Primary-outcome results across pivotal trials
Per-arm reported values from Phase 2/3 and Phase 3 trials with results posted to ClinicalTrials.gov.
| Trial | Indication | Primary endpoint | Arm | Value |
|---|---|---|---|---|
| NCT02200770 | Neuromyelitis Optica | Time to Adjudication Committee (AC)-Determined Neuromyelitis Optica Spectrum Disorder (NMOSD) Attack During RCP Day 1 (Baseline) through Day 197 | Inebilizumab/Inebilizumab | NA Days |
| Placebo/Inebilizumab | NA Days | |||
| NCT04524273 MINT | Myasthenia Gravis | Change From Baseline at Week 26 in Myasthenia Gravis Activities of Daily Living (MG-ADL) Score in the Overall Study Population Baseline and Week 26 | Overall: Inebilizumab 300 mg | -4.2 Score on a scale |
| Overall: Placebo | -2.2 Score on a scale | |||
| NCT04540497 | Immunoglobulin G4-Related Disease | RCP: Time to Disease Flare Up to Week 52 | Inebilizumab 300 mg | NA Days |
| Placebo | 246.0 Days |