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Alzamend Neuro Regains Compliance with Nasdaq Listing Standards ATLANTA, GA

Key Takeaway: Alzamend Neuro has announced that it has regained compliance with Nasdaq's listing standards after meeting the minimum stockholders' equity requirement. The company received a written notice from Nasdaq confirming its compliance after an appeal process that began when it failed to meet the requirements in 2023. This development allows Alzamend to continue its listing on the Nasdaq Capital Market and supports its ongoing clinical trials aimed at treating Alzheimer's disease and other conditions. Alzamend is now focused on advancing its product candidates with plans to initiate phase II clinical trials in 2025.

Market Sentiment Analysis

POSITIVE FACTORS

  • Alzamend Neuro has regained compliance with Nasdaq listing standards.
  • The company successfully executed its strategic plan to demonstrate compliance.
  • Positive funding progress with $25 million securities purchase agreement.

Full Press Release Details

Alzamend Neuro Regains Compliance with Nasdaq
ATLANTA, GA, October 15, 2024 -- Alzamend Neuro,
Inc. (Nasdaq: ALZN) ("Alzamend"), a clinical-stage biopharmaceutical company focused on developing novel products for
the treatment of Alzheimer's disease ("Alzheimer's"), bipolar disorder ("BD"), major
depressive disorder ("MDD") and post-traumatic stress disorder ("PTSD"), today announced that it
has received formal written notice from The Nasdaq Stock Market, LLC's Office of General Counsel ("Nasdaq")
that Alzamend has demonstrated compliance with the minimum stockholders' equity requirement as set forth in Nasdaq Listing Rule
5550(b)(1) (the "Equity Rule"), which requires a minimum stockholders' equity of $2,500,000.
As previously reported, on September 26, 2023,
Alzamend was notified by Nasdaq that it did not meet the minimum market value of listed securities requirement for continued listing
on Nasdaq under Nasdaq Listing Rule 5550(b)(2), or any other continued listing standard, such as the Equity Rule, and was provided 180
calendar days, or until March 25, 2024, to regain compliance. Alzamend had not regained compliance by March 25, 2024, and Nasdaq determined
to delist Alzamend's common stock. Alzamend appealed the delisting determination to a Hearings Panel (the "Panel").
In May 2024, the Panel granted Alzamend's request to continue its listing on The Nasdaq Capital Market, subject to Alzamend demonstrating
compliance, on or before September 23, 2024, with the Equity Rule and satisfying all applicable requirements for continued listing on
Earlier this year, Alzamend entered into a securities
purchase agreement to provide for the sale of $25 million of Alzamend's Series A Convertible Preferred Stock ("Series A
Preferred") over a period of time. To date, the investor has purchased $8 million of Series A Preferred, with (i) an additional
$2 million to be funded within the next 30 days, as Alzamend has achieved the milestones for such payment and (ii) the investor is obligated
to purchase $1 million of Series A Preferred each month going forward, subject to the terms and conditions set forth in the purchase agreement,
until January 2026. Accordingly, on October 14, 2024, the Panel provided Alzamend with written notice that it had regained compliance
with the Equity Rule and determined to continue the listing of Alzamend's securities on Nasdaq.
Stephan Jackman, CEO of Alzamend, stated,
"We are very pleased to announce that Alzamend has regained compliance with Nasdaq's listing standards. We presented a strategic
plan of compliance to the Panel at our hearing in May, which we have successfully executed upon. Regaining compliance with Nasdaq listing
standards was an important goal for Alzamend, and we appreciate the Panel's confirmation that we were able to deliver on our commitment.
We remain focused on moving forward with our five phase II clinical trials of AL001 in partnership with Massachusetts General Hospital,
which we intend to initiate in 2025."
About Alzamend Neuro
Alzamend Neuro is a clinical-stage biopharmaceutical
company focused on developing novel products for the treatment of Alzheimer's, BD, MDD and PTSD. Our mission is to rapidly develop
and market safe and effective treatments. Our current pipeline consists of two novel therapeutic drug candidates, AL001 - a patented ionic
cocrystal technology delivering lithium via a therapeutic combination of lithium, salicylate and L-proline, and ALZN002 - a patented method
using a mutant-peptide sensitized cell as a cell-based therapeutic vaccine that seeks to restore the ability of a patient's immunological
system to combat Alzheimer's by removing beta-amyloid from the brain. The latter is a second-generation active-immunity approach
designed to mitigate the disadvantages of approved passive immunity marketed antibody products, particularly by reducing the required
frequency and costs of dosing associated with antibody products. Both of our product candidates are licensed from the University of South
Florida Research Foundation, Inc. pursuant to royalty-bearing exclusive worldwide licenses.
Forward-Looking Statements
This press release contains "forward looking
statements" within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange
Act of 1934, as amended. These forward-looking statements generally include statements that are predictive in nature and depend upon or
refer to future events or conditions, and include words such as "believes," "plans," "anticipates,"
"projects," "estimates," "expects," "intends," "strategy," "future,"
"opportunity," "may," "will," "should," "could," "potential,"
or similar expressions. Statements that are not historical facts are forward-looking statements. Forward-looking statements are based
on current beliefs and assumptions that are subject to risks and uncertainties. Forward-looking statements speak only as of the date they
are made, and Alzamend undertakes no obligation to update any of them publicly in light of new information or future events. Actual results
could differ materially from those contained in any forward-looking statement as a result of various factors. More information, including
potential risk factors, that could affect Alzamend's business and financial results are included in Alzamend's filings with
the U.S. Securities and Exchange Commission. All filings are available at www.sec.gov and on Alzamend's website at www.Alzamend.com.
Email: Info@Alzamend.com or call: 1-844-722-6333

Frequently Asked Questions

What recent compliance update did Alzamend Neuro announce?

Alzamend Neuro confirmed it has regained compliance with Nasdaq's equity requirement.

What is Alzamend Neuro's focus area?

Alzamend Neuro develops treatments for Alzheimer's, bipolar disorder, MDD, and PTSD.

How much capital has Alzamend raised through Series A Preferred?

Alzamend has raised $8 million, with an additional $2 million expected soon.

What is Alzamend's key product candidate?

AL001 is a novel treatment using ionic cocrystal technology for Alzheimer's.

When does Alzamend plan to initiate clinical trials for AL001?

Alzamend intends to begin its phase II clinical trials for AL001 in 2025.

Last updated: Oct 15, 2024