July 23, 2024
Biodexa Pharmaceuticals PLC
Announces Closing of $5.0 Million
Registered Direct Offering and Concurrent Private
Placement
Biodexa Pharmaceuticals PLC (“Biodexa” or the
“Company”) (Nasdaq: BDRX), an acquisition-focused clinical stage
biopharmaceutical company developing a pipeline of innovative
products for the treatment of diseases with unmet medical needs,
today announced the closing of its previously announced registered
direct offering of an aggregate of (i) 5,050,808 American
Depositary Shares (the “Depositary Shares”) (each Depositary Share
representing 400 of the Company’s ordinary shares, nominal value
£0.001 per share) and (ii) 278,975 pre-funded warrants exercisable
for Depositary Shares, at a purchase price of $0.94 per Depositary
Share (or $0.9399 per pre-funded warrant).
The net proceeds from the offering were
approximately $4.2 million, after deducting placement agent fees
and other offering expenses. The Company anticipates that the
proceeds of this offering will be used to fund its development
programs, including to provide the final match payment with respect
to a $17 million grant from the Cancer Prevention Research
Institute of Texas (CPRIT) and initiate the Phase 3 clinical trial
of eRapa in Familial Adenomatous Polyposis (FAP), for working
capital and for general corporate purposes.
In a concurrent private placement, the Company
also issued and sold unregistered Series J warrants to purchase up
to an aggregate of 5,329,783 Depositary Shares (the “Series J
Warrants”) and unregistered Series K warrants to purchase up to an
aggregate of 5,329,783 Depositary Shares (the “Series K
Warrants”).
The pre-funded warrants have an exercise price
of $0.0001 per Depositary Share, are immediately exercisable and do
not expire. The Series J Warrants have an exercise price of $1.00
per Depositary Share, are immediately exercisable and expire on the
fifth anniversary of the issuance date. The Series K Warrants have
an exercise price of $1.00 per Depositary Share, are immediately
exercisable and expire on the first anniversary of the issuance
date.
Ladenburg Thalmann & Co. Inc. acted as sole
placement agent in connection with the offering.
In connection with the offering, the Company
also agreed to amend the exercise price of existing Series E
warrants to purchase an aggregate of 978,233 Depositary Shares,
existing Series G warrants to purchase an aggregate of 2,443,995
Depositary Shares and existing Series H warrants to purchase an
aggregate of 3,236,345 Depositary Shares that were previously
issued in December 2023, May 2022 and May 2022, respectively, held
by investors participating in the offering, such that the amended
warrants now have an exercise price of $1.00 per share.
The Depositary Shares (or pre-funded warrants in
lieu thereof) were offered pursuant to a shelf registration
statement on Form F-3 (File No. 333-267932), which was declared
effective by the United States Securities and Exchange Commission
(“SEC”) on October 26, 2022. A prospectus supplement relating to
the Depositary Shares and pre-funded warrants has been filed with
the SEC and is available on the SEC’s website located at
http://www.sec.gov. Electronic copies of the prospectus supplement
relating to the registered direct offering, together with the
accompanying prospectus, may be obtained, when available, from
Ladenburg Thalmann & Co. Inc., Prospectus Department, 640 Fifth
Avenue, 4th Floor, New York, New York 10019 or by email at
prospectus@ladenburg.com.
The private placement of the Series J Warrants
and Series K Warrants was made in a transaction not involving a
public offering and the securities sold in the private placement
have not been registered under the Securities Act of 1933, as
amended (the “Securities Act”), or any state or other applicable
jurisdiction’s securities laws, and may not be offered or sold in
the United States absent registration or an applicable exemption
from the registration requirements of the Securities Act and
applicable state or other jurisdictions’ securities laws. Pursuant
to the securities purchase agreement, the Company has agreed to
file a registration statement with the SEC registering the resale
of the ordinary shares underlying the Depositary Shares issuable
upon the exercise of the Series J Warrants and Series K Warrants
issued in the private placement.
This press release shall not constitute an offer
to sell or the solicitation of an offer to buy these securities,
nor shall there be any offer, solicitation or sale of these
securities in any jurisdiction in which such offer, solicitation or
sale would be unlawful. Any offering of the securities under the
resale registration statement will only be made by means of a
prospectus.
About the Cancer Prevention and Research Institute of
Texas
CPRIT was created by the Texas Legislature and
approved by a statewide vote in 2007 to lead the Lone Star State’s
fight against cancer. In 2019, Texas voters again voted
overwhelmingly to continue CPRIT with an additional $3 billion for
a total $6 billion investment in cancer research and prevention. To
date, CPRIT has awarded over $3 billion in grants to Texas research
institutions and organizations through its academic research,
prevention and product development research programs. CPRIT has
also recruited more than 281 distinguished researchers to Texas,
supported the establishment, expansion or relocation of 51
companies to Texas and generated over $7.66 billion in additional
public and private investment. CPRIT funding has advanced
scientific and clinical knowledge and provided over 8.1 million
life-saving cancer prevention and early detection services to
Texans in all 254 counties. Learn more
at https://cprit.texas.gov.
About Biodexa Pharmaceuticals PLC
Biodexa Pharmaceuticals PLC (listed on NASDAQ:
BDRX) is a clinical stage biopharmaceutical company developing a
pipeline of innovative products for the treatment of diseases with
unmet medical needs. The Company’s lead development programs
include eRapa, under development for Familial Adenomatous Polyposis
and Non-Muscle Invasive Blader Cancer: tolimidone, under
development as a for the treatment of type 1 diabetes; and MTX110,
which is being studied in aggressive rare/orphan brain cancer
indications.
eRapa is a proprietary oral tablet formulation
of rapamycin, also known as sirolimus. Rapamycin is an mTOR
(mammalian Target Of Rapamycin) inhibitor. mTOR has been shown to
have a significant role in the signalling pathway that regulates
cellular metabolism, growth and proliferation and is activated
during tumorgenesis.
Tolimidone is an orally delivered, potent and
selective inhibitor of Lyn kinase. Lyn is a member of the Src
family of protein tyrosine kinases, which is mainly expressed in
hematopoietic cells, in neural tissues, liver, and adipose tissue.
Tolimidone demonstrates glycemic control via insulin sensitization
in animal models of diabetes and has the potential to become a
first in class blood glucose modulating agent.
MTX110 is a solubilised formulation of the
histone deacetylase (HDAC) inhibitor, panobinostat. This
proprietary formulation enables delivery of the product via
convection-enhanced delivery (CED) at chemotherapeutic doses
directly to the site of the tumor, by-passing the blood-brain
barrier and potentially avoiding systemic toxicity.
Biodexa is supported by three proprietary drug
delivery technologies focused on improving the bio-delivery and
bio-distribution of medicines. Biodexa’s headquarters and R&D
facility is in Cardiff, UK. For more information visit
www.biodexapharma.com.
Forward-Looking Statements
Certain statements in this announcement may
constitute “forward-looking statements” within the meaning of
legislation in the United Kingdom and/or United States. Such
statements are made pursuant to the safe harbor provisions of the
Private Securities Litigation Reform Act of 1995 and are based on
management’s belief or interpretation. All statements contained in
this announcement that do not relate to matters of historical fact
should be considered forward-looking statements including, but not
limited to, the anticipated net proceeds, and the anticipated use
of proceeds therefrom, and projected cash runway. In certain cases,
forward-looking statements can be identified by the use of words
such as “plans”, “expects” or “does not anticipate”, or “believes”,
or variations of such words and phrases or statements that certain
actions, events or results “may”, “could”, “would”, “might” or
“will be taken”, “occur” or “be achieved.” Forward-looking
statements and information are subject to various known and unknown
risks and uncertainties, many of which are beyond the ability of
the Company to control or predict, that may cause their actual
results, performance or achievements to be materially different
from those expressed or implied thereby, and are developed based on
assumptions about such risks, uncertainties and other factors set
out herein.
Reference should be made to those documents that
Biodexa shall file from time to time or announcements that may be
made by Biodexa in accordance with the rules and regulations
promulgated by the SEC, which contain and identify other important
factors that could cause actual results to differ materially from
those contained in any projections or forward-looking statements.
These forward-looking statements speak only as of the date of this
announcement. All subsequent written and oral forward-looking
statements by or concerning Biodexa are expressly qualified in
their entirety by the cautionary statements above. Except as may be
required under relevant laws in the United States, Biodexa does not
undertake any obligation to publicly update or revise any
forward-looking statements because of new information, future
events or events otherwise arising.
For more information, please contact:
Biodexa Pharmaceuticals PLC |
Stephen Stamp, CEO, CFOTel: +44 (0)29 20480
180www.biodexapharma.com |
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