Budget Impact of Baricitinib for Moderate-to-Severe Atopic Dermatitis Patients with an Inadequate Response to Topical Treatments
Author(s)
Fenske C1, Rosettie K2, Ferrufino C3, Borns M1, Atiya B1, Johnson N1, Wehler E4
1Eli Lilly and Company, Indianapolis, IN, USA, 2IQVIA, Everett, WA, USA, 3IQVIA, Falls Church, VA, USA, 4IQVIA, Plymouth Meeting, PA, USA
Presentation Documents
OBJECTIVES: Systemic therapy for management of moderate-to-severe atopic dermatitis (AD) in patients with inadequate response (IR) to topical treatments has been limited to dupilumab. Given the expected launch of baricitinib, an oral Janus kinase inhibitor indicated for this population, the budget impact of adding baricitinib to a commercial managed-care formulary for treatment of moderate-to-severe AD was estimated from a US payer perspective. METHODS: A budget impact analysis was done using a comparative cost determination framework and a 5-year time horizon. Starting with a hypothetical commercial plan of one million lives, the model estimated the number of baricitinib-eligible patients by disease severity using AD prevalence, topical treatment use, and IR to topical treatments. Baricitinib was assumed to draw market share from dupilumab, with uptake ranging from 2% to 12%, 1% to 5%, and 2% to 11% in the moderate, severe, and moderate-to-severe AD populations, respectively. Treatment costs excluded rebates and cost-sharing and were from published wholesale acquisition costs. Dosing, administration, and monitoring requirements were from product prescribing information. Unit costs were from publicly available fee schedules. One-way sensitivity analyses (OWSA) were performed by varying all parameters by 20%. RESULTS: The net budget impact over 5-years in the moderate AD population was -$4,393,706 (-3.05%) with a -$0.07 per member per month (PMPM). In the severe AD population, the net budget impact was -$372,200 (-1.15%) with a PMPM of -$0.01. In the moderate-to-severe AD population, the net budget impact was -$4,719,710 (-2.68%) with a PMPM of -$0.08. OWSA results were consistent with the base case, with results most sensitive to changes in epidemiological inputs, baricitinib market shares, and monitoring costs. CONCLUSIONS: Adding baricitinib to a formulary would result in cost-savings across all three disease severities, with the greatest relative cost-savings in the moderate AD population, given the lower annual cost compared to dupilumab.
Conference/Value in Health Info
2021-05, ISPOR 2021, Montreal, Canada
Value in Health, Volume 24, Issue 5, S1 (May 2021)
Code
PSY4
Topic
Economic Evaluation
Topic Subcategory
Budget Impact Analysis
Disease
Drugs, Systemic Disorders/Conditions