Myriad Sets Forth Its Case to the Supreme Court

by McDonnell Boehnen Hulbert & Berghoff LLP

MyriadMyriad Genetics filed its responsive  brief with the Supreme Court last Thursday in AMP v. Myriad Genetics ("the Myriad case").  It is a certainly a serviceable brief that makes the patent law arguments that need to be made and cites at least some of the precedent that should be cited.  But reading the brief leaves nothing so much as the impression that Myriad has squandered its opportunity to submit a brief the Supreme Court would listen to.

The brief begins by expanding on the Question Presented by Petitioners (and for which certiorari was granted, i.e., "Are human genes patentable") to the following:

Did the Federal Circuit correctly apply 35 U.S.C. § 101 to conclude that these particular molecules are "product[s] of human ingenuity 'having a distinctive name, character [and] use,'" particularly where the general legal rule followed by courts for 30 years has been to allow such patent claims, where the U.S. Patent and Trademark Office ("USPTO") has issued similar patents since at least 1982 and confirmed in the 2001 Utility Guidelines that such isolated molecules are patent-eligible as human-made inventions under § 101, where investors and technology companies have placed significant reliance in these settled property rights over the last 30 years, where the alternative dividing line is indefensible under law or science, and where the challenged claims do not preempt or preclude the use of alternative technologies to identify a patient's cancer predisposition?

The brief then makes many of the points that have been made by Myriad and its amici throughout this litigation:  that the scope of Section 101 of the Patent Act is broad, the Federal Circuit came to the correct decision, the requirements in Diamond v. Chakrabarty, 447 U.S. 303, 309 (1980), are controlling precedent and Myriad's claims satisfy these requirements, and that the government's and Petitioner's arguments and interpretations of the law are incorrect.  The brief emphasizes the distinctions between isolated DNA and DNA as it exists in nature, and the new utilities imparted upon isolated DNA as the result of its isolation.  Myriad distinguishes claims to isolated human DNA from the unpatentable claims in Funk Bros. Seed Co. v. Kalo Inoculant Co., 333 U.S. 127, 130 (1948) (properly stating that Funk Bros. was a case about "invention," i.e., non-obviousness and not patent-eligibility), and relies heavily on the Court's interpretation of the scope of Section 101 in J.E.M. Ag Supply, Inc. v. Pioneer Hi-Bred International, Inc., 534 U.S. 124 (1996).  The brief makes the following analogy (among many):

No one would doubt the patent-eligibility of a newly-created chemical composition that, when applied in a laboratory to a person's blood or tissue sample, could detect a mutation genetically predisposing her to a risk of breast or ovarian cancer, thereby allowing her to take proactive measures to prolong her life even before cancer actually strikes.  That is what Myriad's patented molecules are -- and they were never available to the world until Myriad's scientists applied their inventive faculties to a previously undistinguished mass of genetic matter in order to identify, define, and create the isolated DNA molecules.

Myriad argues that there are other provisions of the Patent Act that can properly cabin claims to their proper scope, and that what Section 101 requires is "invention," drawing a parallel with analogous concepts in copyright law (specifically, "the eligibility threshold of copyright law, which requires authorial 'originality' -- defined as a "minimal level of creativity."  Feist Pub., Inc. v. Rural Tel. Serv. Co., 499 U.S. 340, 358-59 (1991)).

And the brief reminds the Court that the USPTO has been granting patents on isolated DNA (and the Federal Circuit upholding them) since 1982 as an application of the broad interpretation of patent eligibility enunciated by the Court in Chakrabarty.  Myriad emphasizes efforts by the PTO to ensure that the scope of claims granted on isolated DNA was appropriate, for example, as having "specific, substantial and credible" utility," citing both the 1995 (Utility Examination Guidelines, 60 Fed. Reg. 36,263 (July 14, 1995)) and 2001 (Utility Guidelines. 66 Fed. Reg. 1092 (Jan. 5, 2001)) versions of the Office's Utility Guidelines.  In this regard, Myriad cites numerous precedent to support the statement that "isolates or extracts of natural products may be patented"; examples include digitalis (U.S. Patent No. 1,898,199), rapamycin (U.S. Patent No. 3,929,992) and (perhaps infelicitously) the HIV virus (U.S. Patent No. 5,135,864), among others.

Myriad's response to the government's position is that it is inconsistent with the government's previous position permitting patents on isolated DNA in "[o]ver thirty years of precedent."  Myriad criticizes the government for arguing that the "line" should be drawn between cDNA (patent eligible) and "other isolated DNA molecules (not)."  The line has been drawn elsewhere under established government (PTO) practice, and this "'established general legal rule' -- not to mention the enormous reliance interests and property rights arising from that practice -- is far more worthy of respect than the arbitrary line now being offered as a mere litigating position by the United States" says Myriad, citing Bowen v. Georgetown Univ. Hosp., 488 U.S. 204, 212 (1988).

These arguments are followed in the brief by an argument related to the "[c]ountless companies and investors [that] have risked billions of dollars to research and develop advances under this promise of stable patent protection," followed almost immediately by a disquisition on the differences between isolated DNA and how it exists in nature, and a brief history of "the little biotech company that could" (i.e., Myriad) and the benefits to human health that resulted from the availability of patent protection (although it does not explain how claims to isolated, full-length BRCA1 and BRCA2 genes are relevant to genetic diagnostic testing, then or now).  The brief does Myriad a great service in getting before the Court some of the facts regarding the credit Myriad is amply due in providing genetic diagnostic testing for breast and ovarian cancer and setting forth the reality (as opposed to Petitioners' fantasies) regarding the true costs of the tests and the number of women for whom Myriad's BRCA gene tests are available.  As has been noted by others, Myriad also informs the Court that its "gene patents" have not impeded research, citing the evidence that "since the patents issued, over 18,000 researchers have conducted studies on BRCA1/2 genes, published over 8,000 papers, and conducted over 130 clinical trials."

Turning to Petitioner's arguments, the brief catalogs the many ways that Plaintiffs have mischaracterized the evidence and the law in making their arguments.  This starts, according to Myriad, with focusing on the similarities between isolated and naturally occurring human DNA, because there will always be such similarities with any naturally occurring product.  What is relevant, according to Myriad, are the differences, because it is in the differences that will be illustrated "whether a claimed composition is ''a product of human ingenuity 'having a distinctive name, character and use'' from a natural product," citing Chakrabarty.  The brief uses an analogy plucked from the opinion below to make this point:

A patent-eligible baseball bat, though shaped and formed by human hands, will share the characteristics of the wood embedded in the tree from which the bat was formed.  But the fact that the bat shares the properties of natural wood does not make the resulting, human-made product ineligible for patenting.

And the brief addresses in this regard Petitioner's "information content" argument, i.e., that Myriad's claims are unpatentable because the sequence of the isolated DNA and the DNA as it exists in nature are identical, pointing out that that to be useful the sequence of the DNA:

[I]n combination with the inventors' scientific work and ingenuity in characterizing and defining the molecule's starting and end points, the severing of covalent bonds, and the removal of the specific defined molecule from other materials in its native environment to create new functionality as a probe or primer.  Only because of the addition of human invention do these molecules exist to help patients chart their own course of medical treatments.

(In a short section, the brief also addresses the 1st and 14th amendment arguments with regard to the absence of any threat to a woman's access to information regarding her health.)  Perhaps the most apt application of these principles comes in the brief's argument that, assessed as Petitioner would have patent eligibility assessed, Chakrabarty's bacterium would not have been sufficiently different from naturally occurring Pseudomonas bacteria to be eligible for patenting.

Myriad also has "its day in court" by taking the opportunity to illustrate the fanciful nature of the litigation, citing quotes from lawyers representing the ACLU and the Public Patent Foundation (PubPat) that they were just looking to "sue somebody" over patents to isolated DNA and that the goal was to "rend[er] invalid patents on many other genes . . . .  We just had to pick one case as our case."  However tempting, this portion of the argument, and indeed the entire first section of the brief, is devoted to Myriad's failed attempt below to convince the lower court that the one plaintiff found by the Federal Circuit to have standing (Dr. Harry Ostrer) in fact does not, either by virtue of a lack of "immediacy" in the threat to his activities posed by Myriad's 1998 letter offering a license to Myriad's patents to his then employer, NYU, or by virtue of his move from NYU to Montefiore Hospital at the Albert Einstein College of Medicine (which had never received a "cease and desist" or license offer letter).  This portion of the brief goes over the same ground trod extensively below, and one that the Court dismissed sub silentio by not including it as a basis for granting certiorari (albeit as part of Petitioners' Questions Presented that the Federal Circuit had been overly exclusive in finding a lack of standing among the various Plaintiffs).  If only by emphasizing this argument by primacy of placement Myriad seems to have made a misjudgment on why the Court granted cert. and what it was interested in deciding.

Even ignoring this strange choice in presenting the order of its arguments, the real problem with the brief is that it seems tone deaf to the tenor of this Supreme Court.  Its emphasis on deference -- to the USPTO or earlier precedent, including especially the Federal Circuit's decision below -- ignores frank and explicit statements and signals from this Court that deference is not on its menu.  The brief seemingly ignores the difference between the Chakrabarty Court's understanding of its role as a coequal branch:

Our task, rather, is the narrow one of determining what Congress meant by the words it used in the statute; once that is done our powers are exhausted.  Congress is free to amend §101 so as to exclude from patent protection organisms produced by genetic engineering.  Compare 42 U.S.C. §2181, exempting from patent protection inventions "useful solely in the utilization of special nuclear material or atomic energy in an atomic weapon."  Or it may choose to craft a statute specifically designed for such living things.  But, until Congress takes such action, this Court must construe the language of §101 as it is.

Diamond v. Chakrabarty.

And this Court's:

[W]e must recognize the role of Congress in crafting more finely tailored rules where necessary.  Cf. 35 U.S.C. §§161–164 (special rules for plant patents).  We need not determine here whether, from a policy perspective, increased protection for discoveries of diagnostic laws of nature is desirable.

(i.e., if Congress does not agree with us they can "craft[] more finely tailored rules").  (Indeed, some members of the Court indicated recently at oral argument in Shelby County v. Holder that the Court need not defer to a 98-0 vote in the Senate reauthorizing the Section 5 of the Voting Rights Act.)

The brief's reliance on deference to the PTO's decisions granting gene patents and the rules it has implemented to do so (like the 2001 Utility Guidelines) lose much of its force in view of the brief filed by the government, that these practices were inconsistent with law and these patents should not have been granted.  While the brief notes that the PTO did not join the brief (and the unprecedented nature of this omission), the Court is certain to be familiar with the concept of the "unified Executive" and thus likely to come to the conclusion that the PTO is stubbornly resisting its comeuppance in a hidebound application of incorrect law.  The brief might have more aptly noted that it is this type of changing positions that is not due deference, as argued recently in Par Pharmaceuticals' brief in FTC v. Actavis:

"[W]hatever deference you are entitled to is compromised by the fact that your predecessors took a different position."  Transcript of Oral Argument at 44, Kiobel v. Royal Dutch Petroleum, No.10-1491 (Oct. 1, 2012) (Roberts, C.J.)

Such a citation might have given the Court pause regarding whether the government's position was persuasive, but the opportunity to make that case was lost.

Similarly, the brief focuses on applications of all the other sections of the Patent Act -- §§ 102, 103, 112 -- in making its arguments, with the rationale that these sections are more appropriate or more flexible or more nuanced in their application to the question before the Court.  This type of argument was made in Mayo, by the government, and rejected:

The Government does not necessarily believe that claims that (like the claims before us) extend just minimally beyond a law of nature should receive patents.  But in its view, other statutory provisions -- those that insist that a claimed process be novel, 35 U. S. C. §102, that it not be "obvious in light of prior art," §103, and that it be "full[y], clear[ly], concise[ly], and exact[ly]" described, §112 -- can perform this screening function.  In particular, it argues that these claims likely fail for lack of novelty under §102.

This approach, however, would make the "law of nature" exception to §101 patentability a dead letter.  The approach is therefore not consistent with prior law.

*  *  *

These considerations lead us to decline the Government's invitation to substitute §§102, 103, and 112 inquiries for the better established inquiry under §101.

(emphasis added).

The fact is that the Supreme Court doesn't consider patent questions like you or I, and patent lawyers would do well to recognize and adapt to that fact.  This brief does not, and its persuasive punch before the Court is likely much reduced as a consequence.

Finally, the Court should have put to bed any comprehension that the "settled expectations" or "economic investment" arguments, such as the brief's argument that "[c]ountless companies and investors have risked billions of dollars to research and develop advances under this promise of stable patent protection," will have much traction, in finding more persuasive the arguments of consumers rather than producers of technology and rejecting the position of respondent and amici like the Biotechnology Industry Organization in Mayo:

Patent protection is, after all, a two-edged sword.  On the one hand, the promise of exclusive rights provides monetary incentives that lead to creation, invention, and discovery.  On the other hand, that very exclusivity can impede the flow of information that might permit, indeed spur, invention, by, for example, raising the price of using the patented ideas once created, requiring potential users to conduct costly and time-consuming searches of existing patents and pending patent applications, and requiring the negotiation of complex licensing arrangements.  At the same time, patent law's general rules must govern inventive activity in many different fields of human endeavor, with the result that the practical effects of rules that reflect a general effort to balance these considerations may differ from one field to another.

The ACLU and PubPat have prevailed -- at the District Court and the court of public opinion -- by making this case about everything but patent law.  While in a different time it might have been sufficient to emphasize patent law in this argument, that time has passed (at least for now).  The Court has evinced a concern that its decisions now may inhibit future progress (a salient concern, in view of the Constitutional imperative that patents and patent law "promote the progress"), as noted in Bilski v. Kappos:

It is important to emphasize that the Court today is not commenting on the patentability of any particular invention, let alone holding that any of the above-mentioned technologies from the Information Age should or should not receive patent protection.  This Age puts the possibility of innovation in the hands of more people and raises new difficulties for the patent law.  With ever more people trying to innovate and thus seeking patent protections for their inventions, the patent law faces a great challenge in striking the balance between protecting inventors and not granting monopolies over procedures that others would discover by independent, creative application of general principles.  Nothing in this opinion should be read to take a position on where that balance ought to be struck.

Emphasizing the negative consequences on progress and innovation of a decision in the ACLU's favor would have provided the Court with greater motivation to pause before taking a broad, sweeping and unnecessary position on where the balance should be struck on patenting isolated human DNA.  Myriad's brief gives the Court no basis for doing so.

Written by:

McDonnell Boehnen Hulbert & Berghoff LLP

McDonnell Boehnen Hulbert & Berghoff LLP on:

Readers' Choice 2017
Reporters on Deadline

"My best business intelligence, in one easy email…"

Your first step to building a free, personalized, morning email brief covering pertinent authors and topics on JD Supra:
Sign up using*

Already signed up? Log in here

*By using the service, you signify your acceptance of JD Supra's Privacy Policy.
Custom Email Digest
Privacy Policy (Updated: October 8, 2015):

JD Supra provides users with access to its legal industry publishing services (the "Service") through its website (the "Website") as well as through other sources. Our policies with regard to data collection and use of personal information of users of the Service, regardless of the manner in which users access the Service, and visitors to the Website are set forth in this statement ("Policy"). By using the Service, you signify your acceptance of this Policy.

Information Collection and Use by JD Supra

JD Supra collects users' names, companies, titles, e-mail address and industry. JD Supra also tracks the pages that users visit, logs IP addresses and aggregates non-personally identifiable user data and browser type. This data is gathered using cookies and other technologies.

The information and data collected is used to authenticate users and to send notifications relating to the Service, including email alerts to which users have subscribed; to manage the Service and Website, to improve the Service and to customize the user's experience. This information is also provided to the authors of the content to give them insight into their readership and help them to improve their content, so that it is most useful for our users.

JD Supra does not sell, rent or otherwise provide your details to third parties, other than to the authors of the content on JD Supra.

If you prefer not to enable cookies, you may change your browser settings to disable cookies; however, please note that rejecting cookies while visiting the Website may result in certain parts of the Website not operating correctly or as efficiently as if cookies were allowed.

Email Choice/Opt-out

Users who opt in to receive emails may choose to no longer receive e-mail updates and newsletters by selecting the "opt-out of future email" option in the email they receive from JD Supra or in their JD Supra account management screen.


JD Supra takes reasonable precautions to insure that user information is kept private. We restrict access to user information to those individuals who reasonably need access to perform their job functions, such as our third party email service, customer service personnel and technical staff. However, please note that no method of transmitting or storing data is completely secure and we cannot guarantee the security of user information. Unauthorized entry or use, hardware or software failure, and other factors may compromise the security of user information at any time.

If you have reason to believe that your interaction with us is no longer secure, you must immediately notify us of the problem by contacting us at In the unlikely event that we believe that the security of your user information in our possession or control may have been compromised, we may seek to notify you of that development and, if so, will endeavor to do so as promptly as practicable under the circumstances.

Sharing and Disclosure of Information JD Supra Collects

Except as otherwise described in this privacy statement, JD Supra will not disclose personal information to any third party unless we believe that disclosure is necessary to: (1) comply with applicable laws; (2) respond to governmental inquiries or requests; (3) comply with valid legal process; (4) protect the rights, privacy, safety or property of JD Supra, users of the Service, Website visitors or the public; (5) permit us to pursue available remedies or limit the damages that we may sustain; and (6) enforce our Terms & Conditions of Use.

In the event there is a change in the corporate structure of JD Supra such as, but not limited to, merger, consolidation, sale, liquidation or transfer of substantial assets, JD Supra may, in its sole discretion, transfer, sell or assign information collected on and through the Service to one or more affiliated or unaffiliated third parties.

Links to Other Websites

This Website and the Service may contain links to other websites. The operator of such other websites may collect information about you, including through cookies or other technologies. If you are using the Service through the Website and link to another site, you will leave the Website and this Policy will not apply to your use of and activity on those other sites. We encourage you to read the legal notices posted on those sites, including their privacy policies. We shall have no responsibility or liability for your visitation to, and the data collection and use practices of, such other sites. This Policy applies solely to the information collected in connection with your use of this Website and does not apply to any practices conducted offline or in connection with any other websites.

Changes in Our Privacy Policy

We reserve the right to change this Policy at any time. Please refer to the date at the top of this page to determine when this Policy was last revised. Any changes to our privacy policy will become effective upon posting of the revised policy on the Website. By continuing to use the Service or Website following such changes, you will be deemed to have agreed to such changes. If you do not agree with the terms of this Policy, as it may be amended from time to time, in whole or part, please do not continue using the Service or the Website.

Contacting JD Supra

If you have any questions about this privacy statement, the practices of this site, your dealings with this Web site, or if you would like to change any of the information you have provided to us, please contact us at:

- hide
*With LinkedIn, you don't need to create a separate login to manage your free JD Supra account, and we can make suggestions based on your needs and interests. We will not post anything on LinkedIn in your name. Or, sign up using your email address.