BAY86-5046 (Betaseron), Non Interventional Studies

NCT02121444 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 151

Last updated 2017-10-18

No results posted yet for this study

Summary

This study aims to investigate adherence to therapy among patients treated with Betaferon who are using the BETACONNECT autoinjector.

Conditions

Interventions

DRUG

Interferon beta-1b (Betaferon, BAY 86-5046)

DEVICE

BETACONNECT auto-injector.

Sponsors & Collaborators

Principal Investigators

  • Bayer Study Director · Bayer

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-06-23
Primary Completion
2016-03-09
Completion
2016-06-01

Countries

  • Germany

More Related Trials

Entities

Companies

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 NCT02121444 on ClinicalTrials.gov