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A Study to Assess the Safety and Efficacy of Elezanumab When Added to Standard of Care in Progressive Forms of Multiple Sclerosis

Phase 2
Completed
Conditions
Multiple Sclerosis (MS)
Interventions
Drug: placebo
Drug: elezanumab
Registration Number
NCT03737812
Lead Sponsor
AbbVie
Brief Summary

The purpose of this study is to evaluate the safety and efficacy of elezanumab in participants with progressive Multiple Sclerosis (PMS).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
123
Inclusion Criteria
  • Diagnosis of primary-progressive multiple sclerosis (PPMS) or non-relapsing secondary-progressive multiple sclerosis (SPMS) and no relapses for at least 24 months.
  • Evidence of physical disability according to Expanded Disability Status Scale (EDSS) or Timed 25-Foot Walk (T25FW) or 9-Hole Peg Test.
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Exclusion Criteria
  • Treatment with any of the following within the 6 months prior to Screening: natalizumab; cyclosporine; azathioprine; methotrexate; mycophenolate mofetil; intravenous immunoglobulin (IVIg); any interferon product; and intravenous (IV), oral, or intrathecal corticosteroids for the purposes of disease modification.
  • Treatment with the following within 1 year prior to Screening: cyclophosphamide or alemtuzumab.
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PlaceboplaceboParticipants randomized to receive placebo by intravenous infusion.
Elezanumab 400mg DoseelezanumabParticipants randomized to receive 400mg of elezanumab by intravenous infusion.
Elezanumab 1800 mg DoseelezanumabParticipants randomized to receive 1800mg of elezanumab by intravenous infusion.
Primary Outcome Measures
NameTimeMethod
Mean Overall Response Score (ORS)Week 52

The ORS is a composite score derived from 4 components: Expanded Disability Status Scale (EDSS), Timed 25-Foot Walk (T25FW), 9-Hole Peg Test in the dominant hand (9HPT-D), and 9HPT in the non-dominant hand (9HPT-ND).

Clinically significant worsening = -1, no change = 0, clinically significant improvement = +1.

The ORS is the sum of these scores for the EDSS: Timed 25-Foot Walk, 9-Hole Peg Test-dominant, and 9-Hole Peg Test-nondominant and ranges from -4 to + 4.

Secondary Outcome Measures
NameTimeMethod
Disability Improvement Response RateWeek 52

Disability improvement response rate is assessed based on the Expanded Disability Status Scale Plus (EDSS+). EDSS+ is comprised of Expanded Disability Status Scale (EDSS), Timed 25-Foot Walk (T25FW) and 9-Hole Peg Tests (9HPT).

Overall Response Score (ORS)Week 36

The ORS is a composite score derived from 4 components: Expanded Disability Status Scale (EDSS), Timed 25-Foot Walk (T25FW), 9-Hole Peg Test in the dominant hand (9HPT-D), and 9HPT in the non-dominant hand (9HPT-ND).

Clinically significant worsening = -1, no change = 0, clinically significant improvement = +1.

The ORS is the sum of these scores for the EDSS, Timed 25-Foot Walk, 9-Hole Peg Test-dominant and 9-Hole Peg Test-non-dominant and ranges from -4 to + 4.

Trial Locations

Locations (37)

Central Texas Neurology Consul /ID# 203108

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Round Rock, Texas, United States

Montreal Neurological Institut /ID# 203868

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Montreal, Quebec, Canada

Centre Hospitalier de l'Universite de Montreal - CRCHUM /ID# 203869

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Montreal, Quebec, Canada

West Virginia Univ School Med /ID# 202849

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Morgantown, West Virginia, United States

KCA Neurology - Franklin /ID# 202912

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Franklin, Tennessee, United States

Michigan Institute for Neurological Disorders (MIND) /ID# 202470

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Farmington Hills, Michigan, United States

UCSF School of Medicine - Neurology /ID# 203194

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San Francisco, California, United States

Advanced Neurosciences Institute /ID# 204555

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Franklin, Tennessee, United States

Washington University-School of Medicine /ID# 202899

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Saint Louis, Missouri, United States

International Neurorehabilitation Institute /ID# 213333

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Lutherville, Maryland, United States

Memorial Neurological Institute and Center for Multiple Sclerosis /ID# 206327

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Owosso, Michigan, United States

The MS Center for Innovations in Care at Missouri Baptist Medical Center /ID# 205432

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Saint Louis, Missouri, United States

Cleveland Clinic Lou Ruvo Cent /ID# 204744

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Las Vegas, Nevada, United States

Ridgeview Specialty Clinic Chaska - Neurology /ID# 204384

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Chaska, Minnesota, United States

Ottawa Hospital Research Institute /ID# 203058

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Ottawa, Ontario, Canada

Vladimir Royter MD /ID# 202483

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Hanford, California, United States

Duplicate_Parexel International /ID# 202747

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Baltimore, Maryland, United States

Advanced Neurosciences Research, LLC /ID# 203072

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Fort Collins, Colorado, United States

Rowe Neurology Institute /ID# 202744

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Lenexa, Kansas, United States

Integrated Neurology Services /ID# 202743

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Alexandria, Virginia, United States

Recherche Sepmus Inc. /ID# 212852

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Greenfield Park, Quebec, Canada

Duplicate_London Health Sciences Centre - University Hospital /ID# 203538

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London, Ontario, Canada

Stanford MS Center /ID# 202445

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Palo Alto, California, United States

Sutter East Bay Medical Foundation-Jordon Research and Education Dev. Inst. /ID# 202448

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Berkeley, California, United States

The Research Center of Southern California /ID# 202802

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Carlsbad, California, United States

Neurology Consultants of Dallas - LBJ Fwy /ID# 203102

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Dallas, Texas, United States

Virginia Mason Medical Center /ID# 205439

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Seattle, Washington, United States

Swedish MS Center /ID# 202904

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Seattle, Washington, United States

University of British Columbia - MS & NMO Clinical Trials Group, Djavad Mowafagh /ID# 203536

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Vancouver, British Columbia, Canada

Unity Health Toronto - St. Michael's Hospital /ID# 206213

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Toronto, Ontario, Canada

St. Josephs Hospital and Med Center /ID# 202809

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Phoenix, Arizona, United States

UC Davis Health-Neurological Surgery /ID# 202485

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Sacramento, California, United States

Providence Neurological Specialties - West /ID# 203193

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Portland, Oregon, United States

Froedtert Memorial Lutheran Hospital /ID# 202618

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Milwaukee, Wisconsin, United States

University of Colorado School of Medicine, Dept of Neurology /ID# 202807

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Aurora, Colorado, United States

Oklahoma Med Res. Foundation /ID# 203442

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Oklahoma City, Oklahoma, United States

Evergreen Neuroscience Institute /ID# 204205

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Kirkland, Washington, United States

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