OTTAWA, Jan. 31, 2020 /CNW Telbec/ - Tetra
Bio-Pharma Inc. ("Tetra" or the "Company") (TSXV:
TBP) (OTCQB: TBPMF), a leader in cannabinoid-derived drug discovery
and development, is pleased to announce that it has received a
favorable letter from the United States Food and Drug
Administration ("FDA") with respect to
CAUMZ™. This follows the Company's
previously announced Type B meeting with the FDA for
CAUMZ™. The Company will be issuing a news
release on Monday, February
3rd, explaining the decisions.
About Tetra Bio-Pharma
Tetra Bio-Pharma
(TSX-V:TBP) (OTCQB:TBPMF) is a biopharmaceutical leader in
cannabinoid-based drug discovery and development with a Health
Canada approved, and FDA reviewed and approved, clinical program
aimed at bringing novel prescription drugs and treatments to
patients and their healthcare providers. The Company has several
subsidiaries engaged in the development of an advanced and growing
pipeline of Bio Pharmaceuticals, Natural Health and Veterinary
Products containing cannabis and other medicinal plant-based
elements. With patients at the core of what we do, Tetra Bio-Pharma
is focused on providing rigorous scientific validation and safety
data required for inclusion into the existing bio pharma industry
by regulators, physicians and insurance companies. Could we work in
"existing regulatory standards of safety and clinical evidence for
pharmaceutical products".
For more information visit: www.tetrabiopharma.com
Neither the TSX Venture Exchange nor its Regulation Services
Provider (as that term is defined in the policies of the TSX
Venture Exchange) accepts responsibility for the adequacy or
accuracy of this release.
Forward-looking statements
Some statements in this
release may contain forward-looking information, including
regarding the FDA's decisions regarding CAUMZTM. 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.
SOURCE Tetra Bio-Pharma Inc.