Status:

ACTIVE_NOT_RECRUITING

A Study of Ocrelizumab in Children and Adolescents With Relapsing-Remitting Multiple Sclerosis

Lead Sponsor:

Hoffmann-La Roche

Conditions:

Multiple Sclerosis

Eligibility:

All Genders

10-18 years

Phase:

PHASE2

Brief Summary

This 2-year study will evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamic (PD) effects of ocrelizumab in children and adolescents ages ≥ 10 to ≤ 18 years with relapsing-remitting...

Eligibility Criteria

Inclusion

  • Body weight \>/= 25 kg
  • Children and adolescents must have received all childhood required vaccinations
  • Female participants of childbearing potential must agree to either remain completely abstinent or to use reliable means of contraception
  • Diagnosis of relapsing-remitting multiple sclerosis (RRMS)
  • Expanded Disability Status Scale (EDSS) at screening: 0-5.5, inclusive
  • Neurologic stability for \>/= 30 days prior to screening, and between screening and baseline
  • Participants naive to prior disease-modifying therapy (DMT)
  • Participants who have had at least 6 contiguous months of DMT within the past 1 year must have evidence of disease activity occurring after the full 6-month course of treatment, that is, at least one relapse or \>/= 1 Gd-enhancing lesion(s) on a T1-weighted brain MRI

Exclusion

  • Known presence or suspicion of other neurologic disorders that may mimic MS, including, but not limited to, acute disseminated encephalomyelitis, neuromyelitis optica or neuromyelitis optica spectrum disorders and any neurologic, somatic, or metabolic condition that could interfere with brain function or normal cognitive or neurological development
  • Patients that are aquaporin 4 positive and myelin oligodendrocyte glycoprotein (MOG) antibody positive are not eligible to participate in the study.
  • In case of an ADEM-like appearance of the first MS attack, a second attack with clear MS-like features is required.
  • Infection requiring hospitalization or treatment with IV anti-infective agents
  • History or known presence of recurrent or chronic infection (e.g., HIV, syphilis, tuberculosis)
  • Receipt of a live or live-attenuated vaccine within 6 weeks prior to treatment allocation
  • History or laboratory evidence of coagulation disorders
  • Peripheral venous access that precludes IV administration and venous blood sampling
  • Inability to complete a magnetic resonance imaging (MRI) scan
  • History of cancer, including solid tumors, hematologic malignancies, and carcinoma in situ
  • History of a severe allergic or anaphylactic reaction to humanized or murine monoclonal antibody (mAbs) or known hypersensitivity to any component of ocrelizumab solution
  • Previous treatment with B-cell-targeted therapies
  • Percentage of CD4 \< 30%
  • Absolute Neutrophil Count \< 1.5x1000/microliter
  • Lymphocyte count below the lower limit of normal (LLN) for age- and sex-specific reference range

Key Trial Info

Start Date :

January 9 2020

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 1 2029

Estimated Enrollment :

23 Patients enrolled

Trial Details

Trial ID

NCT04075266

Start Date

January 9 2020

End Date

December 1 2029

Last Update

December 23 2025

Active Locations (12)

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Page 1 of 3 (12 locations)

1

University of Colorado Denver Childrens Hospital Rocky Mountain MS Center

Aurora, Colorado, United States, 80045

2

Childrens National Health Center

Washington D.C., District of Columbia, United States, 20010

3

Boston Childrens Hospital

Boston, Massachusetts, United States, 02115

4

Washington Universtiy school of Medicine

St Louis, Missouri, United States, 63110