PAYER REQUIREMENTS IN THE TREATMENT OF CHRONIC HEART FAILURE

Author(s)

Bergenheim K1, Hellsten Kronander A2, Lauks S3, van Engen A4
1AstraZeneca, Mölndal, Sweden, 2AstraZeneca, Gothenburg, Sweden, 3Quintiles, Reading, UK, 4Quintiles Advisory Services, Hoofddorp, The Netherlands

OBJECTIVES: Given the lack of novel therapies and stagnant survival outcomes, there remains a high unmet need in chronic heart failure (HF). However, after years of limited development, the HF treatment pipeline looks promising. This research investigated the current chronic HF payer landscape, comparing Health Technology Assessment (HTAs) decisions and evidence packages submitted for key products to determine payer requirements and to understand how these requirements may evolve as new, more effective treatments are launched. METHODS: HTAs published by key agencies from 2011-2016 for eplerenone, ivabradine and sacubitril/valsartan in the treatment of chronic HF were identified. Submissions and decision rationale, including economic and clinical critiques, were compared across the products. RESULTS: CONCLUSIONS: With a sizeable patient population and only a limited number of treatment options for chronic HF available, proving clinical efficacy in reducing hospitalisation rates and cost-effectiveness have historically been sufficient for a positive payer recommendation. As superior treatments come to market, pressure from payers for survival endpoints, superiority versus an active comparator, cost-offsets and budget impact data will increase.

Conference/Value in Health Info

2016-10, ISPOR Europe 2016, Vienna, Austria

Value in Health, Vol. 19, No. 7 (November 2016)

Code

PRM18

Topic

Clinical Outcomes, Economic Evaluation, Methodological & Statistical Research, Study Approaches

Topic Subcategory

Clinical Outcomes Assessment, Cost/Cost of Illness/Resource Use Studies, Modeling and simulation

Disease

Cardiovascular Disorders

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