Form 6-K - Report of foreign issuer [Rules 13a-16 and 15d-16]
September 06 2024 - 8:15AM
Edgar (US Regulatory)
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
Form 6-K
Report of Foreign Private Issuer
Pursuant to Rule 13a-16 or 15d-16
under the Securities Exchange Act of 1934
For the month of September 2024
Commission file number: 001-38041
SCISPARC LTD.
(Translation of registrant’s name into English)
20 Raul Wallenberg Street, Tower A,
Tel Aviv 6971916 Israel
(Address of principal executive offices)
Indicate by check mark whether the registrant
files or will file annual reports under cover of Form 20-F or Form 40-F.
Form 20-F ☒ Form
40-F ☐
CONTENTS
On September 6, 2024, SciSparc
Ltd. (the “Company”) issued a press release titled “SciSparc-Clearmind Medicine Collaboration Leads to Publication of
International Patent Application for Innovative MDMA-Based Combination Treatment.” A copy of this press release is furnished herewith
as Exhibit 99.1 to this Report of Foreign Private Issuer on Form 6-K and is incorporated by reference herein.
The first two paragraphs
and the section titled “Forward-Looking Statements” in the press release are incorporated by reference into the Company’s
registration statements on Form F-3 (File No. 333-275305, File No. 333-269839, File No. 333-266047, File No. 333-233417, File No. 333-248670,
File No. 333-255408, and File No. 333-275305) and on Form S-8 (File No. 333-225773) filed with the Securities and Exchange Commission
to be a part thereof from the date on which this Report of Foreign Private Issuer on Form 6-K is submitted, to the extent not superseded
by documents or reports subsequently filed or furnished.
EXHIBIT INDEX
SIGNATURES
Pursuant to the requirements
of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto
duly authorized.
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SciSparc Ltd. |
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Date: September 6, 2024 |
By: |
/s/ Oz Adler |
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Name: |
Oz Adler |
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Title: |
Chief Executive Officer and
Chief Financial Officer |
3
Exhibit 99.1
SciSparc-Clearmind Medicine Collaboration Leads
to Publication of International Patent Application for Innovative MDMA-Based Combination Treatment
Pioneering Therapeutic Approach Aims to Enhance
Safety and Efficacy
in Mental Health and Addiction Treatments
TEL AVIV, Israel, Sept. 06, 2024 (GLOBE
NEWSWIRE) -- 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: CWY0), a biotechnology company focused on discovery and development of novel psychedelic-derived therapeutics to
solve major under-treated mental health problems, an international patent application under the Patent Cooperation Treaty has been
published for the innovative combination of 3,4-Methylenedioxymethamphetamine (MDMA) with N-Acylethanolamines.
As part of their collaboration, SciSparc and Clearmind are researching
innovative combination therapies that combine psychedelic molecules with the N-Acylethanolamines family, including Palmitoylethanolamide
(PEA). To date, thirteen patents related to this collaboration have been filed by Clearmind with the U.S. Patent and Trademark Office,
as well as in several other global jurisdictions.
“The great importance of the cooperation with Clearmind lies
in our unceasing attempts to offer effective and safe treatments and today’s announcement is another demonstration of this methodology,
as we believe that our combined approach may address some of the U.S. Food & Drug Administration’s concerns associated with
MDMA safety,” said Oz Adler, Chief Executive Officer of SciSparc. “By integrating MDMA with N-Acylethanolamines like PEA,
we aim to enhance both the safety and therapeutic potential of these treatments. This combination offers a promising path forward in the
treatment of mental health disorders and addictions, providing an opportunity to overcome regulatory barriers and unlock the full potential
of MDMA in clinical settings.”
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 seed oil-based products on the Amazon Marketplace.
About Clearmind Medicine Inc.
Clearmind is a clinical-stage psychedelic pharmaceutical biotech company
focused on the discovery and development of novel psychedelic-derived therapeutics to solve widespread and underserved health problems,
including alcohol use disorder. Its primary objective is to research and develop psychedelic-based compounds and attempt to commercialize
them as regulated medicines, foods or supplements.
The Company’s intellectual portfolio currently consists of nineteen
patent families including 29 granted patents. The Company intends to seek additional patents for its compounds whenever warranted and
will remain opportunistic regarding the acquisition of additional intellectual property to build its portfolio.
Shares of Clearmind are listed for trading on Nasdaq under the symbol
“CMND” and the Frankfurt Stock Exchange under the symbol “CWY0.”
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 it discusses its belief that the patent publication represents the potential
of the collaboration between Clearmind and SciSparc to offer effective and safe treatments, that the collaboration approach of Clearmind
and SciSparc could address the U.S. Food & Drug Administration’s concerns associated with MDMA safety, that the Company aims
to enhance the safety and therapeutic potential of its treatments, and that this combination offers a promising path forward in the treatment
of mental health disorders and addictions, providing an opportunity to overcome regulatory barriers and unlock the full potential of MDMA
in clinical settings. 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.com
Tel: +972 3-761-7108
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