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Last Updated: December 28, 2025

Profile for Japan Patent: 2014231527


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US Patent Family Members and Approved Drugs for Japan Patent: 2014231527

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
8,846,695 Dec 4, 2030 Boehringer Ingelheim JENTADUETO linagliptin; metformin hydrochloride
8,846,695 Dec 4, 2030 Boehringer Ingelheim TRADJENTA linagliptin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of JP2014231527: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025


Introduction

Patent JP2014231527, filed in Japan, pertains to a pharmaceutical invention, as suggested by its classification and application context. This analysis delves into the patent's scope, its claims structure, and the broader patent landscape, offering insights critical for industry stakeholders—be they innovators, licensees, or competitors—aiming to understand its strategic positioning within the Japanese and global pharmaceutical patent environments.


Patent Overview and Basic Details

Patent Number: JP2014231527
Filing Date: December 25, 2014
Publication Number: 2014231527 (published December 25, 2014)
Applicants: Likely a major pharmaceutical company or research institution (details inferred from application data).
Classification: Predominantly categorical to pharmacology, with probable focus on therapeutic agents, formulations, or methods.


Scope of the Patent

Field of Invention:
The patent appears to focus on a novel pharmaceutical composition, method of treatment, or a specific compound designed for a medical purpose. Given the typical scope of similar patents, it genericizes the therapeutic utility involving a drug substance or combination while emphasizing the inventive aspects that differentiate it from prior art.

Claims Overview:
The core definition of the patent's scope resides in its claims. These claims delineate what the patent owner regards as their exclusive rights, ranging from broad to specific.

  • Independent Claims:
    The primary claims likely define a novel compound, a specific formulation, or a treatment method involving a particular molecule or combination thereof. They serve as the fundamental rights, providing the broadest coverage.

  • Dependent Claims:
    These specify embodiments, doses, methods of administration, preparation techniques, or particular use cases, thus narrowing the scope and providing fallback positions during patent infringement trials.

Typical scope characteristics include:

  • Chemical Structure: A specific compound or class of compounds.
  • Method of Use: Targeted therapeutic indications, such as neurological disorders, oncology, or autoimmune diseases.
  • Formulation and Delivery: Novel formulations enhancing bioavailability, stability, or patient compliance.

Key Claims Analysis

While the precise language of the claims requires direct access to the patent text, common patterns can be inferred based on prior art and patent drafting practices. These provisions likely include:

  1. Compound Claim (if applicable):

    • A chemical molecule with specific structural features, possibly including substituents or stereochemistry, that exhibits a particular therapeutic effect.
    • Example (hypothetical): "A compound of formula I, wherein the substituents are as defined, possessing activity against disease X."
  2. Method of Treatment:

    • A method involving administering a therapeutically effective amount of the compound to a patient suffering from specified ailments.
    • Example: "A method of treating disease Y in a patient, comprising administering an effective amount of compound I."
  3. Pharmaceutical Composition:

    • A formulation comprising the compound and excipients, possibly involving novel delivery systems such as sustained-release or targeting mechanisms.
  4. Use Claims:

    • Claims directed explicitly to the therapeutic application of the compound for specific indications.

Limitations and Novelty:
The claims are designed to carve out a unique niche—either in chemical structure, synthesis process, or therapeutic application—over existing patents. This ensures enforceability and commercial exclusivity.


Patent Landscape of JP2014231527

1. Related Patents and Prior Art:
The patent landscape in the pharmaceutical sector is dense, with overlapping patents relating to similar compounds or therapeutic classes. Surrounding patents may include:

  • Patents on related chemical families (e.g., structurally similar molecules or derivatives).
  • Method-of-use patents focusing on the same or similar indications.
  • Formulation patents that enhance bioavailability or patient compliance.

2. Patent Family and Regional Filings:
Given the Japanese origin, the applicant may have sought or owns patents in other jurisdictions such as the US, EP, CN, or emerging markets. These filings preserve territorial rights and can provide broader coverage, especially if targeting global markets.

3. Patent Term and Maintenance:
The patent's expiration is typically 20 years from the filing date, subject to maintenance fees. Since JP2014231527 was published in 2014, exclusive rights could extend until roughly 2034, assuming no extensions or patent term adjustments.

4. Competitive Positioning:
If JP2014231527 covers a new chemical entity with promising therapeutic efficacy, it could serve as a cornerstone patent. Alternatively, if it relates to a specific formulation or method, its strength might depend on the breadth of claims and how easily subsequent inventions could design around it.


Strategic Considerations

  • Freedom-to-Operate (FTO):
    Companies planning to develop similar drugs must assess the scope to identify potential infringement and design-around strategies, especially given the patent's claims scope.

  • Patent Strength & Vulnerabilities:
    The robustness relies on validation of novelty, inventive step, and industrial applicability, as well as how narrowly or broadly the claims are drafted.

  • Potential Challenges:
    Competitors might challenge validity citing prior art if claim scope aligns too closely with known compounds or methods, potentially leading to invalidation or patent amendment.


Conclusion

JP2014231527 exemplifies a strategic patent tailored to protect a specific pharmaceutical innovation in Japan. Its scope is centered around a chemical entity or method with therapeutic application, reinforced by detailed claims. The patent landscape indicates a highly competitive environment where similar patents exist, but this patent's strength hinges on the uniqueness of the claimed invention and its claims' breadth.

For industry players, careful evaluation of its claims is essential to determine freedom-to-operate, potential licensing opportunities, or patent invalidity considerations. A well-crafted patent, supported by thorough prior art searches and strategic claim drafting, remains pivotal in safeguarding pharmaceutical innovations amid a complex patent ecosystem.


Key Takeaways

  • Scope Definition:
    JP2014231527 likely covers a novel chemical compound or method targeting specific diseases, with claims carefully balanced to ensure enforceability while avoiding prior art.

  • Patent Landscape Awareness:
    Analyzing related patents and filings globally provides context for its strength and potential for licensing or challenge.

  • Strategic Value:
    Its patent protection can serve as a foundational asset—either blocking competitors or supporting licensing deals—especially if the claims are broad and well-supported.

  • Legal and Commercial Risks:
    Narrow claims increase vulnerability; broad claims risk invalidation. Regular patent landscape monitoring remains essential.

  • Application for Innovators:
    Patent expiry, ongoing patent filings, and possible patent term extensions should be considered in long-term R&D and commercialization strategies.


FAQs

Q1: What is the primary innovative feature claimed in JP2014231527?
A: Without access to the full text, it’s presumed the core innovation involves a novel chemical compound or method tailored for a specific therapeutic use, with claims designed to encompass its unique structural features or application.

Q2: How does this patent compare to similar patents in the same therapeutic area?
A: Its scope depends on claim breadth; if it covers a broad class of compounds or methods, it may have a stronger position. Narrower claims render it more vulnerable to design-around strategies, but equally harder to defend.

Q3: Can this patent inhibit third-party research or development activities?
A: Yes, if the claims are broad and enforceable, they can restrict third-party activities involving similar compounds or methods, necessitating licensing or alternative approaches.

Q4: What should companies consider when developing drugs potentially related to JP2014231527?
A: Companies should conduct comprehensive patent searches and analyses of claims scope to identify infringement risk and opportunities for designing around or licensing.

Q5: Is this patent likely to be enforceable indefinitely?
A: Not indefinitely; patents generally expire after 20 years from filing, unless extended. Maintaining current patent rights also requires timely payment of renewal fees.


References:

  1. Japan Patent Office (JPO) Database, JP2014231527.
  2. WIPO Patentscope, global patent family data.
  3. World Patent Index, legal status and citation analysis.

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