Literature DB >> 18504330

N-of-1 trials of expensive biological therapies: a third way?

Richard L Kravitz1, Naihua Duan, Richard H White.   

Abstract

In developing policies for use of expensive agents, such as those used for the treatment of rheumatoid arthritis, managed care organizations have invoked "stepped care," in which physicians and patients must first try more established and less costly agents. N-of-1 clinical trials are multiple crossover trials in a single patient. In this cost-minimization analysis, we show that offering patients with rheumatoid arthritis the opportunity to participate in an n-of-1 trial comparing methotrexate with etanercept could save costs relative to open access while preserving clinical freedom relative to mandatory stepped care. In the primary model, the n-of-1 trial option was 15% more expensive than stepped care but 47% cheaper than open access to etanercept. More research is needed on the acceptability, safety, and generalizability of this promising approach.

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Year:  2008        PMID: 18504330      PMCID: PMC2715700          DOI: 10.1001/archinte.168.10.1030

Source DB:  PubMed          Journal:  Arch Intern Med        ISSN: 0003-9926


  26 in total

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Review 3.  "Stepping-up" from methotrexate: a systematic review of randomised placebo controlled trials in patients with rheumatoid arthritis with an incomplete response to methotrexate.

Authors:  M C Hochberg; J K Tracy; R H Flores
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Review 5.  New drugs for rheumatoid arthritis.

Authors:  Nancy J Olsen; C Michael Stein
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Review 6.  Therapeutic strategies for rheumatoid arthritis.

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Review 9.  Defining and characterizing the late-stage biopharmaceutical pipeline.

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Review 3.  A Useful and Sustainable Role for N-of-1 Trials in the Healthcare Ecosystem.

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5.  What ever happened to N-of-1 trials? Insiders' perspectives and a look to the future.

Authors:  Richard L Kravitz; Naihua Duan; Edmund J Niedzinski; M Cameron Hay; Saskia K Subramanian; Thomas S Weisner
Journal:  Milbank Q       Date:  2008-12       Impact factor: 4.911

6.  Issues in assessing products for the treatment of hemophilia - the intersection between efficacy, economics, and ethics.

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