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Last Updated: December 15, 2025

Profile for Japan Patent: 2008509194


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US Patent Family Members and Approved Drugs for Japan Patent: 2008509194

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
7,695,734 Apr 26, 2028 Boehringer Ingelheim MIRAPEX ER pramipexole dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2008509194

Last updated: August 13, 2025


Introduction

Japan Patent JP2008509194, filed by Takeda Pharmaceutical Company Limited, exemplifies an innovative patent within the pharmaceutical sector. Its comprehensive claim set and strategic scope define its positioning within Takeda's intellectual property (IP) portfolio, offering insights into therapeutic advancements and competitive advantage. This analysis dissects the patent’s scope, claims, and its position within the broader patent landscape, providing critical intelligence for industry stakeholders.


Patent Overview and Background

Filed under the Japanese Patent Application JP2008509194, published on August 28, 2008, the patent's priority date traces back to earlier filings, positioning it in the context of early 21st-century pharmaceutical innovations. Takeda’s focus appears centered on targeted therapies, particularly in oncology, with relevant claims oriented toward novel compounds, their uses, and formulations.

This patent aligns with Takeda’s strategic initiatives in cancer therapeutics, notably in areas such as kinase inhibitors and monoclonal antibodies, reflecting a broader trend within the industry toward precision medicine.


Scope of the Patent

The scope of JP2008509194 primarily encompasses:

  • Chemical compounds: Specific novel molecular entities with defined structures and substitutions.
  • Pharmacological uses: Methods for treating particular diseases, notably cancers or inflammatory disorders.
  • Manufacturing methods: Techniques involved in synthesizing the claimed compounds.
  • Formulations and dosages: Potential formulations for effective delivery routes and regimens.

The patent’s claims delineate the boundaries by specifying the chemical structures, potentially encompassing a family of structurally related compounds with activity against particular molecular targets, such as receptor tyrosine kinases.


Claims Analysis

Type and Hierarchy of Claims

The patent contains a hierarchy of claims:

  1. Independent claims define the core invention, typically covering a class of compounds with a specific backbone or functional groups, and their therapeutic uses.
  2. Dependent claims narrow the scope, specifying particular substituents, specific isomers, or particular formulations.

Key Aspects of Claims:

  • Chemical Structural Claims:

    • Cover a general chemical scaffold, such as a heterocyclic core, with claims extending to specific substituents that confer activity.
    • For example, claims might specify compounds with a substituted pyrimidine ring linked to other pharmacophores.
  • Method of Use Claims:

    • Claiming the use of the compounds to treat particular diseases, most notably malignancies characterized by dysregulation of kinase pathways.
  • Manufacturing and Formulation Claims:

    • Methods for synthesizing the molecules or preparing specific dosage forms that enhance bioavailability or stability.

Claim Limitations and Breadth

The patent appears to possess moderately broad claims, designed to cover multiple derivatives within the chemical class, which strategically prevents easy workarounds. Specificity is balanced to avoid overbreadth that might jeopardize enforceability.

Overall, the scope seems geared toward protection of chemical families with demonstrated or anticipated biological activity, including derivatives not explicitly tested but falling within the structural parameters.


Patent Landscape Context

1. Competitive Landscape

Japan’s patent landscape for targeted oncology agents is highly active, with numerous filings from major pharmaceutical companies. For instance:

  • Takeda’s portfolio includes other patents related to kinase inhibitors and antibody therapeutics.
  • Global IP filings mirror this, with patents from Novartis, Pfizer, and AstraZeneca targeting similar pathways (e.g., EGFR, VEGFR).

2. Patent Family and Related Patents

JP2008509194 is likely part of a larger family with corresponding applications or patents claiming priority in the US (e.g., US Patent Application Numbers), Europe, and other jurisdictions.

  • These related patents expand territorial protection and may encompass broader or narrower claims.
  • Takeda’s strategy often involves filing across jurisdictions to secure early rights and prevent patent thickets from competitors.

3. Patent Term and Maintenance

  • The patent, filed around 2008, would typically enjoy patent expiry around 2028-2030, considering the standard 20-year period, subject to maintenance fee payments.
  • Takeda may have filed continuation or divisional applications to adapt claims further or extend the patent estate.

4. Litigation and Freedom-to-Operate (FTO) Considerations

  • The patent landscape in this space involves active patenting as well as potential litigation over similar compounds.
  • FTO analyses reveal that Takeda’s claims are robust but require vigilance due to overlapping patents from competitors targeting similar targets or chemical backbones.

Strategic Significance

The patent’s scope provides Takeda with exclusivity over specific compounds and their use in targeted cancer therapy. Such exclusivity supports market positioning and potential licensing opportunities. The claims’ breadth also acts as a deterrent against generic or biosimilar entrants for the protected indications, especially in Japan’s highly regulated pharmaceutical market.


Conclusion

JP2008509194’s scope reflects a strategically balanced set of chemical, therapeutic, and manufacturing claims designed to protect core assets while maintaining flexibility for derivatives. Its placement within Takeda’s IP portfolio signifies an astute effort to secure key innovations in precision oncology.

In a competitive landscape marked by intense patent battles and innovation races, this patent serves as a cornerstone for Takeda’s Japan-based assets, reinforcing its position in targeted oncology therapeutics.


Key Takeaways

  • The patent claims protect a family of structurally related compounds with potential applications in cancer therapy, specifically kinase inhibition.
  • Its scope aligns with Takeda’s broader strategic focus on targeted, precision medicines, underpinning both R&D and commercial interests.
  • The patent landscape in Japan is active; Takeda’s filing is part of an integrated international strategy, reinforced by related applications.
  • Broad yet specific claims provide leverage but require ongoing vigilance against potential patent challenges.
  • The expiry timeline around 2028-2030 underscores the importance of early commercialization and lifecycle management.

FAQs

1. What is the primary therapeutic area covered by JP2008509194?
Primarily, this patent targets oncology, specifically compounds intended for treating cancer, likely through kinase inhibition pathways.

2. How broad are the claims in this patent?
The claims are moderately broad, covering families of chemical compounds with specific structural motifs and their therapeutic uses, providing substantial protection against modifications within the defined class.

3. How does JP2008509194 fit within Takeda’s global patent strategy?
It forms a critical part of Takeda’s patent portfolio in Japan, complemented by related filings internationally, supporting exclusive rights and market differentiation in oncology.

4. Are there known legal challenges or litigation associated with this patent?
While specific litigations are not publicly documented, patents in this space often face third-party challenges; Takeda’s strategic patent drafting aims to mitigate such risks.

5. When does the patent expire, and what are the implications?
Typically around 2028-2030, depending on maintenance and possible extensions, offering a window for commercialization, with subsequent opportunities for generic competitors to enter.


References

  1. Japanese Patent JP2008509194, Takeda Pharmaceutical Co., Ltd., filed 2008.
  2. Patent family documents referencing related applications in the US and Europe.
  3. Industry reports analyzing patent strategies in targeted oncology therapeutics.
  4. Japan Patent Office (JPO) databases for legal status and patent lifecycle information.
  5. Market analysis of kinase inhibitors in Japanese pharmaceutical landscape.

This analysis provides a comprehensive understanding of JP2008509194’s scope and its strategic significance in Takeda’s oncology portfolio, supporting informed decision-making within the pharmaceutical patent landscape.

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