The Role of Risk Aversion in Reverse Payment Agreements

AuthorWenqing Li
DOI10.1177/0003603X18770066
Date01 June 2018
Published date01 June 2018
Subject MatterArticles
Article
The Role of Risk Aversion
in Reverse Payment Agreements
Wenqing Li*
Abstract
Both the courts and the economists have identified risk aversion as a justification for reverse payment
agreements, especially the risk aversion of brand-name companies. However, existing economic
researches show whether risk aversion can be a rationale for reverse payment agreements depends on
the type of reverse payment agreements reached. In “complete” settlement agreement where a brand-
name drug manufacturer provides consideration to a generic drug company to completely settle the
patent litigation, with agreed-upon entry dates for the generic, risk aversion does not provide a
justification for reverse payment, but asymmetry in risk aversion can be a rationale for reverse pay-
ment. In “partial” settlement agreement where a branded drug manufacturer provides consideration
to a generic drug company in exchange for the generic to agree not to enter the market while they
continue the patent litigation, it is not the risk aversion of the brand company, but the risk aversion of
the generic company that can facilitate the parties to reach a partial settlement agreement with reverse
payment that serves the procompetitive purpose.
Keywords
reverse payment, pay-for-delay, risk aversion, settlement, pharmaceutical, intellectual property
I. Introduction
Reverse payment agreements in which a brand-name drug manufacturer provides consideration
1
to
a generic drug company to settle their patent litigation, in exchange for the generic to agree not to
enter the market until a certain date, continue to attract enforcement attention. The Federal Trade
*
Director at Epsilon Economics, Chicago, IL, USA
Corresponding Author:
Wenqing Li, 111 South Wacker Drive, 50th Floor, Chicago, IL 60606, USA.
Email: wli@epsiloneconomics.com
1. Consideration can be, for example, a cash payment or a promise by the branded drug company not to launch an authorized
generic during certain period of time.
The Antitrust Bulletin
2018, Vol. 63(2) 237-245
ªThe Author(s) 2018
Reprints and permission:
sagepub.com/journalsPermissions.nav
DOI: 10.1177/0003603X18770066
journals.sagepub.com/home/abx

To continue reading

Request your trial

VLEX uses login cookies to provide you with a better browsing experience. If you click on 'Accept' or continue browsing this site we consider that you accept our cookie policy. ACCEPT