021    326,024    303,201    778,149 
                     
Net loss  $(3,069,036)  $(3,922,388)  $(10,890,980)  $(11,420,691)
                     
Net loss available to common stockholders per share of common stock, basic and diluted  $(0.32)  $(0.47)  $(1.23)  $(1.36)
                     
Weighted average number of shares used in calculating net loss per share, basic and diluted   9,510,447    8,401,047    8,832,630    8,401,047 
Net loss  $(3,069,036)  $(3,922,388)  $(10,890,980)  $(11,420,691)
Other comprehensive income (loss):                    
Reclassification adjustment for interest earned on marketable securities included in net loss   -    (140,567)   -    (430,993)
Change in unrealized gain on marketable securities   -    6,412    -    334,559 
Comprehensive loss  $(3,069,036)  $(4,056,543)  $(10,890,980)  $(11,517,125)

 

 
 

 

Unaudited Condensed Consolidated Statements of Cash Flows

 

   For the Nine Months Ended 
   September 30, 
   2024   2023 
Cash flows from operating activities:          
Net loss  $(10,890,980)  $(11,420,691)
Adjustments to reconcile net loss to net cash used in operating activities:          
Depreciation   735    964 
Stock-based compensation   2,001,727    2,220,413 
Interest earned on marketable securities   -    (430,993)
Changes in operating assets and liabilities:          
Prepaid expenses and other current and non- current assets   634,419    (84,568)
Accounts payable and other current liabilities   (673,829)   (1,088,785)
Operating lease right-of-use asset and liability, net   487    290 
Net cash used in operating activities   (8,927,441)   (10,803,370)
           
Cash flows from investing activities:          
Maturity of marketable securities   -    24,000,000 
Purchase of marketable securities   -    (6,859,432)
Net cash provided by investing activities   -    17,140,568 
           
Cash flows from financing activities:          
Proceeds from issuance of shares of common stock and warrants   3,375,590    - 
Issuance costs   (429,516)   - 
Net cash provided by financing activities   2,946,074    - 
           
Net (decrease) increase in cash and cash equivalents   (5,981,367)   6,337,198 
           
Cash and cash equivalents at beginning of period   13,362,053    9,626,800 
           
Cash and cash equivalents at end of period  $7,380,686   $15,963,998 
           
Noncash investing and financing activities          
Transaction costs in accounts payable and other current liabilities  $129,993   $- 
Change in unrealized gain/loss on marketable securities  $-   $(96,434)
ASC 842 lease renewal option exercise  $-   $236,506 
Reclassification of security deposit  $-   $16,477 

 

 

 

 

 

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