MOG-AD
A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER, PHASE 3, PIVOTAL STUDY WITH AN OPEN-LABEL EXTENSION PERIOD TO EVALUATE THE EFFICACY AND SAFETY OF ROZANOLIXIZUMAB IN ADULT PARTICIPANTS WITH MYELIN OLIGODENDROCYTE GLYCOPROTEIN (MOG) ANTIBODY
- Sex at Birth: Any
- Age: Adult (18 - 64), Older Adult (65+)
- Accepting Healthy People: No
- Type: Interventional / Therapeutic
- Trial Phase: Phase III
- Conditions Being Studied: Brain and Nervous System, Myelin-Oligodendrocyte Glycoprotein
Study Purpose
The purpose of MOG001 is to assess how safe, tolerable (acceptable to you) and effective rozanolixizumab (referred to as 'the study drug' hereafter) is in treating MOG-AD. This study will also help us understand how it acts in your body and how your body reacts to it in MOG001.
Locations
UH Cleveland Medical Center
11100 Euclid Avenue
Cleveland OH, 44106
- UH IRB: SITE00001964
- StudyID: 2023-01162
- ClinicalTrials.gov: NCT05063162
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