Safety and Efficacy in Pediatric MS Patients Prescribed Tysabri

NCT02137109 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 400

Last updated 2015-10-20

No results posted yet for this study

Summary

The primary objective of the study is to evaluate the safety of natalizumab use in the pediatric multiple sclerosis (MS) population.

Conditions

Interventions

DRUG

natalizumab

Administered as specified in the treatment arm.

Sponsors & Collaborators

Principal Investigators

  • Medical Director · Biogen

Eligibility

Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-03-31
Primary Completion
2015-10-31
Completion
2015-10-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02137109 on ClinicalTrials.gov