Study of Tysabri in Early Relapsing Remitting Multiple Sclerosis Participants
NCT04832399 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 60
Last updated 2024-02-05
Summary
The purpose of this study is to evaluate the impact of an early treatment with Natalizumab on the management of the progressive nature of Relapsing Remitting Multiple Sclerosis (RRMS).
Conditions
- Relapsing Remitting Multiple Sclerosis
Interventions
- DRUG
-
Natalizumab
As described in the treatment arm.
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Medical Director · Biogen
Eligibility
- Min Age
- 18 Years
- Max Age
- 55 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-11-12
- Primary Completion
- 2023-10-02
- Completion
- 2023-10-02
- FDA Drug
- Yes
Countries
- Portugal
Study Locations
More Related Trials
-
Tysabri Effects on Cognition and Neurodegeneration in Multiple Sclerosis
NCT01071512 ·Status: COMPLETED ·Phase: NA
-
Tysabri Observational Cohort Study - Multiple Sclerosis (MS) Registries
NCT03399981 ·Status: COMPLETED
-
The Effects of Tysabri Treatment on Vaccination Response and Lymphocyte Subsets in Subjects With Relapsing Forms of Multiple Sclerosis
NCT00536120 ·Status: COMPLETED ·Phase: PHASE4
-
Natalizumab (BG00002, Tysabri) Study in Japanese Participants With Relapsing-Remitting Multiple Sclerosis (RRMS)
NCT01440101 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Cognitive Evolution in Tysabri Treated Multiple Sclerosis Patients
NCT01658384 ·Status: COMPLETED
-
Ireland Natalizumab (TYSABRI) Observational Program
NCT01943526 ·Status: COMPLETED
-
Evaluation of Early Changes Visible to the Diffusion MRI in Response to Two Years of Treatment With Tysabri in Patients With Multiple Sclerosis
NCT02904876 ·Status: TERMINATED ·Phase: PHASE4
-
Evaluation of Natalizumab for thE Relief of MS Associated FatiGue
NCT00464074 ·Status: COMPLETED
-
A Prospective, Open-label, Non-randomized, Clinical Trial to Determine if Natalizumab (Tysabri®) Improves Ambulatory Measures in Relapsing-remitting Multiple Sclerosis (RRMS) Patients
NCT00871780 ·Status: COMPLETED ·Phase: PHASE4
-
Validation of a Laboratory Test Measuring Natalizumab (Tysabri®) Serum Levels in MS
NCT02965170 ·Status: COMPLETED
-
Safety and Efficacy of Natalizumab (BG00002, Tysabri®) in Russian Participants With Relapsing Remitting Multiple Sclerosis (RRMS)
NCT02142205 ·Status: COMPLETED ·Phase: PHASE4
-
The Effect of Natalizumab (Tysabri) on Sexual Dysfunction in Multiple Sclerosis
NCT01455220 ·Status: COMPLETED ·Phase: NA
-
Efficacy and Safety of the Biosimilar Natalizumab PB006 in Comparison to Tysabri®
NCT04115488 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Investigate the Radiological Onset of Action After Treatment Initiation With Subcutaneous (SC) Natalizumab in Participants With Relapsing-Remitting Multiple Sclerosis (RRMS)
NCT05532163 ·Status: TERMINATED ·Phase: PHASE4
-
Canadian Multicenter Observational Study of Tysabri in Early Relapsing Remitting Multiple Sclerosis Participants
NCT01706107 ·Status: TERMINATED
-
COMparison Between All immunoTherapies for Multiple Sclerosis.
NCT03193866 ·Status: COMPLETED
-
Comparing the Safety and Benefit of Natalizumab (Tysabri®) At-home Infusion vs At-hospital Infusion in Multiple Sclerosis
NCT04777539 ·Status: COMPLETED
-
Cognitive Evolution in Tysabri Treated Multiple Sclerosis Patients - A Three Year Extension
NCT02383550 ·Status: COMPLETED
-
Real World Effectiveness of Natalizumab Extended Interval Dosing in a French Cohort
NCT04580381 ·Status: COMPLETED
-
Study Evaluating Rebif, Copaxone, and Tysabri for Active Multiple Sclerosis
NCT01058005 ·Status: TERMINATED ·Phase: PHASE3
-
A Longitudinal Study of Brain Atrophy in MS Patients Over 5 Years
NCT01847287 ·Status: COMPLETED
-
TYGRIS - ROW: TYSABRI Global Observational Program in Safety - Rest of World
NCT00483847 ·Status: COMPLETED
-
Exploratory Study of the Safety, Tolerability and Efficacy of Multiple Regimens of Natalizumab in Adult Participants With Relapsing Multiple Sclerosis (MS)
NCT01405820 ·Status: COMPLETED ·Phase: PHASE2
-
Natalizumab Re-Initiation of Dosing
NCT00306592 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Efficacy in Pediatric MS Patients Prescribed Tysabri
NCT02137109 ·Status: COMPLETED