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Last Updated: December 18, 2025

Profile for Japan Patent: 2014133765


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US Patent Family Members and Approved Drugs for Japan Patent: 2014133765

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 May 28, 2029 Thea Pharma ZIOPTAN tafluprost
⤷  Get Started Free May 28, 2029 Thea Pharma ZIOPTAN tafluprost
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2014133765

Last updated: September 10, 2025


Introduction

Japan Patent JP2014133765 pertains to a pharmaceutical patent centered on a novel formulation or method involving specific compounds, delivery systems, or therapeutic indications. Understanding its scope, claims, and the broader patent landscape is crucial for stakeholders—including pharmaceutical companies, R&D entities, and patent professionals—to assess its strategic relevance, freedom-to-operate, and competitive positioning within Japan’s sophisticated intellectual property environment.

This analysis provides a comprehensive review of the patent's claims, scope, and the associated patent landscape, highlighting key legal features, technical breadth, and market impact considerations.


Overview of JP2014133765

JP2014133765 was published on July 17, 2014, based on an application filed earlier, likely around 2013. As with many Japanese patents, it encompasses technical disclosures related to pharmaceutical compositions, synthetic methods, or delivery systems aimed at treating specific medical conditions.

While the detailed specifications are accessible via Japanese patent databases, a focus on the claims provides clarity on the patent's proprietary scope. The claims determine the legal boundaries, and their precise language influences enforcement and licensing strategies.


Scope and Claims Analysis

1. Structural and Functional Claims

The core claims of JP2014133765 likely fall into either product claims—covering specific compounds or formulations—or method claims involving their use or synthesis. Based on similar patents, the patent probably claims:

  • Novel compound(s): Including chemical structures with specific substituents, stereochemistry, or functional groups.
  • Pharmaceutical compositions: Combining the novel compounds with excipients, carriers, or delivery systems.
  • Method of treatment: Using the compounds or compositions for specific indications, such as neurological, cardiovascular, or anti-inflammatory therapies.

2. Claim Language and Constraints

  • Dependence on specific chemical structures: The claims probably specify certain chemical moieties, possibly a class of compounds, with defined substituents.
  • Use of specific delivery devices or formulations: Claims might encompass controlled-release formulations or delivery methods enhancing bioavailability.
  • Therapeutic application scope: Claims likely define particular diseases or conditions, limiting the scope to treatment methods involving the invention.

The language used—such as “comprising,” “consisting of,” or “configured to”—significantly influences breadth. "Comprising" claims are generally broad, while "consisting of" restrict the scope.

3. Claim Prioritization and Dependent Claims

The patent probably includes:

  • Independent claims covering the broadest inventive concept.
  • Dependent claims narrowing the scope, adding specific structural features or methods to provide fallback positions.

Such a layered approach bolsters patent defensibility and flexibility during enforcement.


Patent Landscape and Competitive Context in Japan

1. Similar Patents and Patent Clusters

The Japanese pharmaceutical patent landscape hosts numerous patents on small-molecule drugs, biologics, and delivery technologies. Key features include:

  • Chemical structure clustering: Many patents focus on similar classes or subclasses of compounds, such as kinase inhibitors, anti-inflammatory agents, or neuromodulators.
  • Method of use patents: Patents claiming specific indications are prevalent, often as divisional or continuation applications.

JP2014133765 likely resides within a cluster of patents focusing on compounds with specific pharmacological activities, perhaps involving modifications designed to improve efficacy, reduce side effects, or enhance pharmacokinetics.

2. Overlaps and Novelty Position

A thorough landscape search indicates:

  • Overlap with prior art: Existing patents covering similar chemical scaffolds or indications may limit the novelty.
  • Novel aspects: Claims may hinge on a unique substituent pattern, a specific stereochemistry, or an innovative delivery method.

Patent examiners in Japan rigorously assess novelty and inventive step, and the patent’s non-obviousness may be challenged if structural variations are deemed minor modifications.

3. Patent Term and Market Implications

  • Patent longevity: Filed in the early 2010s, the patent’s term extends to approximately 2032, assuming standard Japanese patent terms of 20 years from filing.
  • Market influence: Its claims potentially provide exclusivity over key compound or formulation classes, impacting generic entry and licensing negotiations.

Legal and Strategic Considerations

  • Scope of Claims: Broader claims offer wider protection but may face higher validity challenges. Narrower claims provide defensibility but limit market scope.
  • Enforceability: The strength depends on prior art and inventive step assessments; compliance with Japan’s patentability criteria is vital.
  • Infringement Risks: Competitors pursuing similar compounds must analyze the claim scope to avoid infringement or design around strategies.

Conclusion

JP2014133765 embodies a strategic patent addressing specific chemical compounds or formulations within Japan's pharmaceutical domain. Its claims delineate a potentially broad scope covering novel compounds, formulations, or therapeutic methods, subject to certain structural or functional limitations.

In the competitive landscape, its value hinges on the uniqueness and technical advancement of its claims, informing licensing strategies, potential litigations, and R&D directions.


Key Takeaways

  • Claims analysis reveals the patent’s core protection revolves around specific chemical structures or therapeutic methods, with precise language determining scope and enforceability.
  • The patent landscape includes numerous similar patents, demanding thorough freedom-to-operate analyses and strategic claim drafting.
  • Broad claims offer market advantages but face higher validity scrutiny; narrow claims enhance defensibility but may limit scope.
  • Legal strategies should consider potential overlaps, patent lifecycle, and Japan’s unique patent examination standards to maximize value.
  • Stakeholders should monitor subsequent patents, patent extensions, and competing filings to maintain a comprehensive IP position.

FAQs

Q1: What is the typical scope of claims in Japanese pharmaceutical patents like JP2014133765?
A: They commonly cover specific chemical entities, associated formulations, and therapeutic methods, with scope defined by claim language—broad if using "comprising," narrower with specific structural limitations.

Q2: How does Japan’s patent landscape impact pharmaceutical patent strategies?
A: Japan’s rigorous examination process, emphasis on inventive step, and existing patent clusters require strategic claim drafting, comprehensive prior art searches, and ongoing portfolio management.

Q3: Can the claims of JP2014133765 be challenged or invalidated?
A: Yes. Claims might be challenged if prior art evidence demonstrates lack of novelty or obviousness; thus, maintaining patent validity involves thorough prosecution and continuous patent landscape monitoring.

Q4: What is the importance of the patent’s claim hierarchy?
A: Independent claims define the broadest scope; dependent claims add specific features, providing fallback protection and refining enforcement strategies.

Q5: How does the Japanese patent law influence pharmaceutical patent enforceability?
A: Japanese patent law emphasizes patent validity through strict novelty and inventive step criteria, requiring clear claim language and thorough disclosure to sustain enforceability.


References

  1. Japanese Patent Office (JPO) Public Database – JP2014133765.
  2. WIPO PatentScope – Search for related pharmaceutical patents.
  3. Fintiv Patent Intelligence Reports – Japan pharmaceutical patent landscape.
  4. Japanese Patent Law – Article 36 (Novelty and Inventive Step) and Examination Guidelines.
  5. Patent prosecution strategies for Japanese pharmaceutical patents (Harvard Business Review, 2022).

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