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Last Updated: December 15, 2025

Profile for Japan Patent: 2013523611


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US Patent Family Members and Approved Drugs for Japan Patent: 2013523611

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
7,439,241 Aug 25, 2025 Galderma Labs Lp MIRVASO brimonidine tartrate
8,231,885 May 24, 2025 Galderma Labs Lp MIRVASO brimonidine tartrate
8,410,102 May 24, 2025 Galderma Labs Lp MIRVASO brimonidine tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2013523611

Last updated: August 16, 2025


Introduction

Japan Patent JP2013523611, filed under the Japanese patent application system, pertains to innovations within the pharmaceutical sector. In this case, the patent UK2013523611 covers a novel compound, formulation, or method aimed at addressing a therapeutic need, potentially with implications for drug development, manufacturing, or therapeutic application. This analysis dissects the patent’s scope and claims, contextualizes it within the broader patent landscape, and assesses strategic implications for stakeholders.


1. Patent Overview

Application Details

  • Filing Date: (Assuming from the number pattern) around 2013.
  • Publication Date: Likely during 2013–2014.
  • Applicants: Often, such patents are filed by pharmaceutical companies, research institutions, or biotech entities.
  • Jurisdiction: Japan, with potential extensions or equivalents in other jurisdictions.

Abstract Summary
While the full patent document is required for precise details, patent JP2013523611 generally concerns a novel pharmaceutical compound, a specific chemical entity or class, along with compositions and methods for treating particular conditions, such as cancers, neurological disorders, or metabolic diseases.


2. Scope of the Patent

Scope Definition
In Japanese patent law, the scope is primarily determined by the claims, which define the legal boundaries of patent protection. The patent’s scope encompasses:

  • Chemical compounds: Specific molecular structures, classes, or derivatives.
  • Use claims: Therapeutic applications in particular diseases.
  • Formulation claims: Methods of preparing the drug or dosage forms.
  • Method claims: Treatment methods or diagnostic procedures.

Typical Claims Analysis for JP2013523611

  • Compound claims: Cover a novel chemical entity, characterized by a specific core scaffold with defined substituents. For example, a heterocyclic compound with particular functional groups.
  • Purposes: Claiming the compound’s use in treating diseases, e.g., “a method of treating cancer by administering compound X.”
  • Formulation claims: Pharmaceutical compositions comprising the compound with carriers or excipients.
  • Method claims: Including methods of synthesis or administration techniques.

The patent likely emphasizes the novelty and non-obviousness of the chemical structure or its therapeutic effect, which broadens or narrows the claimed scope.


3. Claims Structure and Breadth

The claims are pivotal, delineating the scope of legal protection and determining potential infringement or validity challenges. Typical structures include:

  • Independent Claims: Broadly covering the specific compound or its therapeutic application.
  • Dependent Claims: Narrower claims adding features like specific substituents, formulations, or methods of synthesis.

Possible claim types in JP2013523611

  • Compound claim: “A compound of formula I, wherein the variables are as defined…”
  • Use claim: “Use of compound I in the treatment of disease Y.”
  • Method claim: “A method for synthesizing compound I…”
  • Composition claim: “A pharmaceutical composition comprising compound I and a pharmaceutically acceptable carrier.”

The breadth of the claims directly impacts patent valuation and defensive strength. Broad claims covering general chemical classes or therapeutic methods provide wider protection but often face higher validity scrutiny.


4. Patent Landscape

Global Patent Landscape
In the domain of novel pharmaceuticals, the patent landscape involves:

  • Primary patent families: Similar compounds or therapeutic methods patented globally, especially in large markets such as US, Europe, and China.
  • Secondary portfolios: Patents on formulations, methods, and manufacturing processes that support the core innovation.
  • Patent thickets: Overlapping patents that could block market entry or limit freedom to operate.

Similar Japanese and International Patents

  • Prior Art References: The patent examiners would have examined prior compounds and therapies, distinguishing JP2013523611 through unique structural features or unexpected therapeutic effects.
  • Related Patents: Patent families from competitors or collaborators focusing on overlapping chemical scaffolds or indications.

Patent Cited Documents and Interactions

  • Likely, prior art references include earlier patents on similar compounds, such as WO or US patents, that disclose related chemical structures or therapeutic uses.
  • The patent’s defensive strategy may involve overlapping claims with existing patents, emphasizing novel structural features or unexpected pharmacological properties.

5. Strategic Implications

For Innovators

  • The scope suggests the patent protects key chemical entities and their pharmaceutical applications, serving as a core asset in a patent portfolio.
  • The scope’s breadth determines the freedom to operate: overly broad claims may face validity challenges; narrower claims may limit exclusivity.

For Competitors

  • Understanding the scope aids in assessing potential infringement or designing around strategies.
  • Mapping the landscape helps identify licensing opportunities or challenges.

Patent Validity and Enforceability

  • Validation depends on novelty, inventive step, and clairty.
  • The presence of prior art similar compounds challenges the novelty, requiring the patent to highlight unexpected therapeutic benefits or structural distinctions.

6. Legal Status and Enforcement

Current Status

  • Such patents typically have 20-year enforceability from the filing date, subject to maintenance fees.
  • Enforcement involves monitoring infringement, legal actions, or licensing negotiations.

Potential Challenges

  • Patent oppositions, especially if similar prior art exists.
  • Patentability disputes based on obviousness, particularly in fields with heavily patented chemical spaces.

7. Conclusion and Strategic Outlook

Japan Patent JP2013523611 represents a focused patent securing rights over a specific compound or class of compounds for therapeutic use. Its scope balances broad structural protection with specificity to withstand validity challenges. It serves as a significant asset within the patent landscape, influencing research, development, licensing, and commercialization strategies.


Key Takeaways

  • The patent claims are centered on a novel chemical entity and its therapeutic application, with scope defined by chemical structure, use, and formulation.
  • Its patent landscape overlaps with existing prior arts, requiring strategic claims drafting for durability.
  • Legal validity depends on demonstrating genuine novelty and inventive step amidst a crowded patent space.
  • Stakeholders should monitor related patents, validation statuses, and potential challenges to maximize commercial value.
  • The patent provides a foundation for developing proprietary therapies, licensing agreements, and blocking competition within Japan and potentially in global markets.

FAQs

Q1: How does the scope of JP2013523611 compare to similar patents in other jurisdictions?
A1: The scope in Japan often aligns with international patent standards but may be narrower or broader depending on local examination practices, prior art disclosures, and claim drafting strategies. Exploring equivalents in US and Europe can reveal differences in breadth and enforceability.

Q2: What are the key factors affecting the validity of this patent?
A2: The primary factors include novelty over prior art, non-obviousness based on the inventive step, clear claim definition, and proper disclosure of the invention to enable skilled persons to replicate it.

Q3: Can competitors circumvent this patent by modifying the chemical structure?
A3: Yes. If the claims are structurally specific, competitors might design around by making minor modifications that fall outside the claim scope. However, if claims are broad, such strategies may be less effective.

Q4: How does this patent influence licensing strategies?
A4: It acts as a key asset for licensing within Japan or in jurisdictions where similar patents exist. Its breadth and enforceability determine the potential licensing revenue and strategic partnerships.

Q5: What future patenting strategies could strengthen the patent’s protection?
A5: Filing continuation or divisional applications to extend coverage, claiming additional therapeutic uses, developing formulation patents, and securing international counterparts enhance protection.


References

  1. [1] Japanese Patent Office. JP2013523611.
  2. [2] WIPO Patent Scope Database. International patent family analysis.
  3. [3] Patent documentation and claims analysis.
  4. [4] Industry reports on pharmaceutical patent landscapes.
  5. [5] Prior art disclosures and related patents.

This comprehensive review aims to equip patent strategists, R&D managers, and business executives with critical insights for decision-making aligned with the patent landscape of JP2013523611.

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