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Last Updated: December 14, 2025

Profile for Japan Patent: 2010515490


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US Patent Family Members and Approved Drugs for Japan Patent: 2010515490

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 Feb 26, 2027 Eli Lilly And Co AXIRON testosterone
⤷  Get Started Free Feb 26, 2027 Eli Lilly And Co AXIRON testosterone
⤷  Get Started Free Feb 26, 2027 Eli Lilly And Co AXIRON testosterone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2010515490

Last updated: August 4, 2025

Introduction

Japan Patent JP2010515490, issued in 2010, pertains to a pharmaceutical invention that claims specific formulations or methods linked to a particular drug or therapeutic approach. As a significant asset within Japan’s intellectual property (IP) environment, understanding its scope, claims, and its position within the larger patent landscape is crucial for stakeholders involved in pharmaceutical R&D, licensing, or strategic patent management.

This article provides a comprehensive examination of the patent’s claims, their legal scope, and the surrounding patent landscape, referencing the relevant Japanese patent doctrines, prior art, and recent patent trends in the pharmaceutical sector.


Scope of the JP2010515490 Patent

Patent Overview

JP2010515490 is categorized as a composite pharmaceutical formulation or method of treatment, reflecting the typical focus of patents in this sector. Its scope likely covers specific compounds, compositions, or methods of use intended for treating particular diseases or conditions.

The scope of a patent can be distilled into independent claims—which define the broadest rights—and dependent claims—which narrow or specify particular aspects. While the precise language of these claims is necessary for definitive analysis, typical scope considerations for such patents involve:

  • Compound-specific claims: Covering chemical entities, their derivatives, or combinations.
  • Use-specific claims: Covering methods of administration, dosage forms, or therapeutic indications.
  • Formulation claims: Covering specific carriers, excipients, or delivery mechanisms.

Legal Boundaries and Limitations

In Japan’s patent law, the scope is bounded by novelty, inventive step, and industrial applicability [1]. Any prior art, especially earlier Japanese or international patents, could limit or render invalid certain claims if they are deemed anticipated or obvious.

The claims likely aim to balance breadth—covering as much ground as possible to deter competitors—and specificity—to withstand validity challenges. Japanese courts and patent examination standards favor clear, well-defined claims that align with the inventor’s contribution to the art.


Analysis of the Claims

Independent Claims

The core of JP2010515490 revolves around independent claims that define the broadest scope. These claims potentially cover:

  • A novel chemical compound or class thereof.
  • A unique pharmaceutical composition comprising the compound and specific excipients.
  • A method of treating a specific disease, such as a metabolic disorder, using the compound or composition.

The language used likely emphasizes the chemical structure, method of use, or administration protocol, with limitations tailored to avoid invalidation, such as avoiding overly broad "all-encompassing" formulations.

Dependent Claims

Dependent claims refine the independent claims by:

  • Narrowing the scope to specific dosage ranges or formulations.
  • Including particular derivatives, salts, or polymorphs.
  • Detailing manufacturing processes or delivery systems (e.g., sustained-release formulations).

This layered claim structure enables patentees to enforce rights across varying degrees of specificity, creating a hierarchical infringement and validity framework.

Scope of the Claims

The claims, as typical for pharmaceutical patents, likely feature a moderate breadth balancing between comprehensive coverage and legal defensibility:

  • Broad claims may cover the class of compounds or their use in treating a disease.
  • Narrower claims secure protection over specific embodiments or formulations.

Potential challenges to scope include claim definiteness, written description, and enablement requirements under Japanese patent law, which necessitate specific disclosure.


Patent Landscape and Competitive Environment

Japanese Patent Environment in Pharmaceuticals

Japan hosts a dynamic pharmaceutical patent landscape, characterized by:

  • High levels of patent filings, particularly by domestic pharmaceutical giants like Takeda, Daiichi Sankyo, and Astellas.
  • Active patenting in drug delivery, formulations, and synthesis processes.
  • Increasing emphasis on orphan drug, biologics, and personalized medicine.

The Asia-Pacific region's expanding patent activity makes Japanese patents strategically significant, especially if they cover key molecules or methods.

Related Patents and Prior Art

Given the filing date (2010), JP2010515490’s validity depends heavily on prior art, including:

  • Earlier Japanese patents and publications.
  • International patents within the same therapeutic area.
  • Scientific literature describing similar compounds or methods.

Recently issued patents might be viewed as blocking patents, necessitating careful freedom-to-operate assessments.

Patent Family and International Patent Strategy

It is common for valuable Japanese pharmaceutical patents to belong to international patent families—filings in other jurisdictions (e.g., US, Europe, China)—to safeguard global market rights.

The Patent Cooperation Treaty (PCT) application associated with JP2010515490 could reveal more extensive international protection, with claims covering broader territories and formulations.

Litigation and Licensing Trends

While Japanese pharmaceutical patents are often maintained through licensing agreements, litigation remains infrequent compared to the US or Europe. However, patent validity challenges, especially in the pharmacological field, are common, emphasizing the importance of thorough prior art searches and comprehensive claim drafting.


Legal and Commercial Implications

The scope and claims of JP2010515490 directly influence:

  • Infringement risks: Determining if a competitor’s product infringes involves detailed claim construction.
  • Patent validity: Narrow or overly broad claims face invalidation risks if challenged by prior art.
  • Market exclusivity: Effective claims extending rather than narrowing coverage enhance patent life and profit margins.
  • Research considerations: Potential infringement or freedom-to-operate issues might impact R&D direction.

In the context of Japanese patent law, securing robust claims aligned with the inventive contribution is critical in defending patent rights amidst intense competition.


Key Takeaways

  • JP2010515490’s claims likely cover specific chemical entities, formulations, or therapeutic methods with moderate breadth, balancing scope and validity.
  • A comprehensive understanding of its patent claims requires detailed claim language review to assess literal infringement and scope.
  • The patent landscape in Japan is highly active, with strategic filings, especially in biologics, drug delivery, and proprietary compounds.
  • Validity of the patent relies on a thorough prior art search across Japanese and international sources, considering recent filings.
  • Effective patent strategy involves aligning claims with innovation while ensuring freedom to operate in competitive markets.

FAQs

1. Does JP2010515490 cover a broad class of drugs or specific compounds?

While the exact language is necessary for precision, it likely covers a specific chemical compound or class, with claims possibly extending to formulations and uses. Broad class coverage is common but depends on detailed claim language.

2. How does Japan’s patent law influence the scope of pharmaceutical patents like JP2010515490?

Japanese patent law emphasizes clear, precise claims that demonstrate an inventive step and industrial applicability. The scope must be supported by the disclosure, and overly broad claims may face challenges during examination or litigation.

3. Can JP2010515490 be enforced against competitors?

Yes, if infringement is demonstrated based on the patent claims, the patent holder can enforce rights through infringement actions in Japan. However, enforcement depends on the patent’s validity and claim scope.

4. How does the patent landscape impact strategic R&D decisions in Japan?

A dense patent environment encourages innovators to file narrow, well-supported patents and engage in licensing or cross-licensing agreements. Understanding existing patents like JP2010515490 helps shape R&D pathways to avoid infringement and secure competitive advantages.

5. What strategies can companies use to navigate patent risks associated with JP2010515490?

Conducting comprehensive patent clearance searches, designing around broad claims, and developing novel derivatives can mitigate risks. Additionally, pursuing opposition, patent invalidation procedures, or licensing can optimize the patent portfolio.


References

[1] Japanese Patent Law, Article 36–39.

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