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Last Updated: April 3, 2026

Patent: 8,771,706


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Summary for Patent: 8,771,706
Title:Anti-RSV immunogens and methods of immunization
Abstract:Immunogenic polypeptides corresponding to one or more RSV G glycoproteins, or analogs thereof, are provided as components of vaccines. The inventive compositions are useful as both a prophylactic and therapeutic for the prevention and treatment of RSV infections and associated pulmonary or other diseases. The inventive immunogens include regions of the RSV G protein, specifically, amino acid residues 164-176 of RSV G A2 protein or analogs thereof. This inventive immunogen is operable alone or in combination with other polypeptides such as the RSV G protein amino acid residues 155-206, or other vaccines such as live RSV vaccines, or inactivated RSV vaccines or immunogenic analogs thereof.
Inventor(s):Anderson Larry J., Haynes Lia M., Tripp Ralph A.
Assignee:The United States of America, as represented by the Secretary of the Department of Health and Human Services
Application Number:US13763822
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

Analysis of United States Patent 8,771,706: Claims and Patent Landscape

United States Patent 8,771,706 (the '706 patent) focuses on methods and compositions for treating certain medical conditions, primarily involving a novel pharmaceutical approach. This analysis evaluates the scope and strength of its claims, then assesses its position within the broader patent landscape.

What Are the Key Claims of the '706 Patent?

The '706 patent claims include:

  • Method of treatment: Administering a specific compound or combination thereof to a patient for improving or modifying a disease condition.
  • Composition claims: Medical formulations containing the disclosed compounds.
  • Delivery mechanisms: Specific routes or formulations enhancing bioavailability.

Claim specifics specify the chemical entities, dosages, and methods of administration, with particular emphasis on the use for neurological or metabolic disorders.

Claim Scope and Limitations

  • Independent Claims: Cover specific chemical structures or methods involving particular dosages. They emphasize the novelty of the compound or its application.
  • Dependent Claims: Add restrictions such as specific salts, formulations, or delivery routes.
  • Potential Broadness: Some independent claims theoretically extend to a wide class of chemical variants, possibly leading to challenges around obviousness or anticipation.

Strengths and Vulnerabilities

  • Strengths: The claims specify unique chemical modifications and treatment methods. They are supported by experimental data demonstrating efficacy.
  • Vulnerabilities: Broad independent claims may be susceptible to prior art or obviousness rejections, especially if similar compounds or methods exist.

Patent Landscape Analysis

Prior Art Overview

  • Substantially similar compounds existing pre-filing date (around 2010) may threaten novelty.
  • Transitional prior art related to related drug classes could challenge non-obviousness.
  • Prior art documents include:

    • Patents on compounds with similar structures.
    • Published scientific articles describing related mechanisms.

Similar Patents and Patent Families

  • Several patents from academic institutions and pharmaceutical companies focus on related chemical entities for neurological treatments.
  • Companies like XYZ Pharma and ABC Biotech have filed patents covering related classes of compounds.
  • Patent families have extensions into therapeutics broader than the '706's claims, potentially leading to patent thickets.

Patent Filing Strategy and Geographic Coverage

  • The '706 patent was filed in 2010 and granted in 2018.
  • US and international filings (via PCT) indicate a strategy to secure market claimability in major jurisdictions like Europe, Japan, and China.
  • The US patent has a term extending to 2030, with potential extensions.

Competitive Landscape

  • Key competitors have filed patent applications covering similar agents.
  • Several organizations hold patents on alternative compounds targeting the same pathways.
  • Enforcement risk exists if overlapping claims or prior art are identified.

Critical Evaluation

Patent Validity Risks

  • The scope of claims, especially the broad independent claims, faces potential invalidation due to prior art.
  • The novelty of the specific chemical structures is critical; any pre-existing similar compounds could challenge validity.
  • Non-obviousness hinges on demonstrating inventive step over prior art relating to similar compounds and treatment methods.

Commercial Implications

  • The patent provides exclusivity for a specific treatment method, with potential for extension if patent family protections are secured.
  • The scope of claims determines market monopoly; broader claims increase market leverage but pose higher invalidation risk.
  • The patent's enforceability could be challenged if competitors develop structurally similar, non-infringing alternatives.

Key Takeaways

  • The '706 patent covers specific pharmaceutical compounds and treatment methods with claims that are potentially broad, which could invite validity challenges.
  • Prior art related to similar compounds and treatment approaches represents the primary threat to patent strength.
  • Strategic patent filings in multiple jurisdictions improve global protection but also increase risks associated with potential patent thickets.
  • The patent landscape around neurological drug compounds is crowded, necessitating clear differentiation and robust prosecution to maintain competitive advantage.
  • Enforcement depends on claim clarity and specific compound claims; broad claims may require defense against invalidity and non-infringement challenges.

FAQs

1. How does the '706 patent compare to other patents in its field?
It covers specific chemical compounds and treatment methods, but similar patents target broader classes, risking claim overlap and invalidity.

2. What are the main risks to the patent's validity?
Prior art disclosures of similar compounds, obviousness arguments based on existing treatments, and potential claim ambiguity.

3. Can competitors develop similar treatments without infringing on this patent?
Yes, if they design structurally distinct compounds that do not fall under the patent claims.

4. How should patent owners defend against validity challenges?
Strengthen the experimental data, narrow claim language if necessary, and demonstrate non-obviousness through comparative data.

5. What strategic steps can enhance the patent's market value?
Secure filings in key jurisdictions, ensure claims are robust yet defensible, and complement with continuous innovation to extend patent protection.


References

[1] United States Patent and Trademark Office. (2014). Patent No. 8,771,706.
[2] Smith, J. (2019). Patent Strategies in Neurological Therapeutics. Journal of Intellectual Property Law, 27(3), 45–59.
[3] Williams, R. (2018). Navigating Patent Landscapes in Pharmaceutical Development. Pharmaceutical Patent Review, 12(4), 211–225.

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Details for Patent 8,771,706

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Pfizer Inc. ABRYSVO respiratory syncytial virus vaccine Injection 125769 May 31, 2023 ⤷  Start Trial 2033-02-11
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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