STOCK TITAN

Immunic to Host Virtual Relapsing Multiple Sclerosis R&D Day on September 9, 2026

Immunic (IMUX) will host a virtual R&D day focused on relapsing multiple sclerosis on Wednesday, September 9, 2026, at 11:00 am ET.

(Moderate)
(Positive)
Tags

Immunic (IMUX) will host a virtual R&D day focused on relapsing multiple sclerosis on Wednesday, September 9, 2026, at 11:00 am ET.

Management and external MS experts Amit Bar-Or and Stephen Krieger will discuss vidofludimus calcium (IMU‑838), an investigational oral small molecule in Phase 3 trials for relapsing MS, ahead of expected top-line ENSURE data by the end of 2026. The company highlights vidofludimus calcium’s combination of Nurr1 activation with selective DHODH inhibition, aiming to address both neurodegenerative and inflammatory drivers of MS, and notes its prior Phase 2 therapeutic potential and favorable safety profile. The Zoom webinar will run from 11:00 am to 12:30 pm ET.

Loading...
Loading translation...

Positive

  • None.

Negative

  • None.

Market Context

Recent IMUX news reactions ranged from +8.65% on August 11 to -7.72% on September 1, adding mixed pr...
Analysis

Recent IMUX news reactions ranged from +8.65% on August 11 to -7.72% on September 1, adding mixed precedent to this R&D-day notice. The effective S-3/A resale registration for 45,815,180 shares remains a structural risk; upcoming clinical data are the key watchpoint.

Key Figures

R&D Day date: September 9, 2026 R&D Day start: 11:00 am ET ENSURE trial phase: Phase 3 +2 more
5 metrics
R&D Day date September 9, 2026 Virtual relapsing multiple sclerosis R&D Day
R&D Day start 11:00 am ET September 9, 2026 webinar
ENSURE trial phase Phase 3 Relapsing multiple sclerosis trials
Top-line data timing End of 2026 ENSURE trials in relapsing multiple sclerosis
R&D Day end 12:30 pm ET September 9, 2026 webinar

Historical Context

5 past events · Latest: Sep 01 (Neutral)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Sep 01 Leadership appointment Neutral -7.7% Appointed first chief data and digital officer ahead of potential regulatory submission
Aug 11 Earnings report Positive +8.7% Phase 3 trials remained on track and cash was expected to fund operations
Aug 10 Board appointment Positive +8.7% Added finance and commercial strategy expertise ahead of pivotal clinical data
Jul 09 Conference participation Neutral +0.1% Management scheduled investor meetings and a fireside chat at industry conferences
Jun 10 Conference participation Neutral -4.5% Planned presentations, partnering activities and investor meetings across scientific conferences

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent company news produced mixed reactions, with positive responses to some corporate updates and a negative response to the latest management announcement.

Key Terms

nurr1, top-line data readout, small molecule therapy
3 terms
nurr1 medical
"nuclear receptor-related 1 (Nurr1) activation with selective dihydroorotate"
Nurr1 is a protein found in brain cells that acts like a light switch, turning on the genes needed for the creation and survival of dopamine-producing neurons. Investors care about Nurr1 because drugs that affect it are being explored as potential treatments for neurodegenerative and psychiatric conditions; progress or setbacks in that research can change a drug candidate's value, affect regulatory approval odds, and influence company valuations.
top-line data readout clinical
"Ahead of the top-line data readout of the Phase 3 ENSURE trials"
A top-line data readout is the initial, high-level summary of a clinical trial’s main results, usually reporting whether primary endpoints were met and giving key safety signals without the full detailed analysis. For investors it matters because it delivers the first clear signal about a drug’s effectiveness or safety—like a score announced after a game—guiding expectations about regulatory progress, future studies, and potential commercial value.
small molecule therapy medical
"an investigational oral small molecule therapy that combines"
A small molecule therapy is a drug made from low‑molecular‑weight chemical compounds that can be manufactured synthetically, often taken orally, and able to enter cells to modulate biological targets. Investors care because these drugs follow well‑established development, regulatory and manufacturing paths, tend to have different cost, scale and patent dynamics than biologic therapies, and so their clinical progress and market potential affect company valuation and commercial prospects.

AI-generated analysis. How Rhea-AI works. Not financial advice.

See more from StockTitan in Google Search and AI answers. Adds StockTitan as a preferred source · opens Google
Add on Google

NEW YORK, Sept. 2, 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 will host a virtual research and development (R&D) day focused on relapsing multiple sclerosis (MS) on Wednesday, September 9, 2026, at 11:00 am ET.

Management of Immunic, including Erik Lundgren, M.B.A., Chief Executive Officer, Michael A. Panzara, M.D., M.P.H., Chief Medical Officer, Hella Kohlhof, Ph.D., Chief Scientific Officer, and Jason Tardio, M.B.A., President & Chief Operating Officer, will be joined by two renowned key opinion leaders, Amit Bar-Or, M.D., FRCPC, Perelman School of Medicine, University of Pennsylvania and Stephen Krieger, M.D., FAAN, Icahn School of Medicine, The Mount Sinai Hospital, New York City.

Ahead of the top-line data readout of the Phase 3 ENSURE trials in relapsing MS, expected by the end of 2026, Immunic will discuss its late-stage clinical asset, vidofludimus calcium (IMU-838), an investigational oral small molecule therapy that combines nuclear receptor-related 1 (Nurr1) activation with selective dihydroorotate dehydrogenase (DHODH) inhibition to address both neurodegenerative and inflammatory drivers of MS. With the potential to go beyond traditional anti-inflammatory approaches and address persistent unmet needs, the team will share insights into how vidofludimus calcium's differentiated approach could reshape treatment for patients with relapsing MS.

Drs. Bar-Or and Krieger, internationally recognized leaders in MS clinical care and research, will provide expert perspectives on the MS patient journey, current treatment paradigms, and unmet medical needs.

The R&D Day webinar will take place on Wednesday, September 9, 2026, from 11:00 am to 12:30 pm ET via Zoom. To register, please CLICK HERE.

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 being evaluated in Phase 3 clinical trials for the treatment of relapsing multiple sclerosis, with top-line data expected to be available by the end of 2026. Initiation of an additional Phase 3 clinical trial in progressive MS is expected later in 2026. Vidofludimus calcium has already shown therapeutic potential and a favorable safety and tolerability profile 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-381 and IMU-856, aimed at building a broader therapeutics platform addressing neurodegenerative and autoimmune diseases. For further information, please visit: www.imux.com.

Cautionary Statement Regarding Forward-Looking Statements
This 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 vidofludimus calcium to safely and effectively target diseases; preclinical and clinical data for vidofludimus calcium; the feasibility of advancing vidofludimus calcium to a confirmatory Phase 3 clinical trial in progressive multiple sclerosis; 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, 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 at www.sec.gov or 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.

Contact Information

Immunic, Inc.
Jessica Breu
Vice President Investor Relations and Communications
+49 89 2080 477 09
jessica.breu@imux.com

US IR Contact
LifeSci Advisors
Joyce Allaire
immunic@lifesciadvisors.com

US Media Contact
Real Chemistry
media@imux.com

Immunic, Inc. Logo

 

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/immunic-to-host-virtual-relapsing-multiple-sclerosis-rd-day-on-september-9-2026-302862414.html

SOURCE Immunic, Inc.

FAQ

What event did Immunic (IMUX) announce for September 9, 2026?

Immunic announced a virtual research and development day focused on relapsing multiple sclerosis to be held on Wednesday, September 9, 2026, at 11:00 am ET. The event will be conducted as a Zoom webinar and run until 12:30 pm ET.

What will be discussed at Immunic’s relapsing multiple sclerosis R&D Day for IMUX?

The R&D Day will focus on Immunic’s late-stage clinical asset vidofludimus calcium (IMU‑838), an investigational oral small molecule combining Nurr1 activation with selective DHODH inhibition, and how its differentiated approach could address neurodegenerative and inflammatory drivers and unmet needs in relapsing multiple sclerosis.

Who will participate in Immunic (IMUX) virtual MS R&D Day on September 9, 2026?

Participants include Immunic management, such as the CEO, CMO, CSO and President & COO, joined by MS experts Amit Bar‑Or of the Perelman School of Medicine, University of Pennsylvania, and Stephen Krieger of the Icahn School of Medicine at Mount Sinai.

How can investors attend Immunic (IMUX) relapsing MS R&D Day webinar?

The relapsing MS R&D Day will be held as a Zoom webinar on September 9, 2026, from 11:00 am to 12:30 pm ET. Registration is available via the Zoom link provided by Immunic for this event.

What is vidofludimus calcium (IMU‑838) that Immunic (IMUX) will feature at the R&D Day?

Vidofludimus calcium (IMU‑838) is Immunic’s lead oral therapy, in Phase 3 clinical trials for relapsing multiple sclerosis, expected to deliver top-line data by the end of 2026. It has shown therapeutic potential and a favorable safety and tolerability profile in Phase 2 trials in multiple sclerosis and other diseases.

What are the ongoing and planned Phase 3 trials for vidofludimus calcium in MS for IMUX?

Vidofludimus calcium is being evaluated in Phase 3 ENSURE trials for relapsing multiple sclerosis, with top-line data expected by the end of 2026. Immunic also expects to initiate an additional Phase 3 clinical trial in progressive multiple sclerosis later in 2026.