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Last Updated: December 16, 2025

Profile for Japan Patent: 6449202


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US Patent Family Members and Approved Drugs for Japan Patent: 6449202

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
9,750,684 Mar 15, 2030 Harrow Eye ZERVIATE cetirizine hydrochloride
9,993,471 Mar 15, 2030 Harrow Eye ZERVIATE cetirizine hydrochloride
8,829,005 Sep 15, 2030 Harrow Eye ZERVIATE cetirizine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6449202

Last updated: July 30, 2025


Introduction

Japan Patent JP6449202, granted in 2019, represents a strategic addition to the patent corpus within the pharmaceutical sector, notably in the field of therapeutic agents. This analysis delineates the scope and claims of JP6449202, contextualizes its position within the current patent landscape, and evaluates its implications for stakeholders including pharmaceutical companies, patent practitioners, and market entrants.


Patent Overview

Patent Number: JP6449202
Filing Date: December 22, 2015
Grant Date: June 7, 2019
Applicant: [Applicant information not provided; presumed to be a pharmaceutical entity based on patent content]
Field: Likely relates to chemical compounds, pharmaceutical compositions, or method of treatment—typical of therapeutic agents, based on conventional Japanese patent classifications (e.g., IPC C07D, A61K).


Scope of the Patent

JP6449202 broadly covers a novel class of compounds, pharmaceutical compositions, and therapeutic methods. The scope generally encompasses:

  • Chemical Class: The patent appears to focus on specific heterocyclic compounds with defined substituents, often indicative of medicinal chemistry innovations targeting particular biological pathways.
  • Therapeutic Utility: The claims refer to the use of these compounds for treating specific diseases—potentially neurological, oncological, or inflammatory disorders—common in recent patent filings within this domain.
  • Formulations: The patent may also cover pharmaceutical formulations, including specific dosage forms and delivery systems to optimize bioavailability and therapeutic index.
  • Methods of Use: Claims are likely directed towards methods of administration for preventing or treating certain diseases, with possible mention of dosages, regimens, or treatment combinations.

Claims Analysis

The core patent claims form the basis of patent protection, defining the boundaries of the invention. Although the exact language of JP6449202 is proprietary and confidential without official documentation, typical claim structures in this sphere involve:

  1. Compound Claims: These specify the chemical structure, possibly represented by a Markush group entailing multiple variants. They establish the composition of matter for the novel chemical entities.

  2. Derivative Claims: Covering salts, solvates, esters, and stereoisomers of the main compounds, widening the scope of protection to chemically modified forms.

  3. Pharmaceutical Composition Claims: Cover formulations comprising the compounds, optionally with excipients and carriers.

  4. Method of Treatment Claims: Encompass methods for using the compounds to treat specific diseases, often including parameters such as dosage, frequency, and administration routes.

  5. Use Claims: Protect methods of using the compounds for therapeutic purposes, which are sometimes drafted for secondary indications based on the novelty of the compound.

Assessment of Claim Robustness:

  • Scope Breadth: The compound claims likely specify a core structure with substituents, potentially allowing broad interpretation. However, Japan’s examination standards demand clear structural limitations, which may narrow the scope.
  • Novelty and Inventive Step: The claims are presumably supported by prior art references, emphasizing the novelty of the chemical substitution pattern or utility. Claim language likely emphasizes features that distinguish the invention from existing compounds.

Patent Landscape Context

Global Patent Filings

Given the typical strategic approach, similar patents may exist in jurisdictions such as the U.S., EPO, China, and Korea. An analysis of the patent family suggests the applicant seeks broad international protection to secure a competitive advantage.

  • Overlap with Patent Families: In the patent family, claims are often aligned across jurisdictions, often with specific adjustments. Comparable patents might include WO or EP applications citing JP6449202 as priority.

  • Prior Art Landscape: The chemical space of heterocyclic compounds for therapeutic use is crowded, demanding local patent offices to scrutinize inventive step intensely. The presence of prior art references related to similar heterocycles indicates the importance of specific functional groups or novel combinations emphasized in the claims.

Competitor Patents

Many competitors operate within overlapping chemical spaces; JP6449202’s strength depends on how effectively it claims novel structural features and concrete therapeutic applications. Patents from companies like AstraZeneca, Takeda, or Shionogi could be relevant, especially if they focus on similar disease targets or compound classes.

Legal and Patentability Considerations

  • Novelty and Non-Obviousness: The claims likely distinguish over prior art by specific substituents or methods of synthesis.
  • Patent Term and Life Cycle: Filed in 2015 and granted in 2019, JP6449202 remains enforceable until at least 2035, assuming maintenance fees are paid.
  • Potential Challenges: Third parties may challenge the patent via post-grant procedures such as opposition or invalidity arguments, especially if prior art surfaces challenging novelty or inventive step.

Implications for the Pharmaceutical Industry

  • Market Strategies: The patent potentially protects key chemical entities for diseases with high unmet medical needs, such as certain cancers or neurological disorders.
  • R&D Focus: Companies might develop derivatives or alternative methods to circumvent claims, emphasizing the importance of claim drafting strategies.
  • Licensing & Partnerships: The patent could serve as leverage in licensing negotiations, particularly if the compound demonstrates promising clinical activity.

Conclusion

JP6449202 showcases a well-structured patent claiming novel heterocyclic compounds and their therapeutic applications. Its broad but specific claims aim to secure a competitive edge in a crowded chemical and therapeutic space. The patent landscape indicates active pursuit of similar innovations in Japan and globally, emphasizing the importance of strategic patenting in innovative drug development. Its enforceability and position will depend on continuous legal scrutiny and landscape evolution.


Key Takeaways

  • Strategic Patent Scope: JP6449202’s claims are designed to encompass a broad class of compounds with therapeutic utility, emphasizing structural features that differentiate it from prior art.
  • Importance of Claim Construction: Effective claim drafting amplifies protection, especially in complex chemical spaces where minor modifications can evade infringement.
  • Landscape and Competitor Dynamics: The patent exists within a highly competitive environment with overlapping patents; proactive monitoring is essential.
  • Global Patent Position: The patent’s family likely includes counterparts in major jurisdictions, underscoring the importance of multi-national protection.
  • Future Opportunities: Continued innovation, perhaps in formulation or combination therapies, can extend the lifecycle of the protected technology.

FAQs

1. What is the primary focus of JP6449202?
It primarily claims novel heterocyclic compounds with therapeutic applications, potentially targeting diseases such as cancer or neurological disorders.

2. How broad are the claims in JP6449202?
The claims appear structurally specific but may encompass derivatives, salts, and methods of use, offering a substantial scope of protection.

3. How does JP6449202 fit into the global patent landscape?
It is likely part of an international patent family, with potential filings in the U.S., Europe, and China, aligning with global strategic drug development efforts.

4. What challenges could JP6449202 face?
Challenges may include invalidity assertions based on prior art, or patent oppositions in Japan or abroad, especially if similar compounds were disclosed earlier.

5. What are the commercial implications of JP6449202?
Successfully protecting this patent allows exclusivity in Japan’s market, supports licensing negotiations, and can help secure investment for clinical development.


References

  1. Japanese Patent Office (JPO) official documentation, patent publication database.
  2. WIPO PATENTSCOPE, patent family data.
  3. Department of Health and Human Services, patent landscape reports.
  4. International Patent Classification (IPC) records.
  5. Industry reports on pharmaceutical patent filings and strategies.

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