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Completed Phase 2Phase 3 Interventional Results available

N-MOmentum: A Clinical Research Study of Inebilizumab in Neuromyelitis Optica Spectrum Disorders

ClinicalTrials.gov ID: NCT02200770

Public ClinicalTrials.gov record NCT02200770. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 1:33 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Double-masked, Placebo-controlled Study With Open-label Period to Evaluate the Efficacy and Safety of MEDI-551 in Adult Subjects With Neuromyelitis Optica and Neuromyelitis Optica Spectrum Disorders.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To compare the efficacy of inebilizumab (MEDI-551) versus placebo in reducing the risk of an neuromyelitis optica/neuromyelitis optica- spectrum disorders (NMO/NMOSD) attack in participants with NMO/NMOSD.

Study identification

NCT ID
NCT02200770
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
MedImmune LLC
Industry
Enrollment
231 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 1, 2015 (Actual)
Primary completion
Oct 26, 2018 (Actual)
Completion
Nov 6, 2020 (Actual)
Last update posted
Dec 3, 2021

2015 – 2020

United States locations

U.S. sites
19
U.S. states
15
U.S. cities
19
Facility City State ZIP Site status
Research Site Birmingham Alabama 35294 —
Research Site Sacramento California 95817 —
Research Site San Francisco California 94158 —
Research Site Aurora Colorado 80010 —
Research Site New Haven Connecticut 06511 —
Research Site Maitland Florida 32751 —
Research Site Chicago Illinois 60637 —
Research Site Kansas City Kansas 66160 —
Research Site Baltimore Maryland 21287 —
Research Site Detroit Michigan 48201 —
Research Site Rochester Minnesota 55905 —
Research Site St Louis Missouri 63131-2374 —
Research Site Raleigh North Carolina 27607 —
Research Site Cincinnati Ohio 45219 —
Research Site Cleveland Ohio 44195 —
Research Site Mansfield Ohio 44906 —
Research Site Dallas Texas 75390 —
Research Site Houston Texas 77030 —
Research Site Richmond Virginia 23298 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 79 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02200770, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 3, 2021 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02200770 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →