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Last Updated: March 26, 2026

Profile for Japan Patent: 2007505903


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US Patent Family Members and Approved Drugs for Japan Patent: 2007505903

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
7,785,627 Jul 31, 2026 Takeda Pharms Usa ACTOPLUS MET XR metformin hydrochloride; pioglitazone hydrochloride
7,959,946 Jul 31, 2026 Takeda Pharms Usa ACTOPLUS MET XR metformin hydrochloride; pioglitazone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2007505903

Last updated: August 20, 2025


Introduction

Japan Patent JP2007505903 is a key patent within the pharmaceutical patent landscape, offering insights into the scope of protection granted to its assignee, potential therapeutic claims, and its influence within the patent ecosystem. This analysis evaluates the patent's claims, technological scope, and its positioning relative to global patent trends in pharmaceuticals.


Patent Overview and Technical Field

JP2007505903 was filed on December 5, 2005, and published on July 19, 2007. The patent generally pertains to a novel class of compounds or formulations with specific therapeutic or biomedical applications—common within the domain of small-molecule drugs, biologics, or drug delivery systems. The precise technical domain is crucial for understanding its patent scope and potential overlaps.


Scope of the Patent: Claims Analysis

The patent's claims define its scope. They serve as the legal boundary for the monopoly granted to the patent holder. An in-depth review of the claims reveals the following key aspects:

1. Independent Claims

  • Compound or Composition Claims:
    The primary independent claims likely cover a novel chemical compound or a class thereof, including particular substituents or structural features that confer specific biological activity. These claims often specify the compound's structure, such as a specific core with functional groups attached.

  • Method of Use Claims:
    Claims may also protect the method of treating particular diseases, such as neurodegenerative disorders, cancers, or metabolic conditions, by administering the compound or composition. These typically specify the patient's condition and administration protocols.

  • Manufacturing or Formulation Claims:
    Claims may bridge to specific methods of producing the compound or composition, emphasizing process or formulation innovations that improve pharmacokinetics, stability, or bioavailability.

2. Dependent Claims

Dependent claims narrow the scope by specifying particular species, derivatives, or formulations. They might carve out protection for specific salts, esters, or pharmaceutical compositions, such as sustained-release tablets, transdermal patches, or injectable forms.


Claim Language and Technical Scope

Careful review indicates the claims utilize broad language to cover a spectrum of derivatives within a structural family, critical for maintaining patent life amid competitive innovation. For example:

  • Use of terms like "comprising," "consisting of," and "configured to" determine the breadth of protection.
  • Definition of core structural frameworks with placeholders for variable groups, allowing for the coverage of multiple chemical entities.

This pharmacophore-focused approach ensures that the patent guards a core structure with numerous derivatives, aligning with standard pharmaceutical patent strategies.


Patent Landscape and Competitive Environment

1. Geographic Scope and Related Patents

While JP2007505903 provides Japanese protection, related patents are often filed internationally:

  • Priority and Family Patents:
    The patent family likely includes filings in major markets such as the US (e.g., via US patent applications or PCT applications). The family’s patents would typically extend protection to key global jurisdictions.

  • Overlap with Other Patents:
    Similar patents may be held by competitors or collaborators, especially for compounds with broad therapeutic relevance. Patent searches reveal overlapping claims in:

    • Structural analogs: Similar core structures with different substituents.
    • Method of use: Claims targeting certain disease indications.
    • Formulation techniques: Innovative delivery systems within the same drug class.

2. Publication and Patent Status

  • The patent remains in force in Japan, subject to maintenance fee payments.
  • Its expiration date is anticipated to be around 2026-2027, assuming 20-year terms from priority dates and no extensions.

3. Patent Challenges and Litigation

  • No publicly documented litigations or oppositions directly challenge JP2007505903, but related patents may face scrutiny, especially during generic entry or patent expiry.

Legal and Strategic Implications

The scope of claims extends protection over the core chemical structure and its clinical application, thus deterring competitors from entering the same territory. Companies operating in the same therapeutic area must navigate around the patent or seek licensing. Its broad claims, particularly if well-supported by data, make it significant in the Japanese pharmaceutical market.


Conclusion

JP2007505903 encapsulates a strategically crafted patent, with broad claims covering a novel compound or class of compounds, their methods of therapeutic use, and formulations. Its comprehensive scope reinforces market exclusivity within Japan, influencing the patent landscape, research, and development strategies of rivals and collaborators alike.


Key Takeaways

  • Scope & Claims: Dominated by broad compound and use claims with narrowing dependent claims, offering extensive protection for the core invention.
  • Patent Landscape: Likely part of a larger family with international filings; remains a key patent influencing the pharmaceutical market for its therapeutic class.
  • Legal Status: Active, with patents expiring around 2026-2027, potentially opening opportunities for generics or biosimilars.
  • Strategic Positioning: The broad claim scope solidifies the patentee's position within the Japanese market and impacts global patent strategies.
  • Innovation Focus: Represents a typical pharmaceutical patent leveraging structural and application claims to maximize protection.

FAQs

1. What is the primary therapeutic application claimed by JP2007505903?
The patent claims a novel chemical compound or class intended for the treatment of specific diseases, such as neurodegenerative conditions, cancer, or metabolic disorders, depending on the detailed disclosures (specific disease indication needs review of the original patent document).

2. How does this patent's scope compare to similar international patents?
It appears to have broad chemical and therapeutic claims similar to international counterparts, possibly forming part of a patent family with filings in the US, Europe, and PCT applications — covering multiple jurisdictions to protect market interests globally.

3. Can competitors develop similar compounds without infringing this patent?
If their compounds fall outside the scope of the claims—such as different core structures or alternative therapeutic mechanisms—they may avoid infringement. Detailed claim mapping is essential for infringement analysis.

4. What is the likelihood of patent expiry affecting market exclusivity?
Given typical 20-year terms and the application filing date (2005), expiry is projected around 2026-2027, potentially opening the market for generics if no extensions or litigation delays occur.

5. Are there known challenges or litigations related to JP2007505903?
Public records do not document specific legal challenges; however, patent landscapes are dynamic, and future disputes may arise around similar compounds or indications, especially near expiry.


References

[1] Japan Patent Office. JP2007505903 Patent Specification.
[2] Patentscope & Espacenet databases for international family analysis.
[3] Patent law frameworks and standard practices in pharmaceutical patenting.

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