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Clinical Trials/NCT04580381
NCT04580381
Completed
Not Applicable

Real World Effectiveness of Natalizumab Extended Interval Dosing in Relapsing-Remitting Multiple Sclerosis in a French Cohort

University Hospital, Caen5 sites in 1 country500 target enrollmentSeptember 1, 2020

Overview

Phase
Not Applicable
Intervention
Natalizumab Injection [Tysabri]
Conditions
Multiple Sclerosis, Relapsing-Remitting
Sponsor
University Hospital, Caen
Enrollment
500
Locations
5
Primary Endpoint
Annualized Relapse Ratio
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Natalizumab (NTZ) use in Multiple Sclerosis (MS) in highly active patients has been largely established during the last Rationale 10 years in both clinical trials and real-world practice. Along with its efficacy, NTZ use has been limited by potential risk of progressive multifocal leukoencephalopathy (PML). Thus, several studies have tried to assess how to minimize this risk.

One suggested approach is to move from the standard interval dose (SID) of 4 weeks to an extended interval dose (EID) of 5 weeks or longer. Extending the dosing interval of NTZ has been practiced by some physicians with the intention of improving the benefit/risk of the treatment by reducing the exposure-dependent risk of progressive multifocal leukoencephalopathy (PML) while maintaining efficacy. We propose to retrospectively analyze data from clinical records coming from RRMS patients treated in France at 5 different centers; Caen, Nice, Bobigny and Toulouse hospitals as well as Percy Military Hospital, to evaluate the effectiveness of natalizumab EID in subjects who have previously been treated with natalizumab SID for 12 months, in relation to continued SID treatment. In the clinical practice of these centers, patients are shifted after minimum 12 months under SID to an EID of 6 weeks regardless antibody JC serum status. Clinical, magnetic resonance imaging (MRI) and serum anti-JCV antibody status data are collected when available.

The objective of this study is to assess the efficacy in term of ARR and safety.

Registry
clinicaltrials.gov
Start Date
September 1, 2020
End Date
October 30, 2021
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients receiving at least 11 infusions of natalizumab as disease-modifying monotherapy for RRMS that is consistent with the approved dosing

Exclusion Criteria

  • Patients for whom the NTZ infusion history and/or MRI and clinical history is not available.
  • Patients with dosing gap defined as \>=12 weeks between any two doses.
  • Patients with over dose defined as \<3 weeks between any two doses.
  • Pregnancy during the follow-up period

Arms & Interventions

Standard Interval Dosing (SID)

Patients continuing Natalizumab treatment with standard interval dosing defined as \> 11 infusions per year

Intervention: Natalizumab Injection [Tysabri]

Extended Interval Dosing (EID)

Patients switching to extended interval dosing defined as ≤ 10 infusions per year

Intervention: Natalizumab Injection [Tysabri]

Outcomes

Primary Outcomes

Annualized Relapse Ratio

Time Frame: baseline to 12 month follow-up

relapse rate per patient per year

Secondary Outcomes

  • Radiological activity(baseline to 12 month follow-up)
  • NEDA-3 achievement(baseline to 12 month follow-up)
  • Disability progression(baseline to 12 month follow-up)

Study Sites (5)

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