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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) August 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
August 12, 2024, Indaptus Therapeutics, Inc. (the “Company”) issued a press release announcing its financial results for
the quarter ended June 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.
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:
August 12, 2024
|
INDAPTUS
THERAPEUTICS, INC. |
|
|
|
By: |
/s/
Nir Sassi |
|
Name: |
Nir Sassi |
|
Title: |
Chief
Financial Officer |
Exhibit 99.1
Indaptus
Therapeutics Reports Second Quarter 2024 Financial Results and Provides Corporate Update
NEW
YORK (August 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 second quarter ended June 30, 2024, and provided a corporate update.
Jeffrey
Meckler, Indaptus Therapeutics’ Chief Executive Officer, commented, “During the second quarter we had multiple opportunities
to share our findings regarding our Phase 1 clinical trial to date, and to demonstrate the unique approach that our Decoy platform offers.
These included impactful conferences such as the American Association for Cancer Research (AACR) annual meeting and the American Society
of Clinical Oncology (ASCO) annual meeting, which are considered among the top annual oncology conferences. Further, our founder was
once again recognized by the industry when he was named chair of the STING & TLR-Targeted Therapies Summit. We are encouraged by
the results we have reported, along with the data we are seeing as we continue the multi-dose stage of the Phase 1 clinical trial. As
Decoy20 continues to be well-tolerated in our Phase 1 clinical trial, we expect to progress to dosing multiple patients simultaneously.
This will increase the data we receive and, as a result, is expected to accelerate the progress of the trial. We look forward to demonstrating
continued impactful outcomes in the second half of the year.”
Key
recent highlights:
| ● | Completed
a $3 million registered direct offering and concurrent private placement on August 8, 2024,
for net proceeds of approximately $2.5 million |
| | |
| ● | Advancing
clinical trial from single to weekly doses of Decoy20, the company completed one month of
weekly dosing in three patients at the 3 x 10^7 Decoy20 dose |
| | |
| ● | Completed
a single dose cohort at the higher dose of 7 x 10^7 Decoy20 and intend to initiate weekly
dosing later this year |
| | |
| ● | Presented
poster outlining data from 3 x 10^7 and 7 x 10^7 dose at the ASCO annual meeting on June
1, 2024, in Chicago |
| | |
| ● | Presented
poster outlining new mechanism of action data for Decoy platform at the AACR annual meeting
in April 2024 |
| | |
| ● | Founder
and Chief Scientific Officer, Michael Newman, Ph.D. presented additional data on the Company’s
lead product candidate, Decoy20, at the 5th Annual STING & TLR-Targeted Therapies
Summit in San Diego on June 19-20, 2024, where he was also named chair of the Summit |
Financial
Highlights for the Second Quarter Ended June 30, 2024
Research
and development expenses for the three months ended June 30, 2024, were approximately $1.7 million, an increase of approximately $0.2
million compared with approximately $1.5 million in the three months ended June 30, 2023. The increase for the three-month period was
primarily due to payroll and related expenses and stock-based compensation. Research and development expenses for the six months ended
June 30, 2024, were approximately $3.3 million, a decrease of approximately $0.1 million compared with approximately $3.4 million in
the six months ended June 30, 2023. The decrease for the six-month period was primarily due to a decrease of approximately $0.5 million
in our manufacturing processes of Decoy20 that were conducted in 2023 and was offset by an increase of approximately $0.4 million in
our Phase 1 clinical trial and in payroll and related expenses.
General
and administrative expenses for the three months ended June 30, 2024, were approximately $2.4 million, an increase of approximately $0.4
million compared with approximately $2.0 million in the three months ended June 30, 2023. The increase was primarily due to payroll and
related expenses, legal fees and investor relations expenses. General and administrative expenses for the six months ended June 30, 2024,
were approximately $4.7 million, an increase of approximately $0.1 million compared with approximately $4.6 million in the six months
ended June 30, 2023. The increase for the six-month period was primarily due to payroll and related expenses and stock-based compensation.
Loss
per share for the three months ended June 30, 2024, was approximately $0.47 compared with approximately $0.39 for the three months ended
June 30, 2023. Loss per share for the six months ended June 30, 2024, was approximately $0.92 compared with approximately $0.89 per share
for the six months ended June 30, 2023.
As
of June 30, 2024, the Company had cash and cash equivalents of approximately $7.3 million and on August 8, 2024, the Company raised $3.0
million in a registered direct offering of 1,643,837 shares of common stock at a purchase price of $1.825 per share and a concurrent
private placement, in which the Company also issued to the purchasers in the offering unregistered warrants to purchase 1,643,837 shares
of common stock. The warrants have an exercise price of $1.70 per share, are immediately exercisable, and will expire five years from
the date of issuance. The total net proceeds of the registered direct offering and the private placement were approximately $2.5 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 $6.4 million for the six months ended June 30, 2024, compared with net cash used
in operating activities of approximately $7.1 million for the six months ended June 30, 2023. The decrease of approximately $0.7 million
in net cash used was primarily attributable to a settlement fee that was paid in February 2023.
There
was no net cash provided by or used in investing activities in the six months ended June 30, 2024. Net cash provided by investing activities
was approximately $10.1 million for the six months ended June 30, 2023, which was related to the maturity of $17.0 million in marketable
securities, offset by net investment of approximately $6.9 million in marketable securities.
Net
cash provided by financing activities for the six months ended June 30, 2024, was approximately $0.4 million, which was provided by issuance
and sale of our common stock under the At The Market Offering Agreement. There was no net cash provided by or used in financing activities
in the six months ended June 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. 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 Phase 1 clinical trial of Decoy20, including the timing and design thereof and expected immune responses as we dose more patients
in the multi-dosing part of the trial; 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 June 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
| |
June 30, 2024 | |
December 31, 2023 | |
Assets | |
| | |
| | |
Current assets: | |
| | |
| | |
Cash and cash equivalents | |
$ | 7,301,751 | |
$ | 13,362,053 | |
Prepaid expenses and other current assets | |
| 186,726 | |
| 633,156 | |
| |
| | |
| | |
Total current assets | |
| 7,488,477 | |
| 13,995,209 | |
| |
| | |
| | |
Non-current assets: | |
| | |
| | |
Property and equipment, net | |
| - | |
| 735 | |
Right-of-use asset | |
| 128,630 | |
| 173,206 | |
Other assets | |
| 504,728 | |
| 754,728 | |
| |
| | |
| | |
Total non-current assets | |
| 633,358 | |
| 928,669 | |
| |
| | |
| | |
Total assets | |
$ | 8,121,835 | |
$ | 14,923,878 | |
| |
| | |
| | |
Liabilities and stockholders’ equity | |
| | |
| | |
Current liabilities: | |
| | |
| | |
Accounts payable and other current liabilities | |
$ | 1,824,825 | |
$ | 2,672,327 | |
Operating lease liability, current portion | |
| 103,223 | |
| 101,705 | |
| |
| | |
| | |
Total current liabilities | |
| 1,928,048 | |
| 2,774,032 | |
| |
| | |
| | |
Non-current liabilities: | |
| | |
| | |
Operating lease liability, net of current portion | |
| 27,579 | |
| 73,348 | |
| |
| | |
| | |
Total non-current liabilities | |
| 27,579 | |
| 73,348 | |
| |
| | |
| | |
Total liabilities | |
| 1,955,627 | |
| 2,847,380 | |
| |
| | |
| | |
Commitments and contingencies | |
| | |
| | |
| |
| | |
| | |
Stockholders’ equity: | |
| | |
| | |
Common stock: $0.01 par value, 200,000,000 shares authorized as of June 30, 2024 and December 31, 2023; 8,553,047 shares issued and outstanding as of June 30, 2024 and 8,401,047 shares issued and outstanding as of December 31, 2023 | |
| 85,531 | |
| 84,011 | |
Additional paid in capital | |
| 59,319,777 | |
| 57,409,643 | |
Accumulated deficit | |
| (53,239,100 | ) |
| (45,417,156 | ) |
| |
| | |
| | |
Total stockholders’ equity | |
| 6,166,208 | |
| 12,076,498 | |
| |
| | |
| | |
Total liabilities and stockholders’ equity | |
$ | 8,121,835 | |
$ | 14,923,878 | |
Unaudited
Condensed Consolidated Statements of Operations and Comprehensive Loss
| |
Three Months Ended June 30, | | |
Six Months Ended June 30, | |
| |
2024 | | |
2023 | | |
2024 | | |
2023 | |
Operating expenses: | |
| | | |
| | | |
| | | |
| | |
Research and development | |
$ | 1,713,973 | | |
$ | 1,480,485 | | |
$ | 3,305,115 | | |
$ | 3,360,385 | |
General and administrative | |
| 2,394,912 | | |
| 2,014,777 | | |
| 4,747,009 | | |
| 4,590,043 | |
| |
| | | |
| | | |
| | | |
| | |
Total operating expenses | |
| 4,108,885 | | |
| 3,495,262 | | |
| 8,052,124 | | |
| 7,950,428 | |
| |
| | | |
| | | |
| | | |
| | |
Loss from operations | |
| (4,108,885 | ) | |
| (3,495,262 | ) | |
| (8,052,124 | ) | |
| (7,950,428 | ) |
| |
| | | |
| | | |
| | | |
| | |
Other income, net | |
| 93,618 | | |
| 250,197 | | |
| 230,180 | | |
| 452,125 | |
| |
| | | |
| | | |
| | | |
| | |
Net loss | |
$ | (4,015,267 | ) | |
$ | (3,245,065 | ) | |
$ | (7,821,944 | ) | |
$ | (7,498,303 | ) |
| |
| | | |
| | | |
| | | |
| | |
Net loss available to common stockholders per share of common stock, basic and diluted | |
$ | (0.47 | ) | |
$ | (0.39 | ) | |
$ | (0.92 | ) | |
$ | (0.89 | ) |
| |
| | | |
| | | |
| | | |
| | |
Weighted average number of shares used in calculating net loss per share, basic and diluted | |
| 8,543,919 | | |
| 8,401,047 | | |
| 8,493,394 | | |
| 8,401,047 | |
Net loss | |
$ | (4,015,267 | ) | |
$ | (3,245,065 | ) | |
$ | (7,821,944 | ) | |
$ | (7,498,303 | ) |
Other comprehensive income (loss): | |
| | | |
| | | |
| | | |
| | |
Reclassification adjustment for interest earned on marketable securities included in net loss | |
| - | | |
| (161,197 | ) | |
| - | | |
| (290,426 | ) |
Change in unrealized gain on marketable securities | |
| - | | |
| 117,895 | | |
| - | | |
| 328,147 | |
Comprehensive loss | |
$ | (4,015,267 | ) | |
$ | (3,288,367 | ) | |
$ | (7,821,944 | ) | |
$ | (7,460,582 | ) |
Unaudited
Condensed Consolidated Statements of Cash Flows
|
|
For
the Six Months Ended |
|
|
|
June
30, |
|
|
|
2024 |
|
|
2023 |
|
Cash
flows from operating activities: |
|
|
|
|
|
|
|
|
Net
loss |
|
$ |
(7,821,944 |
) |
|
$ |
(7,498,303 |
) |
Adjustments
to reconcile net loss to net cash used in operating activities: |
|
|
|
|
|
|
|
|
Depreciation |
|
|
735 |
|
|
|
643 |
|
Stock-based
compensation |
|
|
1,557,543 |
|
|
|
1,455,610 |
|
Interest
earned on marketable securities |
|
|
- |
|
|
|
(290,426 |
) |
Changes
in operating assets and liabilities: |
|
|
|
|
|
|
|
|
Prepaid
expenses and other current assets |
|
|
696,430 |
|
|
|
614,172 |
|
Accounts
payable and other current liabilities |
|
|
(847,502 |
) |
|
|
(1,350,222 |
) |
Operating
lease right-of-use asset and liability, net |
|
|
325 |
|
|
|
(455 |
) |
Net
cash used in operating activities |
|
|
(6,414,413 |
) |
|
|
(7,068,981 |
) |
|
|
|
|
|
|
|
|
|
Cash
flows from investing activities: |
|
|
|
|
|
|
|
|
Maturity
of marketable securities |
|
|
- |
|
|
|
17,000,000 |
|
Purchase
of marketable securities |
|
|
- |
|
|
|
(6,859,432 |
) |
Net
cash provided by investing activities |
|
|
- |
|
|
|
10,140,568 |
|
|
|
|
|
|
|
|
|
|
Cash
flows from financing activities: |
|
|
|
|
|
|
|
|
Issuance
of shares of common stock |
|
|
375,588 |
|
|
|
- |
|
Issuance
costs |
|
|
(21,477 |
) |
|
|
- |
|
Net
cash provided by financing activities |
|
|
354,111 |
|
|
|
- |
|
|
|
|
|
|
|
|
|
|
Net
(decrease) increase in cash and cash equivalents |
|
|
(6,060,302 |
) |
|
|
3,071,587 |
|
|
|
|
|
|
|
|
|
|
Cash
and cash equivalents at beginning of period |
|
|
13,362,053 |
|
|
|
9,626,800 |
|
|
|
|
|
|
|
|
|
|
Cash
and cash equivalents at end of period |
|
$ |
7,301,751 |
|
|
$ |
12,698,387 |
|
|
|
|
|
|
|
|
|
|
Noncash
investing and financing activities |
|
|
|
|
|
|
|
|
Change
in unrealized gain/loss on marketable securities |
|
$ |
- |
|
|
$ |
37,721 |
|
ASC
842 lease renewal option exercise |
|
$ |
- |
|
|
$ |
236,506 |
|
Reclassification
of security deposit |
|
$ |
- |
|
|
$ |
16,477 |
|
v3.24.2.u1
Cover
|
Aug. 12, 2024 |
Cover [Abstract] |
|
Document Type |
8-K
|
Amendment Flag |
false
|
Document Period End Date |
Aug. 12, 2024
|
Entity File Number |
001-40652
|
Entity Registrant Name |
INDAPTUS
THERAPEUTICS, INC.
|
Entity Central Index Key |
0001857044
|
Entity Tax Identification Number |
86-3158720
|
Entity Incorporation, State or Country Code |
DE
|
Entity Address, Address Line One |
3
Columbus Circle
|
Entity Address, Address Line Two |
15th
Floor
|
Entity Address, City or Town |
New
York
|
Entity Address, State or Province |
NY
|
Entity Address, Postal Zip Code |
10019
|
City Area Code |
(646)
|
Local Phone Number |
427-2727
|
Written Communications |
false
|
Soliciting Material |
false
|
Pre-commencement Tender Offer |
false
|
Pre-commencement Issuer Tender Offer |
false
|
Title of 12(b) Security |
Common
Stock, $0.01 par value
|
Trading Symbol |
INDP
|
Security Exchange Name |
NASDAQ
|
Entity Emerging Growth Company |
false
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