Immunic, Inc. Announces Closing of Oversubscribed $65 Million Underwritten Public Offering
- Secured significant initial funding of $65 million through the offering
- Potential for additional $130 million if all warrants are exercised
- Strong institutional investor participation including BVF Partners, Coastlands Capital, and Janus Henderson
- Funds will support clinical trials and operations advancement
- Potential dilution for existing shareholders upon warrant exercise
- Complex warrant structure with different exercise periods may create market uncertainty
- Significant dependence on future warrant exercises for additional funding
Insights
Immunic secured $65M in funding with potential for $130M more, substantially strengthening its financial position for clinical development.
Immunic has successfully closed an oversubscribed $65 million public offering through a complex warrant structure that could potentially bring in an additional $130 million if all warrants are fully exercised. This significant capital infusion represents a substantial financial strengthening for a clinical-stage biotech company developing oral therapies for inflammatory and autoimmune diseases.
The structure of this deal is particularly noteworthy, using pre-funded warrants alongside Series A warrants (exercisable until December 2025) and Series B warrants (exercisable from October 2025 through June 2030). This tiered approach provides Immunic with immediate capital while creating incentives for investors to exercise additional warrants, potentially doubling the total raise.
The quality of participating investors is impressive, with the offering co-led by BVF Partners and Coastlands Capital, alongside participation from established institutional investors including Aberdeen Investments, Adage Capital Partners, and Janus Henderson. This level of institutional backing signals strong confidence in Immunic's clinical pipeline and business strategy.
This financing significantly bolsters Immunic's ability to advance its clinical programs for inflammatory and autoimmune conditions. With these funds allocated to clinical trials and operations, the company has secured a stronger financial foundation to progress its pipeline of oral small molecule therapies through critical development stages without immediate capital constraints.
The Pre-Funded Warrants are immediately exercisable, and may be exercised at any time after their original issuance. The Series A Warrants are immediately exercisable any time after their original issuance until December 31, 2025. The Series B Warrants will be exercisable beginning on October 1, 2025, or earlier if certain thresholds are met, until June 3, 2030. The Series A and B Warrants will immediately expire in proportion to the extent that the corresponding Pre-Funded Warrant offered hereby is exercised on or prior to September 30, 2025, subject to certain exceptions.
The initial proceeds to Immunic from the offering were approximately
The financing was co-led by BVF Partners and Coastlands Capital, and included participation from Aberdeen Investments, Adage Capital Partners LP, Janus Henderson Investors, and other institutional investors.
Leerink Partners acted as the sole bookrunner for the offering. B. Riley Securities and Brookline Capital Markets, a division of Arcadia Securities, LLC, acted as co-managers, and William Blair & Company, L.L.C. served as financial advisor to the Company.
The Company intends to use the net proceeds from the offering to fund its clinical trials and operations and for other general corporate purposes.
This press release shall not constitute an offer to sell or the solicitation of an offer to buy, nor shall there be any sale of, these securities in any state or jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of such state or jurisdiction.
About Immunic, Inc.
Immunic, Inc. (Nasdaq: IMUX) is a biotechnology company developing a clinical pipeline of orally administered, small molecule therapies for chronic inflammatory and autoimmune 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 end of 2026. It has already shown therapeutic activity in phase 2 clinical trials in patients suffering from relapsing-remitting multiple sclerosis and progressive multiple sclerosis. 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). IMU-856, which targets the protein Sirtuin 6 (SIRT6), is intended to restore intestinal barrier function and regenerate bowel epithelium, which could potentially be applicable in numerous gastrointestinal diseases, such as celiac disease as well as inflammatory bowel disease, Graft-versus-Host-Disease and weight management. IMU-381, which currently is in preclinical testing, is a next generation molecule being developed to specifically address the needs of gastrointestinal diseases.
Cautionary Note 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 the receipt of additional proceeds from the offering if the Series A Warrants and Series B Warrants are exercised in full for cash, 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 and anticipated clinical milestones; 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
Contact Information
Immunic, Inc.
Jessica Breu
Vice President Investor Relations and Communications
+49 89 2080 477 09
jessica.breu@imux.com
US IR Contact
Rx Communications Group
Paula Schwartzs
+1 917 633 7790
immunic@rxir.com
US Media Contact
KCSA Strategic Communications
Caitlin Kasunich
+1 212 896 1241
ckasunich@kcsa.com
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SOURCE Immunic, Inc.