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Valuing Trial Designs from a Pharmaceutical Perspective Using Value‐Based Pricing

Listed author(s):
  • Penny Breeze
  • Alan Brennan
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    Our aim was to adapt the traditional framework for expected net benefit of sampling (ENBS) to be more compatible with drug development trials from the pharmaceutical perspective. We modify the traditional framework for conducting ENBS and assume that the price of the drug is conditional on the trial outcomes. We use a value‐based pricing (VBP) criterion to determine price conditional on trial data using Bayesian updating of cost‐effectiveness (CE) model parameters. We assume that there is a threshold price below which the company would not market the new intervention. We present a case study in which a phase III trial sample size and trial duration are varied. For each trial design, we sampled 10 000 trial outcomes and estimated VBP using a CE model. The expected commercial net benefit is calculated as the expected profits minus the trial costs. A clinical trial with shorter follow‐up, and larger sample size, generated the greatest expected commercial net benefit. Increasing the duration of follow‐up had a modest impact on profit forecasts. Expected net benefit of sampling can be adapted to value clinical trials in the pharmaceutical industry to optimise the expected commercial net benefit. However, the analyses can be very time consuming for complex CE models. © 2014 The Authors. Health Economics published by John Wiley & Sons Ltd.

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    Article provided by John Wiley & Sons, Ltd. in its journal Health Economics.

    Volume (Year): 24 (2015)
    Issue (Month): 11 (November)
    Pages: 1468-1482

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    Handle: RePEc:wly:hlthec:v:24:y:2015:i:11:p:1468-1482
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