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Immunic Regains Compliance with Nasdaq Minimum Bid Price Requirement

Key Takeaway: Immunic, Inc. announced it has regained compliance with Nasdaq's minimum bid price requirement. The company achieved this as its stock price remained above $1.00 for at least 20 consecutive business days. This compliance is crucial for its continued listing on the Nasdaq Capital Market. Immunic is focused on developing therapies for neurologic diseases, with its lead program currently in phase 3 trials.
Price reaction · baseline $11.1 (2026-03-31 close) · hit after-hours · clean, no other IMUX news in the window
day 0 close · peak
+3.6%

Market Sentiment Analysis

POSITIVE FACTORS

  • Immunic has regained compliance with Nasdaq listing requirements.
  • The company's stock price has been stable at $1.00 or greater for 20 days.
  • Immunic's lead program is in phase 3 trials with promising results.

Full Press Release Details

NEW YORK,April 1, 2026/PRNewswire/ --Immunic, Inc.(Nasdaq:IMUX), a late-stage biotechnology company pioneering the development of novel oral therapies for neurologic diseases, today announced that it received written notice (the "Notice") from the Listing Qualifications Department of The Nasdaq Stock Market LLC ("Nasdaq") on March 27, 2026, informing the company that it has regained compliance with the minimum bid price requirement under Nasdaq Listing Rule 5550(a)(2) for continued listing on The Nasdaq Capital Market.
According to the Notice, Immunic has regained compliance with the minimum bid price requirement, because the closing bid price of the Company's common stock was at $1.00 per share or greater for at least 20 consecutive business days, satisfying the Nasdaq requirement on March 26, 2026. As a result, the matter was closed.
About Immunic, Inc.Immunic, Inc. (Nasdaq:IMUX) is a late-stage biotechnology company pioneering the development of novel oral therapies for neurologic diseases. The company's lead development program, vidofludimus calcium (IMU-838), is currently in phase 3 clinical trials for the treatment of relapsing multiple sclerosis, for which top-line data is expected to be available by the end of 2026. It has already shown therapeutic activity in phase 2 clinical trials in relapsing-remitting multiple sclerosis, progressive multiple sclerosis and other diseases. Vidofludimus calcium combines neuroprotective effects, through its mechanism as a first-in-class nuclear receptor-related 1 (Nurr1) activator, with additional anti-inflammatory and anti-viral effects, by selectively inhibiting the enzyme dihydroorotate dehydrogenase (DHODH). The company's development pipeline also includes earlier-stage programs, including IMU-856 and IMU-381, aimed at building a broader therapeutics platform addressing neurodegenerative, chronic inflammatory, and autoimmune-related diseases. For further information, please visit:www.imux.com.
Cautionary Statement Regarding Forward-Looking StatementsThis press release contains "forward-looking statements" that involve substantial risks and uncertainties for purposes of the safe harbor provided by the Private Securities Litigation Reform Act of 1995. All statements, other than statements of historical facts, included in this press release regarding strategy, future operations, future financial position, future revenue, projected expenses, sufficiency of cash and cash runway, expected timing, development and results of clinical trials, prospects, plans and objectives of management are forward-looking statements. Examples of such statements include, but are not limited to, statements relating to Immunic's development programs and the targeted diseases; the potential for Immunic's development programs to safely and effectively target diseases; preclinical and clinical data for Immunic's development programs; the timing of current and future clinical trials, anticipated clinical milestones and regulatory approvals; the nature, strategy and focus of the company and further updates with respect thereto; and the development and commercial potential of any product candidates of the company. Immunic may not actually achieve the plans, carry out the intentions or meet the expectations or projections disclosed in the forward-looking statements and you should not place undue reliance on these forward-looking statements. Such statements are based on management's current expectations and involve substantial risks and uncertainties. Actual results and performance could differ materially from those projected in the forward-looking statements as a result of many factors, including, without limitation, increasing inflation, tariffs and macroeconomics trends, impacts of the Ukraine – Russia conflict and the conflict in the Middle East on planned and ongoing clinical trials, risks and uncertainties associated with the ability to project future cash utilization and reserves needed for contingent future liabilities and business operations, the availability of sufficient financial and other resources to meet business objectives and operational requirements, and the ability to raise sufficient capital to continue as a going concern, the fact that the results of earlier preclinical studies and clinical trials may not be predictive of future clinical trial results, any changes to the size of the target markets for the company's products or product candidates, the protection and market exclusivity provided by Immunic's intellectual property, risks related to the drug development and the regulatory approval process and the impact of competitive products and technological changes. A further list and descriptions of these risks, uncertainties and other factors can be found in the section captioned "Risk Factors," in the company's Annual Report on Form 10-K for the fiscal year ended December 31, 2025, filed with the SEC on February 26, 2026, and in the company's subsequent filings with the SEC. Copies of these filings are available online atwww.sec.govor ir.imux.com/sec-filings. Any forward-looking statement made in this release speaks only as of the date of this release. Immunic disclaims any intent or obligation to update these forward-looking statements to reflect events or circumstances that exist after the date on which they were made. Immunic expressly disclaims all liability in respect to actions taken or not taken based on any or all of the contents of this press release.

Immunic, Inc.Jessica BreuVice President Investor Relations and Communications+49 89 2080 477 09[email protected]

US IR ContactRx Communications GroupPaula Schwartz+1 917 633 7790[email protected]

US Media ContactKCSA Strategic CommunicationsCaitlin Kasunich+1 212 896 1241[email protected]

Frequently Asked Questions

What did Immunic announce regarding Nasdaq compliance?

Immunic announced it has regained compliance with Nasdaq's minimum bid price requirement.

How long did Immunic's stock stay above the required price?

Immunic's stock price was at $1.00 or greater for at least 20 consecutive business days.

What is Immunic's lead development program?

Immunic's lead program is vidofludimus calcium, currently in phase 3 trials for multiple sclerosis.

What is the significance of the Nasdaq compliance?

Regaining compliance is crucial for Immunic's continued listing on the Nasdaq Capital Market.

Last updated: Apr 1, 2026