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Tag Archives: Gene

Supreme Court Oral Arguments in ACLU Myriad Gene Patent Case

Posted in 101; Myriad; Supreme Court Decisions

On April 15, 2013, the Supreme Court heard oral arguments in one of the most controversial and publicized biotech patent cases–the “ACLU/Myriad” gene patent case (e.g., The Association For Molecular Pathology v. USPTO). While it is always risky to predict the outcome of a Supreme Court case from the oral arguments, the Justices seemed to have accepted the U.S. Solicitor General’s arguments that cDNA molecules satisfy § 101, but seem unlikely to find that human genes can be patented.Continue reading this entry

Briefing The Supreme Court In Myriad

Posted in 101; Myriad; Personalized Medicine; Supreme Court Decisions

March 15, 2013 was a big deadline for patent applicants seeking to secure first-to-invent filing dates for U.S. patent applications, but April 15 will be a big day for the biotechnology industry, when the Supreme Court hears oral arguments in The Association of Molecular Pathology v. Myriad Genetics, Inc. (also known as the ACLU/Myriad “gene patent” case). Here I provide a brief summary of the parties’ briefs to the Supreme Court.Continue reading this entry

Supreme Court Grants Cert In Myriad To Decide If Human Genes Can Be Patented

Posted in 101; Myriad; Supreme Court Decisions

On November 30, 2012, the Supreme Court granted certiorari in the “ACLU/Myriad” gene patenting case (Association for Molecular Pathology v. Genetics, Inc.), guaranteeing that the debate over the patent-eligibility of human genes will continue for another round. The Court will review the August 16, 2012 Federal Circuit decision that held for the second time that Myriad’s claims directed to isolated DNA sequences satisfy 35 USC § 101.

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Deja Vu All Over Again In Federal Circuit’s August 16 Myriad Decision

Posted in 101; Federal Circuit Decisions; Myriad; Personalized Medicine

On August 16, 2012, just four weeks after it heard oral arguments, the Federal Circuit issued its second decision in Association for Molecular Pathology v. Myriad Genetics, Inc. (the ACLU ”gene patenting”/BRCAI case), which was on remand in view of the Supreme Court’s March 20, 2012 decision in Mayo v. Prometheus. The same three-judge panel heard the case on remand, and the judges reached essentially the same results on the interpretation of 35 USC § 101 as set forth in their July 29, 2011 decision. Thus, once again, Judge Lourie wrote the opinion for the court, Judge Moore concurred in the result, and Judge Bryson concurred in part and dissented in part.

All judges agree that at least one plaintiff has standing, that the diagnostic method claims based on “comparing” or “analyzing” DNA sequences are not patent-eligible, and that the drug screening method claim is patent-eligible. The court again held that all of the “isolated DNA” claims are patent-eligible, including those encompassing genomic DNA. Judge Bryson once again dissented with regard to the genomic DNA claims, but agreed with the majority that the cDNA claims satisfy 35 USC § 101.

While it is not surprising that the Federal Circuit reached the same conclusion in this decision, many will be relieved that they maintained the status quo as we move one step closer to final resolution of the issues by the Supreme Court.

For a more detailed review of the decision, please see this August 16, 2012 Foley & Lardner LLP Legal News Alert.

Non-Legal Perspectives On Isolated DNA: The Watson And Holman Amicus Briefs In The Myriad Remand

Posted in 101; Myriad

The most interesting briefs in the Federal Circuit remand of Association for Molecular Pathology v. Myriad Genetics, Inc. (the ACLU “gene patenting”/BRCA1 case) may be those submitted by James D. Watson and Christopher M. Holman, which each present non-legal perspectives on the issues before the court.Continue reading this entry

Myriad Calls ACLU Bluff On Standing

Posted in 101; Myriad; Personalized Medicine

As I wrote yesterday, the ACLU filed a Petition for Panel Rehearing in Association for Molecular Pathology v. USPTO, also known as the ACLU/Myriad “gene patenting” case, alleging factual and legal errors in the court’s July 29, 2011 decision on both the standing issue and the patent-eligibility issue. I was not impressed by the ACLU’s standing arguments, and now Myriad has filed its own Petition for Panel Rehearing challenging the standing of the ACLU plaintiffs. Because standing is a threshold issue, and because the factual basis of standing has changed, it is possible that the Federal Circuit will grant Myriad’s motion and rehear the case, at least on the standing issue.

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ACLU Files Petition For Panel Rehearing In Myriad

Posted in 101; Myriad; Personalized Medicine

As reported by Kevin Noonan on Patent Docs, plaintiffs-appellees (e.g., the ACLU) have filed a Petition for Panel Rehearing in Association for Molecular Pathology v. USPTO, also known as the ACLU/Myriad “gene patenting” case. The Petition alleges factual and legal errors in the court’s July 29, 2011 decision on both the standing issue and the patent-eligibility issue, but is not likely to be granted. While the petition may foreshadow the arguments being formulated for Supreme Court review, its most likely effect will be to delay that review, further extending the period of uncertainty that is hanging over isolated DNA claims.

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More On Myriad: Judge Moore’s Concurrence

Posted in 101; Federal Circuit Decisions; Myriad

I wrote previously on the apparent scientific basis for the differing opinions of Judge Lourie and Judge Bryson on the patent-eligibility of isolated genomic DNA claims in Association for Molecular Pathology v. USPTO. Here, I look at Judge Moore’s concurring opinion, which appears to agree in principal with Judge Bryson’s legal analysis, but places more emphasis on policy concerns to reach agreement with Judge Lourie.

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More On Myriad: The Chemical Divide–Judge Bryson

Posted in 101; Federal Circuit Decisions; Myriad

As I wrote previously, one interesting aspect of the recent Federal Circuit decision in Association for Molecular Pathology v. USPTO, is the apparent scientific basis for the differing opinions of Judge Lourie and Judge Bryson on the patent-eligibility of isolated genomic DNA claims. Unlike many concurring and dissenting opinions that are spurred by a different view of the law, Judge Lourie and Judge Bryson also appear to part ways based on different views of the science.

In this second part of a three-part series, I focus on the views of Judge Bryson.

Judge Bryson’s Dissent

Judge Bryson joined the court’s decision regarding standing, the method claims, and the cDNA claims, but disagreed with the holding that the “BRCA gene claims” are patent-eligible.

Judge Bryson read the Supreme Court’s Chakrabarty decision as requiring consideration of two factors:

  1. [T]he similarity in structure between what is claimed and what is found in nature and
  2. [T]he similarity in utility between what is claimed and what is found in nature.

(This appears to be the same test that Judge Moore applies, although she finds that the isolated genomic DNA claims are patent-eligible for policy reasons.)

Considering genomic DNA, Judge Bryson finds its to be “the same, structurally and functionally, in both the native gene and the isolated form of the gene.” Thus, Judge Bryson believes that claims directed to isolated genomic DNA (as opposed to cDNA) do not satisfy § 101.

The Insignificance Of Breaking Covalent Bonds

Judge Bryson acknowledges that covalent bonds are broken to obtain isolated genomic DNA from its natural state, but does not believe that this difference answers the patent-eligibility question. Quoting Linus Pauling, Judge Bryson writes,

[T]here is no magic to a chemical bond that requires us to recognize a new product when a chemical bond is created or broken, but not when other atomic or molecular forces are altered. . . . A chemical bond is merely a force between two atoms or groups of atoms strong enough “to make it convenient for the chemist to consider [the aggregate] as an independent molecular species.”

Judge Bryson criticizes Judge Lourie’s test for conferring patent eligibility based on the breaking of covalent bonds, but not other types of chemical bonds such as hydrogen bonds or ionic bonds, finding no logical reason or precedent for drawing such a distinction.

Using Genetics, Not Chemistry, To Evaluate The Claims

Judge Bryson suggests that Judge Lourie’s analysis took a wrong turn when it used principles of chemistry to evaluate the claimed subject matter. Judge Bryson explains that the both the language of the claims at issue and the focus of the claimed invention warrant the use of genetic principles instead.

For example, Judge Bryson points out the that the broadest gene claims do not recite specific DNA sequences, but rather recite isolated DNA coding for specific amino acid sequences. Because those claims encompass “[a]n almost incalculably large number” of DNA molecules that “share only one unifying characteristic,” they should be evaluated based on that shared, genetic characteristic—encoding the naturally occurring BRCA1 gene.

Applying such a framework, isolated genomic DNA is no different from the naturally occurring gene:

The isolated BRCA genes are identical to the BRCA genes found on chromosomes 13 and 17. They have the same sequence, they code for the same proteins, and they represent the same units of heredity.

Judge Bryson also emphasizes that isolated genomic DNA has been isolated according to its natural boundaries:

In the case of the BRCA genes . . . nature has defined the genes as independent entities by virtue of their capacity for protein synthesis and, ultimately, trait inheritance. Biochemists extract the target genes along lines defined by nature so as to preserve the structure and function that the gene possessed in its natural environment. In such a case, the extraction of a product in a manner that retains the character and function of the product as found in nature does not result in the creation of a human invention.

Similar Function More Important Than Different Structure

Judge Bryson’s views on the relative importance of structure and function are completely opposite from Judge Lourie’s. While Judge Lourie found structural differences alone sufficient to support patent-eligibility, Judge Bryson reached the opposition conclusion:

The structural differences between the claimed “isolated” genes and the corresponding portion of the native genes are irrelevant to the claim limitations, to the functioning of the genes, and to their utility in their isolated form. The use to which the genetic material can be put, i.e., determining its sequence in a clinical setting, is not a new use; it is only a consequence of possession. In order to sequence an isolated gene, each gene must function in the same manner in the laboratory as it does in the human body. Indeed, that identity of function in the isolated gene is the key to its value.

Judge Bryson concludes:

The naturally occurring genetic material thus has not been altered in a way that would matter under the standard set forth in Chakrabarty. For that reason, the isolation of the naturally occurring genetic material does not make the claims to the isolated BRCA genes patent-eligible.

The Hypothetical Analogies Are Instructive

While Judge Lourie was not concerned with the analogies of a “leaf plucked from a tree” or elemental lithium, Judge Bryson indicates that these analogies should not be ignored.

Judge Bryson believes that “extracting a gene is akin to snapping a leaf from a tree,” and so does not confer patent-eligibility.

[T]o argue that the isolated BRCA gene is patentable because in its native environment it is part of a much larger structure is no more persuasive than arguing that although an atom may not be patentable, a subatomic particle is patentable because it was previously part of a larger structure, or that while a tree is not patentable, a limb of the tree becomes a patentable invention when it is removed from the tree.

Thus, Judge Bryson bases his decision that the isolated, genomic DNA claims do not satisfy § 101 on his understanding that an isolated gene does not exhibit a materially different function from a native gene. Judge Bryson also would have invalidated the claims reciting fragments of genomic DNA, because the claims use open-ended language that encomasses naturally occurring, full-length sequences.

More On Myriad: The Chemical Divide–Judge Lourie

Posted in 101; Federal Circuit Decisions; Myriad

One interesting aspect of the recent Federal Circuit decision in Association for Molecular Pathology v. USPTO, is the apparent scientific basis for the differing opinions of Judge Lourie and Judge Bryson on the patent-eligibility of isolated genomic DNA claims.  Unlike many concurring and dissenting opinions that are spurred by a different view of the law, Judge Lourie and Judge Bryson also appear to part ways based on different views of the science.

In this first part of a three-part series, I focus on the views of Judge Lourie.

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Federal Circuit Issues Mixed Decision On Myriad Claims

Posted in 101; Federal Circuit Decisions; Myriad; Personalized Medicine; Prometheus

On July 29, 2011, the Federal Circuit issued its decision in Association for Molecular Pathology v. USPTO, also known as the ACLU/Myriad “gene patenting” case. In a mixed decision, the court held that “isolated DNA” claims are patent-eligible under 35 USC § 101, but that the “comparing” or “analyzing” method claims are not. With a 55 page opinion authored by Judge Lourie, a 31 page concurrence-in-part authored by Judge Moore, and a 19 page dissent-in-part authored by Judge Bryson, there is much to be analyzed before the full impact of this decision—and the contours of the holdings—will be understood.

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Diagnostic Test For Genetic Mutation Fails Written Description Requirement Where Mutation Was Not Disclosed

Posted in Federal Circuit Decisions

In Billups-Rothenberg, Inc. v. Associated Regional And University Pathologists, Inc., the Federal Circuit affirmed the district court’s grant of summary judgment of invalidity based on a lack of written description. The claims at issue were directed to methods of diagnosing a disease by detecting a specific genetic mutation associated with that disease, but the patent did not disclose any such genetic mutation.

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Federal Circuit Hears Oral Arguments in Myriad

Posted in 101; Myriad; Personalized Medicine

On April 4, 2011, Judges Lourie, Bryson and Moore at the U.S. Court of Appeals for the Federal Circuit heard oral arguments in Association for Molecular Pathology v. USPTO, also known as the ACLU/Myriad “gene patenting” case. This case has garnered extraordinary attention from the biotech, pharmaceutical, and health care industries, from academic and government researchers, from breast cancer patients and their families, and from the U.S. Department of Justice (DOJ) itself.

These groups disagree on the fundamental legal question of whether isolated DNA should be eligible for a patent, and also disagree on the fundamentally political question of whether the patenting of genes promotes or stifles innovation and development of new diagnostics and therapies. While the Federal Circuit’s decision in this case will be important, further resolution of the issues is likely to come from the Supreme Court. The ultimate decision could have a profound effect on existing intellectual property rights, and could impact current and future patent strategies, particularly in biotechnology-related fields.

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Solicitor General Asks To Argue Myriad on April 4

Posted in 101; Myriad; Personalized Medicine

In an unusual (if not unprecedented) move, the Solicitor General of the United States wrote a letter to the Federal Circuit asking that oral argument in Association for Molecular Pathology v. Myriad Genetics be scheduled for April 4, 2011. The Solicitor General (Neal Katyal) noted that “the United States will file an unopposed motion to participate in the oral argument” and that he intends to ”personally be presenting the oral argument on behalf of the United States.”

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Testing The Separation Of Powers: Will The Federal Circuit Rule Against The Department Of Justice On The Patent-Eligibility of DNA Claims?

Posted in 101; Myriad; Personalized Medicine

In a move that surprised many in the U.S. patent community, the Department of Justice filed a brief in the Federal Circuit appeal of Association for Molecular Pathology v. USPTO, arguing against the patentability of isolated genomic DNA sequences. This brief may raise the stakes in the appeal, and certainly shines a brighter spotlight on a case that already has garnered far more general media attention than any other patent case.

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Board Finds IBM Method of Analyzing Genomic Data Is Not Patent-Eligible

Posted in 101; Bilski; USPTO Board Decisions

Last week, Dennis Crouch highlighted recent decisions from the Patent Office Board of Appeals and Interferences that evaluated the patent-eligibility of claims under 35 USC § 101. One case with relevance to biotech and pharmaceutical applicants upheld the § 101 rejection of IBM claims directed to methods for clustering genes having potential functional similarity by comparing gene expression profiles based on both the time and intensity of gene expression. In that case, In re Kelkar, the Board found that the claims failed the “machine or transformation test” (MOT) and were directed to an abstract idea, despite language that invoked the use of a computer.

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