[Ip-health] 'Government Patent Use': A Legal Approach to Reducing Drug Spending

Jamie Love james.love at keionline.org
Tue May 3 14:04:45 PDT 2016

The uncertainly over the compensation is uncertainly about how much less
the government would pay when using 28 USC 1498.   If the government use of
the product is insensitive to the price, then 28 USC 1498 is more
appealing, because you would have bought the product anyway, at a high
price.  But if you intend to use it more intensively if the price is lower,
such as treating everyone who has HCV, rather than patients with advanced
disease, or stockpiling Cipro, then the compensation becomes a risk to
consider.  Having read a lot of 1498(a) cases, the compensation is hard to
predict.  I agree that the rules for the government have some attractive
features, but depending upon the context and the judge, there can be some
unpleasant surprises too.


On Tue, May 3, 2016 at 10:46 PM, Kapczynski, Amy <amy.kapczynski at yale.edu>

> Agree that legislation that clarified the appropriate level of
> compensation would be very beneficial. A test case could also establish
> more certainty.
> But I don’t think there’s any way that the gov would be worse off
> employing this statute than it would be if it doesn’t — there is strong
> caselaw rejecting the lost profits approach here, meaning companies can
> only obtain a reasonable royalty. Even if a court rejected that approach
> and chose lost profits, those profits would logically and legally have to
> be capped at the doses the gov actually would have bought — i.e., the
> current spending.
> Btw, I am working on a law review article with some colleagues describing
> how we think courts should approach the compensation question.  Would
> welcome thoughts on that,
> Best
> Amy
> On May 3, 2016, at 4:29 PM, Jamie Love <james.love at keionline.org> wrote:
> Our own take on 28 USC 1498 is that it can be useful, but it is not
> necessarily well suited for dealing with drug patent cases, given the case
> law on compensation to patent holders, which includes uncertainty on what
> can be big ticket items.
> If 28 USC 1498 is what you have to work with, you use it.  Al Engelberg
> and others proposed this in 2001 for Ciprofloxcin, and we supported that
> effort then.  (http://www.cptech.org/ip/health/cl/cipro/
> <https://urldefense.proofpoint.com/v2/url?u=http-3A__www.cptech.org_ip_health_cl_cipro_&d=AwMFaQ&c=-dg2m7zWuuDZ0MUcV7Sdqw&r=-ddH8Zceq1hAY-PYLwkNHeKcPT9OK3Kb_YdJ7DDd_Uo&m=MPw9Wmrmv4VhfbYbUzWUPhnME7KSUFcM7ifS-biAz9Q&s=PMr-mbrcm11aOCiB0ymUOqmT29faV20hPyP77L3A-3k&e=>).
>  1498 was also used for drugs earlier by DoD.
> When Bernie Sanders proposed that the Department of Veterans Affairs use
> 1498 for HCV drugs, the issue of compensation to Gilead was a concern.
> Sanders offered a still to be considered legislative reform that would have
> fixed this.    Zack Struver did an informative video about the issue here:
> https://www.youtube.com/watch?v=xAY4Ua7B2mQ
> <https://urldefense.proofpoint.com/v2/url?u=https-3A__www.youtube.com_watch-3Fv-3DxAY4Ua7B2mQ&d=AwMFaQ&c=-dg2m7zWuuDZ0MUcV7Sdqw&r=-ddH8Zceq1hAY-PYLwkNHeKcPT9OK3Kb_YdJ7DDd_Uo&m=MPw9Wmrmv4VhfbYbUzWUPhnME7KSUFcM7ifS-biAz9Q&s=HZO__4HratjjmnVcaUYBGGRfcL4OCad3x3lynxGxp-A&e=>
> On Tue, May 3, 2016 at 8:04 PM, Kapczynski, Amy <amy.kapczynski at yale.edu>
> wrote:
>> Aaron Kesselheim and I just published this in Health Affairs:
>> http://content.healthaffairs.org/content/35/5/791.full
>> <https://urldefense.proofpoint.com/v2/url?u=http-3A__content.healthaffairs.org_content_35_5_791.full&d=AwMFaQ&c=-dg2m7zWuuDZ0MUcV7Sdqw&r=-ddH8Zceq1hAY-PYLwkNHeKcPT9OK3Kb_YdJ7DDd_Uo&m=MPw9Wmrmv4VhfbYbUzWUPhnME7KSUFcM7ifS-biAz9Q&s=tQqlLY5P8HkR8FTNd0ei6-sdXSxCe_psB0uS6f9WR48&e=>
>> Abstract:
>> The high cost of patent-protected brand-name drugs can strain budgets and
>> curb the widespread use of new medicines. An example is the case of
>> direct-acting antiviral drugs for the treatment of hepatitis C. While
>> prices for these drugs have come down in recent months, they still create
>> barriers to treatment. Additionally, prescribing restrictions imposed by
>> insurers put patients at increased risk of medical complications and
>> contribute to transmission of the hepatitis C virus. We propose that the
>> federal government invoke its power under an existing “government patent
>> use” law to reduce excessive prices for important patent-protected
>> medicines. Using this law would permit the government to procure generic
>> versions of patented drugs and in exchange pay the patent-holding companies
>> reasonable royalties to compensate them for research and development. This
>> would allow patients in federal programs, and perhaps beyond, to be treated
>> with inexpensive generic medicines according to clinical need—meaning that
>> many more patients could be reached for no more, and perhaps far less,
>> money than is currently spent. Another benefit would be a reduction in the
>> opportunity for companies to extract monopoly profits that far exceed their
>> risk-adjusted costs of research and development.
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> --
> James Love.  Knowledge Ecology International
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> <https://urldefense.proofpoint.com/v2/url?u=http-3A__twitter.com_jamie-5Flove&d=AwMFaQ&c=-dg2m7zWuuDZ0MUcV7Sdqw&r=-ddH8Zceq1hAY-PYLwkNHeKcPT9OK3Kb_YdJ7DDd_Uo&m=MPw9Wmrmv4VhfbYbUzWUPhnME7KSUFcM7ifS-biAz9Q&s=Q1UUTA0lc49cYeBgmUH4zj_EVNpbKMsGXhZXBiGOAcA&e=>

James Love.  Knowledge Ecology International
KEI DC tel: +1.202.332.2670, US Mobile: +1.202.361.3040, Geneva Mobile:
+41.76.413.6584, twitter.com/jamie_love

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