Multiple Sclerosis Clinical Trial

Impact of the BETACONNECT Auto-injector on BETASERON Therapy Adherence and Patient Satisfaction

Summary

The primary objective of this study is to assess adherence and persistence to BETASERON therapy in patients who are using the BETACONNECT auto-injector device (BETACONNECT device).

The secondary objective of this study is to assess patient-reported satisfaction with the BETACONNECT device.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Male and females greater than or equal to 18 years of age
Diagnosis of RRMS according to revised McDonald Criteria (2010) or (CIS)
Prescribed BETASERON (note: decision to treat with BETASERON must be made independent of participation in this study)
Confirmation of insurance coverage for BETASERON treatment
Access to a personal computer to complete online patient satisfaction survey at Week 6

Exclusion Criteria:

Currently enrolled in a clinical trial or other observational study for Multiple Sclerosis treatment
Documented substance abuse within the previous 6 months prior to study enrollment
Any major laboratory value abnormality that the investigator believes would preclude the patient from participating in the study
Any medical disorder, condition or history that in the opinion of the investigator would impair the patient's ability to participate in or complete the study
Pregnant or nursing

Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

146

Study ID:

NCT02652091

Recruitment Status:

Completed

Sponsor:

Bayer

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There are 21 Locations for this study

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Cullman Alabama, 35058, United States

Boca Raton Florida, 33428, United States

New Port Richey Florida, 34653, United States

Tampa Florida, 33609, United States

Atlanta Georgia, 30309, United States

Fulton Maryland, 20759, United States

Foxboro Massachusetts, 02035, United States

Deckerville Michigan, 48427, United States

Saint Louis Missouri, 63131, United States

Stratford New Jersey, 08084, United States

Teaneck New Jersey, 07666, United States

Staten Island New York, 10306, United States

Medford Oregon, 97504, United States

Medford Oregon, , United States

Bala-Cynwyd Pennsylvania, 19004, United States

Lititz Pennsylvania, 17543, United States

Franklin Tennessee, 37064, United States

Memphis Tennessee, 38104, United States

Nashville Tennessee, 37212, United States

Lubbock Texas, 79430, United States

Round Rock Texas, 78681, United States

Fairfax Virginia, 22031, United States

Virginia Beach Virginia, , United States

How clear is this clinincal trial information?

Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

146

Study ID:

NCT02652091

Recruitment Status:

Completed

Sponsor:


Bayer

How clear is this clinincal trial information?

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