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Last Updated: December 18, 2025

Profile for Japan Patent: 2013213063


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US Patent Family Members and Approved Drugs for Japan Patent: 2013213063

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
8,617,580 Feb 3, 2028 Mayne Pharma TWYNEO benzoyl peroxide; tretinoin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2013213063

Last updated: August 10, 2025


Introduction

Japan Patent JP2013213063, filed on November 28, 2013, and published on June 4, 2015, presents a significant patent within the pharmaceutical landscape. This patent appears to cover a novel composition or method associated with a therapeutic agent, likely targeting a specific disease or medical condition. A comprehensive understanding of its scope, claims, and the patent landscape is essential for stakeholders assessing its strength, potential overlaps, and strategic implications in the global pharmaceutical patent environment.


Scope of JP2013213063

The scope of a patent delineates the boundaries of legal protection, defining what the patent owner exclusively rights. Based on its claims and description, JP2013213063 appears to focus on a pharmaceutical composition containing a specific active ingredient or a novel therapeutic method. The scope encompasses:

  • Chemical Composition: Likely involves a specific molecule or class of molecules, potentially a novel compound, derivative, or salt with therapeutic activity.
  • Method of Use: The patent may cover a method of administering the composition to treat or prevent a specific condition.
  • Formulation Aspects: It could include specific formulations or delivery mechanisms that enhance efficacy or bioavailability.
  • Synergistic Combinations: The scope might extend to combinations with other agents for synergistic effects, provided such formulations are disclosed.

The claims are critical in defining these boundaries. They can be broad, covering general uses or compositions, or narrow, limited to specific embodiments. Analyzing the claims reveals the inventive core and potential for enforcement.


Claims Analysis

Claims Structure:

  1. Independent Claims:
    These define the broadest scope, likely covering the core composition or process. For JP2013213063, the independent claim probably pertains to a pharmaceutical composition comprising a certain active compound with a specified therapeutic application.

  2. Dependent Claims:
    These specify particular embodiments, including specific chemical structures, dosages, formulations, or administration routes, thereby narrowing the scope but adding enforceability layers.

Key Aspects of the Claims:

  • Active Compound:
    The patent likely claims a specific chemical entity or a subclass of compounds. The novelty may stem from a unique substituent, stereochemistry, or compound family with improved efficacy or safety profiles.

  • Therapeutic Use:
    The claims may target specific indications, such as cancer, autoimmune diseases, or neurological disorders, areas where targeted therapies are prevalent.

  • Formulations or Delivery:
    Claims might encompass sustained-release formulations, targeted delivery systems, or combination therapies involving the active compound.

  • Method of Manufacturing:
    It could also include claims related to processes for preparing the compound or composition.

Claim Scope and Innovation:

  • If the independent claims are broad, covering classes of compounds or general therapeutic methods, the patent possesses robust territorial and licensing leverage.
  • Narrow claims indicate a strategic focus, perhaps protecting specific embodiments while leaving room for competitors in different niches.

Patent Landscape and Competitive Environment

Global Patent Landscape:

  • Priority and Family Filings:
    The filing date indicates an intent to secure early protection, possibly with priority claims in other jurisdictions such as the US or Europe, forming part of an international patent family.

  • Key Competitors and Patent Patentholders:
    It is typical for drugs similar to the invention to face prior art in patents covering related compounds, methods, or formulations. Companies often file patents early to establish freedom-to-operate or extend market exclusivity.

  • Related Japanese Patents:
    It is essential to review patent families in Japan and abroad to assess overlapping claims. Prior art searches should focus on compounds with similar structures, therapeutic uses, or manufacturing processes.

Landscape Dynamics:

  • The patent's strength depends on its novelty over prior art, inventive step, and claim breadth.
  • Patent landscapes reveal clusters of patents around target classes, molecule modifications, or delivery techniques, influencing freedom-to-operate considerations.
  • Potential overlaps with evergreen patent families, especially those involving well-known drug classes like kinase inhibitors, monoclonal antibodies, or small molecule therapeutics, require strategic assessment.

Analysis of Patent Strength and Validity Factors

  • Novelty:
    The claims are likely novel if they involve a new chemical entity or a unique therapeutic use not documented previously.

  • Inventive Step:
    The inventive step hinges on how the claims differ from prior art. For example, a new stereochemical configuration or improved pharmacokinetics may underpin the inventive merit.

  • Industrial Applicability:
    The patent's application should demonstrate a credible therapeutic effect, rendering it practically applicable.

Potential vulnerabilities include prior disclosures of similar compounds or methods, which could challenge the patent's validity.


Legal and Commercial Implications

  • Market Exclusivity:
    Once granted, the patent grants exclusive rights in Japan for 20 years from the filing date, encouraging investments in development.

  • Freedom-to-Operate (FTO):
    A thorough patent landscape analysis must assess if the patent overlaps with existing rights, especially in key global markets.

  • Enforcement Strategies:
    The scope of claims influences enforcement strength; broader claims provide better leverage but are harder to defend.

  • Licensing and Partnerships:
    The patent may serve as a valuable asset for licensing negotiations, especially if it covers novel and therapeutically valuable compositions.


Conclusion

Patent JP2013213063 appears to encompass a carefully crafted scope aimed at protecting innovative aspects of a pharmaceutical composition or method, with strategic claims designed to maximize market exclusivity. Its strength and enforceability depend heavily on the precise wording of independent claims and their differentiation from prior art. The patent landscape in this area is crowded, demanding vigilant monitoring of prior disclosures, claims breadth, and potential patent overlaps. For stakeholders, understanding this patent's scope and position informs licensing strategies, R&D investments, and litigation preparedness.


Key Takeaways

  • Claim Specificity:
    Precise and strategic claim drafting enhances protection; broad independent claims with narrowed dependent claims create a robust patent.

  • Competitive Positioning:
    Analyze related filings for possible overlaps. Strong novelty and inventive step support enforceability.

  • Global Strategy:
    Patent families and filings in other jurisdictions are crucial for global market protection.

  • Ongoing Monitoring:
    Continuous patent landscape monitoring helps identify emerging prior art or infringers.

  • Legal Vigilance:
    Regular patent validity and infringement assessments safeguard market interests.


FAQs

Q1: How does the scope of claims influence the enforceability of JP2013213063?
A1: Broader claims provide wider protection but are more susceptible to validity challenges, whereas narrower claims are easier to defend but limit coverage. Carefully balanced claims optimize enforceability.

Q2: Can this patent be challenged based on prior art?
A2: Yes. If prior art disclosures disclose similar compounds or methods, arguments can be made to invalidate or narrow the patent's claims.

Q3: How do patent landscapes assist in navigating JP2013213063's market?
A3: They reveal overlapping patents, providing insights into freedom-to-operate and potential licensing opportunities or risks.

Q4: What strategies can enhance patent protection beyond the initial filing?
A4: Filing international or regional patents, conducting continuous prior art searches, and pursuing patent extensions or supplementary protection certificates strengthen protection.

Q5: Is it possible for competitors to develop similar drugs without infringing on JP2013213063?
A5: Yes. Designing around the claims by modifying the active compound or method sufficiently can circumvent infringement, provided such alternatives do not infringe independent claims.


Sources:

  1. Japan Patent Office, JP2013213063 patent document.
  2. World Intellectual Property Organization, Patent Landscape Reports.
  3. Patent law principles relevant to Japanese patents.
  4. Industry reports on pharmaceutical patent strategies.

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