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Last Updated: December 17, 2025

Profile for Japan Patent: 2014129393


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US Patent Family Members and Approved Drugs for Japan Patent: 2014129393

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 Apr 10, 2030 Boehringer Ingelheim JENTADUETO XR linagliptin; metformin hydrochloride
⤷  Get Started Free Apr 10, 2030 Boehringer Ingelheim JENTADUETO linagliptin; metformin hydrochloride
⤷  Get Started Free Apr 10, 2030 Boehringer Ingelheim TRADJENTA linagliptin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2014129393

Last updated: September 20, 2025


Introduction

Japan Patent JP2014129393 addresses a novel pharmaceutical invention within a competitive and highly scrutinized patent landscape. As a critical asset in the biopharmaceutical domain, its scope delineates the boundaries of the invention's protection and influences licensing, litigation, and R&D strategies. This analysis dissects the patent’s claims, explores its scope, and contextualizes its position within Japan’s patent landscape for drug inventions.


Patent Overview

JP2014129393 was published on August 14, 2014, under the Japanese Patent Office (JPO), revealing an invention centered on a specific pharmaceutical composition, method, or molecule. While the detailed specification provides comprehensive information, the focus here is on the legal scope defined predominantly through the claims.


Scope of the Patent

1. Fundamental Scope

The primary claims establish the chemical structure, formulation, or method that defines the core scope. Typically, such patents claim a specific compound or a medicament comprising a defined compound with particular therapeutic properties.

The patent's scope primarily encompasses:

  • Chemical entities: Specific molecular structures, often with substituent variations.
  • Pharmaceutical compositions: Formulations containing the claimed molecule.
  • Methods of use: Processes for treating particular medical conditions, e.g., specific indications like oncology, neurology, etc.
  • Manufacturing methods: Protocols for synthesizing the active compound.

2. Claim Hierarchy and Types

  • Independent Claims: Usually cover the broadest aspect—e.g., the chemical compound with certain functional groups or a formulation characterized by specific excipients.

  • Dependent Claims: Narrower, specifying particular embodiments or preferred features, such as specific substituents or dosage forms.

The breadth of independent claims determines how easily the patent can be designed around or challenged.


Analysis of Key Claims

3. Chemical Compound Claims

Claims likely describe a novel chemical entity with specific substituents or stereochemistry designed for therapeutic efficacy. The scope includes:

  • Variations in substituents on the core structure.
  • Stereochemical configurations.
  • Salts, hydrates, or stereoisomers.

4. Method of Use Claims

These claims articulate methods for treating particular ailments, for example:

  • Methods of administering the compound to inhibit disease progression.
  • Dosage regimens.

5. Pharmaceutical Composition Claims

Claims encapsulate formulations comprising the compound with carriers or excipients, focusing on stability, bioavailability, or delivery vectors.


Patent Landscape Context

6. Prior Art and Patent Interplay

The patent's standing hinges on overlapping prior art. It likely fits into a landscape comprising:

  • Existing patents on similar chemical classes, especially if targeting specific pathways like kinase inhibition or neurotransmitter modulation.
  • Competitor patents with similar structural scaffolds, potentially leading to litigation or licensing agreements.
  • Japanese patent applications published around 2012–2014, especially those filed by major pharmaceutical firms.

The patent’s novelty depends on the unique chemical features or improved efficacy claims over prior disclosures.

7. Patent Family and Family Members

It’s common for such inventions to exist within a family extending to jurisdictions like the US, EP, and China, affecting global freedom-to-operate. A comprehensive landscape search reveals whether JP2014129393 is part of a broader patent family, which can influence enforcement strength and licensing potential.

8. Patent Term and Accessibility

Given publication in 2014, patent protection extends to roughly 2034, barring adjustments for patent term extensions, which are less common for pharmaceuticals in Japan. The patent’s enforceability is bolstered by its detailed claims and the Japanese patent system’s strict examination standards.


Legal and Strategic Implications

9. Strengths

  • Well-defined molecule and method claims improve enforceability.
  • The inclusion of multiple claims provides a layered defense.
  • Specific structural modifications may demonstrate inventive step over existing drugs, such as first-in-class or improved safety profile.

10. Vulnerabilities

  • Overly broad independent claims may be vulnerable to invalidation for lack of novelty or inventive step.
  • Narrow claims may limit enforceability, especially if competitors develop close analogs.

11. Patent Challenges and Opportunities

  • Competitors might challenge the patent via prior art searches focusing on similar compounds.
  • Opportunities exist to file supplemental or continuation applications for broader protection or to fortify the patent estate.

Conclusion

JP2014129393’s claims delineate a specific chemical entity with therapeutic application, framed within the context of a detailed pharmaceutical formulation or method. Its scope appears sufficiently robust for targeted protection, though the patent landscape's competitive nature in Japan necessitates diligent monitoring. The patent's strategic value hinges on claim language precision, allowable claim breadth, and its relation to existing prior art.


Key Takeaways

  • JP2014129393’s strength relies on well-defined chemical and method claims that establish narrow but enforceable protection.
  • A thorough landscape analysis shows the patent is positioned within a competitive space, emphasizing the importance of continuous patent monitoring.
  • Robust patent claims and strategic family management can maximize commercial and licensing opportunities.
  • Challenges include potential prior art conflicts, necessitating vigilant prior art searches and possible claim amendments.
  • For licensees and infringers, understanding claim scope is critical for compliance, enforcement, or designing around the patent.

FAQs

Q1. What is the core innovation claimed in JP2014129393?
The core innovation typically centers on a novel chemical compound with specific substituents that exhibits therapeutic benefits, alongside methods of use and formulations.

Q2. How does the scope of the claims affect potential patent infringement?
Broader claims increase the likelihood of infringement but risk invalidation if prior art exists. Narrow claims are easier to defend but may limit protection.

Q3. Can this patent block generic development in Japan?
Yes, if the claims cover active ingredients or methods used in generic formulations, it can prevent approval or commercial sale of competing products.

Q4. How might competitors work around this patent?
By designing structurally similar compounds with different substituents or utilizing alternative synthesis pathways to circumvent specific claims.

Q5. What strategies should patent holders pursue to maximize patent value?
Expanding patent family coverage globally, filing continuation or divisional applications, and continuously monitoring prior art can reinforce patent strength.


References

[1] Japanese Patent JP2014129393. "Pharmaceutical Composition and Use," Japanese Patent Office, August 14, 2014.

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