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Participants Preferences to Disease Modifying Agents in Relapsing Remitting Multiple Sclerosis Condition

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Roche

Status

Completed

Conditions

Multiple Sclerosis, Relapsing-Remitting

Study type

Observational

Funder types

Industry

Identifiers

NCT02598167
ML29715

Details and patient eligibility

About

This multi-center non-interventional, observational, cross-sectional study in adult participants with relapsing remitting multiple sclerosis (RRMS) will evaluate the participants' preferences for disease modifying treatments (DMT) in routine clinical practice.

Enrollment

223 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participants aged greater than or equal to (>/=) 18 years
  • Participants who have a diagnosis of RRMS as documented in their medical records
  • Participants who have been prescribed a DMT for at least 3 months
  • Participants who have an expanded disability status scale (EDSS) score of 1-6 points

Exclusion criteria

  • Participants with any personal or medical condition that in opinion of the investigator would interfere with or make impossible proper participation in the study

Trial design

223 participants in 1 patient group

RRMS Population
Description:
Participants with a diagnosis of RRMS and being prescribed with a DMT for a period of at least 3 months according to standard local clinical practice will be included.

Trial contacts and locations

18

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Data sourced from clinicaltrials.gov

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