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 IRLouie
Tomalouie@coreir.com
Media Contact:Cuttlefish CommunicationsShira
Derasmoshira@cuttlefishpr.com917-280-2497
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 |
|
Indaptus Therapeutics (NASDAQ:INDP)
Historical Stock Chart
Von Dez 2024 bis Jan 2025
Indaptus Therapeutics (NASDAQ:INDP)
Historical Stock Chart
Von Jan 2024 bis Jan 2025