Impact of Fingolimod Adherence on Outcomes
What it found
We found no results in the registry or in papers.
This trial finished 5 years ago. We found no results in the registry or in any paper that cites it.
What was tested
Treatment tested
What it measured
Main measures
Number of Multiple Sclerosis (MS) relapses
Month 7 to Month 18 (12 months) of the post-index period. The date of the first fingolimod claim was the index date (01 January 2012 through 10 May 2018)
RelapsesQuality of life (reported by participants)
Other measures (5)
Number of Multiple Sclerosis-related inpatient admission
Month 7 to Month 18 (12 months) of the post-index period. The date of the first fingolimod claim was the index date (01 January 2012 through 10 May 2018)
Quality of life (reported by participants)Number of Multiple Sclerosis-related Emergency Room (ER) visits
Month 7 to Month 18 (12 months) of the post-index period. The date of the first fingolimod claim was the index date (01 January 2012 through 10 May 2018)
Quality of life (reported by participants)All-cause total (medical plus pharmacy) health care costs
Month 7 to Month 18 (12 months) of the post-index period. The date of the first fingolimod claim was the index date (01 January 2012 through 10 May 2018)
All-cause medical health care costs
Month 7 to Month 18 (12 months) of the post-index period. The date of the first fingolimod claim was the index date (01 January 2012 through 10 May 2018)
Quality of life (reported by participants)All-cause total (medical plus pharmacy) health care costs excluding fingolimod
Month 7 to Month 18 (12 months) of the post-index period. The date of the first fingolimod claim was the index date (01 January 2012 through 10 May 2018)
Quality of life (reported by participants)
Who could take part
MS (type not specified) · 18 to 85
Inclusion Criteria: * ≥18 years old during year of index date with valid gender and geographic information * Continuous enrollment (CE) in the health plan with medical and pharmacy benefits for ≥6 months (180ii days) before the index date (pre-index period) * CE with medical and pharmacy benefits for ≥18 months (540 days) beginning on the index date (post-index period) * All patients had uniform 6-month pre-index and 18-month post-index periods * ≥1 medical claim with an MS diagnosis codei in any position during the pre-or post-index periods * ≥1 claim for fingolimod after the index date (i.e., from index date +1 to 539 days post-index) * By requiring ≥1 medical claim with an MS diagnosis code and ≥2 claims with an NDC for fingolimod, the inclusion criteria essentially incorporated the preferred/overall best performing MS case-finding definition validated by Culpepper et al. The criteria for that definition required at least 3 separate encounters from any of the following: MS-related ambulatory visits, MS-related inpatient stays, and DMT claims during a 12-month period. Slightly higher accuracy was found when a 24-month period was used. Exclusion Criteria: •≥1 pharmacy or medical claim for any MS DMT during the pre-index period
As registered. Criteria can change, so ask the trial team or your neurologist.
About this trial
In the sponsor's words
This study was a retrospective observational claims data study of commercial and Medicare Advantage with Part D (MAPD) patients initiating fingolimod.
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History
Started
May 2020
Main results due
Nov 2020
Finished
Nov 2020
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