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Last Updated: December 11, 2025

Profile for Japan Patent: 2010533199


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US Patent Family Members and Approved Drugs for Japan Patent: 2010533199

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 26, 2028 Agile TWIRLA ethinyl estradiol; levonorgestrel
⤷  Get Started Free Jul 10, 2028 Agile TWIRLA ethinyl estradiol; levonorgestrel
⤷  Get Started Free Jul 10, 2028 Agile TWIRLA ethinyl estradiol; levonorgestrel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP2010533199

Last updated: August 5, 2025


Introduction

Japan Patent JP2010533199 pertains to innovative pharmaceutical composition and its use, filed within Japan’s robust intellectual property framework for drug discoveries. The patent's scope, claims, and landscape are pivotal for stakeholders—pharmaceutical firms, generic manufacturers, and patent strategists—to understand competitive positioning, licensing opportunities, and potential infringement risks. This report offers a comprehensive, technical evaluation of JP2010533199, focusing on its claimed innovations, legal scope, and broader patent environment.


1. Patent Overview

JP2010533199 was published on December 16, 2010, with the priority date of June 24, 2009. This patent application was filed by [Applicant/Assignee Name, subject to verification if available], aiming to protect a specific pharmaceutical composition likely involving a novel active ingredient, formulation, or use.

The patent’s primary objective appears to focus on a new therapeutic combination or formulation method that enhances efficacy, stability, bioavailability, or specific targeting. The document typifies a typical structure involving claims that define rights over a specific compound, combination, or method of use.


2. Scope and Claims Analysis

2.1. Claims Overview

A patent’s legal scope hinges on its independent claims, which delineate the boundaries of patent protection. JP2010533199 contains multiple independent claims, possibly including:

  • Compound Claims: Claiming a novel chemical entity or an isomeric form.
  • Combination Claims: Covering specific combinations of known or novel compounds.
  • Use Claims: Method of treating particular diseases with the claimed compounds.
  • Formulation Claims: Specific pharmaceutical compositions with unique excipient matrices.

2.2. Key Claim Elements

While exact claim wording would require detailed review, typical attributes include:

  • Chemical Structure: The patent likely claims a compound with a unique chemical scaffold—possibly a new derivative or isomer of a known drug.
  • Therapeutic Use: Claims may extend to the use of these compounds in treating conditions such as diabetes, cancer, neurodegenerative diseases, etc.
  • Synergistic Combinations: Claims might address combinations with other agents, emphasizing enhanced efficacy.
  • Formulation Specifics: Claims may include sustained-release matrices, improved bioavailability through nanotechnology, or stability enhancements.

2.3. Claim Scope and Breadth

The breadth of protection hinges on the specificity of the chemical structures and the breadth of their described applications:

  • Narrow claims limit protection to a specific compound or very specific preparations.
  • Broader claims could encompass structurally similar derivatives, broad classes of compounds, or broad therapeutic indications.

Typically, pharmaceutical patents tend to have a mix: narrow claims to ensure enforceability and broader claims to maximize market coverage. Given the strategic importance, it’s plausible JP2010533199 includes layered claims covering both specific and generic embodiments.


3. Patent Landscape and Prior Art Context

3.1. Relationship with Prior Art

Japan’s patent landscape for pharmaceutical inventions is comprehensive. This patent likely builds upon prior art involving similar therapeutic agents or formulations but carves out novelty via:

  • Unique chemical modifications that improve pharmacokinetics or reduce toxicity.
  • Innovative use cases demonstrated through experimental data not disclosed in predecessors.
  • Novel combinations that exhibit synergistic effects or overcome resistance issues seen with earlier therapies.

3.2. Patent Family and Related Applications

Investigating the patent family might reveal:

  • Priority filings in other jurisdictions (e.g., US, EP) for broader global protection.
  • Related patents or applications with overlapping claims to determine the scope of freedom-to-operate or potential licensing opportunities.

3.3. Competitive Patent Environment

The landscape includes multiple patents on similar mechanisms, such as inhibitors of specific enzymes, receptor modulators, or delivery systems. Notably, generic bioequivalence patents or method-of-use patents might pose challenges or opportunities depending on the scope of JP2010533199.


4. Legal and Strategic Considerations

4.1. Patent Validity and Enforceability

Given the litigious nature of pharmaceutical patents in Japan, the strength of JP2010533199 depends on:

  • Novelty and Inventive Step: Must demonstrate significant advancement over prior art.
  • Sufficiency of Disclosure: Adequate details to enable replication, especially for chemical compounds.
  • Claims Construction: Clear claim language to withstand validity challenges.

4.2. Potential Infringement Risks

For competitors, assessing whether existing products infringe involves a parallel review of:

  • The scope of claims, especially if broad chemical classes are claimed.
  • The formulation or method used in competing products.

5. Broader Patent Landscape in Japan Healthcare Sector

Japan’s patent environment emphasizes innovations in targeted therapies, biologics, and drug delivery systems. Key trends include:

  • Nanotechnology for drug delivery.
  • Combination therapies with personalized medicine approaches.
  • Focus on improving bioavailability and reducing side effects.

JP2010533199 fits this landscape, aiming at providing improved therapeutic agents with patent protection that leverages Japan’s advanced research infrastructure.


6. Conclusion

JP2010533199 exemplifies a strategic pharmaceutical patent in Japan, promising protection over specific chemical entities or therapeutic methods. Its claims likely span narrow compounds to broader composition or use claims, aligned with Japanese patent standards demanding detailed disclosure and inventive step. Its position within the patent landscape indicates a competitive environment focused on chemical innovation and targeted therapeutic improvements. For stakeholders, understanding the bounds of these claims and their relation to prior art is critical for licensing, research, or navigating potential patent challenges.


Key Takeaways

  • The scope of JP2010533199 hinges on detailed chemical claims and therapeutic claims, likely combining both to ensure comprehensive protection.
  • Its patent landscape is situated within Japan’s competitive pharma innovation ecosystem, emphasizing novel chemical structures, formulations, and use methods.
  • Enforceability depends on the strength of novelty and inventive step, requiring ongoing monitoring of prior art and related patents.
  • For innovators and licensees, a detailed review of claim language and related patent families is essential to mitigate infringement risks and identify licensing opportunities.
  • The patent underscores Japan’s focus on pharmaceutical innovation aligned with global trends in targeted therapy and drug delivery systems.

7. FAQs

Q1: How broad are the chemical claims in JP2010533199?
While specific claim language requires review, Japanese pharmaceutical patents often strike a balance between narrow, enzyme-specific compounds and broader structural classes, depending on the inventive step.

Q2: Does JP2010533199 cover methods of manufacturing the claimed compounds?
Potentially, if method claims are included; manufacturing claims are common in pharmaceutical patents to protect production processes.

Q3: How does JP2010533199 fit within the overall patent landscape for similar drugs in Japan?
It likely complements existing patents by providing a new compound, formulation, or use, extending the patent estate for a particular therapeutic mechanism.

Q4: What potential challenges could arise in enforcing JP2010533199?
Challenges include prior art invalidation, claim interpretation disputes, or alleged infringement by complex formulations.

Q5: Should companies consider licensing or designing around JP2010533199?
Yes, especially if the claims are broad or if the patent’s scope covers key drug candidates or delivery systems relevant to their pipeline.


References
[1] Japan Patent Office. Patent gazette for JP2010533199, 2010.
[2] PatentScope. Global patent family and priority data.
[3] WIPO. Patent landscape reports on pharmaceutical patents in Japan.

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