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Profile for Japan Patent: 2017141296


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US Patent Family Members and Approved Drugs for Japan Patent: 2017141296

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
RE48468 Oct 27, 2028 Sarepta Theraps Inc EXONDYS 51 eteplirsen
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2017141296

Last updated: August 24, 2025

Introduction

Japan Patent JP2017141296 pertains to a novel pharmaceutical invention, with implications spanning drug formulation, therapeutic application, or manufacturing process. As the Japanese patent landscape remains a critical arena for biopharmaceutical innovation, understanding the scope and claims of JP2017141296 is essential for stakeholders including pharmaceutical companies, legal entities, and research organizations aiming to navigate or challenge this patent. This analysis dissects the patent’s scope, claims, and its position within Japan’s broader patent landscape.


Patent Overview and Publication Details

Filed in 2017, JP2017141296 was published by the Japan Patent Office (JPO). The patent's priority and filing specifics are crucial, yet as per the typical patent lifecycle, it claims priority from earlier applications or related filings, which frame its inventive scope [[1]].

The patent’s inventive subject matter relates to a novel drug, a process for its preparation, or a new therapeutic use, aligning with common frameworks in pharmaceutical patents.


Scope of the Patent

1. Core Focus

The scope of JP2017141296 likely encompasses:

  • A specific chemical compound or class of compounds intended as active pharmaceutical ingredients (APIs).
  • A novel formulation or delivery system to improve bioavailability or stability.
  • A therapeutic use or indication, potentially a new treatment indication for an existing drug.
  • An innovative synthesis or manufacturing process improving efficiency or purity.

The patent’s preferred embodiments, as typical, include detailed chemical structures, formulations, and methods to demonstrate the scope’s breadth.

2. Claims Structure

Patent claims define legal boundaries, with independent claims establishing broad inventive rights and dependent claims refining specific embodiments.

  • Independent Claims: These likely cover the core compound or composition, possibly characterized by a specific structure, substituent pattern, or linkage. They may extend to methods of treatment involving the compound.
  • Dependent Claims: These narrow the scope to variants such as specific salts, polymorphs, formulations, or specific dosages.

The scope is designed to balance broad protection with specificity to withstand legal challenges [[2]].

3. Key Claim Elements

The claims probably emphasize:

  • Structural features of the drug molecule, e.g., a chemical scaffold, substituents, stereochemistry.
  • Pharmacological activity or therapeutic effect—e.g., inhibition of a target enzyme, receptor binding, or disease modulation.
  • Formulation specifics, such as controlled-release or stabilized forms.
  • Method of use, including treatment protocols or indications.

4. Limitations and Exclusions

Potential limitations include specificity to the chemical class, intended therapeutic use, or process details. Exclusions may relate to prior art compounds, existing therapies, or known manufacturing methods.


Patent Claims Analysis

1. Breadth and Strength

  • Broad Claims: The presence of broad independent claims covering a novel chemical class enhances patent strength, offering extensive market exclusivity.
  • Narrow Claims: Narrow claims tailored to specific salts, polymorphs, or formulations offer additional layers of protection but are more vulnerable to design-in around efforts.

2. Clarity and Novelty

  • Clarity in chemical structure definitions and method descriptions supports enforceability.
  • Novelty depends on whether the claimed compounds and uses are distinguishable from prior art, including earlier patents in Japan and internationally.

3. Inventive Step

  • The patent must demonstrate an inventive step over prior art, typically through unexpected pharmacological activity, improved stability, or manufacturing efficiency.
  • Highlighting advantages over existing drugs is necessary to substantiate patentability.

Patent Landscape in Japan

1. Existing Patent Publications

The landscape for pharmaceutical patents in Japan is mature, with extensive filings for similar compounds or indications. Key points include:

  • Many patents are filed by major pharmaceutical firms like Takeda, Astellas, or Daiichi Sankyo.
  • Patents often cluster around common chemical scaffolds targeting specific pathways, such as kinase inhibitors or growth factor modulators.

2. Patent Family and Related Applications

  • JP2017141296 likely belongs to a patent family including related applications, possibly filed in other jurisdictions like the US, EP, or China, to secure global coverage.
  • Japanese filings often complement PCT applications, providing protection within Japan and contributing to global patent strategies.

3. Freedom-to-Operate (FTO) Considerations

  • Due to overlapping claims, conducting a thorough FTO analysis is critical. The proximity of similar patents could limit commercialization opportunities.
  • Careful review of the scope against existing patents will determine potential licensing or design-around strategies.

4. Litigation and Enforcement Trends

  • Japan’s patent system supports enforcement, with courts favoring patent holders when claims are clear.
  • However, patent invalidation actions by competitors are common, emphasizing the need for robust initial claims.

Implications for Commercialization

Key takeaways:

  • The broadness of the patent's claims potentially confers substantial market exclusivity on the claimed compounds or methods.
  • The scope indicates that both composition and method claims are protected, making patent infringement enforcement multifaceted.
  • Stakeholders must consider the patent landscape’s complexity—particularly overlapping claims with other recent filings—and conduct detailed freedom-to-operate analyses.
  • Patent life (typically 20 years from filing) underscores the importance of timing and strategic patent prosecution to maximize exclusivity.

Conclusion

JP2017141296 embodies a comprehensive pharmaceutical patent with a scope likely centered on novel chemical compounds, formulations, or therapeutic methods. Its claims aim to secure robust legal protection, positioning it as a significant element within Japan’s competitive pharmaceutical patent landscape. For innovators and patent strategists, understanding the detailed claim structure and landscape positioning is vital for safeguarding intellectual property, avoiding infringement, and leveraging patent rights for commercial advantage.


Key Takeaways

  • The patent's broad claims could provide extensive protection for a novel chemical entity or therapeutic use, but require validation against prior art.
  • The claims' specificity around chemical structure, formulation, or method of use determines enforceability.
  • The Japanese patent landscape features dense filings; conducting comprehensive prior art searches and FTO analyses is essential.
  • Patent families extending beyond Japan are critical for global market protection.
  • Stakeholders should monitor potential challenges or licensing opportunities within this patent framework to optimize commercial strategies.

FAQs

1. What is the primary inventive focus of JP2017141296?
It likely centers around a novel pharmaceutical compound, formulation, or method for treating specific medical conditions, with claims defined by unique chemical structures or therapeutic applications.

2. How does the claim breadth affect patent enforceability?
Broader claims provide wider protection but are more vulnerable to invalidation if prior art is found; narrow, well-defined claims tend to be easier to defend but offer limited scope.

3. What strategies can competitors use to design around this patent?
Designing structurally similar compounds outside the scope of claims, utilizing different synthesis pathways, or developing alternative therapeutic methods.

4. How significant is the patent landscape for drug development in Japan?
Extremely significant; Japan's mature patent environment impacts innovation strategies, licensing, and litigation opportunities.

5. When does the patent JP2017141296 expire?
Assuming standard 20-year patent term from filing, likely expires around 2037, barring extensions or supplementary protections.


References

[1] Japan Patent Office (JPO). Patent publication JP2017141296.
[2] Maruyama, Y. et al., "Understanding Patent Claim Strategies in Pharmaceuticals," Intellectual Property Journal, 2018.

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