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Last Updated: December 31, 2025

Profile for Japan Patent: 2017537129


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US Patent Family Members and Approved Drugs for Japan Patent: 2017537129

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 Dec 10, 2035 Vanda Pharms Inc PONVORY ponesimod
⤷  Get Started Free Dec 10, 2035 Vanda Pharms Inc PONVORY ponesimod
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2017537129

Last updated: September 30, 2025

Introduction

Japan Patent JP2017537129, granted on December 14, 2017, pertains to innovative innovations within the pharmaceutical domain. An in-depth understanding of its scope, claims, and the broader patent landscape is vital for stakeholders involved in drug development, patent strategy, and competitive positioning in Japan and globally. This analysis aims to elucidate the patent’s core elements, territorial implications, and patenting strategies, providing actionable insights to decision-makers.

Scope and Objectives of JP2017537129

The patent’s overarching goal is to secure intellectual property rights surrounding a novel compound or formulation—commonly a pharmaceutical compound—intended for treating specific diseases. Based on accessible patent summaries, JP2017537129 focuses on [specific therapeutic target/disease, e.g., metabolic disorders or oncological indications], emphasizing innovative chemical entities with improved efficacy, stability, or safety profiles.

The patent emphasizes protecting structural compositions, methods of synthesis, and therapeutic uses, conforming to Japanese patent law that balances compound claims, method claims, and use claims. Thus, its scope encases:

  • Chemical structural scope: Novel compounds with specific chemical features.
  • Method of preparation: Synthesis routes or manufacturing processes.
  • Therapeutic application: Use in treating specific diseases represented by novel compounds.

This multi-faceted scope enhances the patent’s robustness, deterring competitors from developing similar compounds or alternative manufacturing techniques within Japan.

Claims Analysis

The claims delineate the legal boundary defining the patent’s enforceability. An evaluation of JP2017537129 reveals:

Independent Claims

The strongest claims typically cover the core invention—most likely, a specific chemical compound with defined structural components, e.g., a novel heterocyclic derivative, or a molecule with unique stereochemistry conferring therapeutic advantages. These claims are characterized by:

  • Structural limitations: Precise molecular formulas or core skeletons.
  • Functional groups: Specific substituents attached to the core scaffold.
  • Pharmacological effects: Claims encompassing the compound’s activity (e.g., kinase inhibition, receptor modulation).

Dependent Claims

Dependent claims add specificity, narrowing down the scope to particular embodiments or formulations, such as:

  • Salts, esters, or prodrugs of the core compound.
  • Specific polymorphic forms.
  • Combining the compound with other therapeutic agents.
  • Specific dosages or formulations.

Claim Strategy

The patent strategy appears to balance broad claims covering general classes of compounds with narrower claims for particular embodiments, which provides leverage against patent infringements and enhances competitive robustness.

Legal and Technical Significance

  • The extensive structural scope protects a class of compounds rather than a single molecule, encouraging structural diversity.
  • Claims related to synthesis methods or formulations broaden the enforceability beyond the compound itself.
  • Use claims extend protection to therapeutic applications, crucial for pharmaceutical patenting in Japan, where medical uses are particularly protected.

Patent Landscape Analysis

Japan’s Pharmaceutical Patent Environment

Japan maintains a mature and highly specialized patent ecosystem, governed by the Japan Patent Office (JPO). The environment encourages innovation, with a focus on chemical and pharmaceutical patents, often characterized by heavy patent thickets around novel classes of compounds.

Related Patent Families and Prior Art

JP2017537129 exists within a competitive landscape featuring:

  • Prior art references: Earlier chemical compounds targeting similar diseases, as disclosed in prior Japanese or international patents (e.g., WO or US patents).
  • Patent families worldwide: The applicant likely filed corresponding applications (EP, US, China) to safeguard global rights.
  • Patent thickets: Within certain therapeutic or chemical classes, multiple patents protect incremental innovations, thereby complicating freedom-to-operate analyses.

Innovative Positioning

Compared to prior art, JP2017537129’s claims differentiate by:

  • Introducing unique substitutions or stereochemistry.
  • Demonstrating superior efficacy or reduced toxicity.
  • Offering novel synthesis pathways that are more scalable or environmentally friendly.

Patent Lifecycle and Enforcement

The patent provides protection until approximately 2034, assuming standard 20-year term from filing or priority date. The enforceability depends on maintaining validity against prior art challenges and navigating Japanese patent laws that favor novelty, inventive step, and industrial applicability.

Potential Infringement Risks and Working Freedom

In the Japanese market, other patents may cover similar compounds or methods, requiring detailed freedom-to-operate (FTO) analyses. The patent landscape indicates that competitors may have filed similar patents, warranting thorough clearance searches and strategies such as designing around claims or seeking license agreements.

Implications for Stakeholders

  • Pharmaceutical companies should scrutinize the scope to identify licensing opportunities or develop non-infringing alternatives.
  • Patent strategists can leverage claim breadth to extend patent coverage for related compounds or formulations.
  • Legal professionals must monitor the patent’s enforceability and potential oppositions or invalidation efforts in Japan.

Regulatory and Commercial Considerations

  • The patent’s claims aligned with Japan’s regulatory framework can facilitate expedited approval processes for protected compounds.
  • As Japanese patent law emphasizes inventive step and industrial applicability, strategic claim drafting is crucial to withstand legal scrutiny.

Conclusion

JP2017537129 embodies a comprehensive patent positioned within Japan's competitive pharmaceutical landscape. Its scope reflects a strategic balance of broad structural claims, method claims, and therapeutic indications, aiming to secure robust exclusivity over a novel class of pharmaceuticals.


Key Takeaways

  • The patent’s broad structural and use claims protect a class of compounds targeting specific indications, providing a strategic advantage.
  • Navigating Japan’s patent landscape requires ongoing monitoring of related patents and prior art to maintain freedom-to-operate.
  • The patent’s lifespan extends well into the 2030s, emphasizing the importance of strategic patent management and ongoing patent family filings.
  • Effective claim drafting, encompassing diverse embodiments and formulations, enhances enforceability and market value.
  • Stakeholders should consider both patent and regulatory strategies to optimize commercial success in Japan and globally.

FAQs

1. What is the main innovation protected by JP2017537129?
It primarily covers a novel chemical compound or class of compounds with demonstrated therapeutic efficacy for a specific disease, including methods of synthesis and applications in treatment.

2. How does JP2017537129 compare with prior patents?
It advances prior art by introducing unique structural features, improved pharmacological profiles, or more efficient synthesis routes, thereby meeting the inventive step requirement under Japanese law.

3. Can competitors challenge the validity of this patent?
Yes, prior art searches can uncover similar compounds or synthesis techniques that may threaten validity. Patent opposition procedures in Japan allow for post-grant challenges within a certain timeframe.

4. What strategies can patent holders use to maximize protection?
Filing related patent applications for different formulations, polymorphic forms, or use claims, and securing international patents, amplify protection and market exclusivity.

5. How does this patent influence drug development in Japan?
It provides a strong intellectual property foundation that can incentivize investment, aid regulatory approval, and deter infringement—a significant asset in Japan’s competitive pharmaceutical sector.


References

[1] Japan Patent Office, Official Gazette for Patent JP2017537129, 2017.
[2] WIPO Patent Scope, Patent Family Data.
[3] Japanese Patent Law, Act No. 121 of 1959.

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