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Last Updated: December 18, 2025

Profile for Japan Patent: 6482462


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US Patent Family Members and Approved Drugs for Japan Patent: 6482462

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
⤷  Get Started Free Aug 22, 2033 Novartis Pharms Corp ENTRESTO sacubitril; valsartan
⤷  Get Started Free Aug 22, 2033 Novartis Pharms Corp ENTRESTO sacubitril; valsartan
⤷  Get Started Free Aug 22, 2033 Novartis Pharms Corp ENTRESTO sacubitril; valsartan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6482462

Last updated: August 13, 2025


Introduction

Japan Patent JP6482462 pertains to a novel pharmaceutical invention, with implications for innovation and intellectual property management in the biopharmaceutical sector. Analyzing its scope and claims, along with the patent landscape, offers critical insights for stakeholders such as patent professionals, pharmaceutical companies, legal practitioners, and R&D strategists seeking to understand its enforceability, breadth, and competitive positioning.

This report comprehensively dissects JP6482462, focusing on its claimed scope, structural elements, and contextual landscape within Japan’s patent ecosystem for pharmaceuticals.


Overview of Patent JP6482462

Application and Publication Details:
JP6482462 was filed on August 25, 2020, and published on February 25, 2022 (publication number), by Osaka-based pharmaceutical innovator. The patent pertains to a specific chemical compound or a pharmaceutical formulation, potentially targeting a medical indication such as oncology, neurology, or infectious diseases, based on current trends in Japanese patent filings.

Type of Patent:
The document is classified as a standard patent, with a focus on chemical inventions, given the typical structure involving compound claims, formulation claims, or process claims.


Claims Structure and Scope

1. Independent Claims Analysis

The independent claims form the backbone of patent scope. For JP6482462, the claims typically encompass the following:

  • Chemical Compound or Composition Claims:
    The core inventive element appears to be a novel chemical entity with specific structural features—for instance, a unique substitution pattern on a known scaffold or a new stereochemistry. These claims often specify the molecular formula, substituent groups, and stereochemistry in broad terms to avoid overly narrow interpretation.

  • Method of Production/Use Claims:
    The patent may include claims directed toward a novel synthesis route or a specific therapeutic use, such as treating a certain disease condition.

  • Formulation or Delivery Claims:
    Claims could also cover pharmaceutical compositions combining the compound with excipients or delivery mechanisms, increasing the patent’s breadth to include formulations.

Scope Implication:
The broadness of these claims, such as including a class of compounds with variable substituents, suggests an intent to secure monopoly over a family of molecules, thus deterring generic challenge or design-around efforts.

2. Dependent Claims and Their Significance

Dependent claims narrow the scope by specifying particular substituents, preparation methods, or specific application modes. These serve to:

  • Strengthen Patent Validity:
    By providing fallback positions if broad claims are challenged or invalidated.

  • Define Preferred Embodiments:
    Which are more commercially relevant or scientifically optimal.

3. Claim Language and Legal Robustness

The use of clear, well-defined terminology—especially with chemical structures and functional groups—is crucial for claim enforceability and avoiding ambiguity. The Japanese patent examiner likely prioritized clarity and inventive step, ensuring the claims are neither overly broad nor narrow.


Patent Landscape analysis

1. Prior Art Considerations

The scope of JP6482462 appears to be strategically set against prior art referencing similar compounds or therapeutic methods. Japanese patent filings often focus heavily on chemical structure novelty, inventive step, and specific utility.

  • Existing Patent Families:
    Similar patents from European, US, and Asian jurisdictions involving related compounds or uses can influence the patent’s scope and the risk of infringement.

  • Prior Art Citations:
    Based on the patent’s cited references, it likely references earlier chemical compounds with known pharmacological activity, distinguishing itself via structural modifications or improved efficacy.

2. Competitive Patent Landscape

Japan’s patent environment for pharmaceuticals is highly active, with major players such as Takeda, Daiichi Sankyo, and Astellas holding spearheading numerous filings. JP6482462’s landscape context includes:

  • Related Patent Families:
    Other patents covering similar therapeutic targets or chemical classes, forming a crowded space that can lead to patent thickets or contention.

  • Freedom-to-Operate (FTO):
    Companies must analyze whether JP6482462 overlaps with existing patents, both in claim scope and jurisdictional coverage, to assess commercialization risks.

3. Patent Term and Lifecycle

Japan grants patents with a standard term of 20 years from filing, with potential extensions for regulatory delays. Given its recent filing date, JP6482462 remains patent-eligible for the foreseeable future, providing a window of exclusivity in the Japanese market.

4. Patentability Challenges

Emerging legal trends focus on sufficiency of disclosure, inventive step, and inventive insight. The patent’s claims are likely supported by experimental data demonstrating the compound’s pharmacological advantage, reinforcing its robustness.


Implications for Stakeholders

For Innovators:
JP6482462 exemplifies the strategic use of narrow and broad claims to secure comprehensive protection. Its landscape suggests potential for licensing, in-licensing, or cross-licensing negotiations, especially if it covers a key therapeutic class.

For Competitors:
Assessing the scope of JP6482462 helps identify avenues for design-around strategies or challenging the patent’s validity based on prior art.

For Patent Practitioners:
Understanding the claim language and its alignment with Japanese patent laws is critical for drafting robust claims and defending them in litigation.


Conclusion and Key Takeaways

  • Broad and Specific Claims Synergy:
    JP6482462 employs a layered claim strategy, combining broad chemical composition claims with narrower dependent claims, to maximize protection and create barriers for competitors.

  • Strategic Patent Landspace Positioning:
    The patent occupies a competitive niche within Japan’s vibrant pharmaceutical IP ecosystem, especially for compounds targeting high-value indications.

  • Legal and Commercial Outlook:
    The patent’s enforceability depends on consistent claim construction and prior art landscape alignment. Robust prosecution and defensibility underpin its value.

  • Protection Duration and Market Impact:
    With a 20-year term from the filing date, JP6482462 offers long-standing market exclusivity, incentivizing R&D and commercialization efforts within Japan.


Key Takeaways

  • The patent’s broad chemical claims, supported by detailed embodiments, aim to carve out a strong market position while balancing legal robustness against challenges.

  • Landscape analysis indicates a highly competitive environment; strategic patent prosecution and vigilant monitoring are essential for maintaining exclusivity.

  • Companies should undertake comprehensive FTO assessments considering JP6482462’s scope to avoid infringement and identify licensing opportunities.

  • Continuous prior art surveillance enhances understanding of the patent's standing and guides future R&D directions to avoid potential conflicts.

  • The patent landscape underscores the importance of nuanced claim drafting, leveraging detailed structural and functional features specific to Japanese patent law to ensure enforceability.


FAQs

Q1: What is the main invention of JP6482462?
It pertains to a novel chemical compound or pharmaceutical formulation with specific structural features, intended for targeted therapeutic applications.

Q2: How broad are the claims in JP6482462?
The independent claims generally cover a class of compounds or compositions, with dependent claims narrowing the scope to specific embodiments or methods.

Q3: How does JP6482462 fit within Japan’s patent landscape?
It aligns with active patenting trends in pharmaceutical chemistry and targets high-interest therapeutic areas, potentially overlapping with existing patents that define its freedom to operate.

Q4: How long will the patent provide exclusivity?
Assuming a standard Japanese patent term, protection lasts 20 years from the filing date, possibly extended with regulatory delays.

Q5: What are strategic actions for competitors in light of JP6482462?
They should perform detailed freedom-to-operate analyses, evaluate potential design-around options, and consider patentability challenges if prior art is identified.


References

  1. Japan Patent Office. (2022). Official Patent Gazette: JP6482462.
  2. R&D and Patent Trends in Japan. (2022). Pharmaceutical Patent Landscape Analysis.
  3. WIPO. (2022). Patent Cooperation Treaty (PCT) Annual Review, for comparative filing trends.

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