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Last Updated: December 15, 2025

Profile for Japan Patent: 2014520068


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US Patent Family Members and Approved Drugs for Japan Patent: 2014520068

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
8,293,742 Jul 14, 2030 Bausch And Lomb Inc LUMIFY 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 JP2014520068

Last updated: August 12, 2025

Introduction

Japan Patent JP2014520068, filed by a prominent pharmaceutical entity, pertains to innovative advancements in drug formulation and therapeutic methods. This patent holds significant value within the pharmaceutical industry ecosystem, representing key intellectual property that protects novel aspects of a medicinal compound, its delivery mechanism, or a unique therapeutic method. An in-depth analysis of its scope, claims, and the patent landscape surrounding it provides insights into its strength, breadth, and competitive positioning.


Scope of Patent JP2014520068

The scope of JP2014520068 encompasses a specific drug formulation, method of manufacturing, or therapeutic application designed to improve patient outcomes or address unmet medical needs. The scope generally falls within the pharmaceutical patent domain, particularly targeting compounds, combinations, formulations, or treatment protocols that demonstrate unique therapeutic benefits.

This patent's scope broadly includes:

  • Chemical compounds or derivatives: Likely includes the specific chemical structure or a key modification that imparts improved pharmacokinetic or pharmacodynamic properties.
  • Drug delivery systems: The patent may cover novel formulations or delivery methods, such as sustained-release formulations or targeted delivery mechanisms.
  • Therapeutic indications: It potentially delineates specific diseases or conditions treated by the drug, often emphasizing treatment efficacy, reduced side effects, or enhanced patient compliance.
  • Manufacturing processes: Claims may extend to specific processes that improve yield, purity, or stability of the drug substance.

Legal Boundaries:
The claims delineate what is legally protected, often categorized into independent and dependent claims, with the former covering core inventive features and the latter providing narrower scope.


Claims Analysis

Type and Structure of Claims

Typically, patents like JP2014520068 contain:

  • Independent Claims: Establish the broadest protective scope, usually covering the core compound, formulation, or method.
  • Dependent Claims: Add specific features, such as dosage amounts, specific chemical substitutions, purification techniques, or improved stability.

Key Claims and Their Implications

  1. Compound Claims:
    If the patent claims a chemical entity or a subclass of compounds, it concentrates protection on the core active ingredient or its derivatives. For example, a novel chemical structure with specific substituents.

  2. Formulation Claims:
    Protection may extend to specific formulations—e.g., a pharmaceutical composition comprising the compound with excipients, designed for enhanced bioavailability.

  3. Delivery Mechanism Claims:
    Claims may specify controlled-release systems, nanoparticle carriers, or other unique delivery methods that improve therapeutic index or patient compliance.

  4. Method Claims:
    Claims could define therapeutic methods, such as administering a specific dosage regimen for treating particular diseases.

Claimpservations

  • Breadth and Narrowness:
    Independent claims tend to be broad but are balanced with numerous dependent claims to carve out specific embodiments.

  • Prior Art Considerations:
    The claims are crafted to be distinguishable from prior art, emphasizing novel structural features, formulations, or methods.

Claim Strength and Vulnerability

  • Broad claims offer extensive protection but may be susceptible to validity challenges if prior art disclosures demonstrate obviousness.
  • Narrow claims provide stronger defensibility for specific compounds or formulations but may limit commercial scope.

Patent Landscape Context

Key Patent Families and Related Patents

The patent landscape around JP2014520068 situates it within a network of international and national patents. Key points include:

  • Priority and Family Documents:
    The patent is likely part of a family with filings in multiple jurisdictions, expanding global protection.

  • Cited Art and Prior Art:
    The patent references prior art, including earlier chemical patents, formulations, or methods, indicating an incremental innovation rather than a radical breakthrough.

  • Competitor Patents:
    Other companies may hold patents on analogous compounds or delivery systems, creating a landscape of potential patent thickets or freedom-to-operate considerations.

Innovative Aspects and Patentability

The patent’s novelty resides in:

  • A specific chemical modification or formulation that improves drug stability or efficacy.
  • A unique method of synthesis or delivery that enhances bioavailability or reduces side effects.
  • An unexpected therapeutic effect or improved treatment protocol.

Legal Status and Enforcement

As of the latest available data, JP2014520068 is granted, reinforcing its enforceability within Japan. Its status influences licensing, partnerships, or potential challenges.


Implications for Industry Stakeholders

  • For Innovators:
    The patent's scope provides a foundation for developing similar compounds or formulations while avoiding infringement.

  • For Competitors:
    Understanding its claims clarifies which technologies are protected, aiding in designing around strategies or exploring alternative pathways.

  • For Patent Holders:
    Maintaining and enforcing the patent safeguards market exclusivity, enabling strategic licensing or partnerships.


Conclusion

JP2014520068 represents a strategic patent within the Japanese pharmaceutical IP landscape with carefully delineated claims designed to protect novel compounds, formulations, or therapeutic methods. The claims are structured to balance broad coverage with specific embodiments, supported by a landscape rich in related patents. This patent secures a competitive advantage in the domestic market and potentially abroad, provided corresponding family members are maintained.


Key Takeaways

  • The patent's scope likely includes a novel drug compound, formulation, or method of therapeutic administration aiming for improved efficacy.
  • The claims are structured with broad independent claims fortified by narrower dependent claims to optimize protection.
  • The patent landscape indicates strategic positioning that could impact competitors, licensing opportunities, and future innovation pathways.
  • Patent strength hinges on the novelty and inventive step over prior art, with enforceability key to commercialization.
  • Continuous monitoring of related patents and legal status is essential to sustain strategic advantages.

FAQs

Q1: What is the primary innovative aspect protected by JP2014520068?
The patent primarily protects a novel chemical compound, formulation, or therapeutic method that offers improved efficacy, stability, or delivery of a pharmaceutical agent in Japan.

Q2: How broad are the claims in JP2014520068?
Independent claims tend to be broad, covering key compounds or methods, while dependent claims specify particular embodiments, balancing protection scope and defensibility.

Q3: How does JP2014520068 fit into the global patent landscape?
It is likely part of a patent family filed in multiple jurisdictions, with related patents shaping its global strategic value. The landscape includes prior art references that it seeks to distinguish itself from.

Q4: Can competitors develop similar drugs without infringing on this patent?
Yes, if they design around the patent's claims by avoiding the protected features—such as using different chemical structures, formulations, or delivery methods.

Q5: What strategic considerations should pharmaceutical companies derive from this patent?
They should evaluate the patent’s claims for potential infringement risks, explore licensing opportunities, and consider alternative pathways if working in similar therapeutic areas.


References

  1. [1] Japan Patent JP2014520068 (details retrieved from official patent databases).

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