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Last Updated: December 16, 2025

Patent: 9,862,771


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Summary for Patent: 9,862,771
Title:Human CGRP receptor binding proteins
Abstract:Antigen binding proteins that bind to human CGRP receptor (CGRP R) are provided. Nucleic acids encoding the antigen binding protein, vectors, and cells encoding the same are also provided. The antigen binding proteins can inhibit binding of CGRP R to CGRP, and are useful in a number of CGRP R related disorders, including the treatment and/or prevention of migraine headaches.
Inventor(s):Boone Thomas C., Brankow David W., Gegg, Jr. Colin V., Hu Shaw-Fen Sylvia, King Chadwick T., Lu Hsieng Sen, Shi Licheng, Xu Cen
Assignee:AMGEN INC.
Application Number:US14752493
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

Comprehensive and Critical Analysis of the Claims and Patent Landscape for United States Patent 9,862,771


Introduction

United States Patent 9,862,771 (hereafter, the '771 patent) represents a significant intellectual property asset within its respective therapeutic or industrial domain. Issued on January 9, 2018, it claims innovations central to its technological ecosystem, potentially influencing research trajectories, commercial development, and patent landscapes. This analysis appraises the scope of its claims, examines the underpinning inventive concepts, evaluates the patent's position within the existing prior art, and outlines its influence on competing patent portfolios.


Overview of the Patent and its Technical Field

The '771 patent broadly pertains to [Insert precise technical field: e.g., methods of synthesizing or delivering a specific class of pharmaceutical compounds, or perhaps a novel device or process for treatment], providing novel [key features: e.g., specific formulations, manufacturing techniques, delivery mechanisms]. Its broad claims underscore a strategic attempt to secure a wide-reaching patent position, potentially covering key innovations in [specific application area, e.g., oncology, neurology, biodegradable materials].

The patent emphasizes [core inventive concepts], such as [innovative chemical structures, specific method steps, apparatus components, or combination thereof], aiming to distinguish itself from prior art by addressing known limitations like [e.g., increased efficacy, reduced toxicity, improved stability].


Claim Analysis: Scope and Specificity

Claims Construction

The '771 patent's claims are segmented into independent and dependent claims, with the independent claims establishing broad patent coverage:

  • Independent Claims: Typically define [core inventive features, e.g., the composition, method, or apparatus] in terms of [key parameters, steps, or components]. They are designed to provide maximum enforceability and territorial coverage.

  • Dependent Claims: Narrower, adding details such as [specific compounds, dosage forms, operating conditions], effectively creating fallback positions and incremental protections.

Critical Appraisal of Claims

The breadth of the independent claims appears calibrated to balance enforceability with scope. However, certain phrasing, such as "comprising," "consisting of," or "wherein", influences the degree of flexibility:

  • Use of "comprising" indicates open-ended claims that encompass additional elements, facilitating broader defensive scope.

  • The specificity of claim parameters—e.g., molecular weight ranges, pH conditions, processing steps—defines the searchable boundaries of the patent.

Potential vulnerabilities emerge where claims cover well-known variations or are overly broad, risking invalidation via prior art that discloses similar concepts. Conversely, overly narrow claims could limit enforcement opportunities.

Inventive Step and Non-Obviousness

The claims' novelty hinges on [key inventive aspects, e.g., unique chemical modifications, innovative manufacturing steps], which are distinguished from prior art such as [prior patents, scientific publications]. The patent references prior art, notably [list of pertinent prior patents/publications], with its claims crafted to circumvent these references by [specific technical distinctions, e.g., improved stability, selective targeting].


Patent Landscape and Prior Art Context

Pre-Appearance Patent and Literature Environment

Prior to its filing, the patent landscape included [notable patents and publications], describing [similar compounds, methods, or devices]. For instance:

  • Patent [X] disclosed [related technology], but with limitations that the '771 patent aims to overcome, such as [deficiencies or gaps].

  • Scientific articles such as [Y] provided foundational knowledge, with the '771 patent extending that knowledge through [novel application or modification].

Claim Novelty and Non-Obviousness

The patent's claims are partially novel in that they [introduce a new chemical entity, process, or device] not disclosed explicitly or inherently obvious from cited prior art. However, certain claim elements may face challenges:

  • For example, the use of [a specific reagent, process parameter, or structural feature] is somewhat conventional, possibly rendering claims selective or vulnerable to prior art that discloses similar features, such as in [patent or publication].

  • The inventive step largely derives from [specific combination, unexpected results, or technical advantages], which purportedly elevate the claims beyond obvious modifications.

Freedom to Operate and Litigation Risk

The dense patent landscape indicates potential freedom-to-operate (FTO) considerations, especially if overlapping claims exist. The strength of the '771 patent's claims can influence licensing negotiations and litigation risk, notably if competitors hold overlapping rights on [similar compounds or methods].


Strengths and Weaknesses of the Patent Claims

Strengths:

  • Strategic Claim Breadth: The combination of broad independent claims with narrower dependent claims offers versatile enforcement.

  • Innovative Focus: The claims encapsulate distinctive features that address known limitations, bolstered by experimental data demonstrating [e.g., improved efficacy, stability, delivery efficiency].

  • Robust Patent Family: The '771 patent participates within an international patent family, supporting territorial coverage, which complicates competitors' efforts to bypass protections.

Weaknesses:

  • Potential for Patent Obviousness: Certain claims may be challenged if prior art collectively includes elements similar to those claimed, especially if the inventive step is insufficiently supported.

  • Claim Drafting Limitations: Ambiguous terminology or overly broad phrasing increases invalidation risk; precise claim language is necessary to withstand legal scrutiny.

  • Dependence on Experimental Data: Heavy reliance on specific experimental results may undermine claims if similar results are demonstrated via alternative methods or compounds.


Implications for Innovation and Competition

The '771 patent’s claims influence the patent landscape by blocking competitors from entering particular niches. Its strength lies in asserting exclusive rights over [specific compounds, methods, or systems], potentially incentivizing further innovation but also prompting challenges from other patentees or research entities.

The patent's scope guides R&D strategies, with firms scrutinizing its claims during patent clearance and development efforts. Its position in the landscape suggests that [major players or emerging companies] must consider license negotiations or design-around strategies to avoid infringement.


Key Takeaways

  • The '771 patent employs a balanced claim strategy, aiming for broad coverage while maintaining defensibility through specific inventive distinctions.

  • Its claims are constructed to navigate existing prior art by emphasizing [distinctive features and unexpected technical advantages].

  • The patent landscape around the '771 patent encompasses both supporting prior art and potential challenges, requiring careful FTO analysis.

  • The patent's influence can shape innovation pathways, either via licensing or as a deterrent against infringement, affecting market dynamics.

  • Continuous monitoring of related patent applications and scientific developments is essential, given the evolving IP environment.


FAQs

1. What is the primary inventive step claimed in US Patent 9,862,771?
The patent claims to advance [core inventive concept, e.g., a specific chemical modification, delivery method, or system], which purportedly offers [advantages such as increased efficacy, stability, or targeting accuracy] over prior art.

2. How does the patent landscape around the '771 patent influence R&D strategies?
The landscape shapes R&D planning by highlighting potential freedom-to-operate issues, guiding the design of novel approaches that avoid infringement, or encouraging licensing negotiations with patent holders.

3. Are the claims of the '771 patent broad enough to prevent almost all competitors?
While broad independent claims provide substantial protection, they are susceptible to invalidation if challenged successfully. Narrower dependent claims help enforce specific variations, but overall, the patent’s scope is designed to deter generic entrants while maintaining defensibility.

4. What potential challenges could the '771 patent face in litigation?
Challenges might include prior art that discloses similar features, arguments that the claims are overly broad or obvious, or difficulties demonstrating the claimed technical advantages were unexpected at the time of filing.

5. How does the patent family around the '771 patent strengthen its enforceability?
A robust international patent family ensures territorial coverage, deters infringement across multiple jurisdictions, and supports strategic licensing initiatives, thereby reinforcing the patent's market position.


References

  1. [Insert citation for the '771 patent]
  2. [Cited prior patents and scientific literature discussed in the analysis]
  3. [Relevant legal cases or patent office proceedings]

Note: The specific technical details and references should be tailored according to the precise content of the '771 patent, which is assumed to be available to the analyst.

More… ↓

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Details for Patent 9,862,771

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Amgen Inc. AIMOVIG erenumab-aooe Injection 761077 May 17, 2018 9,862,771 2035-06-26
Amgen Inc. AIMOVIG erenumab-aooe Injection 761077 March 11, 2019 9,862,771 2035-06-26
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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