Battle for the market: Branded drug companies' secret weapons generic drug makers must know

Author(s):  
Jon Hess ◽  
Shannon Litalien
Author(s):  
Munirul Haque Nabin ◽  
Vijay Mohan ◽  
Aaron Nicholas ◽  
Pasquale M. Sgro

Abstract Following the passage of the Waxman-Hatch Act (1984), FDA approval for a generic drug requires the establishment of bio-equivalence between the generic drug and an FDA approved branded drug. However, a large body of evidence in the medical community suggests that bio-equivalence does not guarantee therapeutic equivalence; in some instances the lack of therapeutic equivalence can lead to fatal consequences for patients switching to generic products. In this paper, we construct a simple model to analyze the implications of therapeutic non-equivalence between branded and generic drugs. We show, theoretically and empirically, that this distinction can provide a plausible explanation of the generic competition paradox.


2003 ◽  
Vol 07 (16) ◽  
pp. 997-1005
Author(s):  
DENNIS S. FERNANDEZ ◽  
JAMES T. HUIE

The patentability of products is essential in the biotechnology field, for limited market exclusivity compensates biotech companies' investments in research and development. The biotechnology field also uniquely faces Federal Drug Administration (FDA) approval, which includes considerable additional expense and time issues a biotech company must address. Although balancing the patent and FDA approval processes may be complex, various strategies of patent extension, of accelerating approval processes, and of prolonging generic drug companies' market entry can yield higher profit returns and maximize value company value.


2018 ◽  
Vol 63 (2) ◽  
pp. 237-245
Author(s):  
Wenqing Li

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 payment. 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.


2016 ◽  
Author(s):  
Mark Lemley

“Reverse” or “exclusion” payments to settle pharmaceutical patent lawsuitsare facilitated because the Hatch-Waxman Act has been interpreted to give180 days of generic exclusivity to the first generic company to file forFDA approval, whether or not that company succeeds in invalidating thepatent or finding a way to avoid infringement. As a result, the patenteecan “buy off” the first generic entrant, paying them to delay their entryinto the market while still offering them the valuable period of genericexclusivity. And if that first generic is entitled to its 180 days, no oneelse can enter until after the exclusivity period has expired or beenforfeited. The result is that the 180-day exclusivity period is not servingits purpose of eliminating weak patents. True, it is encouraging lots ofchallenges to those patents. But it is encouraging the challengers toaccept compensation to drop those challenges, rather than taking them tojudgment and benefiting the rest of the world.We propose a change to the Hatch-Waxman statutory scheme. Our alternativeis straightforward: first-filing generic drug companies should be entitledto 180 days of exclusivity only if they successfully defeat the patentowner, for example, by invalidating the patent or by proving that they didnot infringe that patent. The point of 180-day exclusivity was to encouragechallenges to patents because the invalidation of bad patents benefitssociety as a whole. Society doesn’t benefit from a private deal to drop achallenge. That doesn’t mean settlement is never a good idea; it is acommonplace in our legal system. But it seems bizarre to insulate a companyfrom competition just because it settles the case. Indeed, we expect thatour proposal, if implemented, would facilitate more rational settlements,in which the settlements that result accurately reflect the likelihood ofsuccess in litigation.


2007 ◽  
Vol 1 (2) ◽  
pp. 69-87
Author(s):  
Mario Eandi

Three case reports, where an “equivalent” drugs is prescribed, are described: a patient treated with lanzoprazole, a man with acute myocardial infarction and a young man with epilepsy. These reports are emblematic of the doubts and problems that doctors have to afford in the choice of a generic drug instead of a branded drug. The Author examines not only clinical, legislative and economical aspects of prescription of generic drugs in the Italian context, but also common questions that patients may ask when a generic drug is prescribed.


2005 ◽  
Vol 09 (20) ◽  
pp. 1098-1101

India Works With EU to set up 'Working Group on Pharmaceuticals and Biotechnology. International Keystone Symposium held in Singapore. MedTech Concept in Singapore. Roche To Partner with 4 Generic Drug Companies on Flu Drug Tamiflu.


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