Immunic Stock Plunges 6.41% to 2025 Low Amid Vidofludimus Trial Uncertainty

Generated by AI AgentMover TrackerReviewed byAInvest News Editorial Team
Tuesday, Nov 4, 2025 1:35 am ET1min read
Aime RobotAime Summary

- Immunic's stock plunged 6.41% to its lowest since July 2025 amid uncertainty over its lead MS candidate vidofludimus calcium.

- The 10.93% four-day decline reflects heightened sensitivity to clinical risks for the dual-mechanism drug targeting a $3-7B market.

- With $55.3M cash through 2026 and no revenue-generating assets, the stock remains vulnerable despite analysts' $4.00 price target.

- Market participants balance the drug's neuroprotection potential against high regulatory hurdles and uncertain trial outcomes expected by late 2026.

The share price fell to its lowest level since July 2025 today, with an intraday decline of 6.41%.

Immunic’s stock has declined 10.93% over four consecutive sessions, extending its slide amid uncertainty around its lead candidate, vidofludimus calcium. The drug, in Phase 3 trials for relapsing-remitting multiple sclerosis, remains central to investor sentiment, though recent volatility reflects heightened sensitivity to clinical and regulatory risks. The compound’s dual mechanism—neuroprotection via Nurr1 activation and anti-inflammatory DHODH inhibition—positions it as a potential blockbuster in the $3–7 billion MS market, but final data from the ENSURE-1 and ENSURE-2 trials, expected by late 2026, will be critical to unlocking value.


The company’s financial runway, with $55.3 million in cash as of June 2025, supports operations through 2026, but the absence of revenue-generating assets leaves the stock vulnerable to cash flow pressures. Analysts maintain a “buy” consensus, citing a $4.00 median price target (80.5% upside from recent levels), though earnings projections—Q3 2025 losses of $0.17 per share—highlight ongoing operational challenges. Competitive differentiation in oral MS therapies, combined with a favorable safety profile, underscores long-term potential, yet near-term risks from trial outcomes and capital-raising needs remain elevated. Market participants are balancing the promise of neuroprotection-driven differentiation against the high bar for regulatory approval and commercial execution.


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