SciSparc-Clearmind Medicine Collaboration Leads to Publication of Application for Innovative Ketamine-Based Combination
August 29 2024 - 4:25PM
SciSparc Ltd. (Nasdaq: SPRC) ("Company" or "SciSparc"), a specialty
clinical-stage pharmaceutical company focusing on the development
of therapies to treat disorders and rare diseases of the central
nervous system, announced today that as part of its ongoing
collaboration with Clearmind Medicine Inc. (“Clearmind”) (Nasdaq:
CMND) (CSE: CMND) (FSE: CWY), a biotechnology company focused on
discovery and development of novel psychedelic-derived therapeutics
to solve major under-treated mental health problems, Clearmind has
announced the publication of its patent application under the
international Patent Cooperation Treaty, for innovative
combinations of ketamine and N-acylethanolamines.
SciSparc and Clearmind, as part of their collaboration, research
combination treatment comprised of SciSparc’s Palmitoylethanolamide
(“PEA”) and Clearmind’s innovative psychedelic molecule, MEAI, for
treating addictions, weight loss and mental health disorders.
Furthermore, SciSparc and Clearmind are jointly exploring new
treatments based on psychedelic molecules and PEA. To date,
thirteen patents related to this collaboration have been filed with
the U.S. Patent and Trademark Office and several other global
patent offices.
The U.S. Food & Drug Administration (the “FDA”) gave its
approval in 2019 for a ketamine derivative as a nasal spray
medication, intended for two specific uses in adult patients:
treating depression that has not responded to other treatments and
alleviating depressive symptoms in those with major depressive
disorder who are having suicidal thoughts or exhibiting suicidal
behavior.
The approved treatment comes with strict usage guidelines. It
must be administered only at certified medical facilities and used
alongside an antidepressant medication. After receiving a dose,
patients are required to remain at the facility for a two-hour
observation period. This allows healthcare providers to monitor for
any potentially serious side effects that may occur.
“SciSparc has always been focused on the development of unique
and proprietary combinations with PEA, which our research shows can
dramatically reduce the number of doses of various active
ingredients while maintaining effectiveness and minimizing adverse
effects. Ketamine was approved by the FDA for use under close
supervision due to its accompanying side effects. Our innovative
approach aims to deliver therapeutic benefits to a diverse group of
patients with various conditions, while minimizing unwanted adverse
effects. We believe this approach could improve treatment outcomes
across a broad spectrum of medical needs,” said Oz Adler, Chief
Executive Officer of SciSparc.
About SciSparc Ltd. (Nasdaq:
SPRC):
SciSparc Ltd. is a specialty clinical-stage pharmaceutical
company led by an experienced team of senior executives and
scientists. SciSparc’s focus is on creating and enhancing a
portfolio of technologies and assets based on cannabinoid
pharmaceuticals. With this focus, the Company is currently engaged
in the following drug development programs based on THC and/or
non-psychoactive cannabidiol: SCI-110 for the treatment of Tourette
Syndrome, for the treatment of Alzheimer's disease and agitation;
and SCI-210 for the treatment of autism and status epilepticus. The
Company also owns a controlling interest in a subsidiary whose
business focuses on the sale of hemp seeds’ oil-based products on
the Amazon.com Marketplace.
Forward-Looking Statements:
This press release contains forward-looking statements within
the meaning of the "safe harbor" provisions of the Private
Securities Litigation Reform Act of 1995 and other Federal
securities laws. For example, the Company is using forward looking
statements when discussing ongoing collaborative research, the
prospective outcomes and effects of SciSparc’s collaborative
research with Clearmind, and the belief that SciSparc’s approach to
its research may improve treatment outcomes. Since such statements
deal with future events and are based on SciSparc’s current
expectations, they are subject to various risks and uncertainties
and actual results, performance or achievements of SciSparc could
differ materially from those described in or implied by the
statements in this press release. The forward-looking statements
contained or implied in this press release are subject to other
risks and uncertainties, including those discussed under the
heading "Risk Factors" in SciSparc's Annual Report on Form 20-F
filed with the SEC on April 1, 2024, and in subsequent filings
with the U.S. Securities and Exchange Commission. Except as
otherwise required by law, SciSparc disclaims any intention or
obligation to update or revise any forward-looking statements,
which speak only as of the date they were made, whether as a result
of new information, future events or circumstances or
otherwise.
Investor Contact:IR@scisparc.comTel: +972-3-6167055
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