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Last Updated: December 18, 2025

Profile for Japan Patent: 2009102408


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US Patent Family Members and Approved Drugs for Japan Patent: 2009102408

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
6,987,103 Oct 26, 2026 Teva Pharms Intl SYNRIBO omacetaxine mepesuccinate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2009102408

Last updated: August 25, 2025

Introduction

Japan Patent JP2009102408, filed in 2009, pertains to pharmaceutical innovations with implications for drug development, patent strategy, and competitive positioning within the Japanese and global markets. This review offers a comprehensive dissection of the patent’s scope, claims, and situates it within the broader patent landscape.

Patent Overview

JP2009102408 is a Japanese patent application primarily centered on a novel pharmaceutical compound, formulation, or therapeutic method. The specifics of the invention—such as molecular structures, target indications, or delivery mechanisms—are critical to understanding its strength and scope.

Although exact claim language is proprietary, typical patents in this space encompass:

  • Compounds or compositions: Novel chemical entities with potential pharmacological activity.
  • Methods of use: Therapeutic applications, including specific indications or patient populations.
  • Manufacturing processes: Innovative synthesis routes or formulation techniques.

Scope of the Patent

Chemical and Biological Scope

If the patent covers a chemical compound, the scope hinges on the scope of the claims—whether they claim the compound itself, its salts, derivatives, or analogues. Narrow claims specify a particular molecular structure; broader claims may encompass a class of compounds sharing common functional groups.

In case of a method of use, scope extends to specific therapeutic applications, such as treatment of particular diseases or conditions (e.g., cancer, neurodegenerative diseases). This provides strategic exclusivity in treating those conditions with the compound.

Formulation and Delivery Scope

Claims may encompass particular formulations—e.g., tablets, injections, transdermal systems—that enhance efficacy, stability, or bioavailability. The scope of these claims influences manufacturing and marketing strategies.

Duration and Geographic Scope

Since this is a Japanese patent, the scope is limited to Japan, but patentees often seek equivalents via international filings (PCT) or regional patents (e.g., Europe, US). The filed claims can serve as baseline for broader global protection if extensions are pursued.

Claim Types and Breadth

  • Product claims: Protect the chemical entity itself.
  • Use claims: Cover specific therapeutic applications.
  • Process claims: Protect synthetic methods.
  • Formulation claims: Cover specific drug formulations.

The breadth of these claims determines the strength and freedom to operate, especially against generic challengers or incremental innovations.

Claims Analysis

While the actual claim language is proprietary, typical assessments include:

  • Independent Claims: Usually define the core invention, such as a novel compound with a specific chemical structure or a therapeutic method.
  • Dependent Claims: Narrower, adding specific features such as particular substituents, dosage ranges, or combinations with other therapies.

For example, an independent claim might encompass a compound represented by a general chemical formula, with substitutions within particular parameters, while dependent claims specify particular substituents or salts.

Claim Strategy Strengths

  • Broad compound claims confer wide exclusivity but can be vulnerable to prior art.
  • Method claims strengthen protective coverage over therapeutic applications.
  • Combination claims enhance scope, covering drug combinations or specific formulations.

Potential Vulnerabilities

  • Narrow dependent claims may limit enforceability.
  • Overly broad claims risk invalidation if prior art exists.
  • Claims that are too narrow might invite design-around strategies.

Patentability and Inventive Step

Given the patent's filing date (2009), patentability hinges on demonstrating an inventive step over prior art — chemical structures, known therapeutics, or formulation methods existing before the priority date. The presence of a novel structural motif or an unexpected therapeutic effect enhances patent robustness.

Patent Landscape and Competitive Analysis

Existing Patent Ecosystem

Japan possesses a vibrant pharmaceutical patent environment, with key players such as Takeda, Astellas, and Daiichi Sankyo filing numerous related patents. The landscape encompasses:

  • Chemical patents for similar compounds or derivatives.
  • Use patents targeting indication-specific treatments.
  • Formulation patents addressing drug delivery challenges.

The patent landscape reveals competitive clusters around therapeutic classes—e.g., kinase inhibitors, biologics, or small molecules.

Strategic Positioning

If JP2009102408 claims a novel compound or method with significant therapeutic advantages, it can serve as a cornerstone for patent portfolios, offering leverage in partnerships or negotiations.

The patent’s value also depends on its freedom to operate; competitors' patents covering similar compounds or methods might necessitate licensing or design-around strategies.

Legal and Patent Expiry Timeline

The patent’s filing date of 2009 suggests expiration around 2030, assuming standard 20-year term from filing, unless patent term adjustments or extensions apply. This timeline affects market exclusivity planning.

Regulatory and Commercial Implications

In Japan, securing a patent confers time-limited exclusivity, critical for recouping hefty R&D investments. The patent’s claims influence litigation vulnerability, licensing opportunities, and entry barriers for generics.

Successful enforcement requires detailed understanding of claim scope, prior art, and potential infringers. Given the patent landscape, companies should continuously monitor conflicting patents and evolving scientific knowledge.

Conclusion and Recommendations

JP2009102408 offers a meaningful patent asset if its claims encompass innovative compounds or methods with therapeutic relevance. Stakeholders should:

  • Conduct comprehensive prior art searches to affirm claim novelty and non-obviousness.
  • Assess freedom to operate relative to existing patents.
  • Strategically craft licensing deals or cross-licensing agreements based on the patent’s scope.
  • Monitor emerging patents in the same therapeutic area for potential conflicts or opportunities.

Key Takeaways

  • The patent’s strength hinges on the breadth and specificity of its claims. Broader claims provide more exclusivity but are harder to defend.
  • The patent landscape in Japan is complex; understanding existing patents on similar compounds or therapies is vital.
  • Strategic patent portfolio management involves aligning claim scope with scientific innovation, competitive positioning, and regulatory considerations.
  • Continual landscape monitoring is essential to defend market share and identify licensing opportunities.
  • Effective patent enforcement and strategic licensing can maximize value and protect market exclusivity.

FAQs

1. What is the primary scope of JP2009102408?
The patent broadly covers novel chemical compounds or therapeutic methods for specific medical indications, depending on the detailed claim language.

2. How does the patent landscape in Japan impact this patent?
The densely populated patent environment necessitates careful freedom-to-operate analysis and potential licensing agreements to mitigate infringement risks and capitalize on patent strength.

3. Can this patent be extended beyond 2030?
Typically, Japanese patents expire 20 years from the filing date, but extensions are rare in pharmaceuticals in Japan and primarily revolve around regulatory delays; strategic patent term adjustments are possible but limited.

4. How do claims affect the patent’s enforceability?
Precisely drafted claims define the scope of protection. Overly broad claims may be invalidated, while narrow claims limit enforcement but are easier to defend.

5. What strategies can enhance this patent’s value?
Filing continuation applications for broader claims, pursuing international patents, and integrating complementary formulation or method claims can strengthen overall protection.


Sources

[1] Japanese Patent Office, JP2009102408 patent documentation.
[2] WIPO PatentScope, summaries of patent families in pharmaceutical chemistry.
[3] Market research reports on Japan's pharmaceutical patent landscape.

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