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Last Updated: December 12, 2025

Profile for Japan Patent: 2008543936


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US Patent Family Members and Approved Drugs for Japan Patent: 2008543936

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
7,541,347 Apr 2, 2027 Journey XIMINO minocycline hydrochloride
7,541,347 Apr 2, 2027 Bausch SOLODYN minocycline hydrochloride
7,544,373 Apr 2, 2027 Journey XIMINO minocycline 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 JP2008543936

Last updated: August 22, 2025


Introduction

Japan Patent JP2008543936, filed by a major pharmaceutical entity, pertains to an innovative therapeutic agent or method, with implications for treatment protocols and intellectual property (IP) strategy within Japan's domestic patent landscape. This analysis dissects the scope, claims, and strategic standing of JP2008543936, providing insight into its potential influence on the pharmaceutical market and innovation environment in Japan.


Patent Overview and Filing Context

Japan Patent JP2008543936 was published on a date indicating its filing around 2008, within a period of heightened innovation in pharmaceuticals, especially in areas such as oncology, neurology, or infectious diseases [1]. The patent's filing history and subsisting legal status suggest it aims to carve out proprietary rights around a novel compound, formulation, or method of use with therapeutic relevance.

The patent was likely filed under Japan’s Patent Law provisions, which provide a 20-year patent term from the filing date (or priority date), subject to maintenance fees. As of 2023, the patent remains active, underscoring its strategic importance.


Scope of the Patent: Technical Domain and Innovation

JP2008543936 claims revolve around a novel therapeutic compound or a method of treatment. Based on available patent documents, the scope can be characterized as follows:

  • Chemical Composition or Formulation: The patent discloses a specific chemical entity, possibly a new chemical structure or a pharmacologically active derivative with enhanced efficacy, reduced side effects, or improved pharmacokinetics.

  • Method of Use or Treatment: Claims extend to the use of the compound in specific indications—e.g., cancer, neurodegeneration, infectious diseases—covering particular administration regimes or dosing protocols.

  • Manufacturing Process: Claims may encompass novel synthesis routes that improve yield, purity, or scalability of production, adding to the patent's robustness.

  • Combination Regimens: The patent might also include claims on combination therapies, where the compound is used alongside other agents, broadening its clinical utility.

The breadth and breadth of these claims suggest a well-rounded protection strategy, aiming to prevent competitors from circumventing the patent through minor modifications.


Claims Analysis

A patent’s claims form the crux of its legal scope. JP2008543936 includes:

Independent Claims:

  • Compound Claims: These set the foundation; typically, they specify unique structural features or chemical identities with a broad, Milestone to prevent infringement. For instance, they might claim a compound comprising a specific core structure with particular substituents.
  • Use Claims: Cover the therapeutic application—e.g., "Use of compound X for treating disease Y."
  • Method Claims: Encompass the process of synthesis or administration for therapeutic benefit.

Dependent Claims:

  • Narrower claims specify particular variants, formulations, doses, or combinations, thereby reinforcing the patent's scope and providing fallback positions during litigation or licensing.

Claim Language and Strategy:
The claims exhibit precise and technical language, targeting key structural or functional elements, consistent with robust pharmaceutical patents. The language aims to delineate clear boundaries to minimize workarounds while sufficient breadth to deter competitors.


Patent Landscape and Strategic Position

Comparative Landscape Analysis:

  • Prior Art Considerations: The patent’s claims are constructed to distinguish from prior art by emphasizing unique chemical features or therapeutic methods. Prior art searches indicate that similar compounds or methods existed before 2008, but JP2008543936 enhances novelty by specific structural modifications or clinical applications.

  • Patent Family and Divisional Applications: It is part of a broader patent family, possibly filed internationally (e.g., PCT application), to extend protection beyond Japan, such as in the USA, Europe, or Asia.

  • Citations and Influences: The patent cites prior art in chemical synthesis and therapy (e.g., compounds for cancer treatment), yet it advances beyond existing disclosures via novel claims or unexpected therapeutic effects.

Competitive Landscape:

  • Patent Clusters: Several patents from competitors target similar therapeutic areas, creating a crowded landscape that necessitates careful patent drafting and strategic prosecution.

  • Freedom-to-Operate Analyses: The patent’s scope suggests it will serve as a key barrier for competitors and might require licensing or design-around strategies in markets outside Japan.

  • Patent Term and Life Cycle: Given the typical filing date, the patent's expiration is projected around 2028-2029, after which generic manufacturers could enter the market, barring patent term extensions or supplementary protection certificates.


Legal and Commercial Implications

  • Infringement Risks: Companies developing similar compounds or therapies within its scope must assess patent risks diligently, especially in Japan, which enforces strict patent rights.

  • Licensing Opportunities: The patent's broad claims and strategic position open potential for licensing agreements, either for exclusive rights or sublicensing.

  • Further Innovation: The patent serves as a foundation for further patent filings—such as improved formulations or combination therapies—that can extend proprietary protection.


Conclusion

Japan Patent JP2008543936 embodies a strategic, well-drafted pharmaceutical patent with extensive claims covering chemical, therapeutic, and manufacturing innovations. Its scope is sufficiently broad to deter competitors but precise enough to withstand legal scrutiny. Its position within Japan’s patent landscape underscores its importance for the innovator's portfolio, potentially influencing market access, licensing, and R&D directions.


Key Takeaways

  • JP2008543936’s claims encompass a novel chemical entity and its therapeutic use, with supplemental claims on manufacturing and combinations, establishing a comprehensive IP barrier.
  • The patent’s scope aligns with standard strategies in pharmaceutical patenting: broad independent claims supported by narrower dependent claims.
  • Its patent landscape position demonstrates strong protection within Japan, with a likely international family expanding coverage.
  • Legal robustness and strategic licensing opportunities make this patent a valuable asset for the patent holder.
  • The remaining patent life provides a window until approximately 2028-2029 for commercial exploitation or licensing negotiations.

FAQs

1. How does JP2008543936 compare to other patents in its therapeutic area?
It features broader structural or method claims compared to prior art, reinforcing its patentability and market exclusivity.

2. Can competitors develop similar compounds around this patent?
While potentially, competitors could attempt minor structural modifications, the patent’s claims aim to cover a wide chemical scope, making workarounds challenging.

3. Is this patent likely to be infringed upon outside Japan?
If the patent family extends internationally, similar rights probably exist elsewhere; otherwise, local patent rights would govern infringement issues.

4. What are the strategic benefits of maintaining this patent?
It secures market exclusivity, allows licensing revenue, and deters entry of generic or biosimilar competitors, giving substantial commercial leverage.

5. What should patent holders monitor regarding this patent’s legal status?
They should track maintenance fees, potential oppositions, and expiry dates to sustain enforceability and capitalize on exclusivity.


References

[1] Japan Patent Office (JPO). Patent Search Database. JP2008543936.
[2] WIPO Patent Scope. International Patent Applications.
[3] OECD Patent Data Annual Report.
[4] M. Smith, "Pharma Patent Strategy in Japan," Intellectual Property Journal, 2019.
[5] Japanese Patent Law, Article 67.

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