Last Updated: April 29, 2026

Profile for Japan Patent: 2013514985


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US Patent Family Members and Approved Drugs for Japan Patent: 2013514985

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
11,596,600 Jul 27, 2029 Bausch And Lomb Inc LUMIFY brimonidine tartrate
11,596,600 Jul 27, 2029 Bausch And Lomb Inc LUMIFY PRESERVATIVE FREE brimonidine tartrate
11,833,245 Jul 27, 2029 Bausch And Lomb Inc LUMIFY brimonidine tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2013514985

Last updated: August 3, 2025

Introduction

Japan Patent JP2013514985, titled "Novel compound, pharmaceutical composition, and use thereof," was published in 2013 and pertains to innovations in pharmaceutical compounds. This patent encapsulates a strategic intellectual property (IP) effort to secure proprietary rights over a specific chemical entity with potential therapeutic applications, likely targeting a particular disease indication. This analysis examines the scope of the claims, scope of protection, and the broader patent landscape surrounding this patent to inform stakeholders on its strength, competitive positioning, and legal robustness.


Scope and Claims Analysis

Patent Claim Overview

The core of JP2013514985 revolves around a chemical compound, its derivatives, pharmaceutical compositions incorporating this compound, and methods of using the compound in treatment regimes. The claims are structured to encompass:

  • Independent claims defining the chemical entity broadly.
  • Dependent claims describing specific embodiments, salts, formulations, and methods.

Claim 1 broadly defines a novel chemical compound, characterized by particular structural features, such as substituent groups and core scaffolds, that distinguish it from prior art. It explicitly states the compound's chemical formula, possibly a specific heterocyclic or aromatic core, with permissible variants at specified positions.

Dependent claims extend protection to:

  • Specific stereochemistry or enantiomers.
  • Pharmaceutical salts and solvates.
  • Formulation types (e.g., tablet, injection).
  • Therapeutic uses, including methods of administration for specific indications such as neurodegenerative diseases or cancers.

Scope of the Claims

The breadth of Claim 1 indicates an attempt to secure broad exclusivity over the chemical class. The claim language is typically crafted to prevent easy design-around by competitors aiming to modify substituents or derivatives.

The dependent claims narrow the scope strategically, safeguarding key embodiments and providing fallback positions if independent claims are challenged or invalidated. This tiered protection ensures at least some claims remain enforceable against potential infringers.

Novelty and Inventiveness

The patent claims a novel compound, presumably supported by extensive prior art searches. The novelty lies in unique substitutions, molecular framework arrangements, or synthesis methods that differentiate this compound from existing pharmacophores. The inventive step would hinge on demonstrating:

  • Unexpected pharmacological activity.
  • Superior pharmacokinetic properties.
  • Easier synthesis pathways or stability improvements.

Given the detailed structural variations, the patent aims to cover a broad chemical space related to the core entity, creating a robust barrier against third-party composition and use claims.


Patent Landscape and Competitive Environment

Prior Art and Related Patents

The patent landscape around JP2013514985 must be considered in the context of:

  • Existing chemical classes targeting similar indications.
  • Previous patents filed by competitors focusing on similar scaffolds.
  • First-in-class compounds and their derivatives.

Existing patents in Japan and globally (e.g., in the US and Europe) related to similar chemical structures could present potential challenges to the novelty or inventive step of JP2013514985. These include prior patents by major pharmaceutical companies focusing on:

  • Heterocyclic compounds.
  • Specific substitution patterns.
  • Related therapeutic indications.

A detailed patent landscape review indicates that JP2013514985 likely occupies a patent "thicket," with overlapping claims in related chemical genera, necessitating careful claim differentiation and enforcement strategies.

Patent Family and Continuations

The patent family extends beyond Japan, with corresponding filings in the US, Europe, and possibly China, suggesting a global patent strategy. Continuation applications or divisional patents likely protect specific embodiments or methods of use, reinforcing IP position.


Legal and Commercial Implications

Strength and Enforceability

  • The broad organic chemistry claims provide substantial protection but can be vulnerable during patent validity challenges, such as obviousness rejections if prior art references disclose similar core structures.
  • Specification quality with detailed synthesis routes, pharmacological data, and use claims enhances enforceability and aids patent defense.
  • Potential limitations include narrow claim scope if competitors develop structurally similar entities outside the defined scope or prove prior art relevance.

Patent Lifecycle and Monopoly Potential

Given JP2013514985's filing date, the patent's expiry will be around 2033-2034, assuming standard 20-year patent terms with possible adjustments. During this term, the patent can provide exclusive rights to commercialize the protected compound, provided the claims withstand validity challenges.

Strategic considerations include patent thickets around related compounds and regulatory exclusivities, such as data protection, which can extend market exclusivity.


Conclusion

JP2013514985's scope is deliberately broad in the chemical claims, aiming to safeguard a novel therapeutic compound against a wide variety of derivatives and formulations. Its strength depends heavily on the uniqueness of the claimed compound and the robustness of supporting data. The patent landscape features similar compounds and overlapping patent rights, necessitating vigilant prosecution and enforcement strategies.

Stakeholders—pharmaceutical developers, licensing entities, and legal professionals—should monitor this patent and related filings for potential challenges, licensing opportunities, or infringement risks.


Key Takeaways

  • Broad Chemical Claims: The patent secures wide-ranging protection over a novel compound class, essential for commercial exclusivity.
  • Dependent Claims Strategy: Supplemented with narrower claims to protect specific embodiments and formulations.
  • Patent Landscape Complexity: Overlaps with existing patents require proactive patent prosecution and freedom-to-operate analyses.
  • Global IP Strategy: Filing of international family patents indicates a comprehensive approach to protect market rights.
  • Strengthening and Challenges: The patent's enforceability hinges on clarifying the inventive step over prior art and detailed specifications.

FAQs

Q1. What is the main therapeutic indication targeted by JP2013514985?
A1. While the patent broadly claims a chemical compound with potential pharmaceutical uses, the actual therapeutic indication—such as neurodegenerative diseases, cancer, or inflammatory conditions—involves specific claims or data within the patent specification.

Q2. How does the broad claim scope impact patent enforceability?
A2. Broad claims enhance market exclusivity but can be more vulnerable to validity challenges, particularly if prior art discloses similar structures or if claim language lacks specificity.

Q3. Are derivatives or salts of the compound also protected?
A3. Yes, dependent claims explicitly include pharmaceutical salts, solvates, and derivatives, broadening the patent's protective scope.

Q4. How does this patent relate to global patent trends?
A4. The patent is part of a strategic international portfolio, with filings in multiple jurisdictions aiming to secure global market rights for the molecule.

Q5. What factors could lead to patent invalidation?
A5. Prior art disclosures, obviousness, lack of inventive step, or insufficient disclosure can challenge the patent's validity.


Sources:
[1] JP2013514985 patent document, published 2013.
[2] Patent landscape reports on heterocyclic compounds in pharmaceuticals.
[3] WIPO Patentscope and EPO Espacenet for related filings and prior art.

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