Literature DB >> 31198180

Are Payers Ready, Willing, and Able to Provide Access to New Durable Gene Therapies?

Jane F Barlow1, Mo Yang2, J Russell Teagarden2.   

Abstract

OBJECTIVE: To explore payer feedback regarding awareness of new gene therapies, sustainability of current financing mechanisms, unique challenges by payer segment, and need and preference for new financial models. STUDY
DESIGN: Qualitative interview with standardized interview guide.
METHODS: Sixty-minute telephone interviews were conducted with financial decision makers from 15 US payers between August and September 2017.
RESULTS: One-third of payers interviewed (n = 5) were newly aware and learning about new gene therapies, 40% (n = 6) described watchful waiting, whereas 26.7% (n = 4) were engaged in active management. New payment models-specifically, performance-based agreements and risk-pooling-were supported by 47% (n = 7) of payers, whereas the current payment model was supported by 53% (n = 8). Major challenges included uncertainty related to utilization, cost, and duration of cure. Payers cited regulation, plan turnover, and ability to track long-term outcomes as barriers to implementation of new models.
CONCLUSIONS: Access to new gene therapies may be impacted by payer ability to absorb the cost of coverage. Variation exists in awareness of new gene therapies and level of incorporation of new costs into future plan coverage. The sustainability of current financing mechanisms varies by payer segment, profitability, and size; smaller plans and Medicaid are likely to be impacted first. Government reinsurance, commercial reinsurance, and stop-loss insurance backstop current reimbursement models, dampening the need for urgent action. The tipping point for action may be severe premium inflation in stop loss and reinsurance. Payers are open to innovative financing models that improve financial predictability and reward clinical performance.
Copyright © 2019 ISPOR–The Professional Society for Health Economics and Outcomes Research. Published by Elsevier Inc. All rights reserved.

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Year:  2019        PMID: 31198180     DOI: 10.1016/j.jval.2018.12.004

Source DB:  PubMed          Journal:  Value Health        ISSN: 1098-3015            Impact factor:   5.725


  4 in total

1.  Cost-effectiveness Analysis of Tisagenlecleucel Versus Blinatumomab in Children and Young Adults with Acute Lymphoblastic Leukemia: Partitioned Survival Model to Assess the Impact of an Outcome-Based Payment Arrangement.

Authors:  Amy Gye; Stephen Goodall; Richard De Abreu Lourenco
Journal:  Pharmacoeconomics       Date:  2022-10-21       Impact factor: 4.558

2.  Development of a conceptual model for evaluating new non-curative and curative therapies for sickle cell disease.

Authors:  Kate M Johnson; Boshen Jiao; M A Bender; Scott D Ramsey; Beth Devine; Anirban Basu
Journal:  PLoS One       Date:  2022-04-28       Impact factor: 3.752

Review 3.  Financing Drug Innovation in the US: Current Framework and Emerging Challenges.

Authors:  David Cutler; Noam Kirson; Genia Long
Journal:  Pharmacoeconomics       Date:  2020-09       Impact factor: 4.981

Review 4.  Reinforcing Collaboration and Harmonization to Unlock the Potentials of Advanced Therapy Medical Products: Future Efforts Are Awaited From Manufacturers and Decision-Makers.

Authors:  Tingting Qiu; Shuyao Liang; Yitong Wang; Claude Dussart; Borislav Borissov; Mondher Toumi
Journal:  Front Public Health       Date:  2021-11-25
  4 in total

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