Last updated: July 28, 2025
Introduction
Patent JP2019112462, filed in Japan, pertains to a pharmaceutical invention aimed at addressing specific medical needs through novel compounds, formulations, or methods. As a "drug patent," its scope and claims significantly influence market competition, licensing opportunities, and patent litigation risk management.
This article provides a comprehensive, detailed analysis of JP2019112462, focusing on its scope, claims, and position within the japan drug patent landscape.
Patent Overview
Filing and Publication Details
- Application Number: JP2019112462
- Filing Date: Presumably mid-2019 (based on the publication number)
- Publication Date: Likely around 2019-2020
- Inventors/Applicants: [Information not provided in the prompt]
Subject Matter
Although the full patent text isn't visible, based on standard practice and typical pharmaceutical patent structures, JP2019112462 likely relates to:
- A novel compound or a class of compounds
- A specific pharmaceutical formulation or delivery method
- A therapeutic use or method of treatment for a particular condition
Such patents often aim to extend patent life cycles, secure exclusive rights over innovative molecules, or improve existing therapies.
Scope of the Patent
Scope refers to the breadth of the patent's statutory rights as conferred by its claims. It defines what is protected and what actions constitute infringement.
Key features:
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Independent Claims:
Usually, the main claim encompasses the core invention—e.g., a chemical compound or composition with specific structural features and intended use.
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Dependent Claims:
Detail particular embodiments, formulations, methods of synthesis, or specific therapeutic applications. Typically, these narrow the scope but provide fallback positions.
Potential Scope Elements for JP2019112462:
Considering Japanese patent conventions and pharmaceutical patents, the scope may include:
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Chemical Structure:
- A specific chemical formula, possibly a new heterocyclic compound or derivative.
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Pharmaceutical Composition:
- Combinations with excipients or carriers suitable for oral, injectable, or topical administration.
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Method of Use:
- Methods for treating a disease, e.g., neurodegenerative disorders, cardiovascular diseases, or cancers with the claimed compound.
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Synthesis or Manufacturing Process:
- Novel methods or intermediates for producing the claimed compound efficiently.
Assessment of Scope Breadth
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Broad Claim Strategies:
If the independent claim claims a generic chemical class or a wide therapeutic application, the patent's scope is broad, offering extensive exclusivity.
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Narrow Claim Strategies:
Specific compounds, dosages, or narrowly defined indications limit the scope, but may be easier to defend or enforce.
Analysis of the Claims
Understanding the Claims
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Independent Claims:
Typically define the core invention—e.g., the chemical entity or method.
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Dependent Claims:
Cover variations, specific embodiments, or particular implementations.
Key Considerations:
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Claim Language and Limitations
- Structural Definitions: Are the chemical structures narrowly or broadly defined?
- Functional Limitations: Does the claim specify particular functional properties?
- Use Claims: Are therapeutic methods claimed, and if so, how specifically?
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Claim Scope and Patentability
- Novelty:
Does the claim define a novel compound or use?
- Inventive Step:
Is the claimed invention non-obvious over prior art?
- Utility:
Does the claim specify a plausible therapeutic benefit?
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Potential Overlaps or Conflicts
- Constraints from prior patents or existing therapeutics could restrict claim scope.
Implication of Claim Structure
- If JP2019112462's independent claims cover a broad chemical class, they could effectively block similar compounds with minor modifications.
- Narrower claims, limited to specific compounds or uses, allow for carve-outs for competitors but provide less overarching protection.
Patents Landscape Analysis in Japan
Japanese Pharmaceutical Patent Environment
Japan ranks among the world's leading pharmaceutical markets, with a robust patent system aligning with international standards (TRIPS agreement). Key features include:
- Patent Term: 20 years from filing date, with extensions possible for certain pharmaceuticals to compensate for regulatory delays.
- Data Exclusivity: 6 years for new drugs, influencing innovation incentives.
- Patent Examination: Rigorous, with an option for accelerated examination for certain pharmaceuticals.
Market & Innovation Trends
- Increasing filings for biologics and biosimilars.
- Focus on personalized medicine and targeted therapies.
- Growing patent litigation, especially regarding process versus product claims.
Position of JP2019112462 in Landscape
- Likely part of a broader portfolio of chemical or therapeutic patents.
- May face prior art hurdles if related existing patents cover similar compounds or uses.
- Potential for licensing or partnership opportunities if the compound shows promising efficacy.
Patentability and Prior Art Considerations
Prior Art Search
- Review of existing patents and publications evaluating similar compounds or methods (e.g., WO, US, EP patents).
- Common references include previous chemical patents (e.g., KR patents, Chinese patents), scientific literature, and clinical data.
Key Patentability Factors
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Novelty:
The claimed compound must differ significantly from existing compounds or uses.
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Inventive Step:
Demonstrating an inventive step requires showing the invention is not obvious to a person skilled in the art based on prior art disclosures.
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Utility:
The claimed method or compound must have demonstrated or plausible therapeutic efficacy.
Potential Obstacles
- Prior art compounds with similar structures or uses could limit scope.
- Prior disclosures of synthesis methods affecting patent defensibility.
- Challenges may arise in establishing sufficient inventive step if similar compounds are known.
Patent Landscape & Competitive Position
Comparative Analysis
- Patent families similar to JP2019112462 may exist in the US, Europe, or China.
- Broader claims might be challenged or invalidated if prior art overlaps.
- Narrow, strategically drafted claims can provide niche protection while avoiding prior art pitfalls.
Licensing and Commercialization
- Depending on the scope, the patent can serve as a foundation for licensing, co-development, or exclusivity in specific indications.
Conclusion
JP2019112462 likely protects a specific chemical entity or therapeutic method with a meticulously drafted set of claims. Its value and scope depend on:
- The breadth of independent claims—whether it covers a broad class of compounds or narrowly defined molecules.
- The robustness against prior art challenges, influenced by claim language and inventive step.
- Its positioning within Japan's patent landscape, considering existing patents and clinical needs.
A well-structured patent focusing on a novel, non-obvious compound or method with clear utility, aligned with the requirements under Japanese patent law, can secure valuable market exclusivity and facilitate strategic partnerships.
Key Takeaways
- Scope varies based on claim drafting: Broader claims offer wider protection but are more vulnerable; narrower claims are safer but limit coverage.
- Patent landscape understanding is crucial: Knowledge of prior art, existing patents, and market needs guides effective patent strategy.
- Japanese patent law emphasizes novelty and inventive step: Ensuring claims overcome prior art hurdles is essential.
- Protecting therapeutic innovations: Claiming specific compounds and uses enhances enforceability in Japan.
- Strategic patent planning: Combination of product, process, and use claims optimizes market position and mitigates infringement risks.
FAQs
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What is the significance of the scope of claims in a pharmaceutical patent?
The scope determines the extent of legal protection, influencing infringement risks, licensing potential, and competitive advantage.
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How does Japanese patent law impact pharmaceutical patents like JP2019112462?
Japan emphasizes novelty, inventive step, and utility. Proper claim drafting aligned with these criteria ensures patent validity and enforceability.
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Can similar compounds outside Japan infringe a patent like JP2019112462?
Patent rights are territorial; infringement depends on whether the claimed invention is made, used, or sold within Japan. Similar compounds abroad are subject to their respective patents.
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What strategies can strengthen the patent landscape for a new drug in Japan?
Filing combination patents, covering both compounds and methods, and conducting comprehensive prior art searches can establish a stronger patent position.
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What role does patent landscape analysis play in drug development?
It guides R&D focus, helps avoid infringement, and facilitates strategic licensing and commercialization planning.
References
- Japanese Patent Office (JPO) Patent Documentation
- WIPO PATENTSCOPE database for international prior art searches
- D. Philips et al., "Strategies for Effective Pharmaceutical Patent Claim Drafting," Journal of IP Law, 2020.