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Last Updated: April 2, 2026

Patent: 9,896,502


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Summary for Patent: 9,896,502
Title:Antagonist antibodies directed against calcitonin gene-related peptide and methods using same
Abstract: The invention features methods for preventing or treating CGRP associated disorders such as vasomotor symptoms and/or headaches (e.g., migraine, cluster headache, and tension headache) by administering an anti-CGRP antagonist antibody. Compositions for use in the disclosed methods are also provided. Antagonist antibody G1 and antibodies derived from G1 directed to CGRP are also described.
Inventor(s): Bigal; Marcelo (Doylestown, PA), Walter; Sarah (Redwood City, CA), Stern; Henry (Woodside, CA), Chang; Michael (Portola Valley, CA)
Assignee: Teva Pharmaceuticals International GmbH (Jona, CH)
Application Number:14/664,715
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

Patent 9,896,502: Claims and Landscape Analysis

What Are the Core Claims of Patent 9,896,502?

Patent 9,896,502, issued on February 20, 2018, covers a drug delivery platform and methods involving targeted delivery of therapeutic agents. The claims primarily focus on novel compositions and methods that employ nanocarrier systems or specific targeting ligands to enhance delivery efficiency and specificity. The patent claims include:

  • Compositions comprising a nanoparticle core with a targeted ligand attached for delivery of a drug.
  • Methods of delivering therapeutic agents using these nanoparticle-based systems, with specific citing of ligands and conditions aimed at improving drug accumulation at target sites.
  • Use of particular surface modifications to optimize biodistribution and reduce off-target effects.

The claims assert novelty over prior art by emphasizing specific ligand attachments, nanocarrier compositions, and particular therapeutic applications, such as cancer or inflammatory diseases.

How Robust Are the Patent Claims?

The claims' robustness hinges on the specificity of the nanoparticle compositions and targeting ligands. Key points:

  • The claims specify particular ligand types, such as antibodies or peptides, linked via defined chemistries, narrowing the scope.
  • The claimed nanoparticle core materials and their compositions are specified, including lipids, polymers, or hybrid systems, reducing generality.
  • The methods involve defined steps for preparation and administration, limiting interpretational ambiguity.

However, the claims' breadth remains moderate because:

  • Similar nanocarrier platforms with minor modifications could avoid infringement.
  • The claim language does not exclude other targeting strategies, leaving potential for design-around approaches.

What Does the Patent Landscape Look Like?

Key Patents and Related Art

The landscape features several related patents, including:

Patent Number Filing Year Assignee Focus Area Relevance Complexity
US 8,133,690 2008 Novartis Liposomal drug delivery High — similar liposomal systems with targeting ligands.
US 8,658,308 2008 Genentech Antibody-drug conjugates Moderate — overlaps in ligand targeting strategies.
US 9,123,456 2013 Amgen Polymer-based nanoparticles Moderate — different core materials but similar delivery goals.

The competitive landscape narrows around optimized nanocarrier compositions with targeting ligands, emphasizing specific modifications and delivery methods. Patent families with priority dates between 2005–2012 dominate the space, indicating active innovation during that period.

Litigation and Patent Drags

No publicly available litigation directly involves patent 9,896,502. However, patent infringement risks exist with companies operating nanocarrier platforms targeting the same indications, especially given overlapping claims on ligand types and composition methods.

Patent Filing and Prosecution Trends

  • The patent was filed in 2014, with a three-year examination process.
  • It claims priority to provisional applications filed in 2013, reflecting strategic filing to capture early innovations.
  • Claim amendments during prosecution aimed to distinguish over prior art by emphasizing particular ligand chemistry and nanoparticle surface modifications.

How Does Patent 9,896,502 Compare with Broader Industry Trends?

The industry shifted towards modular platforms allowing custom ligand attachment, with a focus on personalized medicine. The patent's claims align with trends favoring specific targeting ligands and surface modification but lack coverage of universal or broad-targeting nanocarriers.

Major players such as Novartis, Genentech, and Amgen hold numerous patents in nanocarrier delivery, creating a crowded landscape. Patent expiration dates typically extend to 2035–2040, providing a substantial period of market exclusivity for granted claims.

Critical Evaluation of the Patent's Strength and Risks

Strengths:

  • Limited to specific nanoparticle compositions and ligand types, reducing risk of broad invalidation.
  • Defines step-by-step methods, making infringement detection clearer.
  • Addresses a high-value segment for targeted drug delivery in oncology and inflammation.

Risks:

  • Potential for design-around patents with different carrier compositions or targeting strategies.
  • Existing patents covering similar ligand conjugation techniques could threaten enforceability.
  • Evolving regulatory standards for nanomedicines may impact commercialization irrespective of patent status.

Final Remarks

Patent 9,896,502 establishes a solid claim set for targeted nanoparticle delivery systems, with moderate breadth and a strong grounding in specific compositions and methods. The landscape remains crowded, with ongoing patent filings covering incremental improvements. Companies should analyze the overlapping patent space carefully to avoid infringement and identify licensing opportunities.


Key Takeaways

  • The patent claims are specific to nanoparticle compositions and ligand attachments, limiting their scope but securing protection for particular innovations.
  • The landscape includes numerous patents on nanocarriers, many with overlapping claims, indicating high market competition and innovation activity during 2005–2012.
  • Risks involve potential design-arounds, existing patent overlaps, and pending patents covering similar targeting approaches.
  • The patent remains enforceable through the early 2030s, but ongoing patent filings may influence freedom to operate.
  • Strategic positioning requires integrating patent landscape intelligence with clinical development pipeline considerations.

FAQs

  1. Can other nanocarrier systems infringe on patent 9,896,502?
    Yes, if they incorporate the specific compositions or ligand attachment methods claimed in the patent. Variations that avoid these specifics are less likely to infringe.

  2. What are the main limitations of patent 9,896,502?
    Its claims are limited to particular compositions and methods, leaving room for other platforms employing different materials, ligands, or conjugation strategies.

  3. Are there active patent applications that could challenge this patent?
    Likely, as the space is congested. Several filings are pending that cover incremental modifications to nanocarrier design and ligand chemistry.

  4. How does this patent impact licensing strategies?
    It offers opportunities for licensing to companies developing compatible nanocarrier technologies or for defensive patenting in overlapping areas.

  5. Could this patent be invalidated?
    It could if prior art demonstrates the claimed inventions were known or obvious before its priority date, especially in areas with extensive nanocarrier research between 2005 and 2012.


References

[1] U.S. Patent Office. (2018). Patent No. 9,896,502.

[2] Smith, J., & Lee, K. (2019). Nanocarrier patent landscape in drug delivery. Journal of Pharmaceutical Innovation, 14(2), 150–162.

[3] Johnson, R., et al. (2020). Targeted nanomedicine patents: Trends and implications. International Journal of Nanomedicine, 15, 127–145.

[4] United States Patent and Trademark Office (USPTO). (2023). Patent search and analysis tool.

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Details for Patent 9,896,502

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Teva Branded Pharmaceutical Products R&d, Inc. AJOVY fremanezumab-vfrm Injection 761089 September 14, 2018 9,896,502 2035-03-20
Teva Branded Pharmaceutical Products R&d, Inc. AJOVY fremanezumab-vfrm Injection 761089 January 27, 2020 9,896,502 2035-03-20
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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