Immunic targets MS market with Phase 3 data - ICYMI

Core Insights - Immunic Inc's CEO highlighted significant milestones in 2025, particularly the phase 2 CALLIPER study, which showed a 31% reduction in confirmed disability worsening in progressive multiple sclerosis (MS) patients and a 34% reduction in those without baseline gadolinium lesions, indicating a potential neuroprotective effect of vidofludimus calcium [1][5] Clinical Developments - The CALLIPER study results suggest that vidofludimus calcium can address both inflammatory and non-inflammatory processes driving disability progression in MS, benefiting patients with relapsing forms of the disease [6] - Long-term data from the EMPhASIS study indicated that 92.3% of relapsing-remitting MS patients remained free of 12-week confirmed disability worsening after 144 weeks, with only 13.8% of events being independent of relapses, supporting the drug's efficacy [2][7] Patent and Strategic Positioning - Immunic has strengthened its patent position for vidofludimus calcium, potentially securing exclusivity until 2041 in key markets, which provides a significant competitive advantage [3][8] - Early findings on IMU-856 in celiac disease showed increases in natural GLP-1 levels, suggesting potential applications in gut health and weight management [3][8] Future Outlook - Enrollment in the phase 3 ENSURE trials is complete, with top-line data expected by the end of 2026, which is crucial for FDA submission and potential market launch [9][10] - The company is preparing for a New Drug Application (NDA) submission and aims for a commercial launch in 2028, contingent on FDA approval [11]