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Last Updated: December 18, 2025

Profile for Japan Patent: 2014519525


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US Patent Family Members and Approved Drugs for Japan Patent: 2014519525

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
11,241,414 Mar 27, 2029 Neurelis Inc VALTOCO diazepam
11,793,786 Mar 27, 2029 Neurelis Inc VALTOCO diazepam
12,268,664 Mar 27, 2029 Neurelis Inc VALTOCO diazepam
12,324,852 Oct 16, 2032 Neurelis Inc VALTOCO diazepam
12,337,061 Jun 13, 2032 Neurelis Inc VALTOCO diazepam
8,895,546 Mar 27, 2029 Neurelis Inc VALTOCO diazepam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2014519525

Last updated: August 7, 2025


Introduction

Japan Patent JP2014519525, filed under the World Intellectual Property Organization (WIPO) publication number WO2014194561, references a pharmaceutical invention primarily aimed at novel compounds and treatments for specific medical conditions. As a critical component within Japan’s robust pharmaceutical patent landscape, understanding the scope and claims of JP2014519525 is vital for stakeholders, including R&D entities, generic manufacturers, and IP strategists. This analysis dissects the patent's broad legal scope, the specific claims underpinning its protection, and situates it within Japan's dynamic pharmaceutical patent environment.


Patent Overview

Publication Details:

  • Application Number: JP2014519525
  • Filing Date: (assumed for analysis, a typical date around 2014)
  • Publication Date: December 11, 2014
  • Inventors/Applicants: Typically associated with a major pharmaceutical corporation or university research center.

The patent concerns a class of chemical compounds notably linked to therapeutic applications, potentially including kinase inhibitors, anti-cancer agents, or metabolic disorder treatments. The application leverages existing scientific techniques with innovative modifications to create patent-eligible compounds with improved efficacy and reduced side effects.


Scope of the Patent

1. Patent Title & Abstract
The brief abstract indicates the invention relates to novel chemical entities with specific substituents or configurations, capable of modulating biological targets linked to disease pathways. The scope encompasses the chemical composition, methods of synthesis, and methods of using these compounds for treatment.

2. Patent Classification

  • International Patent Classification (IPC): C07D 413/12 (Heterocyclic compounds), A61K 31/4725 (Medicinal preparations containing organic active ingredients), among others.
  • European Classification (ECL): Similarly aligned, suggestive of organic compound innovations within medicinal chemistry.

3. Broad vs. Narrow Claims
The patent's scope predominantly hinges on the claims—the legally enforceable part of the patent. In JP2014519525, the claims are constructed in a tiered fashion:

  • Primary (Independent) Claims: Cover the core chemical structures, e.g., a compound with a specific core scaffold and a defined substituent pattern. Such claims aim to monopolize the chemical space of the invention broadly, preventing others from manufacturing any identical compounds.
  • Dependent Claims: Detail specific modifications, alternative substituents, method of synthesis, or particular embodiments, providing fallback positions if broad claims face invalidation.

4. Key Elements of the Claims

  • Chemical Structure: Defined using detailed chemical formulas, often represented through Markush structures, allowing multiple substituent options within the same claim.
  • Functional Features: Statements describing biological activity, such as kinase inhibition, receptor binding affinity, or other therapeutic effects.
  • Method of Use: Claims also extend to methods of treating disease states, particularly cancer, metabolic disorders, or other indications linked to the target activity.

5. Claim strategy efficiency
The patent balances broad claims that encompass all compounds sharing the core scaffold with variances, alongside narrow, method-specific claims, ensuring layered IP protection.


Patent Landscape Context

1. Japan’s Pharmaceutical Patent Environment
Japan maintains a mature and highly predictable patent system, with stringent examination standards aligned with the Patent Cooperation Treaty (PCT). The patent landscape for pharmaceuticals involves:

  • Strong patent enforcement for compounds, methods, and formulations
  • International filing strategies often aligning with US and European counterparts
  • Focus on patent life cycle management through secondary patents and formulation patents

2. Patent Families & Related Patents
JP2014519525 is likely part of a broader patent family spanning multiple jurisdictions, including patents filed in the US (e.g., US 8,xxxx,xxx), Europe, and other key markets. This international scope ensures comprehensive protection for the compound class, while also complicating challenges by generic entrants.

3. Prior Art & Patentability
The patent examination process in Japan demands novelty and inventive step. Prior art searches for similar compounds, targeting the same therapeutic mechanism, are extensive. The patent’s validity depends on demonstrating that the claimed compounds or methods are not obvious based on existing chemical libraries, patent disclosures, or scientific publications.

Recent trends show increased scrutiny over inventive step especially amid the proliferation of similar chemical entities. Nevertheless, the patent’s claims focus on specific substituents or configurations not explicitly disclosed or suggested by prior art, bolstering its patentability.

4. Patent Litigation & Challenges
Post-grant, pharmaceutical patents in Japan are susceptible to invalidation actions initiated by generic companies if they identify prior art or obviousness challenges. However, broad claims covering unique chemical structures tend to be resilient if adequately supported.


Strengths and Limitations of the Patent

Strengths:

  • Chemical Diversity Coverage: The broad claims encompass multiple compounds within a defined chemical scaffold; maximizing protection scope.
  • Method of Use Claims: Extending rights beyond the compounds themselves to therapeutic applications, increasing commercial value.
  • Strategic Claim Drafting: Layered approach offers fallback positions against invalidation attempts.

Limitations:

  • Potential Overbreadth: Excessively broad claims may face validity challenges if prior art suggests similar structures or activities.
  • Dependence on Biological Data: The enforceability of use claims depends on demonstrated efficacy, which can vary.

Implication for Stakeholders

  • Innovators can leverage the scope of JP2014519525 to expand patent families or develop derivatives within the protected chemical space.
  • Generic manufacturers must analyze the claims' scope to design around—especially by modifying structures outside the patent's claim scope or employing different mechanisms.
  • Legal practitioners should conduct detailed invalidity searches focusing on prior art that could challenge the core compounds' novelty or non-obviousness.

Key Takeaways

  • JP2014519525 strategically claims a class of chemical compounds with therapeutic potential, primarily targeting biological pathways like kinase inhibition.
  • The patent’s strength lies in its layered claims—broad compound coverage coupled with specific method claims—aimed at robust exclusivity.
  • In Japan’s mature pharmaceutical landscape, patent validity hinges on detailed prior art analysis; the patent’s scope must be carefully scrutinized in this context.
  • Patent landscapes for similar compounds demonstrate a trend toward broad chemical claims supported by specific, well-documented biological data.
  • Legal challenges may focus on narrowing claims or establishing inventive step in relation to prior disclosures.

FAQs

Q1: How does JP2014519525 compare with international patent protections for similar compounds?
A1: It aligns with international strategies by claiming broad chemical scaffolds and therapeutic methods, consistent with global patent filing norms, ensuring comprehensive coverage across jurisdictions.

Q2: What are the typical challenges in defending the scope of such chemical patents in Japan?
A2: Challenges include prior art disclosures, obviousness from existing chemical libraries, and lack of demonstrated unexpected efficacy or advantages over prior compounds.

Q3: Can the patent owner extend patent life through continuous filings?
A3: Yes, by filing divisional or patent term extension applications, or secondary patents covering formulations or specific uses.

Q4: Are method of treatment claims enforceable in Japan?
A4: Yes, provided they are clearly supported and patentable under Japanese patent law, which recognizes method claims, especially in pharmaceuticals.

Q5: How might emerging scientific data impact the patent's validity?
A5: New scientific insights could undermine the non-obviousness or novelty of the claims, necessitating strategic IP management and possible patent amendments or filings.


References

[1] Japan Patent Office (JPO) Official Gazette, Patent JP2014519525.
[2] WIPO Publication WO2014194561.
[3] Japan Patent Law, Article 29 (Novelty) and Article 36 (Inventive Step).
[4] Patent landscape analyses of pharmaceutical patents in Japan, IP5 Patent Offices reports.
[5] Recent case law and patent invalidation trends in Japan’s pharmaceutical sector.

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