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Published in: PharmacoEconomics 10/2012

01-10-2012 | Leading Article

Private Manufacturers’ Thresholds to Invest in Comparative Effectiveness Trials

Authors: Anirban Basu, PhD, David Meltzer

Published in: PharmacoEconomics | Issue 10/2012

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Abstract

The recent rush of enthusiasm for public investment in comparative effectiveness research (CER) in the US has focussed attention on these public investments. However, little attention has been given to how changing public investment in CER may affect private manufacturers’ incentives for CER, which has long been a major source of CER. In this work, based on a simple revenue maximizing economic framework, we generate predictions on thresholds to invest in CER for a private manufacturer that compares its own product to a competitor’s product in head-to-head trials. Our analysis shows that private incentives to invest in CER are determined by how the results of CER may affect the price and quantity of the product sold and the duration over which resulting changes in revenue would accrue, given the time required to complete CER and the time from the completion of CER to the time of patent expiration. We highlight the result that private incentives may often be less than public incentives to invest in CER and may even be negative if the likelihood of adverse findings is sufficient. We find that these incentives imply a number of predictions about patterns of CER and how they will be affected by changes in public financing of CER and CER methods. For example, these incentives imply that incumbent patent holders may be less likely to invest in CER than entrants and that public investments in CER may crowd out similar private investments. In contrast, newer designs and methods for CER, such as Bayesian adaptive trials, which can reduce ex post risk of unfavourable results and shorten the time for the production of CER, may increase the expected benefits of CER and may tend to increase private investment in CER as long as the costs of such innovative designs are not excessive. Bayesian approaches to design also naturally highlight the dynamic aspects of CER, allowing less expensive initial studies to guide decisions about future investments and thereby encouraging greater initial investments in CER. However, whether the potential effects we highlight of public funding of CER and of Bayesian approaches to trial design actually produce changes in private investment in CER remains an empirical question.
Footnotes
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1 Throughout the paper, we will refer to ‘trials’ as randomized controlled trials or other designs, investments in which are readily transparent to other stakeholders. Private manufacturers may engage in comparative observational studies to generate priors for comparative effects. However, they are more likely to keep such investments and the resulting information private, especially when there are unfavourable results in terms of effectiveness. However, current laws do prevent hiding of such information when there is evidence of harm.
 
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2 It is worth noting that certain types of adaptive trials, such as adaptive assignment of treatments within a trial, are well suited to study and estimate the extent of such heterogeneous treatment effects.
 
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3 This is also facilitated by the coverage decision.
 
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4 Newer entrants usually spend large amounts on detailing and advertisement, especially highlighting selected dimensions of outcomes where their products may be better than the generics.
 
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5 This is especially true in competitive product markets where it is difficult for one manufacturer to negotiate with payers for a lower price and a larger share of the market.
 
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6 Sometimes CER results may lead to new indications for a product, thereby expanding its market. We will ignore such complications for now.
 
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7 Price erosion may be limited for biologics since the generic market expansion for biologics will be limited by regulatory and manufacturing hurdles as well as competition from the introduction of next-generation biotherapeutics.
 
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8 The multiplier effect arises mainly because the demand curve may become more inelastic when pushed outward, thereby increasing the difference between demand prices (co-pays) and supply prices (reimbursements).
 
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9 We continue to assume a two-competitor market. Our general results extend to a market where there are multiple competitors.
 
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10 Such prior development can occur with investments in observation studies and Bayesian indirect treatment comparisons that are considerably less expensive than RCTs.
 
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11 It is possible that sometimes an incumbent may benefit from a well done Bayesian adaptive CER study that shows substantial previously unreported benefits for an older product that helps extend the ‘effective’ patent life of the product at very little cost to the innovator. However, such favourable outcomes at the middle or tail-end of a product life-cycle are usually hard to come by and such investments must ride on strong priors of benefits.
 
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Metadata
Title
Private Manufacturers’ Thresholds to Invest in Comparative Effectiveness Trials
Authors
Anirban Basu, PhD
David Meltzer
Publication date
01-10-2012
Publisher
Springer International Publishing
Published in
PharmacoEconomics / Issue 10/2012
Print ISSN: 1170-7690
Electronic ISSN: 1179-2027
DOI
https://doi.org/10.2165/11597730-000000000-00000

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