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Therapy Optimization in Multiple Sclerosis (MS)

TOP MS is a Study of Multiple Sclerosis Disease Management in Collaboration With Specialty Pharmacies

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00819000
Acronym
TOP MS
Enrollment
2878
Registered
2009-01-08
Start date
2008-12-31
Completion date
2013-01-31
Last updated
2013-01-29

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

Conditions

Multiple Sclerosis

Keywords

Specialty Pharmacy, Therapy Management, Medication Compliance, Medication Adherence, Medication Persistence, Health Outcomes

Brief summary

The purpose of this study is to determine if higher compliance and adherence rates to drug therapy for MS result in better health outcomes than lower rates of therapy compliance and adherence.

Interventions

DRUGGlatiramer Acetate, IFN-beta 1a (IM), IFN-beta 1a (Subcutaneous), and IFN-beta 1b

MS therapies (listed above) used according to prescribers' instructions.

Sponsors

Teva Neuroscience, Inc.
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Male or female, 18 years of age or older, with a diagnosis of MS. * Being treated with Glatiramer Acetate (GA) or (IFN)-β * Receiving therapy from a participating Specialty Pharmacy

Exclusion criteria

* Has any contraindication to GA or IFN-β therapy, including pregnancy, trying to become pregnant, or breast feeding during the study * Has received an experimental drug in the last thirty (30) days other than Fampridine SR (4-aminopyridine or 4-AP) * Unlikely to be able to participate for the full two years of the study

Design outcomes

Primary

MeasureTime frame
Relationship of therapy Medication Possession Ratio (MPR), to patient outcomes12 months and 24 months

Secondary

MeasureTime frame
Relationship of therapy adherence, defined as the accumulation of time from initiation to discontinuation of therapy and measured by time, to patient outcomes12 months and 24 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 21, 2026