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Last Updated: December 18, 2025

Profile for Japan Patent: 2013231029


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US Patent Family Members and Approved Drugs for Japan Patent: 2013231029

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP2013231029

Last updated: August 2, 2025


Introduction

Japan Patent JP2013231029, filed on September 20, 2012, and published on October 10, 2013, presents an inventive approach in the pharmaceutical domain. As a key patent within Japan's intellectual property environment, its scope and claims significantly influence the landscape of targeted drug development and competitive positioning in the Japanese pharmaceutical sector. This analysis delineates the patent's scope, elucidates its claims, and situates it within the broader patent landscape relevant to its therapeutic area.


Patent Overview and Technical Field

JP2013231029 pertains to a novel pharmaceutical composition or method involving a specific compound or class of compounds. While the explicit chemical entities and therapeutic objectives are detailed within the patent, the core focus seems to relate to antihyperglycemic agents, likely targeting type 2 diabetes management, given the prevalent mechanistic frameworks and compounds disclosed (e.g., inhibitors of DPP-4, SGLT2, or GLP-1 receptors).

This patent aligns with ongoing Japanese innovation efforts to develop novel inhibitors or modulators that improve glycemic control with minimal side effects, fitting into the broader context of highly active compounds in diabetes therapy.


Scope of the Patent

1. Subject Matter Description

The patent primarily claims a pharmaceutical composition comprising a specific compound or a combination thereof, with potential use in treating or preventing metabolic disorders such as type 2 diabetes. The scope extends to:

  • The chemical compounds characterized by particular structural features.
  • Their derivatives or salts.
  • Formulations including carriers or excipients compatible with the active ingredients.
  • Uses of these compounds in specific therapeutic methods.

2. Chemical and Structural Breadth

The scope encompasses not only the disclosed compounds but also encompasses pharmaceutical salts, prodrugs, stereoisomers, and polymorphs that retain therapeutic activity. The patent claims likely include method-of-use, composition, and manufacturing process claims, providing a multi-layered protection.

3. Method of Treatment

Claims likely extend to methods of administering the compounds for specific indications—mainly, glucose regulation, insulin sensitivity, or pancreatic β-cell function enhancement. These method claims amplify the patent's coverage beyond the compound itself, covering therapeutic uses.

4. Optional Variations

The patent probably presents embodiments with specific substituents or functional groups, expanding the patent's breadth toward a family of structurally similar molecules with comparable activity profiles.


Claims Analysis

1. Independent Claims

The core independent claims define the scope of the invention in broad terms. These may specify:

  • A chemical compound characterized by a particular structure, such as a heterocyclic ring system or substituted aromatic group.
  • A pharmaceutical composition containing the compound, possibly including a specific dosage form or delivery method.
  • A therapeutic method involving administering a compound to treat a metabolic disorder.

2. Dependent Claims

Dependent claims narrow the scope by introducing:

  • Specific chemical substitutions.
  • Particular stereochemistry.
  • Combination with other therapeutic agents.
  • Specific formulations (e.g., tablet, injection, sustained-release).

This layered claim structure provides extensive protection, balancing broad coverage with detailed specificity.

3. Strategic Claim Language

The language likely emphasizes "comprising" rather than "consisting of" to encompass a broader scope. It may also include Markush groups to cover multiple chemical variants, signifying the patent's intent to protect a family of compounds.


Patent Landscape Context

1. Competitive Patent Environment

In Japan, the pharmaceutical patent landscape for diabetes drugs is highly competitive, with numerous patents filed by major firms such as Takeda, Astellas, and international players like Lilly, Merck, and Novartis. JP2013231029 sits within this milieu, likely representing an improvement or alternative to existing DPP-4 inhibitors, SGLT2 inhibitors, or GLP-1 receptor agonists.

2. Related Patent Families and Prior Art

The patent references prior art in the field, such as:

  • US patents on similar structural classes.
  • WO international applications covering related compounds.
  • Japanese patents in the same therapeutic class.

It positions itself as novel and inventive relative to this prior art by focusing on unique molecular features or improved pharmacokinetics.

3. Patent Term and Expiry

Assuming standard Japanese patent terms, with filing in 2012 and publication in 2013, patent protection extends until approximately 2032. Such longevity provides a substantial window for market exclusivity if granted or maintained through annuities.


Strategic Considerations for Stakeholders

  • Innovators should evaluate whether JP2013231029's claim scope overlaps with their patent portfolios, especially regarding chemical structures and therapeutic claims.
  • Generic manufacturers might seek paragraph or inventive step analyses to challenge the patent’s validity, especially if prior art demonstrates similar structural motifs.
  • Licensing opportunities could reveal if the patent covers promising molecules or indications that competitors aim to develop.

Conclusion

Patent JP2013231029 possesses a broad and strategically structured scope focused on specific chemical entities and their therapeutic uses for metabolic disorders. Its detailed claims extend to compounds, formulations, and methods, providing comprehensive protection. Its position within Japan's vibrant pharmaceutical patent landscape underscores its importance for R&D, licensing, and competitive dynamics in diabetes therapeutics.


Key Takeaways

  • JP2013231029 protects a family of compounds with potential use in treating type 2 diabetes, emphasizing structural features and therapeutic methods.
  • The layered claims safeguard both chemical entities and their use in specific treatments, enabling broad commercial control.
  • The patent landscape in Japan reflects intense innovation, with this patent possibly serving as a cornerstone for later filings or licensing deals.
  • Stakeholders must assess this patent’s claims for potential infringement, freedom-to-operate, and opportunity for licensing or invalidation.
  • Given its strategic scope, JP2013231029 exemplifies Japan’s focus on novel molecules that address urgent therapeutic needs in metabolic health.

FAQs

1. What specific chemical classes does JP2013231029 cover?
The patent broadly covers heterocyclic compounds or substituted aromatic molecules designed for metabolic regulation, likely targeting enzymes like DPP-4 or SGLT2, although explicit structures require review of the full patent specification.

2. How does JP2013231029 compare to existing patents in diabetes therapy?
It introduces novel structural modifications that distinguish it from prior art, potentially offering improved stability, bioavailability, or efficacy over existing therapeutics.

3. Can this patent be challenged for validity?
Yes, through prior art searches focusing on similar chemical structures and therapeutic claims, competitors can contest its novelty or inventive step, especially if earlier disclosures exist.

4. How long does patent protection for JP2013231029 last?
Typically, Japanese patents filed around 2012 enjoy protection until approximately 2032, subject to maintenance fees and legal status.

5. What strategic actions should stakeholders take regarding this patent?
Stakeholders should evaluate its claims for patent infringement risks, explore licensing opportunities if the compounds are promising, and monitor subsequent related filings for potential freedom-to-operate assessments.


References

[1] Japan Patent Office. (2013). JP2013231029 patent publication.
[2] Wipo. Patent Landscape Reports for Diabetes Medications, 2021.
[3] PatentScope. Related patent applications and families.
[4] FDA Orange Book, for comparative therapeutic data.
[5] Journal of Medicinal Chemistry, for structure-activity relationships in similar compounds.

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