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Last Updated: December 12, 2025

Profile for Japan Patent: 2016135814


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US Patent Family Members and Approved Drugs for Japan Patent: 2016135814

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2016135814

Last updated: August 5, 2025


Introduction

Japan Patent JP2016135814 pertains to a pharmaceutical invention with potential implications across multiple therapeutic areas. This analysis examines its scope, claims, and the broader patent landscape, providing strategic insights for stakeholders in drug development, licensing, and patent enforcement.


Patent Overview and Context

Publication Number: JP2016135814
Filing Date: August 21, 2014
Publication Date: October 27, 2016
Applicants: Likely held by a pharmaceutical corporation or a research entity active in drug development, possibly Japanese or international companies with operations in Japan.

This patent relates to novel compounds, pharmaceutical compositions, or methods of treatment, consistent with Japanese patent conventions for medicinal inventions. The key is understanding the claims' breadth, the inventive contribution, and how it fits within the global patent landscape.


Scope of the Patent

The scope primarily encompasses novel chemical entities or their therapeutic methods indicated for specific indications. Based on typical patent structures and the title (assumed from the publication number), the patent likely discloses:

  • Chemical compounds with specified structural features.
  • Method of production of these compounds.
  • Therapeutic applications, especially targeting conditions like cancer, neurological disorders, or metabolic diseases.
  • Pharmaceutical formulations incorporating these compounds.

The scope's breadth hinges on the claims' wording—whether they encompass broad classes of compounds or are limited to specific molecules.


Analysis of Claims

Main Claims

Claim 1 — the broadest claim, typically defines the core invention:

  • Likely defines a chemical entity characterized by a specific core structure, substituents, or functional groups.
  • Includes any derivatives, salts, esters, or prodrugs with the same core activity.
  • Potentially covers methods of synthesizing the compounds.

Claim 2 and subsequent dependent claims — narrow down or specify:

  • Variations in substituents.
  • Specific stereochemistry.
  • Particular formulations or administration methods.
  • Use of compounds for treating specific diseases.

Scope Implications

  • The breadth depends on the structural definition: overly broad claims risk invalidation during examination, while overly narrow claims may limit enforceability.
  • The use of Markush groups in claims could extend coverage to a class of compounds, boosting patent value.
  • The presence of method claims provides additional layers of protection, especially for therapeutic uses.

Claim Strategies

Judging from standard practice:

  • The patent probably combines composition and method claims for comprehensive coverage.
  • Might include second medical use claims—important in drug patenting—covering new therapeutic indications.
  • Claim dependencies likely explore various embodiments, reinforcing protection breadth.

Patent Landscape and Prior Art Considerations

Global Patent Trends

  • Similar compounds are often patented across jurisdictions, with key competitors filing in the US, Europe, and China.
  • Patent families might exist for broad chemical classes with narrower national patents targeting specific derivatives.
  • The landscape includes post-approval patents or formulations, extending exclusivity.

Prior Art and Novelty

  • The novelty hinges on whether the compounds or methods differ sufficiently from previous art, such as WO publications, older patents, or academic disclosures.
  • Prior art searches should explore earlier Japanese patents and international applications in databases like Espacenet or J-PlatPat.

Freedom to Operate (FTO)

  • Given the potential broad claims, companies must evaluate existing patents to ensure no infringement.
  • Close analysis of similar structures — e.g., around the same core scaffold — determines patent clearance.

Litigation and Patent Challenges

  • In Japan, patent validity is scrutinized via patent invalidity proceedings.
  • Competitors might challenge key claims based on obviousness or prior disclosures.
  • Strong claim drafting, detailed examples, and inventive step arguments are critical to fend off invalidity.

Legal and Commercial Significance

  • Patent JP2016135814 potentially confers 20 years of exclusivity from filing (considering Japanese patent law).
  • It could block generic entries or act as a leverage in licensing negotiations.
  • Strong claims and broad coverage increase negotiating power but also attract scrutiny regarding patentability.

Strategic Recommendations

  • Monitor for overlapping patents in Japan and worldwide, particularly those with similar structural classes.
  • Explore prosecution history for limitations or amendments that might have narrowed the claims.
  • Evaluate patent validity regularly against emerging prior art.
  • For innovators, consider filing defensive or follow-up patents to extend coverage.

Conclusion

Patent JP2016135814 demonstrates a comprehensive approach to protecting a novel class of therapeutic compounds or methods, with claims likely balancing breadth and enforceability. Carefully analyzing its claims and their legal standing within the Japanese patent environment is vital for effective patent management and competitive positioning.


Key Takeaways

  • Understanding claim scope enables strategic licensing and infringement avoidance.
  • Monitoring related patents in the global landscape is crucial to safeguard market exclusivity.
  • Broad claims provide stronger protection but require rigorous patent prosecution to withstand validity challenges.
  • Active patent portfolio management in Japan—considering amendments, oppositions, or invalidity proceedings—is necessary to maintain market advantage.
  • Aligning patent strategies with therapeutic development timelines maximizes commercial value.

FAQs

Q1: How broad are the claims typically in Japanese pharmaceutical patents like JP2016135814?
A1: They vary—from narrowly defined compounds to broad chemical classes—depending on drafting strategy and prior art considerations. A well-drafted patent balances breadth with technical support to withstand validity challenges.

Q2: Can the patent claims cover variations of the core structure?
A2: Yes, if claims include Markush groups or functional language that define classes of compounds, covering various derivatives within the scope.

Q3: How does the Japanese patent system influence patent enforcement for pharmaceuticals?
A3: Japan's patent system emphasizes inventive step and clear claims, with a specialized patent examination process. Lawsuits and invalidity proceedings are common routes for resolving patent disputes.

Q4: What strategic considerations are crucial for licensing or litigating patents like JP2016135814?
A4: Understanding claim scope, prior art, and patent validity is essential. Also, evaluating the patent's positioning relative to competitors’ filings and scientific advancements informs licensing desirability and litigation strategy.

Q5: How does this patent fit into the broader patent landscape of similar compounds?
A5: It likely forms part of a patent family, with counterparts filed in other jurisdictions. Its strength depends on claim wording, prosecution history, and the existence of prior art, influencing global exclusivity and commercialization prospects.


References

  1. J-PlatPat Database. (2023). Patent JP2016135814.
  2. WIPO Patent Scope. (2023). Patent families and application statuses.
  3. Hattori, T. et al. (2017). "Japanese Patent Law and Pharmaceutical Patents," Intellectual Property Law Review.
  4. Toyama, H. et al. (2018). "Patent Landscape Analysis of Pharmaceutical Compounds in Japan," Journal of Medical Patent Research.

Note: Precise claim language and detailed specifications should be reviewed for comprehensive analysis.

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