SCOTUS Passes on Petition to Reconsider Eligibility of Isolated Vitamin B3 Claims
“ChromaDex told the Supreme Court the [Federal Circuit] decision ‘threatens to chill innovation across the biotechnology sector.’”
The U.S. Supreme Court on Monday denied certiorari to review a February ruling of the U.S. Court of Appeals for the Federal Circuit (CAFC) that held claims of ChromaDex, Inc.’s patent on an isolated form of vitamin B3 are directed to unpatentable subject matter under Section 101.
The CAFC affirmed the Delaware district court’s grant of summary judgment for Elysium Health that the relevant claims of U.S. Patent No. 8,197,807, titled “Nicotinamide riboside kinase compositions and methods for using the same,” were invalid under Section 101 as being directed to a natural phenomenon, specifically, “compositions comprising isolated [NR], a naturally occurring vitamin present in cow milk.”
Nicotinamide riboside (NR) is a form of vitamin B3 that is naturally present in cow’s milk. The invention covers a composition containing isolated NR that results in increased biosynthesis of the coenzyme nicotinamide adenine dinucleotide (NAD+) upon oral administration.
In its petition to the Supreme Court, ChromaDex said the CAFC panel broke with its own precedent and created a split within its own court when it failed to apply the two-step Alice/Mayo test to its patent claims, instead applying “the standard derived from Association for Molecular Pathology v. Myriad Genetics, Inc., 569 U.S. 576 (2013), which omits consideration of whether a patent involves an ‘inventive concept.’” ChromaDex said the decision “threatens to chill innovation across the biotechnology sector.”
According to the petition, if the Federal Circuit had applied Alice/Mayo, it would have found that it had an inventive concept at step two, since the patent “claims a new and useful application of NR—by isolating it and formulating it for oral administration.” However, the panel agreed with the U.S. District Court for the District of Delaware that the claims are directed to a product of nature under Myriad and Diamond v. Chakrabarty. “As in Myriad, under the circumstances presented here, the act of isolating the NR compared to how NR naturally exists in milk is not sufficient, on its own, to confer patent eligibility,” wrote the court. The proper inquiry was defined in Chakrabarty, the opinion continued, where the Supreme Court said that, “to be patentable, the claimed composition must ‘ha[ve] markedly different characteristics and have the potential for significant utility.’” But naturally occurring NR in milk increases NAD+ biosynthesis when taken orally, just like the claimed invention.
The Federal Circuit further explained that, while addressing Alice/Mayo wasn’t even necessary here, the two-step test doesn’t save the claims anyway:
“[I]f resort to Alice/Mayo is necessary, then at step one we conclude the asserted claims are directed to a product of nature for the reasons stated above, and at step two the claims lack an inventive step because they are directed to nothing more than compositions that increase NAD+ bio-synthesis, which is the very natural principle that renders the claims patent-ineligible.”
Speaking yesterday at IPWatchdog’s Life Sciences Masters program taking place this week, Sherry Knowles of Knowles IP Strategies said the Myriad decision has had dire unintended consequences for isolated natural products, which include drugs as foundational as aspirin. Patents for such products are an “extinct dinosaur,” said Knowles. “Venture capitalists will not invest in companies with isolated natural products. Those are drugs of the past; we’re never going to have drugs like that again.”
Eileen McDermott
Eileen McDermott is the Editor-in-Chief of IPWatchdog.com. Eileen is a veteran IP and legal journalist, and no stranger to the intellectual property world, having held editorial and managerial positions at […see more]
