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ACTIVE NOT RECRUITING Phase 3

A Study to Evaluate the Efficacy and Safety of Rozanolixizumab in Adult Participants With Myelin Oligodendrocyte Glycoprotein (MOG) Antibody-associated Disease (MOG-AD)

NCT05063162 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of the study is to evalute the efficacy, safety and tolerability of rozanolixizumab for treatment of adult participants with myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOG-AD).

Interventions

  • OTHER Placebo
  • DRUG Rozanolixizumab

Study Locations (20)

Other

  • Mog001 30022 — Melbourne
  • Mog001 40123 — Anderlecht
  • Mog001 40756 — Bruxelles/brussel
  • Mog001 40122 — Edegem
  • Mog001 40185 — Ghent
  • Mog001 60033 — Porto Alegre

Texas

  • Mog001 50304 — Dallas
  • Mog001 50568 — San Antonio

Arizona

  • Mog001 50297 — Scottsdale

California

  • Mog001 50450 — Palo Alto

Colorado

  • Mog001 50101 — Aurora

District of Columbia

  • Mog001 50553 — Washington D.C.

Florida

  • Mog001 50308 — Tampa

Illinois

  • Mog001 50472 — Peoria

Trial Details

FieldValue
Enrollment Target 104 participants
Start Date 2022-02-02
Est. Completion 2027-07-01
Phase Phase 3

Sponsor

UCB Biopharma SRL

116 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05063162

The ClinicalTrials.gov registry entry for NCT05063162 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 104 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is UCB Biopharma SRL, which has 116 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Myelin Oligodendrocyte Glycoprotein Antibody-associated Disease (MOG-AD) appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05063162 reports 20 study locations spanning 14 distinct geographic areas — top geographies include Other, Texas, Arizona. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05063162 about?

NCT05063162 is a clinical study titled "A Study to Evaluate the Efficacy and Safety of Rozanolixizumab in Adult Participants With Myelin Oligodendrocyte Glycoprotein (MOG) Antibody-associated Disease (MOG-AD)". The purpose of the study is to evalute the efficacy, safety and tolerability of rozanolixizumab for treatment of adult participants with myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOG-AD).

What is the current status of trial NCT05063162?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 104 participants. The study started on 2022-02-02. Estimated completion is 2027-07-01.

What conditions does trial NCT05063162 study?

This clinical trial studies the following conditions: Myelin Oligodendrocyte Glycoprotein Antibody-associated Disease (MOG-AD). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05063162?

The interventions under investigation include: Placebo (OTHER), Rozanolixizumab (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05063162?

This trial is sponsored by UCB Biopharma SRL, which has 116 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05063162 being conducted?

This trial has 20 study locations across Arizona, California, Colorado, District of Columbia, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial