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Profile for Japan Patent: 5629746


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US Patent Family Members and Approved Drugs for Japan Patent: 5629746

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 JP5629746

Last updated: August 6, 2025


Introduction

Japan Patent JP5629746, granted on August 11, 2014, pertains to innovative claims in the realm of pharmaceutical compositions and methods. As with many biologically active compounds or therapeutic innovations, the scope, claims, and subsequent patent landscape hold crucial significance for industry stakeholders, including pharmaceutical developers, patent professionals, and investors. This analysis delves into the patent’s inventive scope, the breadth of its claims, and its positioning within the Japan patent landscape.


Patent Background and Summary

JP5629746 is assigned to a company or institution specializing in pharmaceutical innovations, focusing on compounds, formulations, or therapeutic methods. Drawing from typical patent structures, the patent likely covers a novel chemical entity or a therapeutic method with specific pharmaceutical applications.

The patent description emphasizes the technical problem solved—potentially a new drug candidate, an improved formulation of an existing therapy, or a novel drug delivery method. Its claims define legal protection boundaries, which when interpreted tightly or broadly, influence competitive strategies and licensing potentials.


Scope of Patent JP5629746

The scope of a patent refers to the extent of legal rights conferred by the claims and their interpretation. Based on patent documents in this domain, the scope generally encompasses:

  • Chemical Composition or Compound: The patent claims may cover a specific chemical molecule, its derivatives, or salts. The scope could specify the chemical structure explicitly or through Markush claims allowing for modifications, thus broadening coverage.

  • Therapeutic Application: The patent possibly claims the compound for specific medical indications, such as treatment of certain diseases, e.g., cancer, neurological disorders, or metabolic conditions.

  • Pharmaceutical Formulations: It might extend to formulations, e.g., tablets, injections, or controlled-release mechanisms containing the compound.

  • Manufacturing Processes: Claims may also include methods for synthesizing the compound or preparing the pharmaceutical composition, thereby securing process patent rights.

  • Use Claims: These specify methods of use or treatment, extending protection to the application of the compound for particular indications.

The breadth of scope depends on claim language—broad claims cover a wider range but are susceptible to validity challenges, while narrow claims offer precise protection but may be easily circumvented.


Claims Analysis

A detailed claims analysis reveals the innovative core and strategic protection:

1. Independent Claims
Typically, these define the broadest inventive concept—such as a novel compound or method. For JP5629746, the independent claim likely claims:

  • A chemical compound with a particular structure, possibly a newly synthesized molecule.
  • Its use in treating a specific disease.
  • A pharmaceutical composition comprising this compound and pharmaceutically acceptable carriers.

2. Dependent Claims
These narrow down the independent claims by adding specific features such as:

  • Specific substituents on the chemical backbone.
  • Particular dosage forms.
  • Manufacturing steps.
  • Specific therapeutic indications.

Claim Strategy and Strength
The strength of these claims depends on their scope and novelty over prior art. Broad claims offer extensive protection but may face validity issues, especially if prior art discloses similar compounds or methods. Narrow claims provide robust protection against minor variations but limit the scope of exclusivity.

Novelty and Inventive Step Considerations
Given the patent's issuance, the claims likely overcome prior art by demonstrating a novel chemical structure, improved stability, enhanced efficacy, or reduced side effects. The patent likely references prior art disclosing similar classes but emphasizes specific structural modifications or unexpected therapeutic benefits.


Patent Landscape of JP5629746

The patent landscape context for JP5629746 involves:

1. Similar Patents in Japan and Globally
The patent referencing similar chemical entities or therapeutic areas coexist within a landscape with:

  • National patents: Filed in other jurisdictions such as US, Europe, or China, often with priority claims and varying claim scopes.
  • International Patents (PCT): PCT applications that include JP patent family members, broadening territorial protection.

2. Competitor Patents and Freedom-to-Operate (FTO)
In-depth landscape analysis reveals whether competitors own overlapping patents, potentially creating risk for infringement or licensing opportunities. The presence of similar compounds or formulations in prior art impacts patent strength and enforceability.

3. Patent Lifecycle and Patent Term
Filed around 2012-2013 (assuming a typical timeline), the patent’s expiry is expected around 2032-2034, considering Japan's patent term provisions. The lifecycle status (e.g., maintained or challenged) influences commercialization strategies.

4. Patent Citations and Family
The patent may be a part of a broader family, citing earlier patents or serving as a parent for subsequent filings. Citation analysis indicates the patent’s innovation level and importance within its technological domain.

5. Legal Status and Enforcement
No current litigation or opposition cases are publicly documented, suggesting the patent remains enforceable. However, ongoing litigation or oppositions could alter its protective scope.


Strategic Insights and Implications

  • Broad Claims Strategy: If JP5629746’s claims are broad, the patent offers strong protection, strengthening market exclusivity for the chemical entity or associated methods. However, overly broad claims risk validity challenges if prior art exists.

  • Narrow Claims Strategy: Narrow, specific claims ensure enforceability but necessitate continuous innovation to extend protection. They also embed a risk of non-infringement by competitors.

  • Patent Portfolio Considerations: A well-rounded patent portfolio around JP5629746, including method patents and formulation claims in other jurisdictions, enhances global protection. Coordinating filings to cover key markets (US, EU, China) is advisable.

  • Potential Workarounds: Competitors might design around narrow claims or develop alternative compounds with similar therapeutic effects. Vigilance in monitoring patent landscapes is essential.


Conclusion

JP5629746 exemplifies a strategic patent securing rights over a specific chemical entity and its applications within Japan. Its scope, defined through carefully crafted claims, balances broad protection with defensibility against prior art. The patent landscape reveals a competitive environment with overlapping patents, emphasizing the importance of continuous monitoring and strategic patenting.

For industry players, understanding its scope facilitates informed decisions on R&D direction, licensing negotiations, and market entry planning. The patent’s strength and position within the global landscape will shape the innovation trajectory and commercial prospects of the protected drug.


Key Takeaways

  • Patent JP5629746 provides protection primarily over a novel chemical compound and its therapeutic applications in Japan, likely extending to formulations and methods.
  • The patent’s claims design influences its enforceability and scope; broad claims maximize protection but may invite validity challenges.
  • The patent landscape indicates a competitive environment with overlapping rights; comprehensive FTO analysis is critical before commercialization.
  • Strategic patent filing, including family members in major jurisdictions, enhances global exclusivity.
  • Ongoing patent monitoring and potential licensing opportunities can maximize the patent's commercial value.

FAQs

  1. What is the typical lifespan of a patent like JP5629746 in Japan?
    The standard term is 20 years from the filing date, generally expiring around 2032–2034, assuming maintenance fees are paid.

  2. Can broad claims in JP5629746 be challenged for validity?
    Yes. Broad claims are vulnerable if prior art precludes such scope. Patent invalidation or opposition proceedings can challenge their validity.

  3. How does the patent landscape affect the development of generic versions?
    Overlapping patents or narrow claims can impact entry. If JP5629746 claims are narrow or expire soon, generics might enter the market, contingent on other patents and regulatory approvals.

  4. Does the patent cover methods of manufacturing as well?
    Likely, yes. Many pharmaceutical patents include process claims to protect manufacturing innovations and prevent imitation.

  5. What steps can a patent holder take to strengthen enforcement around JP5629746?
    The holder can strengthen rights by filing additional patents, monitoring competitor activities, and pursuing infringement litigation or licensing agreements.


Sources

  1. Patent JP5629746. Japan Patent Office database.
  2. WIPO PatentScope. International patent applications referencing JP5629746.
  3. Relevant legal frameworks and patent law commentary (Japanese Patent Law).
  4. Industry reports on pharmaceutical patent strategies.
  5. Patent landscape reports for chemical and pharmaceutical inventions within Japan.

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