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COMPliance With Avonex® PS in Patients With Relapsing-Remitting MS

COMPliance With Avonex® PS in Patients With Relapsing-Remitting MS

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00675883
Acronym
COMPASS
Enrollment
1000
Registered
2008-05-12
Start date
2008-05-31
Completion date
2011-12-31
Last updated
2012-01-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Sclerosis, Relapsing-Remitting

Brief summary

A phase IV, observational, survey-based study to measure compliance with Avonex® PS therapy in patients with Relapsing-Remitting Multiple Sclerosis, and to compare persistence on therapy 22 months after initial prescription of AVONEX® PS between patients enrolled in the current MS AllianceTM program versus patients enrolled in this program prior to October 2007.

Detailed description

Study Design Five hundred patients will be enrolled in the prospective portion of the study, all of whom will receive AVONEX. Patients will join the study by signing the attached Informed Consent Form (Appendix 1) at their doctor's office at the time of prescription. Innomar will provide the drug to approximately 40 new patients per month, so it will take about twelve to fourteen months to enroll all of the study subjects, assuming that all agree to participate. Once the recruitment period is over, it will take another 22 months to complete the study to the 22-months point for the last subject. In the retrospective arm of the study, 500 chart reviews will be completed for patients who had participated in the MS Alliance program two (2) to three (3) years ago to determine persistence to therapy over a similar 22 month period. Study Objectives Primary Objectives: \- To assess patients' compliance (as defined above) with AVONEX therapy in the prospective arm using self-reported patients questionnaire, as well as to compare patients' persistence on therapy (as defined above) between prospective and retrospective arms. Secondary Objective: \- Evaluate patients' satisfaction with new MSA program. Patients and Methods Only patients enrolled in the MSA program will be included in this study. There will be no interventions above the current standard of care with the MSA program. Two distinct patient arms will exist for this study: the prospective arm and the retrospective (chart review) arm. Inclusion Criteria * Diagnosed with Relapsing Remitting Multiple Sclerosis (RRMS) * Prescription of AVONEX® PS (prefilled syringes) * Enrolment in the MS AllianceTM program

Interventions

None listed

Sponsors

Biogen
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosed with Relapsing Remitting Multiple Sclerosis (RRMS) * Prescription of AVONEX® PS (prefilled syringes) * Enrolment in the MS AllianceTM program

Design outcomes

Primary

MeasureTime frame
Compliance with therapy in the prospective armWeek 7-10 and Week 80-83
Persistence on therapy between prospective and retrospective arms22 months

Secondary

MeasureTime frame
Patients' satisfaction with new MSA programWeek 7-10 and Week 80-83

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026