- Tetra strengthens its intellectual property position with
PCT and provisional patent applications for its innovative
therapeutic, ARDS-003.
MONTREAL, Nov. 29,
2022 /PRNewswire/ - Tetra Bio-Pharma Inc. ("Tetra"
or the "Company") (TSX: TBP) (OTCQB: TBPMF) (FRA: JAM1), a
leader in cannabinoid-derived drug discovery and development today
announced the filing of three patent applications for its novel
therapeutic, ARDS-003.
- The Company filed an international patent under PCT (Patent
Cooperation Treaty) related to the methodology, including
improvements, for the synthesis of target synthetic cannabinoid
derivatives, specifically HU308 (known as Onternabez) and HU433.
(Methods, Processes, and Compositions for Improved Preparation of
HU308 and HU433 Application No. PCT/CA2021/051327)
- The Company filed an international PCT application related to
the pharmaceutical methods of production and uses of the
compositions comprising Onternabez, suitable for parenteral
delivery. (Parenteral Cannabinoid Formulations and Uses Thereof
Application No. PCT/CA2021/051882).
- The Company filed a provisional patent application with the
United States Patent and Trademark Office related to crystalline
Onternabez and uses thereof. This application covers identification
of novel polymorphs and cocrystals of Onternabez, which will allow
for extended patent protection on Onternabez and may lead to
improvements in stability and solubility when formulating
Onternabez for future drug products.
Guy Chamberland, CEO and Chief
Regulatory Officer at Tetra commented "This is a significant step
in protecting our novel therapeutic, ARDS-003. It is especially
significant, considering the potential use of this novel
cannabinoid molecule in antiviral and immunomodulator therapies.
These patents would be enforceable once granted and provide
additional protection to investors for up to 20 years from the
filing date."
These three patent applications become part of Tetra's growing
IP portfolio, which includes, 14 granted/issued patents, as well as
one (1) provisional and five (5) PCT applications pending across
international and national jurisdictions.
About ARDS-003
ARDS-003 is a novel First in Human (FIH) drug product containing
the active pharmaceutical agent, Onternabez, a potent and selective
full agonist of the type 2 cannabinoid receptor (CB2R), an
essential immunomodulatory target. ARDS-003 is positioned to
modulate acute systemic inflammation and prevent sepsis, ARDS, and
organ damage. While the clinical profile of ARDS arising from
viral (COVID) or bacterial sepsis can vary, hyperinflammation
involving a dysfunctional immune response is a common mediator of
lung damage. Tetra's pre-clinical studies have demonstrated that
ARDS-003 decreases this hyperinflammatory response and slows
disease progression.
About Tetra Bio-Pharma
Tetra Bio-Pharma (TSX: TBP) (OTCQB: TBPMF) (FRA:JAM1) is a
leader in cannabinoid-derived drug discovery and development with a
FDA and a Health Canada cleared clinical program aimed at bringing
novel prescription drugs and treatments to patients and their
healthcare providers. Their evidence-based scientific approach has
enabled them to develop a pipeline of cannabinoid-based drug
products for a range of medical conditions, including pain,
inflammation, and oncology. With patients at the core of what they
do, Tetra Bio-Pharma is focused on providing rigorous scientific
validation and safety data required for inclusion into the existing
biopharma industry by regulators, physicians and insurance
companies.
For more information visit: www.tetrabiopharma.com
Neither the TSX Exchange nor its Regulation Services Provider
(as that term is defined in the policies of the TSX Exchange)
accepts responsibility for the adequacy or accuracy of this
release.
Forward-looking
statements
Some statements in this release may contain forward-looking
information. All statements, other than of historical fact, that
address activities, events or developments that the Company
believes, expects or anticipates will or may occur in the future
(including, without limitation, statements regarding potential
acquisitions and financings) are forward-looking statements.
Forward-looking statements are generally identifiable by use of the
words "may", "will", "should", "continue", "expect", "anticipate",
"estimate", "believe", "intend", "plan" or "project" or the
negative of these words or other variations on these words or
comparable terminology. Forward-looking statements are subject to a
number of risks and uncertainties, many of which are beyond the
Company's ability to control or predict, that may cause the actual
results of the Company to differ materially from those discussed in
the forward-looking statements. Factors that could cause actual
results or events to differ materially from current expectations
include, among other things, without limitation, the inability of
the Company to obtain sufficient financing to execute the Company's
business plan; competition; regulation and anticipated and
unanticipated costs and delays, the success of the Company's
research and development strategies, including the success of this
product or any other product, the applicability of the
discoveries made therein, the successful and timely completion and
uncertainties related to the regulatory process, the timing of
clinical trials, the timing and outcomes of regulatory or
intellectual property decisions and other risks disclosed in the
Company's public disclosure record on file with the relevant
securities regulatory authorities. Although the Company has
attempted to identify important factors that could cause actual
results or events to differ materially from those described in
forward-looking statements, there may be other factors that cause
results or events not to be as anticipated, estimated or intended.
Readers should not place undue reliance on forward-looking
statements. The forward-looking statements included in this news
release are made as of the date of this news release and the
Company does not undertake an obligation to publicly update such
forward-looking statements to reflect new information, subsequent
events or otherwise unless required by applicable securities
legislation.
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SOURCE Tetra Bio-Pharma Inc.