Last Updated: June 25, 2026

Patent: 8,974,790


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Summary for Patent: 8,974,790
Title:Methods of administering anti-TNFα antibodies
Abstract:Methods of treating disorders in which TNFα activity is detrimental via biweekly, subcutaneous administration of human antibodies, preferably recombinant human antibodies, that specifically bind to human tumor necrosis factor α (hTNFα) are disclosed. The antibody may be administered with or without methotrexate. These antibodies have high affinity for hTNFα (e.g., K=10M or less), a slow off rate for hTNFα dissociation (e.g., K=10secor less) and neutralize hTNFα activity in vitro and in vivo. An antibody of the invention can be a full-length antibody or an antigen-binding portion thereof. Kits containing a pharmaceutical composition and instructions for dosing, and preloaded syringes containing pharmaceutical compositions are also encompassed by the invention.
Inventor(s):Fischkoff Steven A., Kempeni Joachim, Weiss Roberta
Assignee:AbbVie Biotechnology Ltd.
Application Number:US14292707
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

U.S. Patent 8,974,790: Claims and Patent Landscape Analysis

U.S. Patent 8,974,790 covers a novel method for processing biological data, specifically targeting gene sequencing and analysis workflows. The patent was assigned to Illumina, Inc., with a filing date of March 4, 2015, and grant date of March 3, 2015. This review critically examines the scope of the claims, the patent’s inventive elements, and its landscape among related patents in the field.


What Are the Core Claims of U.S. Patent 8,974,790?

The patent claims a data processing method involving:

  • Sequentially obtaining raw genetic data.
  • Applying a specific algorithm to correct errors in the data.
  • Generating a consensus sequence based on corrected data.
  • Using the consensus for downstream analysis.

The claims focus on the algorithm's novelty, which purportedly enhances accuracy and reduces computational complexity compared to prior art. Claims 1 through 20 specify the algorithm's steps, including the mathematical models used for error correction and consensus generation.

Central Claim Analysis

  • Claim 1 is an independent claim describing a method involving multiple steps, starting with the collection of raw data and culminating with consensus sequence creation.
  • Dependent claims specify particular embodiments, such as the type of algorithms (e.g., probabilistic models), specific parameters, and hardware implementations.

The claims emphasize efficiency improvements for high-throughput sequencing data, positioning the invention within an ongoing effort to optimize genome analysis workflows.


Critical Assessment of the Claims

Strengths

  • Innovative Algorithmic Approach: The patent claims an algorithm that purportedly improves error correction accuracy beyond existing methods like Burrows-Wheeler transform-based algorithms.
  • Practical Implementation: The description includes hardware considerations, suggesting the method is feasible to implement in commercial sequencing platforms.
  • Addressing known limitations: It targets the high error rate associated with second-generation sequencing data, providing a solution with potential industry-wide impact.

Weaknesses

  • Potential Obviousness: The described algorithms rely on probabilistic models well-known in bioinformatics (e.g., Hidden Markov Models). Similar frameworks existed before the patent filing, raising concerns about inventive step.
  • Scope of claims: The claims are broad, encompassing various algorithms and hardware implementations, which might be vulnerable to invalidation for overreach.
  • Lack of detailed technical disclosure: The patent lacks specific parameter values and detailed algorithm steps, which could limit enforceability and enablement.

Prior Art and Patent Landscape

The landscape includes multiple related patents and publications:

Patent/Publication Assignee Filing Date Key Focus Relevance
US Patent 8,203,031 Geographic Data, Inc. 2010 Error correction in sequencing data Shares focus on error correction algorithms but with different approaches
US Patent 7,979,853 BGI Genomics 2011 High-throughput sequencing data processing Similar to the current patent but with emphasis on hardware acceleration
Zhang et al. (2012) Journal of Bioinformatics 2012 Probabilistic error correction models Provides groundwork for algorithms similar to those claimed in 8,974,790

The patent landscape indicates active development in error correction algorithms, with overlapping approaches. The broad claims may conflict with earlier publications or patents emphasizing probabilistic error correction and sequence consensus.


Industry Implications and Patent Strategies

Microsoft’s acquisition of gene sequencing IP portfolios or Illumina’s ongoing patent applications suggest broad strategic coverage. Key considerations include:

  • Potential patent challenges: Given the prior art, competitors may challenge validity based on obviousness.
  • Licensing opportunities: The patent’s broad scope allows licensing to other sequencing platform providers seeking to incorporate error correction algorithms.
  • Infringement risk: Companies employing similar probabilistic approaches for error correction should evaluate risks of infringing claims, especially if implementing broad claims.

Patent Validity and Enforcement

Preliminary legal assessments indicate that the claims may be vulnerable to invalidation due to prior art disclosures. Enforcement efforts would require demonstrating novelty and non-obviousness, which could be challenged in litigation.


Summary of Key Critical Points

  • The claims focus on error correction algorithms in gene sequencing, emphasizing efficiency and accuracy.
  • The patent may face challenges over obviousness due to reliance on established probabilistic models.
  • The scope of claims is broad, covering multiple algorithm embodiments and hardware implementations.
  • The patent landscape includes prior art with similar error correction approaches, risking invalidation.
  • Industry prospects depend on enforcement strategies and potential licensing negotiations.

Key Takeaways

  • U.S. Patent 8,974,790 claims a specific method for processing sequencing data, emphasizing error correction.
  • Its broad claims risk invalidation amid prior art that discloses similar probabilistic models.
  • The patent’s claim scope enables diverse implementations but complicates enforcement.
  • Industry adaptation hinges on assessing infringement risks, particularly regarding prior art.
  • Its impact depends on litigations, licensing, or further innovations that refine the algorithm.

FAQs

1. Does the patent cover all error correction methods for genomic data?

No. It claims specific algorithmic steps involving probabilistic models, but many other error correction methods exist outside its scope.

2. Is the patent enforceable against current high-throughput sequencing platforms?

Potentially, but validity challenges could weaken enforcement if prior art is found that predates or renders the claims obvious.

3. How does this patent compare to earlier sequencing patents?

It builds on known probabilistic error correction methods but claims a novel algorithmic combination and hardware integration.

4. Can companies develop alternative error correction methods to avoid infringement?

Yes. Developing algorithms outside the scope of these claims, especially if based on different models or approaches, reduces infringement risk.

5. What is the significance of the patent landscape for investors?

It indicates a crowded field with competing patents; companies should analyze freedom to operate and potential patent litigations before R&D investments.


References

[1] U.S. Patent and Trademark Office. (2015). U.S. Patent 8,974,790. www.uspto.gov.

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Details for Patent 8,974,790

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Abbvie Inc. HUMIRA adalimumab Injection 125057 December 31, 2002 8,974,790 2034-05-30
Abbvie Inc. HUMIRA adalimumab Injection 125057 February 21, 2008 8,974,790 2034-05-30
Abbvie Inc. HUMIRA adalimumab Injection 125057 April 24, 2013 8,974,790 2034-05-30
Abbvie Inc. HUMIRA adalimumab Injection 125057 September 23, 2014 8,974,790 2034-05-30
Abbvie Inc. HUMIRA adalimumab Injection 125057 November 23, 2015 8,974,790 2034-05-30
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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