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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM
8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the Securities Exchange Act
of 1934
Date of report (date of earliest event reported):
May 17, 2023
TONIX PHARMACEUTICALS HOLDING CORP.
(Exact name of registrant as specified in its charter)
Nevada |
001-36019 |
26-1434750 |
(State or Other Jurisdiction
of Incorporation)
|
(Commission
File Number)
|
(IRS Employer
Identification No.)
|
26 Main Street,
Chatham,
New Jersey
07928
(Address of principal executive offices) (Zip Code)
Registrant’s telephone number, including area code:
(862)
904-8182
Check the appropriate box below if the Form 8-K filing is intended
to simultaneously satisfy the filing obligation of the registrant
under any of the following provisions (see General Instruction A.2.
below):
☐ Written communications pursuant to Rule 425
under the Securities Act (17 CFR 230.425)
☐ Soliciting material pursuant to Rule 14a-12
under the Exchange Act (17 CFR 240.14a-12)
☐ Pre-commencement communications pursuant to
Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
☐ Pre-commencement communications pursuant to
Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
Securities registered pursuant to Section 12(b) of the Act:
Title
of each class |
Trading
Symbol(s) |
Name
of each exchange on which registered |
Common Stock |
TNXP |
The
NASDAQ Capital Market |
Indicate by check mark whether the registrant is an emerging growth
company as defined in Rule 405 of the Securities Act of 1933 (§
230.405 of this chapter) or Rule 12b-2 of the Securities Exchange
Act of 1934 (§ 240.12b-2 of this chapter).
Emerging growth company ☐
If an emerging growth company, indicate by check mark if the
registrant has elected not to use the extended transition period
for complying with any new or revised financial accounting
standards provided pursuant to Section 13(a) of the Exchange
Act. ☐
Item
7.01 |
Regulation
FD Disclosure. |
On May 17, 2023, Tonix Pharmaceuticals Holding Corp. (the
“Company”) announced the molecular mechanism of action of
tianeptine, the active ingredient of the Company’s TNX-601 ER
(tianeptine hemioxalate extended-release tablets) product
candidate, currently in Phase 2 clinical development for the
treatment of major depressive disorder (“MDD”). A copy of the press
release which discusses this matter is furnished hereto as Exhibit
99.01, and incorporated herein by reference.
The Company updated its TNX-601 presentation, which it intends to
place on its website and which may contain nonpublic information. A
copy of the presentation is filed as Exhibit 99.02 hereto and
incorporated herein by reference.
The information in this Item 7.01 of this Current Report on
Form 8-K, including Exhibits 99.01 and 99.02 attached hereto,
shall not be deemed “filed” for purposes of Section 18 of the
United States Securities Exchange Act of 1934 (the “Exchange Act”)
or otherwise subject to the liabilities of that section, nor shall
they be deemed incorporated by reference in any filing under the
United States Securities Act of 1933 or the Exchange Act, except as
shall be expressly set forth by specific reference in such a
filing.
On May 17, 2023, the Company announced the molecular mechanism of
action of tianeptine, the active ingredient of TNX-601 ER,
currently in Phase 2 clinical development for the treatment of MDD.
Based on pharmacology and medicinal chemistry experiments,
scientists at the Company have established that tianeptine is an
agonist for the nuclear peroxisome proliferator-activated receptor
(“PPAR”) isoforms PPAR-β/δ and PPAR-γ, and tianeptine’s effects on
these PPAR isoforms account for its ability to induce
neuroplasticity in cultured neurons. The findings upset a long-held
belief that the only way to restore the connectivity of neurons
damaged in the state of depression was to increase the synaptic
levels or activity of neurotransmitters such as the monoamines
serotonin, norepinephrine, and dopamine. The new findings show that
selective activation of nuclear PPAR-β/δ and PPAR-γ in neurons and
supporting glia appears to be a more direct mechanism to achieve
the goal of restoring neuronal connectivity, or neuroplasticity.
Drugs that restore neuroplasticity are called plastogens.
Consequently, tianeptine is a plastogen that acts directly on
nuclear receptors that regulate gene expression in neurons and
microglia.
The new research provides clarity on why tianeptine does not cause
sexual dysfunction, weight gain, or several other
treatment-limiting toxicities associated with traditional
antidepressants. Tianeptine treats depression by activating select
nuclear PPAR isoforms, and has little to do with monoaminergic
neurotransmitters, which are known to be implicated in the most
frequently cited side effects of most marketed antidepressants. Key
experiments were performed by scientists at the Company’s Research
and Development Center in Frederick, Maryland.
In animal models, tianeptine restores neuroplasticity and reverses
stress-induced impairments through activation of select nuclear
PPAR isoforms without modulating synaptic monoamine
neurotransmitters, mimicking naturally occurring polyunsaturated
fatty acid in binding to PPARs.
The Company believes that the proposed mechanism is consistent with
the clinical effects of tianeptine in promoting cognition in
Alzheimer’s disease, Parkinson’s disease and bipolar disorder, and
is considering the development TNX-601 ER as a treatment for these
and other conditions.
The new findings about tianeptine’s mechanism dispel the notion
that tianeptine’s weak µ-opioid receptor activity was central to
its mechanism of treating depression and indicate that there is no
connection between tianeptine’s neuroplastic effects on cultured
neurons and its weak µ-opioid receptor agonism. The Company has
identified a new chemical entity related to tianeptine, TNX-4300,
that restores neuroplasticity in cultured neurons and is free from
µ-opioid receptor activity. The Company intends to submit data
supporting tianeptine’s mechanism of action for presentation at
upcoming scientific conferences and for publication in peer
reviewed journals.
Forward- Looking Statements
This Current Report on Form 8-K contains certain forward-looking
statements within the meaning of Section 27A of the Securities Act
of 1933 and Section 21E of the Securities Exchange Act of 1934 and
Private Securities Litigation Reform Act, as amended, including
those relating to the Company’s product development, clinical
trials, clinical and regulatory timelines, market opportunity,
competitive position, possible or assumed future results of
operations, business strategies, potential growth opportunities and
other statement that are predictive in nature. These
forward-looking statements are based on current expectations,
estimates, forecasts and projections about the industry and markets
in which we operate and management’s current beliefs and
assumptions.
These statements may be identified by the use of forward-looking
expressions, including, but not limited to, “expect,” “anticipate,”
“intend,” “plan,” “believe,” “estimate,” “potential,” “predict,”
“project,” “should,” “would” and similar expressions and the
negatives of those terms. These statements relate to future events
or our financial performance and involve known and unknown risks,
uncertainties, and other factors which may cause actual results,
performance or achievements to be materially different from any
future results, performance or achievements expressed or implied by
the forward-looking statements. Such factors include those set
forth in the Company’s filings with the SEC. Prospective investors
are cautioned not to place undue reliance on such forward-looking
statements, which speak only as of the date of this press release.
The Company undertakes no obligation to publicly update any
forward-looking statement, whether as a result of new information,
future events or otherwise.
Item
9.01 |
Financial
Statements and Exhibits. |
(d) |
|
Exhibit
No.
|
|
Description. |
|
|
99.01
99.02
104
|
|
Press Release of the Company, dated May 17, 2023
TNX-601 Product Presentation
Cover Page Interactive Data File (embedded within the Inline XBRL
document)
|
SIGNATURE
Pursuant to the requirement 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.
|
TONIX
PHARMACEUTICALS HOLDING CORP. |
|
|
Date:
May 17, 2023 |
By: |
/s/
Bradley Saenger |
|
|
Bradley
Saenger |
|
Chief
Financial Officer |
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