Novartis Q4 Results

↓ ↑ Content Click below to navigate through the document MayzentⓇ - S1P1,5 receptor modulator Company overview Financial review Conclusions NCT04926818 NEOS (CBAF312D2301) Multiple sclerosis, pediatrics Phase 3 Indication Phase Patients 180 Annualized relapse rate (ARR) in target pediatric participants Appendix Innovation: Pipeline overview Financial performance Innovation: Clinical trials Cardiovascular, Renal and Metabolic Immunology > Neuroscience Oncology Other Global Health Abbreviations Primary Outcome Measures Arms Intervention Target Patients References Arm 1: Experimental ofatumumab - 20 mg injection/ placebo Arm 2: Experimental siponimod - 0.5 mg, 1 mg or 2 mg/ placebo Arm 3: Active Comparator fingolimod - 0.5 mg or 0.25 mg/ placebo Children/adolescent patients aged 10-17 years old with Multiple Sclerosis (MS). The targeted enrollment is 180 participants with multiple sclerosis which will include at least 5 participants with body weight (BW) ≤40 kg and at least 5 participants with age 10 to 12 years in each of the ofatumumab and siponimod arms. There is a minimum 6 month follow up period for all participants (core and extension). Total duration of the study could be up to 7 years. 2026 Readout Milestone(s) Publication TBD □ NOVARTIS Reimagining Medicine Novartis Q4 Results | January 31, 2024 66

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