Stock Markets February 13, 2026

Immunic Gains After $400M Private Placement; Eyes Phase 3 Readouts and Commercial Transition

Oversubscribed financing led by BVF Partners supplies initial $200M and optional $200M to back MS programs and organizational shift

By Caleb Monroe IMUX
Immunic Gains After $400M Private Placement; Eyes Phase 3 Readouts and Commercial Transition
IMUX

Immunic, Inc. (NASDAQ:IMUX) jumped 20% in early trading after revealing an oversubscribed private placement that could bring up to $400 million to finance late-stage trials of vidofludimus calcium and to support the company's shift toward becoming a commercial entity. The financing provides $200 million upfront with a potential additional $200 million, is led by BVF Partners L.P., and includes participation from several institutional investors. Immunic also announced board and executive leadership changes as it prepares for regulatory filings and potential product launch preparations.

Key Points

  • Immunic announced an oversubscribed private placement that could raise up to $400 million, with $200 million in upfront proceeds and a potential additional $200 million.
  • Financing is led by BVF Partners L.P. and includes Aberdeen Investments, Avidity Partners, OrbiMed, and RA Capital Management; Leerink Partners served as lead placement agent.
  • Funds will support completion of phase 3 ENSURE trials for vidofludimus calcium in relapsing multiple sclerosis, initiation of a phase 3 program in primary progressive multiple sclerosis later this year, and preparations for potential commercial launch and NDA submission in mid-2027.

Immunic, Inc. (NASDAQ:IMUX) saw its shares climb about 20% on Friday morning following the announcement of an oversubscribed private placement that could raise as much as $400 million. The late-stage biotechnology firm said the funds are intended to underwrite its multiple sclerosis drug development programs and to help transition the company into a commercial organization.

The financing is being led by existing investor BVF Partners L.P., and includes commitments from institutional investors Aberdeen Investments, Avidity Partners, OrbiMed, and RA Capital Management. The arrangement provides for $200 million in initial proceeds, with the possibility of an additional $200 million under the terms of the deal.

Immunic specified that the capital will support completion of its ongoing phase 3 ENSURE trials for vidofludimus calcium in relapsing multiple sclerosis. The company reiterated its expectation that top-line data from those trials will be available by the end of 2026. The financing is also intended to enable the company to initiate a phase 3 clinical program in primary progressive multiple sclerosis later this year.

The announcement included changes to the company's leadership. Simona Skerjanec, who previously served as SVP and Global Head of Neuroscience and Rare Diseases at Roche, has been elevated to interim Chairperson of the Board of Directors. Immunic said it will begin a search for a new chief executive officer with commercial experience as current CEO and co-founder Dr. Daniel Vitt prepares to transition into a new senior executive role.

"I could not be prouder of the Immunic team and what we have achieved with vidofludimus calcium," commented Dr. Vitt. "The proceeds from the initial closing are expected to provide sufficient runway through submission of an NDA in the United States in mid-2027 and to start preparations for the potential launch of vidofludimus calcium in RMS."

Immunic said it expects to close the private placement around February 17, 2026, subject to customary closing conditions. Leerink Partners acted as lead placement agent for the financing.


This development affects several segments of the market, including biotechnology companies engaged in neurologic and rare disease drug development, investors focused on late-stage therapeutics, and capital markets that facilitate private placements and crossover financing for companies moving toward commercialization.

Risks

  • Closing of the private placement is subject to customary closing conditions, and the expected funding is not guaranteed until the transaction is closed - this impacts capital markets and investor confidence.
  • Top-line phase 3 ENSURE trial data are not expected until the end of 2026, creating timing uncertainty for regulatory milestones and potential commercialization plans - this affects biotech investors and drug development stakeholders.
  • Leadership transitions, including the search for a new CEO and interim board chair appointment, introduce execution and organizational risk during a critical development and commercialization phase - this impacts corporate governance and strategic execution.

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