Recent Updates
Recently added Catalysts
MTNB Positive Sentiment Score: 80/100

Matinas BioPharma Regains Compliance with NYSE American Continued Listing Standards

Key Takeaway: Matinas BioPharma Holdings, Inc. has announced that it has regained compliance with NYSE American continued listing standards as of March 21, 2024. This comes after the company demonstrated sustained price improvement of its common stock, allowing it to be removed from the NYSE American noncompliant issuers list. Matinas is focused on developing therapies using its lipid nanocrystal delivery technology, notably featuring MAT2203, an oral antifungal treatment that recently met primary endpoints in Phase 2 studies. The company is preparing for further clinical evaluations as it enhances its market position.

Market Sentiment Analysis

POSITIVE FACTORS

  • Matinas BioPharma regained compliance with NYSE listing standards.
  • Shares of common stock showed sustained price improvement.
  • Removal from the noncompliant issuers list indicates financial stability.
  • Positive progress in clinical trials with MAT2203 enhances growth potential.

Full Press Release Details

BEDMINSTER, N.J., March 22, 2024 (GLOBE NEWSWIRE) -- Matinas BioPharma Holdings, Inc. (NYSE American: MTNB), a clinical-stage biopharmaceutical company focused on delivering groundbreaking therapies using its lipid nanocrystal (LNC) platform delivery technology, today announced that on March 21, 2024, the Company received written notification from the NYSE American LLC ("NYSE American") stating that the Company has regained compliance with the NYSE American’s continued listing standards. Specifically, the Company has resolved the continued listing deficiency with respect to the low selling price of its common stock as described in Section 1003(f)(v) of the NYSE American Company Guide due to shares of its common stock demonstrating sustained price improvement.
In the notification, the NYSE American informed the Company that the below compliance (".BC") indicator will no longer be disseminated at the opening of trading on March 22, 2024, and the Company will be removed from the NYSE American noncompliant issuers list on the NYSE American's website.
About Matinas BioPharma
Matinas BioPharma is a biopharmaceutical company focused on delivering groundbreaking therapies using its lipid nanocrystal (LNC) platform delivery technology.
Matinas’ lead LNC-based therapy is MAT2203, an oral formulation of the broad-spectrum antifungal drug amphotericin B, which although highly potent, can be associated with significant toxicity. Matinas’ LNC platform provides oral delivery of amphotericin B without the significant nephrotoxicity otherwise associated with IV-delivered formulations. Combining comparable fungicidal activity with targeted delivery results in a lower risk of toxicity and potentially creates the ideal antifungal agent for the treatment of invasive fungal infections. MAT2203 was successfully evaluated in the completed Phase 2 EnACT study in HIV patients suffering from cryptococcal meningitis, meeting its primary endpoint and achieving robust survival. MAT2203 will be further evaluated in a single Phase 3 registration trial (the “ORALTO” trial) as an oral step-down monotherapy following treatment with AmBisome® (liposomal amphotericin B) compared with the standard of care in patients with invasive aspergillosis who have limited treatment options.
In addition to MAT2203, preclinical and clinical data have demonstrated that this novel technology can potentially provide solutions to many challenges of achieving safe and effective intracellular delivery of both small molecules and larger, more complex molecular cargos including small oligonucleotides such as ASOs and siRNA. The combination of its unique mechanism of action and flexibility with routes of administration (including oral) positions Matinas’ LNC technology to potentially become a preferred next-generation orally available intracellular drug delivery platform. For more information, please visit www.matinasbiopharma.com.
Forward-looking Statements
This press release 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 compliance with the NYSE American’s continued listing standards, product development, clinical and regulatory timelines, market opportunity, competitive position, intellectual property rights, possible or assumed future results of operations, business strategies, potential growth opportunities and other statements 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 that 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 Annual Report on Form 10-K for the year ended December 31, 2022 as well as other documents filed by the Company from time to time thereafter with the Securities and Exchange Commission. 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.
LHA Investor Relations

Frequently Asked Questions

What recent compliance update did Matinas BioPharma receive?

Matinas BioPharma regained compliance with NYSE American’s listing standards.

What is MAT2203 used for?

MAT2203 is an oral formulation for treating invasive fungal infections.

How does the LNC technology benefit MAT2203?

LNC technology enables oral delivery of MAT2203, reducing toxicity risk.

What trial is MAT2203 set to enter next?

MAT2203 will undergo the Phase 3 ORALTO trial for invasive aspergillosis.

What is the goal of Matinas' LNC platform?

The LNC platform aims to enhance safe and effective drug delivery.

Last updated: Mar 22, 2024