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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): October 24, 2024
INMUNE BIO INC. |
(Exact
name of registrant as specified in charter) |
Nevada |
|
001-38793 |
|
47-5205835 |
(State
or other jurisdiction |
|
(Commission
File Number) |
|
(IRS
Employer |
of
incorporation) |
|
|
|
Identification
No.) |
225 NE Mizner Blvd., Suite 640, Boca Raton, Florida 33432
(Address of Principal Executive Offices) (Zip Code)
(858)
964 3720
(Registrant’s
Telephone Number, Including Area Code)
Not
Applicable
(Former
Name or Former Address, If Changed Since Last Report)
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, par value $0.001 per shares |
|
INMB |
|
The
NASDAQ Stock Market LLC |
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 mart 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
8.01. Other Events.
On
October 24, 2024, INmune Bio Inc. (the “Company”), issued a press release announcing the publication of a seminal paper in
the journal Cell Reports that demonstrates XPro1595 promotes remyelination in an animal model of demyelinating disease.
A
copy of the Company’s press release is attached as Exhibit 99.1 to this Current Report on Form 8-K and is incorporated herein by
reference.
Item
9.01 Financial statements and Exhibits
(d)
Exhibits.
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 hereunto duly authorized.
|
INMUNE
BIO INC. |
|
|
Date:
October 25, 2024 |
By: |
/s/
David Moss |
|
Name: |
David
Moss |
|
Title:
|
Chief
Financial Officer |
2
Exhibit 99.1
INmune
Bio Inc. Announces Publication in Cell Reports Demonstrating XPro™ Promotes Remyelination
Data
from Animal Model Study Demonstrate XPro™ converts microglia from a demyelinating cell to a remyelinating cell
Multi-year
study published has implications for many CNS diseases including Alzheimer’s
Boca
Raton, Florida, Oct. 24, 2024 (GLOBE NEWSWIRE) -- INmune Bio, Inc. (NASDAQ: INMB) (the “Company”), a
clinical-stage inflammation and immunology company focused on developing treatments that harness the patient’s innate
immune system to fight disease, announces the publication of a seminal paper in the journal Cell Reports that demonstrates
XPro1595 promotes remyelination in an animal model of demyelinating disease. The study, Microglia Regulate Cortical Remyelination
via ΤNFR1-Dependent Phenotypic Polarization, was performed under the direction of Leslie Probert PhD, Head of Immunology
at the Hellenic Pasteur Institute in Athens Greece, and is the culmination of several years of work supported by EU research grants.
Myelin
is necessary for fast and efficient communication between neurons. Loss of myelin compromises neuron function and communication and is
a key step in the neurodegenerative process of many CNS diseases, including Alzheimer’s Disease.
“Activated
microglia play a central role in both demyelination and remyelination,” said Dr. Probert, senior author of the publication. “Our
data identify solTNF as a critical cytokine checkpoint that converts microglia from a reparative, remyelinating cell to a damaging, demyelinating
cell. These data suggest that blocking soluble TNF is a promising strategy for treating demyelinating diseases.”
“Demyelination
is a core mechanism of neurodegeneration that has been overlooked in Alzheimer's disease, despite the evidence that it’s a critical
element of the disease's pathology,” said RJ Tesi MD, CEO of INmune Bio. “These new data further support the potential for
XPro1595 in neurodegenerative diseases by restoring glia function to improve key components of neurodegeneration at multiple levels,
including restoration of synaptic function, remyelination, and ceasing cell loss.”
INmune
anticipates reporting top-line cognitive results of an ongoing blinded randomized Phase II in Early AD patients in the first half of
2025.
About
Demyelination in Alzheimer's Disease
Research
shows that demyelination occurs in various brain regions critical for cognition in AD patients. This damage is often associated with
the presence of amyloid-beta (Aβ) plaques, suggesting that myelin loss may precede or accompany the classic pathological changes
seen in AD. Changes in myelin structure can be detected even before the onset of typical AD symptoms. Advanced imaging techniques have
revealed alterations in myelin density and integrity in individuals at risk for AD, indicating that demyelination might serve as an early
biomarker for the disease. The mechanisms underlying myelin damage in AD involve oligodendrocyte dysfunction, which can lead to the breakdown
of myelin sheaths. This breakdown not only affects neuronal health but may also contribute to the accumulation of Aβ, creating a
feedback loop that exacerbates both myelin loss and neurodegeneration. Studies utilizing techniques like myelin water fraction imaging
have shown significant reductions in myelin integrity among individuals with mild cognitive impairment and dementia, reinforcing the
notion that demyelination is prevalent in AD.
About
INmune Bio Inc.
INmune
Bio, Inc. is a publicly traded (NASDAQ: INMB), clinical-stage biotechnology company focused on developing treatments that target
the innate immune system to fight disease. INmune Bio has two product platforms that are both in clinical trials: The Dominant-Negative
Tumor Necrosis Factor (DN-TNF) product platform utilizes dominant-negative technology to selectively neutralize soluble TNF, a key driver
of innate immune dysfunction and a mechanistic driver of many diseases. XPRO, the first of several DN-TNF products, is in clinical trials
to determine if it can treat patients with Mild Alzheimer’s disease. Additional therapeutic indications including d treatment-resistant
depression and oncology will be pursued when resources allow. The Natural Killer Cell Priming Platform includes INKmune™, a therapy
developed to prime a patient’s NK cells to treat patients with cancer. INKmune uses a precision medicine approach for the treatment
of a wide variety of hematologic and solid tumor malignancies. The INKmune trial is enrolling patients into a US Phase I/II trial in
men with metastatic castrate resistant prostate cancer. To learn more, please visit www.inmunebio.com.
Forward
Looking Statements
Clinical
trials are in early stages and there is no assurance that any specific outcome will be achieved. Any statements contained in this press
release that do not describe historical facts may constitute forward-looking statements as that term is defined in the Private Securities
Litigation Reform Act of 1995. Any statements contained in this press release that do not describe historical facts may constitute
forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995. Any forward-looking statements
contained herein are based on current expectations but are subject to a number of risks and uncertainties. Actual results and the timing
of certain events and circumstances may differ materially from those described by the forward-looking statements as a result of these
risks and uncertainties. INB03™, XPro1595, and INKmune™ are still in clinical trials or preparing to start clinical trials
and have not been approved by the US Food and Drug Administration (FDA) or any regulatory body and there cannot be any assurance that
they will be approved by the FDA or any regulatory body or that any specific results will be achieved. The factors that could cause actual
future results to differ materially from current expectations include, but are not limited to, risks and uncertainties relating to the
Company’s ability to produce more drug for clinical trials; the availability of substantial additional funding for the Company
to continue its operations and to conduct research and development, clinical studies and future product commercialization; and, the Company’s
business, research, product development, regulatory approval, marketing and distribution plans and strategies. These and other factors
are identified and described in more detail in the Company’s filings with the Securities and Exchange Commission, including the
Company’s Annual Report on Form 10-K, the Company’s Quarterly Reports on Form 10-Q and the Company’s Current Reports
on Form 8-K. The Company assumes no obligation to update any forward-looking statements in order to reflect any event or circumstance
that may arise after the date of this release.
INmune
Bio Contact:
David
Moss, CFO (858) 964-3720
info@inmunebio.com
Daniel
Carlson
Head of Investor Relations
(415) 509-4590
dcarlson@inmunebio.com
Investor Contact:
Mike
Moyer
Managing Director – LifeSci Advisors
mmoyer@lifesciadvisors.com
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