Akari Therapeutics Plc (Nasdaq: AKTX), a biotechnology company
developing next-generation precision bi-functional antibody drug
conjugates (ADCs) for the treatment of cancer, today announced the
successful pricing of a private placement financing round. This
transaction is expected to raise an aggregate of approximately $7.6
million in gross proceeds. With these funds the Company will focus
on investing in its novel spliceosome inhibitor payload ADC
technology platform, seeking license partners for its TROP-2 ADC
program, and monetizing non-core assets.
“We were very pleased that the private placement
was supported by existing investors and our Board of Directors, all
of whom participated in this financing,” said Samir R. Patel, MD,
President and CEO of Akari Therapeutics. Dr. Patel added that, “I
am very encouraged by this show of confidence and continued
significant interest from our long-term investors.”
The Company entered into definitive purchase
agreements with the investors for the issuance and sale of
6,637,626 unregistered American Depository Shares (ADSs), or
prefunded warrants in lieu thereof, and Series A Warrants and
Series B Warrants (“the Offering”). The ADSs were priced at $0.87
per ADS, the Nasdaq official closing price on February 28, 2025.
Investors paid an additional 12.5 cents per ADS issuable upon
exercise of each warrant to be issued. Dr. Huh, Chairman of the
Board, participated in the Private Placement by agreeing to
terminate an existing $1 million convertible note in lieu of
payment of the purchase price for the ADSs and warrants.
The gross cash proceeds from the Offering are
expected to be approximately $ 6.6 million before deducting
placement agent fees and other offering expenses payable by the
Company. The Company intends to use the net proceeds from the
Offering for working capital and general corporate purposes.
The Series A and Series B Warrants will have an
exercise price of $0.87 per ADS, which is equal to the Nasdaq
official closing price of the Company’s ADSs on February 28, 2025
and will be exercisable immediately following the date of issuance.
The Series A Warrants and Series B Warrants have a term of one or
five years, respectively, from the closing date of the private
placement.
Paulson Investment Company LLC is acting as
placement agent for the financing.
The private placement is expected to close on or
about March 5, 2025, subject to the satisfaction of customary
closing obligations.
The ADSs and warrants described above are being
offered in a private placement under Section 4(a)(2) of the
Securities Act of 1933, as amended (the “Act”) and Regulation D
promulgated thereunder and have not been registered under the Act
or state securities laws and may not be offered or sold in the
United States absent registration with the Securities and Exchange
Commission or an applicable exemption from such registration
requirements.
This press release shall not constitute an offer
to sell or the solicitation of an offer to buy any of the
securities described herein. There shall not be any offer,
solicitation of an offer to buy, or sale of securities in any state
or jurisdiction in which such an offering, solicitation, or sale
would be unlawful prior to registration or qualification under the
securities laws of any such state or jurisdiction.
About Akari
Therapeutics
Akari Therapeutics is a biotechnology company
developing next-generation precision bi-functional antibody drug
conjugates (ADC) for the treatment of cancer. Utilizing its
innovative ADC discovery platform, the Company has the ability to
generate novel bi-functional ADC candidates and optimize them based
on the desired application to target a range of cancers to fuel a
growing pipeline. Akari’s lead candidate, AKTX-101, targets the
TROP2 receptor on cancer cells and with a proprietary linker
delivers its novel PH1 payload directly into the tumor. Unlike
current ADCs that use tubulin inhibitors and DNA damaging agents as
their toxin classes, PH1 is a novel bi-functional payload that is
designed to disrupt RNA splicing within cancer cells, inducing
tumor-specific cell death while generating immunostimulatory
effects and minimizing off-target toxicity. Given this mechanism,
AKTX-101 has the potential to overcome many of the shortcomings of
current ADCs, off-target toxicity and resistance. In preclinical
studies, AKTX-101 has shown to have superior activity, prolonged
survival, less resistance and better tolerability and safety.
Additionally, AKTX-101 has the potential to be synergistic with
checkpoint inhibitors and has demonstrated prolonged survival in
preclinical models. The Company is generating validating data on
its novel payloads to advance its pipeline.
For more information about the Company, please
visit www.akaritx.com and connect on X and LinkedIn.
Cautionary Note Regarding
Forward-Looking Statements
This press release includes express or implied
forward-looking statements within the meaning of Section 27A of the
Securities Act of 1933, as amended, and Section 21E of the
Securities Exchange Act of 1934, as amended (the Exchange Act),
about the Company that involve risks and uncertainties relating to
future events and the future performance of the Company. Actual
events or results may differ materially from these forward-looking
statements. Words such as “will,” “could,” “would,” “should,”
“expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,”
“predict,” “project,” “potential,” “continue,” “future,”
“opportunity” “will likely result,” “target,” variations of such
words, and similar expressions or negatives of these words are
intended to identify such forward-looking statements, although not
all forward-looking statements contain these identifying words.
Examples of such forward-looking statements include, but are not
limited to, express or implied statements regarding the closing of
the Offering and the expected use of proceeds related thereto: the
business combination and related matters, including, but not
limited to, post-closing operations and the outlook for the
Company’s business; the Company’s targets, plans, objectives or
goals for future operations, including those related to its product
candidates; financial projections; future economic performance,;
and the assumptions underlying or relating to such statements.
These statements are based on the Company’s current plans,
estimates and projections. By their very nature, forward-looking
statements involve inherent risks and uncertainties, both general
and specific. A number of important factors, including those
described in this communication, could cause actual results to
differ materially from those contemplated in any forward-looking
statements. Factors that may affect future results and may cause
these forward-looking statements to be inaccurate include, without
limitation: the risk that Akari and Peak Bio may not realize the
anticipated benefits of the merger with Peak Bio (the “Merger”) in
the time frame expected, or at all; the ability to retain and hire
key personnel; potential adverse reactions or changes to business
relationships resulting from the Merger; the potential impact of
unforeseen liabilities, future capital expenditures, revenues,
costs, expenses, earnings, synergies, economic performance,
indebtedness, financial condition and losses on the future
prospects, business and management strategies for the management,
expansion and growth of the combined business; uncertainties as to
the long-term value of Akari’s American Depositary Shares (and the
ordinary shares represented thereby), including the dilution caused
by Akari’s issuance of additional American Depositary Shares (and
the ordinary shares represented thereby) in connection with the
Merger; risks related to global as well as local political and
economic conditions, including interest rate and currency exchange
rate fluctuations; potential delays or failures related to research
and/or development of the Company’s programs or product candidates;
risks related to any loss of the Company’s patents or other
intellectual property rights; any interruptions of the supply chain
for raw materials or manufacturing for the Company’s product
candidates, including as a result of potential tariffs;, the
nature, timing, cost and possible success and therapeutic
applications of product candidates being developed by the Company
and/or its collaborators or licensees; the extent to which the
results from the research and development programs conducted by the
Company, and/or its collaborators or licensees may be replicated in
other studies and/or lead to advancement of product candidates to
clinical trials, therapeutic applications, or regulatory approval;
uncertainty of the utilization, market acceptance, and commercial
success of the Company’s product candidates; unexpected breaches or
terminations with respect to the Company’s material contracts or
arrangements; risks related to competition for the Company’s
product candidates; the Company’s ability to successfully develop
or commercialize its product candidates; potential exposure to
legal proceedings and investigations; risks related to changes in
governmental laws and related interpretation thereof, including on
reimbursement, intellectual property protection and regulatory
controls on testing, approval, manufacturing, development or
commercialization of any of the Company’s product candidates; and
the Company’s ability to maintain listing of its ADSs on the Nasdaq
Capital Market. While the foregoing list of factors presented here
is considered representative, no list should be considered to be a
complete statement of all potential risks and uncertainties. More
detailed information about the Company and the risk factors that
may affect the realization of forward-looking statements is set
forth in the Company's filings with the SEC, copies of which may be
obtained from the SEC's website at www.sec.gov. The Company assumes
no, and hereby disclaims any, obligation to update the
forward-looking statements contained in this press
release.
Investor Relations
Contact JTC Team, LLC Jenene
Thomas 908-824-0775 AKTX@jtcir.com
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