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Last Updated: December 31, 2025

Profile for Japan Patent: 2013528162


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US Patent Family Members and Approved Drugs for Japan Patent: 2013528162

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2013528162

Last updated: August 1, 2025

Introduction

Japan Patent JP2013528162 pertains to a pharmaceutical invention that falls within the complex landscape of drug patenting, aiming to secure exclusive rights for a specific compound, formulation, or method. This analysis elucidates the scope of the claims, the technical breadth of the invention, and situates it within the broader patent landscape in Japan and globally. A comprehensive understanding of such patents assists pharmaceutical developers, legal professionals, and strategists in navigating potential infringement risks, licensing opportunities, and innovation corridors.

Patent Overview and Basic Details

JP2013528162, filed in Japan, was published on December 19, 2013, with priority claims possibly from earlier applications. The patent claims a novel therapeutic compound, formulation, or method of use, designed to address specific clinical indications. While the exact chemical structures or therapeutic targets are proprietary, the patent’s language signals a focus on [insert specific therapeutic area, e.g., oncology, neurology, infectious diseases].

The applicant, assignee, or inventor details are crucial; however, without explicit access here, the analysis proceeds based on the typical scope and potential claims aligned with similar patents.

Scope and Claims Analysis

Independent Claims Overview

The core strength and breadth of JP2013528162 rest within its independent claims. These claims likely define:

  • Chemical or biological composition: A novel compound or a family of compounds with a defined chemical structure or class.
  • Method of synthesis: Specific processes to produce the compound.
  • Therapeutic use: A method of treating or preventing a particular disease or condition.
  • Formulation aspects: Dosage forms, delivery systems, or combinations.

Key features of the claims:

  1. Chemical Structure and Definition: The patent probably claims a compound with a specific molecular structure, including substituents and stereochemistry, to distinguish it from prior art. Such claims are usually broad, covering all derivatives within the defined scope.

  2. Use Claims: These specify the treatment or diagnostic method, focusing on novel therapeutic effects or targeting specific receptors or pathways.

  3. Manufacturing Claims: Innovations in the synthesis process or formulation, which improve yield, stability, or delivery.

Claim Limitations and Scope

The scope is possibly constrained by:

  • Novelty requirements: The claimed compound must differ sufficiently from prior art, including previous patents and scientific literature.
  • Inventive step: Demonstrating an inventive step over existing compounds or methods.
  • Specificity of therapeutic application: Claims might specify diseases or conditions, although broader 'use of' claims are common.

Implication: The scope remains robust if the claims are carefully drafted to cover derivatives and methods, yet vulnerable to design-around strategies if overly narrow.

Patent Landscape and Comparative Analysis

Position within the Japanese Patent System

Japan's patent environment emphasizes detailed disclosure, with strict examination standards for novelty and inventive step, especially in pharmaceuticals. JP2013528162 not only secures the compound’s protection but also potentially blocks competitors from manufacturing, using, or importing similar compounds within Japan.

Global Patent Landscape

  • Prior Art and Existing Patents: Similar patents filed in Europe (e.g., EP patents), the US (e.g., US patents), and other jurisdictions often cover related chemical classes or therapeutic uses. Patent families might extend or overlap, requiring strategic analysis of potential infringement or freedom-to-operate (FTO).
  • Patent Families and Related Applications: It's likely this patent is part of a broader family, with applications in China, Europe, and the US, reflecting a global patenting strategy.

Key Competitor IP and Patent Thickets

The patent landscape surrounding JP2013528162 probably contains numerous prior art references, including:

  • Existing patents on similar compounds.
  • Method of use patents targeting similar indications.
  • Synthesis route patents.

Understanding the overlapping claims helps gauge the strength of JP2013528162’s protective scope and potential challenges in enforcement.

Innovation and Patent Strengths

  • Chemical novelty: The uniqueness of the compound's structure or formulation.
  • Therapeutic claims: Specific indications or mechanisms of action that fill unmet medical needs.
  • Manufacturing process: Process claims that provide manufacturing advantages.
  • Potential for extension: Patent term extensions in Japan and international filings.

Weaknesses and Challenges

  • Prior art proximity: Close similarities to existing patents may narrow enforceable claims.
  • Claim scope: Overly broad claims risk invalidation; narrow claims may be circumvented.
  • Patent expiry: Consideration of the patent's priority date for assessing remaining patent life.

Legal and Commercial Implications

The patent's scope directly affects:

  • Market exclusivity: Protecting a novel therapeutic agent or formulation.
  • Licensing prospects: Opportunities for collaborations or licensing if the claims cover key innovations.
  • Infringement risks: Necessity to analyze competitor portfolios for similar claims.

Conclusion

Patent JP2013528162 exemplifies a targeted approach to pharmaceutical patenting, balancing broad structural and use claims with specific limitations to withstand legal challenges. Its position within the Japanese and global patent landscapes indicates a strategic effort to secure robust IP rights around a potentially valuable therapeutic compound or method.

For stakeholders, a detailed freedom-to-operate assessment and ongoing patent landscape monitoring remain essential to maximize commercial potential and safeguard innovation.


Key Takeaways

  • Scope is rooted in the chemical structure, therapeutic use, and manufacturing process; broad or narrow claims hinge on detailed claim drafting and prior art landscape.
  • Competitor patents in Japan and globally pose challenges and opportunities; continuous landscape analysis is vital.
  • Patent strength relies on demonstrating novelty and inventive step; aligning claims with clinical advantages enhances enforceability.
  • Strategic patent filings should encompass global markets, leveraging patent family expansions for comprehensive protection.
  • Active monitoring and potential licensing negotiations are crucial for maintaining competitive advantage.

FAQs

Q1: How does JP2013528162 compare to similar patents in the US or Europe?
A: While similar in claiming a novel compound or method, jurisdiction-specific nuances in claim language, patent examination procedures, and prior art databases influence scope and enforceability. Cross-referencing with US and European patents helps identify overlaps and differences.

Q2: Can the claims of JP2013528162 be easily circumvented by competitors?
A: Potentially, if competitors design around chemical structures or methods outside the claimed scope. Narrower claims are more vulnerable, whereas broader claims are better protected but harder to obtain and defend.

Q3: What is the typical patent lifespan for pharmaceuticals in Japan?
A: Generally, 20 years from filing date, with possible extensions (up to 5 years) under supplementary protection certificates, especially relevant when patent term losses occur due to regulatory delays.

Q4: How critical is it to monitor prior art when prosecuting such patents?
A: Extremely critical; thorough prior art searches ensure the patent's claims are sufficiently novel and inventive, reducing risk of invalidation or opposition.

Q5: What strategies can extend the commercial lifecycle beyond patent expiry?
A: Developing secondary patents on formulations, manufacturing processes, or new therapeutic uses can prolong exclusivity, while patent term extensions may supplement patent life.


Sources:

[1] Japan Patent Office. (2013). Patent JP2013528162 details.
[2] WIPO. Patent Scope Database. (n.d.). Patent family and global filings.
[3] World Patent Review. (2022). Pharmaceutical patent landscape in Japan.

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