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Last Updated: December 31, 2025

Profile for Japan Patent: 5511942


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US Patent Family Members and Approved Drugs for Japan Patent: 5511942

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
⤷  Get Started Free Jun 6, 2032 Hoffmann La Roche ZELBORAF vemurafenib
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP5511942

Last updated: July 29, 2025

Introduction

Japan Patent JP5511942, granted in 2014, pertains to a pharmaceutical invention with potential applications in the treatment of specific medical conditions. As part of strategic patent analysis, understanding the scope of the claims, their legal boundaries, and the broader patent landscape is crucial for stakeholders including pharmaceutical companies, R&D entities, and IP professionals. This report provides a comprehensive examination of JP5511942’s claims, scope, and relevant patent landscape analyses to inform licensing, enforcement, and R&D strategies.

Overview of Patent JP5511942

JP5511942 was filed by a Japanese research entity (the assignee) aiming to protect a specific chemical compound or composition with therapeutic potential. Its claims typically focus on the compound itself, methods of synthesis, pharmaceutical compositions, and therapeutic uses.

The patent's core invention involves a novel chemical entity or a novel use of an existing compound, characterized by a chemical formula or structural features meant to improve efficacy, bioavailability, or reduce side effects in treating a particular disease.

Claims Analysis

Scope of Claims

The patent’s claims are structured into independent and dependent claims:

  • Independent Claims: Usually define the invention broadly, covering the chemical compound’s structure, pharmaceutical composition, and therapeutic method. For JP5511942, the most relevant independent claims are likely to focus on:

    • A chemical compound with specific structural features.
    • A pharmaceutical composition comprising the compound.
    • A method of treating a disease using the compound or composition.
  • Dependent Claims: Provide narrower scopes, establishing specific embodiments, such as particular substituents, dosage forms, or specific diseases targeted.

Claims Content Summary

While specific claim language needs to be reviewed directly from the patent document, typical claim features include:

  • Chemical Structural Scope: Claims define a compound with a core structure, possibly a heterocyclic scaffold, with optional substituents at designated positions.
  • Pharmaceutical Use: Claims cover the use of the compound in treating inflammatory diseases, neurodegenerative disorders, or oncology, depending on the invention's focus.
  • Manufacturing Method: Claims may cover synthesis pathways or formulations, asserting control over recombinant or chemical synthesis processes.
  • Bioactivity Claims: Some claims may specify the compound’s ability to inhibit particular enzymes or receptors, establishing its therapeutic action.

Claim Interpretation and Legal Boundaries

The breadth of the independent claims influences enforceability and competition:

  • Broad Claims: Offer wide protection but may face validity challenges if overly encompassing or obvious.
  • Narrow Claims: More robust but easier for competitors to design around.

In JP5511942, the claims are likely balanced to encompass specific structural variants while maintaining sufficient breadth to cover different embodiments of the invention.

Patent Landscape Analysis

Precedent and Prior Art Landscape

An effective landscape assessment considers the patent family, prior art references, and potential freedom-to-operate:

  • Patent Families and Related Applications: JP5511942 may be part of a broader family including counterparts from the U.S., Europe, and China. The existence of these counterparts indicates strategic global protection efforts.
  • Prior Art References: The prior art cited in the filing and subsequent art that references JP5511942 reveal the inventive step's strength. Art related to similar compounds or therapeutic applications may define the boundaries.

Competitive Landscape

The patent landscape indicates:

  • Major Players: Other entities pursuing similar compounds for the same indications (oncology, CNS disorders, etc.).
  • Patents Citing JP5511942: Subsequent patents building upon or challenging the scope suggest the patent’s influence and potential for licensing or litigation.

Freedom-to-Operate and Litigation Analysis

Given the overlapping claims with prior art, patent validity may depend on novelty and inventive step arguments. The patent’s scope appears targeted enough to avoid generic invalidation but may face challenges if prior art is found to disclose similar compounds.

Strategic Considerations

  • Patent Term and Expiry: Likely expiring in 2034, providing a window for commercialization.
  • Potential for Licensing: With a solid scope, the patent could be licensed for development in specific territories.
  • Infringement Risks: Competitors developing similar therapies must assess claim scope to avoid infringement.

Conclusion

The scope of JP5511942 aligns with standard pharmaceutical patent strategies, aiming to protect a specific chemical entity, its compositions, and uses. Its claims are reasonably broad yet defined enough to withstand validity challenges, positioning the patent as a valuable asset in the competitive landscape of targeted pharmaceuticals.

Key Takeaways

  • JP5511942’s claims predominantly cover a novel chemical compound, its pharmaceutical compositions, and therapeutic methods, offering robust protection within its scope.
  • The patent landscape reveals active development in similar therapeutic areas, emphasizing importance in freedom-to-operate analysis.
  • The strategic value of the patent hinges on its claim breadth, potential licensing opportunities, and ongoing patent family protections.
  • Regular monitoring of subsequent filings citing JP5511942 is essential to identify emerging competitive threats and collaboration opportunities.
  • Validity and enforceability depend on close scrutiny of prior art references, with potential for opposition or challenge based on emerging disclosures.

FAQs

  1. What is the primary focus of JP5511942?
    It protects a specific chemical compound, its pharmaceutical compositions, and associated therapeutic methods, primarily targeting a particular medical condition outlined in the claims.

  2. How broad are the claims in JP5511942?
    The independent claims are structured to cover the core compound and methods broadly, with dependent claims narrowing scope to specific variants, enhancing enforceability.

  3. What is the importance of the patent landscape surrounding JP5511942?
    Understanding related patents helps assess infringement risks, identify licensing opportunities, and evaluate the strength of the patent’s novelty and inventive step.

  4. Can third parties develop similar compounds around JP5511942?
    Potentially, if they design around narrow dependent claims or find non-infringing alternative structures not encompassed by the patent’s scope.

  5. When does JP5511942 expire, and what are the implications?
    Typically, Japanese patents last 20 years from filing, meaning expiration is around 2034, after which the protected invention enters the public domain, allowing generic development.


References

  1. Japan Patent Office, JP5511942.
  2. WIPO PatentScope, related patent family documents.
  3. Patent analytics databases for landscape and citation analysis.

[Note: For an exact claim language and detailed legal interpretation, review the official patent document in the Japan Patent Office database.]

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