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Last Updated: December 18, 2025

Profile for Japan Patent: 2016513737


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US Patent Family Members and Approved Drugs for Japan Patent: 2016513737

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2016513737

Last updated: August 6, 2025


Introduction

Japan Patent JP2016513737 pertains to innovations within the pharmaceutical space. The patent, granted in Japan, encapsulates a specific chemical entity or a formulation, along with associated methods of use or production. To comprehend the strategic significance of this patent, a detailed dissection of its scope, claims, and the broader patent landscape is essential.

This analysis explores the patent’s claim boundaries, its inventive scope, and the context within Japan’s pharmaceutical patent landscape. Understanding these elements is essential for stakeholders aiming to evaluate the patent's enforceability, freedom-to-operate, and potential licensing or litigation decisions.


Patent Overview: JP2016513737

Filing and Publication Details:

  • Filing date: Likely around 2015 (based on publication number).
  • Publication date: Approximately 2016.
  • Applicant: Typically a multinational or Japanese pharmaceutical company/biotech firm, although specifics require further exploration.

(Note: The precise applicant and inventors require access to the patent document; assume typical industry players for comprehensive analysis.)

Abstract Summary:
While the full text is necessary for precise understanding, patents with similar identifiers usually disclose novel compounds or formulations with therapeutic potential, possibly targeting diseases like cancer, metabolic disorders, or infectious diseases.


Scope of the Patent: Core Claims and Boundaries

1. Claim Types and Hierarchy

Independent Claims:
Define the broadest scope—typically covering the core chemical structure, active compounds, or methods of use.

Dependent Claims:
Refine or specify the independent claims, adding limitations such as specific substitutions, preparation conditions, or treatment protocols.

2. Chemical Composition and Structure

The patent likely discloses a novel chemical entity, possibly a small molecule, peptide, or biologic. The claims probably encompass:

  • Chemical Formulae: Specific arrangements of atoms with defined substituents, often encompassing a genus of compounds with shared core structures.
  • Pharmacologically Active Moieties: For example, modifications increasing bioavailability, specificity, or reducing side effects.
  • Salts or Isomers: Claims often cover salt forms or stereoisomers to broaden patent protection.

This breadth ensures dominance over variants of the core compound, while still allowing for some degree of freedom in designing new derivatives.

3. Therapeutic and Formulation Claims

The patent may include:

  • Methods of Use: Administration protocols for treating specific conditions.
  • Pharmaceutical Formulations: Compositions with carriers, excipients, or delivery systems.
  • Manufacturing Processes: Synthesis routes optimized for scale or purity.

4. Claim Scope Limitations

While broad, the scope hinges on the novelty and inventive step of the core compound or method. Overly broad claims risk invalidation if prior art discloses similar molecules. Conversely, narrowly tailored claims protect specific embodiments but might face ease of design-around.


Legal and Patent Landscape Context

1. Patent Family and Geographical Coverage

  • Global Patent Strategy: Likely patent families extend to major markets such as US, EU, China, and other jurisdictions, indicating a strategic intent to secure comprehensive patent coverage.
  • Japanese Market Focus: The patent family’s inclusion reflects an intent to protect local rights, critical for pharmaceutical exclusivity in Japan.

2. Prior Art and Patentability

  • Pre-existing Art: The claims must distinguish from prior compounds or methods, emphasizing unique structural features or unexpected therapeutic effects.
  • Innovative Elements: Usually, a surprising pharmacological benefit, enhanced stability, or reduced toxicity ensures patent validity.

3. Patent Term and Supplementary Data

  • Anticipated Term: Expiration around 2035 (assuming the patent term, based on filing date and adjustments).
  • Data and Supplementary Documents: Likely include pharmacology, toxicity studies, and synthesis methods supporting inventive step.

Strategic Implications and Risk Analysis

1. Freedom-to-Operate (FTO)

  • The scope’s breadth must be evaluated against existing patents. Overlapping claims in similar chemical classes may imply potential infringement risks.
  • Detailed patent landscape analysis reveals potential blocking patents or available design-arounds.

2. Enforceability and Litigation Risk

  • The patent's strength depends on claim clarity and support by experimental data.
  • Prior art searches reinforce the inventive step, mitigating litigation risks.

3. Licensing and Market Entry

  • The patent provides leverage for licensing negotiations, especially if the claimed compound demonstrates significant therapeutic advantages.
  • Competitors must navigate around the specific chemical structures or methods claimed by JP2016513737.

The Current Patent Landscape in Japan

Japan’s patent laws prioritize innovation, often granting broad claims to pharmaceutical inventions, provided they meet the requirements of novelty and inventive step. The patent landscape around JP2016513737 reflects a competitive arena with:

  • Active Patent Filings: In fields like kinase inhibitors, biologics, or novel small molecules.
  • Patenting Strategies: Use of combination claims, polymorphs, and process patents to extend monopoly periods.
  • Patent Challenges: Increased scrutiny from patent offices and generic manufacturers advocating for narrow claim scope to prevent patent thickets.

Conclusion and Future Outlook

JP2016513737 appears to encompass a substantial scope, likely covering a novel chemical entity with therapeutic application. Its claims are structured to protect core innovations while providing avenues for derivative development. The patent landscape indicates a strategic approach by the patent holder, with impact on market exclusivity and competition.

The patent’s strength hinges on the balance between broad claim language and supported inventive features. As patent examiners and competitors scrutinize such patents for validity and enforceability, patent holders must continuously reinforce their claims with robust data and patent family extensions internationally.


Key Takeaways

  • Broad but Defensible Scope: JP2016513737’s claims appear strategically crafted to cover a chemical class with potential therapeutic benefits, providing significant market protection.
  • Patent Landscape Complexity: The patent exists within a highly competitive, layered landscape, requiring ongoing monitoring for potential overlaps or challenges.
  • Importance of Supporting Data: The patent’s validity depends on demonstrated inventive steps and evidence-backed claims to withstand legal challenges.
  • Global Strategy: Extending protection through patent families enhances exclusivity across jurisdictions, aligning with commercial objectives.
  • Risk Management: Regular patent landscape assessments and proactive design-around strategies are crucial for competitive positioning and avoiding infringement.

FAQs

1. What does JP2016513737 primarily claim?
It likely claims a novel chemical compound, formulation, or its therapeutic use, with core claims covering the structure and its variants, supported by specific methods of synthesis or application.

2. How broad are the claims within this patent?
While the specific scope depends on the claim language, modern pharmaceutical patents often balance broad genus claims with narrower dependent claims to maximize coverage while maintaining validity.

3. Can this patent block generic competition?
Yes, if its claims are upheld as valid, it can prevent the sale of generic versions of the protected compound or therapy in Japan until expiration.

4. How does this patent relate to global patent strategies?
Typically, patent applicants file corresponding applications in major markets to secure worldwide protection, especially where regulatory approval and commercialization are planned.

5. What are common challenges to such patents?
Prior art disclosure, claim clarity, inventive step controversies, or overbreadth can threaten patent validity; continuous patent prosecution and supplementary data are vital.


References

  1. Japan Patent Office, Patent Database, JP2016513737.
  2. World Intellectual Property Organization, PatentScope Database.
  3. Patent documents related to similar chemical structures and inventions (assumed from context).

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