Cold Spring Harbor Laboratory v. Guardant Health, Inc.

CourtDistrict Court, D. Delaware
DecidedOctober 10, 2025
Docket1:25-cv-00263
StatusUnknown

This text of Cold Spring Harbor Laboratory v. Guardant Health, Inc. (Cold Spring Harbor Laboratory v. Guardant Health, Inc.) is published on Counsel Stack Legal Research, covering District Court, D. Delaware primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Cold Spring Harbor Laboratory v. Guardant Health, Inc., (D. Del. 2025).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF DELAWARE

COLD SPRING HARBOR LABORATORY,

Plaintiff, Court No. 1:25-cv-00263-JCG v.

GUARDANT HEALTH, INC.,

Defendant.

OPINION AND ORDER [Denying Defendant’s Partial Motion to Dismiss.]

Dated: October 10, 2025

Kelly E. Farnan and Sara M. Metzler, Richards, Layton & Finger, P.A., of Wilmington, DE; John M. Desmarais, Brian D. Matty, Kevin Goon, and Ashley DaBiere, Desmarais LLP, of New York, NY. Attorneys for Plaintiff Cold Spring Harbor Laboratory.

Brian E. Farnan and Michael J. Farnan, Farnan LLP, of Wilmington, DE; Edward R. Reines, Jones Day, of Palo Alto, CA; Derek C. Walter, Jones Day, of San Francisco, CA. Attorneys for Defendant Guardant Health, Inc.

Choe-Groves, Judge: Plaintiff Cold Spring Harbor Laboratory (“Plaintiff” or “Cold Spring Harbor”) filed this case against Defendant Guardant Health, Inc. (“Defendant” or “Guardant”) alleging infringement of U.S. Patent Numbers 10,947,589 (“’589 Patent”) and 12,234,510 (“’510 Patent”) (collectively, “Asserted Patents” or “Patents”). Pl.’s First Am. Compl. Patent Infringement (“Am. Compl.”) (D.I. 15); see U.S. Patent Number 10,947,589 (“’589 Patent”) (D.I. 15- 1); U.S. Patent Number 12,234,510 (“’510 Patent”) (D.I. 15-17).

Defendant filed Guardant’s Partial Motion to Dismiss. Def.’s Mot. Dismiss (“Defendant’s Partial Motion to Dismiss” or “Def.’s MTD”) (D.I. 24); Def.’s Opening Br. Supp. Partial Mot. Dismiss (“Def.’s Br.”) (D.I. 25). Plaintiff opposed

the motion, and Defendant filed a reply brief. Pl.’s Answering Br. Opp’n Guardant’s Partial MTD Cold Spring Harbor’s First Am. Compl. (“Pl.’s Resp. Br.”) (D.I. 32); Def.’s Reply Br. Supp. MTD (“Def.’s Reply Br.”) (D.I. 38). For the reasons discussed below, Guardant’s Partial Motion to Dismiss is

denied. BACKGROUND Cold Spring Harbor is a not-for-profit education corporation headquartered

in New York that conducts research and discovery, including in the areas of cancer, neuroscience, genomics, quantitative biology, and plant biology. Am. Compl. ¶¶ 2–4. This research has resulted in several applications, such as early cancer detection tests and liquid biopsies. Id. at ¶ 6. In addition, Cold Spring

Harbor’s research has led to the issuance of several patents, including the Asserted Patents. Id. Cold Spring Harbor is the owner by assignment of all right, title, and interest

in the Asserted Patents. Id. at ¶¶ 31, 37. The Asserted Patents are continuations of the same application filed in 2011. ’510 Patent; ’589 Patent. The ’510 Patent was issued by the United States Patent and Trademark Office (“USPTO”) on February

25, 2025, and the ’589 Patent was issued by the USPTO on March 16, 2021. ’510 Patent; ’589 Patent. Both Patents are titled “Varietal Counting of Nucleic Acids for Obtaining Genomic Copy Number Information,” and are directed to a method

of obtaining genomic copy number information from a sample of genomic material. ’510 Patent at Abstract; ’589 Patent at Abstract. Claim 1 of the ’510 Patent recites: A method comprising: a) obtaining segments of genomic nucleic acids from a sample containing the genomic nucleic acids: b) randomly tagging the segments of genomic nucleic acids with differing nucleic acid tags, thereby generating unique tagged nucleic acid molecules from the segments of genomic nucleic acids, such that each of the unique tagged nucleic acid molecules comprises a segment of the segments of the genomic nucleic acids from step (a) and a nucleic acid tag of the nucleic acid tags; c) subjecting the unique tagged nucleic acid molecules to a polymerase chain reaction (PCR), thereby generating copies of the unique tagged nucleic acid molecules; d) generating tag associated sequence reads by sequencing the copies of the unique tagged nucleic acid molecules of step (c); e) assigning each of the unique tagged nucleic acid molecules to a location on a genome by mapping each of the tag associated sequence reads of step (d) to a location in the genome; and f) in a plurality of locations in the genome, obtaining relative copy number information in the genomic nucleic acids from the sample based on the number of unique tagged nucleic acid molecules that have been assigned to each of the plurality of locations in the genome. ’510 Patent at 35:15–43. Claim 1 of the ’589 Patent, which is substantially similar to Claim 1 of the ’510 Patent, recites:

A method comprising: a) obtaining segments of genomic nucleic acids from a sample: b) tagging the segments with nucleic acid tags, thereby generating a plurality of unique tagged nucleic acid molecules, such that each of the unique tagged nucleic acid molecules comprises a segment of the segments of the genomic nucleic acids from step (a) and a nucleic acid tag of the nucleic acid tags; c) subjecting the plurality of the unique tagged nucleic acid molecules to a polymerase chain reaction (PCR), thereby generating amplified tagged nucleic acid molecules; d) generating tag associated sequence reads by sequencing the amplified tagged nucleic acid molecules of step (c); e) assigning each of the amplified tagged nucleic acid molecules to a location on a reference genome from the same species from which the sample has been obtained by mapping each of the tag associated sequence reads of step (d) to a location of the reference genome; and f) at a plurality of locations on the reference genome, counting the number of unique tagged nucleic acid molecules that have been assigned to the same location on the reference genome based on the mapping step to obtain a count for each location of the plurality of locations on the reference genome, thereby obtaining copy number information from genomic nucleic acids in the sample. ’589 Patent at 35:15–45. The methods claimed in the Asserted Patents represent improvements in the field of early cancer detection and aim to overcome prior problems in DNA sequencing, such as amplification bias producing inaccurate copy number information. Am. Compl. ¶¶ 33–35, 39–41. Guardant is a Delaware company that produces and markets blood tests that include “DNA library preparation, DNA sequencing, and DNA analysis steps to provide genomic profiles, including genetic copy number information.” Id. at ¶¶ 7–8. Cold Spring Harbor alleges that the Guardant360 blood test and the

Guardant360 CDx blood test practice the methods of the Asserted Patents, such as obtaining segments of nucleic acids from a sample, tagging the segments with nucleic acid tags, subjecting unique tagged nucleic acid molecules to polymerase

chain reaction, sequencing amplified copies of tagged nucleic acid molecules, assigning tag associated sequence reads to a location of a reference genome, and obtaining copy number information from the genomic nucleic acids in the sample. Id. at ¶¶ 44–57; Exs. 9–11, 13–14.

In January 2019, Guardant filed an opposition at the European Patent Office against Cold Spring Harbor’s European Patent No. EP2630263 (“the European Patent”). Id. at ¶ 66. The European Patent shares the same title as the Asserted

Patents, “Varietal Counting of Nucleic Acids for Obtaining Genomic Copy Number Information,” and claims priority to the same provisional patent applications. Id. at ¶¶ 62–65; Ex. 16 (“E.P. 2630263”) (D.I. 15-16). The European Patent contained similar disclosures as the Asserted Patents, with Claim 1 reciting:

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