Currently Browsing CPLRG™ by: Case Name
Browse By: Case Date | Case Number

  1. Pages:
  2. 1
  3. 2
  4. 3
  5. 4
  6. 5
  7. 6
  8. 7
  9. ...
  10. 17

American Invents Act No.3 - CPLRG™ 0078 - Dec. 4, 2011

AIA Analysis: Section-by-Section Review of America Invents Act with Cross-References

The American Invents Act contains 37 sections.  The sections vary greatly in relative length, importance and generality.  For example, Section 3 makes a fundamental change in the priority principle by substituting a “first inventor to file” principle for the historic “first to invent” principle.  In contrast, Section 24 names the new Detroit satellite office of the Patent and Trademark Office.

The substantive amendments to the patent statutes  made by the AIA are best understood against the background of existing law.  Attached is a draft section on the AIA, organized section-by-section.  For each section, it analyzes the changes in the Patent Act made by the AIA and their impact, together with cross references to discussions of the affected subject area in the Chisum on Patents treatise.  The AIA Analysis is here:  AIAOverview

Anascape, Ltd. v. Nintendo of America, Inc. - CPLRG™ 0048 - Apr. 13, 2010

Anascape, Ltd. v. Nintendo of America, Inc., 601 F.3d 1333 (Fed. Cir. 2010) (NEWMAN & Dyk; GAJARSA, concurring)Anascape04132010

MAJOR ISSUES: written description; new matter; continuation-in-part application redesignated as continuation Read CPLRG™ 0048

Ariad Pharmaceuticals, Inc. v. Eli Lilly & Co. - CPLRG™ 0016 - Mar. 22, 2010

Ariad Pharmaceuticals, Inc. v. Eli Lilly & Co., 598 F.3d 1336 (Fed. Cir. 2010) (En Banc) (LOURIE, Michel, Newman, Mayer, Bryson, Gajarsa, Dyk & Prost; NEWMAN, additional views; GAJARSA, concurring; RADER & Linn, dissenting-in-part & concurring-in-part; LINN & Rader, dissenting-in-part & concurring-in-part)

Ariad03222010

MAJOR ISSUES: Written description of invention (Section 112); requirement separate from enablement; original claims; support for generic claims; invention described by biological function Read CPLRG™ 0016

Ass'n for Molecular Pathology v. United States Patent and Trademark Office - CPLRG™ 0073 - Jul. 29, 2011

Ass’n for Molecular Pathology v. United States Patent and Trademark Office, 2011 U.S. App. LEXIS 15649 (Fed. Cir. July 29, 2011) (LOURIE, MOORE, concurring in part; BRYSON, concurring in part and dissenting in part)  MyriadGenetics07292011.fc

Major issues:  claims to isolated genes; claims to comparing gene sequences to detect cancer; Bilski; patent eligible subject matter

In a much-watched case, known generally by the name of the patent owner, Myriad Genetics, a Federal Circuit panel addressed Section 101 issues concerning claims to isolated DNA and to methods of screening for cancer by DNA testing.  The panel also addressed the issue whether the plaintiffs, “an assortment of medical organizations, researchers, genetic counselors, and patients” had “standing under the Declaratory Judgment Act to challenge Myriad’s patents.”
.
On standing, the Federal Circuit held that “at least one plaintiff,” a doctor, had standing.  On the merits, the majority distinguished between claims to isolated genes and screening by cell growth rates and claims to methods of comparing DNA sequences.  The former but not the latter were for patent eligible subject matter.

Pertinent to this decision is the Supreme Courts June 20, 2011 grant of certiorari in Prometheus Laboratories, Inc. v. Mayo Collaborative Services, 628 F.3d 1347, CPLRG 0071 (Fed. Cir. 2010), which involves Section 101 issues on patent claims concerning medical diagnostics.

UPDATE: The Supreme Court reversed in the Prometheus case.  See CPLR 0079.    On March 26, 2012, the Supreme Court remanded the Myriad Genetics case.  Thereafter, on August 16, 2012, the Federal Circuit, in a divided panel decision, affirmed its prior approach.  Myriad2012.fc Thus, applying Mayo, the majority held that the “composition claims to `isolated” DNA molecules” did not “cover patent-ineligible products of nature under § 101 because each of the claimed molecules represents a nonnaturally occurring composition of matter.”  It also held that the “method claim to screening potential cancer therapeutics via changes in cell growth rates of transformed cells” as not “directed to a patent-ineligible scientific principle.”  However, it held that the “method claims directed to `comparing’ or `analyzing’ DNA sequences are patent ineligible” because the “claims include no transformative steps and cover only patent-ineligible abstract, mental steps.”

Read CPLRG™ 0073

Association for Molecular Pathology v. Myriad Genetics, Inc. - CPLRG™ 0085 - Jun. 13, 2013

Association for Molecular Pathology v. Myriad Genetics, Inc., 133 S. Ct. 2107 (2013) (Thomas).  For the Court’s slip opinion, click here.AMPMyriad06132013

AMP is a first-order, high-profile decision by the Supreme Court.  It was front-page news in the general media.

Like last year’s decision in Mayo Collaborative Services v. Prometheus Labs., Inc., 132 S. Ct. 1289 (2012), in which the Court held certain diagnostic methods to be unpatentable “principles of nature,” and unlike the Federal Circuit’s May 10, 2013, decision on Section 101’s application to computer-implemented methods and and systems, CLS Bank International v. Alice Corp. Pty., the Supreme Court was unanimous in an opinion by Justice Thomas.

Only Justice Scalia wrote separately, concurring because of his personal doubts about the full accuracy of the Court’s description of the molecular biology involved.

In AMP, the Court held that  “genes and the information they encode are not patent eligible under §101 simply because they have been isolated from the surrounding genetic material.”  A patent owner had “found an important and useful gene,” to wit, one the mutations of which are indicative of an increased risk of breast cancer, but “separating that gene from its surrounding genetic material is not an act of invention.”  On the other hand, complementary DNA (cDNA) is “patent eligible because it is not naturally occurring.”  Unlike isolated DNA (deoxyribonucleic acid), cDNA omits the non-coding regions (introns) and retains the coding regions (exons) of the natural DNA nucleotide sequence.  It is not an unpatentable product of nature even though nature dictates the nucleotide sequence, to wit, one that contains the same protein-coding information, because “a lab technician unquestionably creates something new when cDNA is made.” Read CPLRG™ 0085

Currently Browsing CPLRG™ by: Case Name
Browse By: Case Date | Case Number

  1. Pages:
  2. 1
  3. 2
  4. 3
  5. 4
  6. 5
  7. 6
  8. 7
  9. ...
  10. 17

©2010 Donald S. Chisum - All Rights Reserved

Website design by Bluegrass Internet Services