A US Claims Database Analysis of the Impact of Fremanezumab on Migraine-Related Health Care Utilization and Costs in Patients with Common Comorbidities, Acute Medication Overuse, or Difficult-to-Treat Migraine

Author(s)

Buse DC1, Driessen MT2, Krasenbaum LJ3, Seminerio MJ4, Carr K4, Ortega M3, Packnett E5
1Albert Einstein College of Medicine, New York, NY, USA, 2Teva Pharmaceuticals, Amsterdam, Netherlands, 3Teva Branded Pharmaceutical Products R&D, Inc., West Chester, PA, USA, 4Teva Branded Pharmaceutical Products R&D, Inc., Parisppany, NJ, USA, 5IBM Watson Health, Cambridge, MA, USA

OBJECTIVES: Patients with common comorbidities, acute medication overuse (AMO), or difficult-to-treat migraine (DTTM) may have high healthcare resource utilization (HCRU) and costs. There are limited real-world data on use of fremanezumab, a fully humanized monoclonal antibody (IgG2Δa) targeting calcitonin gene-related peptide (CGRP), in these patients. This retrospective claims database study evaluated migraine-related HCRU and costs for patients with comorbidities, AMO, or DTTM initiating fremanezumab treatment.

METHODS: Adult patients (≥18 years) initiating fremanezumab treatment between September 1, 2018–June 30, 2019 (date of earliest claim=index date) were identified from the IBM/MarketScan Commercial and Medicare supplemental database, which contains health care service and outpatient prescription data from a convenience sample of individuals with employer-sponsored health insurance in the US. Other inclusion criteria were 12 months of continuous enrollment in the database pre-index, ≥6 months of data post-index, and evidence of comorbidities, AMO, or DTTM pre-index, defined by presence of major depressive disorder, generalized anxiety disorder, cardiovascular disease; potential AMO in the 90 days pre-index; or inadequate response to ≥2 previous preventive medication classes.

RESULTS: 3,193 patients with comorbidities, AMO, or DTTM were included. For post-index versus pre-index, mean (SD) migraine-related HCRU per-patient-per-month (PPPM) was significantly lower for neurologist visits (0.14 [0.17] versus 0.15 [0.18]), outpatient office visits (0.32 [0.35] versus 0.35 [0.31]), and acute medication claims (0.86 [0.87] versus 0.97 [0.90]; all P<0.001). Consequently, post-index versus pre-index, significantly lower mean (SD) migraine-related costs PPPM were reported for office visits ($38 [45] vs $46 [46]), neurologist office visits ($17 [24] vs $21 [28]), acute medication ($74 [219] vs $93 [224]; all P<0.001), and migraine-related health care costs PPPM (excluding fremanezumab costs; $490 [974] versus $541 [858], P=0.003).

CONCLUSIONS: Statistically significant reductions in migraine-related HCRU and migraine-related health care costs were observed in patients with comorbidities, AMO, or DTTM following initiation of fremanezumab treatment.

Conference/Value in Health Info

2022-05, ISPOR 2022, Washington, DC, USA

Value in Health, Volume 25, Issue 6, S1 (June 2022)

Code

EE433

Topic

Economic Evaluation

Disease

Biologics and Biosimilars

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