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Clinical Trials/NCT06159712
NCT06159712
Recruiting
Not Applicable

Comparative Study of High-Efficacy Disease Modifying Treatment of Relapsing Multiple Sclerosis

University of Aarhus1 site in 1 country200 target enrollmentNovember 27, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Relapsing Remitting Multiple Sclerosis
Sponsor
University of Aarhus
Enrollment
200
Locations
1
Primary Endpoint
Changes in B cell populations
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The goal of this prospective, multi-center, non-blinded, non-randomized, non-intervention clinical trial is to compare immunologic, virologic and epigenetic factors in patients with active multiple sclerosis in standard 2.line treatment with ocrelizumab, rituximab, ofatumumab or natalizumab in Region Midt, Denmark. It aims to answer how the immunologic, virologic and epigenetic response in these patients are compared to healthy controls, and analyze their treatment effect in relation to this response. Participants will get an extra blood sample, when they have their routine blood samples taken.

Detailed Description

The CoSHED RMS study will include patients with active multiple sclerosis aged 18-65 years fulfilling the criteria for 2. line treatment and starting treatment with one of the four high-efficacy disease modifying treatments ocrelizumab, rituximab, ofatumumab or natalizumab. Researchers will compare immunologic, virologic and epigenetic parameters in the four treatment groups to a age and gender matched healthy control group. The study duration is 12 months, and patients can continue in an extension phase for additional 12 month. The primary endpoint is changes in B cell populations between the four treatments within 12 months. The study will evaluate a number of efficacy and safety endpoints using clinical, MRI, routine blood samples and research biomarkers.

Registry
clinicaltrials.gov
Start Date
November 27, 2023
End Date
November 2025
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Multiple sclerosis diagnosis and definition of disease course according to the 2017 McDonald criteria
  • Expanded disability status scale (EDSS) ≤6.5
  • Signed written informed consent
  • Fulfilling criteria for active MS: Treatment naïve relapsing remitting multiple sclerosis (RRMS) patients (never treated, or no DMT the previous 2 years):
  • 2 relapse previous 12 months OR
  • 1 relapse previous 12 months with severe residual symptoms and EDSS ≥ 3.0 OR
  • 1 relapse previous 12 months AND ≥9 T2 lesions on brain and/or spinal cord MRI AND
  • contrast-enhancing lesion or ≥1 new or enlarging T2 lesion on brain and/or spinal cord MRI previous 12 month
  • Previously treated RRMS patients:
  • 1 relapse previous 12 months OR

Exclusion Criteria

  • Pregnancy or breast feeding
  • Lack of effective contraception for women of child-bearing potential (effective contraception include oral contraception, intrauterine devices and other forms of contraception with failure rate \<1%)
  • Receipt of a live or live-attenuated vaccine within 6 weeks prior to randomization
  • Known active malignant disease
  • Severe heart failure (New York Heart Association Class IV) or severe, uncontrolled cardiac disease
  • Positive test for HIV, hepatitis B or C, or tuberculosis
  • Negative test for varicella zoster
  • Lymphopenia grade 2 (0.5 to 0.8 × 10\^9/L) or higher grades of lymphopenia (in case of switching from fingolimod lymphopenia grade 2 can be accepted if lymphocytes are rising markedly compared to on treatment levels)
  • Neutropenia grade 2 (1.0 to 1.5 × 10\^9/L) or higher grades
  • Thrombocytopenia grade 2 (50 to 75 × 10\^9/L) or higher grades

Outcomes

Primary Outcomes

Changes in B cell populations

Time Frame: 1 year

Changes in B cell populations in the four treatment groups

Study Sites (1)

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