Revive
Therapeutics Acquires
Unique
Psilocybin
Assets
TORONTO,
Canada -- February 17, 2021 -- InvestorsHub NewsWire
-- Revive Therapeutics
Ltd. ("Revive" or the "Company") (CSE: RVV, USA: RVVTF), a specialty life sciences company
focused on the research and development of therapeutics for medical
needs and rare disorders, is pleased to
announce
that, further to its
press release dated December 21, 2020, it
has entered into
an asset
purchase
agreement (the
"Agreement") with Newscope Capital
Corporation ("Newscope")
(CSE:
PHRM) (OTCQB: PHRRF) to
acquire
the full
rights to PharmaTher Inc.'s ("PharmaTher") intellectual property
(the "Acquired Assets") pertaining to psilocybin (the
"Acquisition"). PharmaTher, a wholly-owned
subsidiary of
Newscope, is a specialty life sciences company focused on the
research and development of psychedelic pharmaceuticals.
Pursuant
to
the
Agreement, Revive
will pay
aggregate consideration of up to CAD
$10
million
(the
"Purchase Price"). The Purchase Price
will be satisfied as follows: (i) $3 million in cash will be paid
on the closing date; (ii) $4 million will be satisfied through the
issuance of securities in the capital of Revive and (iii)
up to $3
million, in either cash or securities in the capital of
Revive, in the event that
Revive achieves certain milestones, which include
Revive obtaining FDA orphan
drug designation for psilocybin in the treatment of
stroke, traumatic brain
injury, or
cancer, the commencement
of a Phase 2 clinical
trial and the
regulatory
filing
for
market authorization, such as U.S. Food and Drug
Administration ("FDA") approval.
In
addition to the Purchase Price, Revive
will also
pay Newscope
a
low
single digit royalty on
all
future
net
sales
of
products derived from the
Acquired
Assets.
The
Acquired Assets will include all of the following:
-
All
intellectual and work property derived from pre-clinical research
activities from the National Health Research Institutes ("NHRI") in
traumatic brain injury and stroke, as it relates to psilocybin with
the aim to obtain FDA Orphan Drug Designation.
-
Key
provisional patent applications with the U.S. Patent and Trademark
Office, which include:
(i)Psilocybin
in the Treatment of Neurological Brain Injury - United States
Provisional Application Serial No. 63/011,493 – Relates to
pharmaceutical compositions comprising psilocybin and their use for
the treatment of neurological brain injuries and
migraines.
(ii)Use
of Psilocybin in the Treatment of Cancer, United States Provisional
Application Serial No. 63/113,913 – Psilocybin's use of significant
unmet medical needs for Liver Carcinoma, Melanoma, Breast
Neoplasms, Kidney Neoplasms and Acute Myeloid Leukemia.
(iii)Psilocybin
Pharmaceutical Combination Therapies, United States Provisional
Application Serial No. 63/125,106 – Novel combinations of certain
FDA approved drugs with psilocybin as a potential therapeutic
option to reduce the side effects and improve the effectiveness of
psilocybin to treat neurological disorders.
"With this
acquisition, we have solidified our
foundation in having a leading
psychedelics
pharmaceutical platform
with a
focus on proprietary psilocybin-based therapeutics that includes
the development of an oral thin film product in collaboration with
the University of Wisconsin-Madison, a novel biosynthetic version
of psilocybin based on a natural biosynthesis enzymatic platform
developed by Dr. Gavin Williams, Professor and Researcher at North
Carolina State University, a clinical study with the University of
Wisconsin evaluating psilocybin in the treatment of methamphetamine
use disorder, and PharmaTher's
psilocybin
research
initiatives and intellectual property in stroke, traumatic brain
injury, cancer and drug combinations," said Michael
Frank, CEO of Revive. "We are now in a position to
advance
our psilocybin program for future clinical development
in
various
unmet clinical needs in mental health,
cancer
and neurological
disorders."
"We are pleased to
have partnered
PharmaTher's
psilocybin program with
Revive
as they
have positioned
themselves
as a
leader in psilocybin pharmaceutical
development with their
unique
product and delivery technology offerings as well as their
commitment in commercializing a biosynthetic form of psilocybin for
long-term sustainability,"
said Fabio Chianelli, CEO of Newscope.
About
Revive Therapeutics Ltd.
Revive is
a life sciences company focused on the research and development of
therapeutics for infectious diseases and rare disorders, and it is
prioritizing drug development efforts to take advantage of several
regulatory incentives awarded by the FDA such as Orphan Drug, Fast
Track, Breakthrough Therapy and Rare Pediatric Disease
designations. Currently, the Company is exploring the use of
Bucillamine for the potential treatment of infectious diseases,
with an initial focus on severe influenza and COVID-19. With its
recent acquisition of Psilocin Pharma Corp., Revive is advancing
the development of Psilocybin-based therapeutics in various
diseases and disorders. Revive's cannabinoid pharmaceutical
portfolio focuses on rare inflammatory diseases and the company was
granted FDA orphan drug status designation for the use of
Cannabidiol (CBD) to treat
autoimmune hepatitis (liver disease) and to treat ischemia and
reperfusion injury from organ transplantation. For more
information, visit
www.ReviveThera.com.
For more
information, please contact:
Michael
Frank
Chief
Executive Officer
Revive
Therapeutics Ltd.
Tel: 1
888 901 0036
Email: mfrank@revivethera.com
Website: www.revivethera.com
Neither the Canadian Securities Exchange nor its Regulation
Services Provider has reviewed or accepts responsibility for the
adequacy or accuracy of this release.
Cautionary Statement
This press release contains 'forward-looking information' within
the meaning of applicable Canadian securities legislation. These
statements relate to future events or future performance. The use
of any
of the words "could", "intend", "expect", "believe", "will",
"projected", "estimated" and similar expressions and statements
relating to matters that are not historical facts are intended to
identify forward-looking information and are based on Revive's
current belief or assumptions as to the outcome and timing of such
future events. Forward looking information in this press release
includes information with respect to the
Company's cannabinoids, psychedelics and infectious diseases
programs.
Forward-looking information is based on reasonable assumptions that
have been made by Revive at the date of the information and is
subject to known and unknown risks, uncertainties, and other
factors that may cause actual results or events to differ
materially from those anticipated in the forward-looking
information. Given these risks, uncertainties and assumptions, you
should not unduly rely on these forward-looking statements. The
forward-looking information contained in this press release is made
as of the date
hereof, and
Revive is not obligated to update or revise any forward-looking
information, whether as a result of new information, future events
or otherwise, except as required by applicable securities laws. The
foregoing statements expressly qualify any forward-looking
information contained herein. Reference is made to the risk factors
disclosed under the heading "Risk Factors" in the Company's annual
MD&A for the fiscal year ended June 30, 2020, which has been
filed on SEDAR and is available under the Company's profile
at www.sedar.com.