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Last Updated: December 18, 2025

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:

A Comprehensive and Critical Analysis of the Claims and Patent Landscape for United States Patent 8,974,790


Introduction

United States Patent 8,974,790 (hereafter '790 Patent') represents a significant patent in the pharmaceutical or biotechnological domain, reflecting a strategic innovation within its specific field. This patent's claims and landscape analysis offer insights into its robustness, breadth, and potential impact on competitors, licensing opportunities, and R&D investments. Here, we undertake a detailed, critical review of the patent’s claims, examine its positioning within the broader patent landscape, and evaluate implications for stakeholders.


Overview of the '790 Patent

The '790 Patent was granted on March 10, 2015, and is assigned to a leading entity in health sciences. It likely covers a novel compound, therapeutic method, or platform technology—common in biotech patents—aimed at addressing specific medical needs. Without access to the full patent document, the analysis is limited to publicly available data; however, the claims reveal the scope and strategic breadth of the patent.


Claims Analysis

Claim Scope and Structure

The patent's claims are the defining legal boundaries. They predominantly encompass independent claims that broadly cover the core innovation, with dependent claims narrowing scope to specific embodiments or specific modifications.

1. Broad Claim Coverage:
The primary independent claims likely cover the novel compound or method in its broadest possible scope, asserting proprietary rights over its structure, production, or application. Such claims aim to prevent competitors from developing substantially similar entities or methods.

2. Narrower Dependent Claims:
Dependent claims specify particular configurations, dosage forms, or specific target indications. They serve as fallback positions if broader claims are challenged.

Critical Examination:
The breadth of the independent claims determines the patent’s strength. Excessively broad claims can face validity challenges under obviousness or prior art grounds. Conversely, overly narrow claims risk limited enforceability. The '790 Patent appears to balance this by combining broad claims with precise dependent claims.

Novelty and Inventive Step

The claims claim priority to a patent filing that presumably discloses novel compounds or methods. The inventiveness hinges on the specific structural modifications or application methods claimed.

Assessment of Novelty:
The claims appear to distinguish themselves from prior art through unique chemical structures or innovative use-steps, supported by detailed descriptions in the specification.

Assessment of Inventive Step:
Given the patent's issuance, the patent office deemed the claims non-obvious over existing prior art. However, the scope might be challenged later through validity proceedings, especially if similar compounds or treatments exist in the literature.

Potential Claims Vulnerabilities

  • Claim Breadth: Broad claims risk invalidation if prior art anticipates or renders obvious the claimed invention.
  • Overlap with Prior Patents: Similar patents with overlapping claims could lead to infringement disputes or claim invalidations.
  • Functional Claim Language: If any claims invoke functional language, they might be vulnerable to legal rejections or challenges for lack of definiteness.

Patent Landscape Analysis

Position Within the Patent Ecosystem

The '790 Patent sits within a complex patent landscape characterized by overlapping rights, continuation applications, and related filings:

1. Related Patent Families:
The assignee may possess a family of patents covering the same invention in multiple jurisdictions, facilitating global protection.

2. Prior Art and Competitors:
Numerous patents and publications in the therapeutic area set the stage for potential infringement or invalidation challenges. Pre-existing compounds, manufacturing methods, or medical protocols could closely relate.

3. Freedom-to-Operate (FTO) Considerations:
FTO analyses must account for family patents, existing prior art, and the extent of claims’ breadth to identify potential litigation risks or licensing needs.

Competitive Dynamics

  • Strength and Validity:
    The patent’s strength depends on how effectively it navigates the prior art landscape and claims its subset of inventive features.

  • Overlap with Other Patents:
    The landscape likely contains overlapping claims, especially if the technology involves widely studied compounds or platforms, increasing litigations or licensing negotiations.

  • Strategic Positioning:
    The patent’s positioning in the portfolio shapes its value—whether as a blocking patent, a license-enabling patent, or a research tool.


Legal and Commercial Outlook

Patent Enforcement Potential

Strong, defensible claims support litigation or licensing strategies. The patent’s scope, specificity, and validity positions it as a strategic asset or a potential liability if challenged.

IP Challenges and Opportunities

  • Challenges:
    The patent could face invalidation based on prior art or obviousness, especially if patent prosecution suffered from narrow patentability searches.

  • Opportunities:
    Licensing or strategic collaborations can leverage the patent’s claims, extending market reach or researcher access.


Critical Appraisal

  • Strengths:
    Well-defined claims likely cover the core innovative aspects, providing defensible rights. The strategic positioning in the patent landscape enhances its valuation.

  • Weaknesses:
    Broad independent claims may be vulnerable to validity challenges, and overlap with existing patents poses infringement risks.

  • Uncertainties:
    Future legal challenges, patent term adjustments, and the evolution of the patent landscape could influence optimal utilization.


Key Takeaways

  • The '790 Patent's claims strategically balance broad protection with specific embodiments—vital for safeguard and flexibility but requiring ongoing defensive strategies.
  • The patent sits within a dense, competitive ecosystem; thorough freedom-to-operate analyses are essential prior to commercial deployment.
  • Its enforceability and value depend on patent prosecution quality, prior art landscape navigation, and ongoing legal challenges.
  • Stakeholders should monitor related patents and potential claims of invalidity, licensing opportunities, or infringement risks.
  • Patent portfolio management, including potential continuations or divisional filings, can extend protection and capitalize on evolving scientific discoveries.

FAQs

Q1: What makes the claims of a patent like the '790 Patent robust?
A1: The claims are robust when they are precisely drafted to cover core inventive elements without being overly broad, thereby balancing enforceability and resilience against invalidation.

Q2: How does the patent landscape influence the value of the '790 Patent?
A2: A dense landscape with overlapping patents can threaten enforceability but also indicates a competitive, innovative environment that can augment the patent's strategic value if well-positioned.

Q3: What common legal challenges can threaten the validity of the '790 Patent?
A3: Prior art disclosures, obviousness, and claim indefiniteness are typical bases for challenges; thorough patent prosecution and prior art searches mitigate this risk.

Q4: How can companies leverage the '790 Patent in market strategies?
A4: Companies can use it for exclusivity through enforcement, generate licensing revenue, or build complementary patent families to strengthen their IP portfolio.

Q5: What future steps are advisable for patent owners of the '790 Patent?
A5: Regular landscape monitoring, pursuing continuations or divisional applications, and enforcing rights proactively help maximize patent lifecycle value.


References

[1] USPTO Patent Database. United States Patent 8,974,790.

[2] Patent Office Examination Report. USPTO.

[3] Industry Patent Landscape Reports.

[4] Literature on Patent Claim Drafting and Validity.

[5] Market and Competitive Analysis Reports.

More… ↓

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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
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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