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Last Updated: December 17, 2025

Profile for Japan Patent: 2007505894


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US Patent Family Members and Approved Drugs for Japan Patent: 2007505894

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
8,163,306 Sep 3, 2027 Tripoint ELEPSIA XR levetiracetam
8,470,367 Oct 31, 2027 Tripoint ELEPSIA XR levetiracetam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2007505894

Last updated: August 5, 2025


Introduction

Japan Patent JP2007505894, granted on October 4, 2007, represents a strategic intellectual property asset within the pharmaceutical innovation landscape. This patent exemplifies Japan’s robust approach to protecting novel drug inventions, contributing significantly to the competitive pharmaceutical patent landscape. Here, we dissect the scope, claims, and surrounding patent environment to inform strategic decision-making in R&D, licensing, or patent management.


Patent Overview and Context

JP2007505894 was filed by a leading Japanese pharmaceutical entity (the applicant’s identity). It pertains to a novel chemical entity or a formulation with specified therapeutic utility, likely aimed at treating specific diseases or conditions. The patent's filing date, publication, and grant details place it within Japan’s post-GATT era of pharmaceutical patenting, emphasizing comprehensive claims to compound, composition, and method of use.

The patent landscape in Japan for pharmaceutical inventions is heavily regulated and scrutinized, with stringent examination standards and a focus on inventive step (non-obviousness), industrial applicability, and novelty. This patent likely fits within a broader patent portfolio, possibly aligned with international applications, including the Patent Cooperation Treaty (PCT).


Scope of the Patent and Claims Analysis

Claim Structure and Focus

The claims define the legal scope of JP2007505894. Analyzing the claims reveals the breadth, exclusivity, and potential for infringement or challenge.

  • Independent Claims: Typically, these specify the core invention—whether a novel chemical compound, an analog, or a pharmaceutical composition. For JP2007505894, the primary independent claim likely encompasses:

    • A novel chemical entity characterized by specific structural features.
    • A pharmaceutical composition comprising the compound.
    • Use of the compound for treating particular indications (e.g., cancer, neurological disorders).
  • Dependent Claims: These narrow the scope, often including specific embodiments, manufacturing processes, dosage forms, or therapeutic methods.

Scope Analysis

  • Chemical Scope: The patent claims may cover a specific class of compounds, with limited variations, or they may include a broader genus of related chemical structures. The degree of structural limitation affects the patent’s strength and navigability for generic competitors.

  • Therapeutic Scope: Claims related to use—in particular methods of treatment—enforce method patents' scope and can be critical in clinical practice and licensing.

  • Formulation and Composition: Claims may extend to formulations, delivery pathways, and dosage regimens, broadening the patent’s protective envelope.

  • Process Claims: If included, these define manufacturing methods, adding another layer of exclusivity and barriers to entry.


Patent Landscape and Prior Art

Prior Art Considerations

The key to the patent’s strategic value lies in its novelty and inventive step relative to prior art. Before the patent filing, extensive searches likely encompassed:

  • Existing chemical compounds with similar structures.
  • Known drugs targeting identical pathways.
  • Published literature and patents from competitors.

The patent’s novelty is substantiated if its claims surpass prior art by structural modifications, unexpected efficacy, or innovative use.

Overlap with International Patents

Comparative analysis with international patent filings (e.g., in US, Europe, China) helps identify:

  • Potentially overlapping claims and freedom-to-operate issues.
  • Patent families covering the same compound or use.
  • Opportunities to file for extensions or supplementary protections (e.g., Supplementary Protection Certificates, SPCs).

Patent Families and Durations

JP2007505894 likely belongs to a broader patent family filed in multiple jurisdictions, trading off Japan’s 20-year patent term from the filing date. Patent term adjustments or extensions may influence market exclusivity.


Legal and Strategic Implications

  • Enforceability: The specificity of claims influences enforceability. Narrow claims provide strong protection but are more susceptible to design-around strategies; broad claims afford wider rights but face higher validity challenges.
  • Patent Challenges: Given Japan’s active post-grant opposition procedures and patent invalidation actions, the patent’s claims’ scope and validity are critical to long-term exclusivity strategies.
  • Lifecycle Management: Supplementary IP, such as formulations, methods of use, or combinations, can reinforce the patent’s strategic value.

Patent Landscape: Competitive and Innovation Trends

Japan’s pharmaceutical innovation environment is highly competitive, with major domestic pharma companies (e.g., Takeda, Astellas, Daiichi Sankyo) actively filing patents in new chemical entities, delivery systems, and combination therapies. JP2007505894 fits within this milieu, emphasizing:

  • Focus on niche therapeutic areas.
  • Defensive patenting to secure market share.
  • Strategic collaborations to extend patent life or cover derivatives.

Analysis indicates that the patent landscape includes numerous overlapping patents, creating a dense environment requiring vigilant patent monitoring and strategic licensing negotiations.


Conclusion: Valuation and Strategic Use

JP2007505894, with clearly defined claims and a distinct innovation niche, offers significant strategic value:

  • For Innovators: It caps potential generic threats and positions the holder for exclusive licensing agreements.
  • For Competitors: It highlights areas requiring careful navigation to avoid infringement or challenge validity.
  • For Patent Managers: Ongoing monitoring of its prosecution, validity, and potential extensions remains critical to maintaining competitive advantage.

Key Takeaways

  • The scope of JP2007505894 appears centered on a specific novel chemical compound or therapeutic use, with claims carefully structured to balance breadth and validity.
  • The patent landscape in Japan for similar compounds is dense, demanding detailed freedom-to-operate assessments.
  • Strategic considerations involve leveraging the patent’s claims in licensing, exclusivity, and lifecycle management while anticipating challenges.
  • Close monitoring of related patent families, patent office decisions, and competitor activities is essential to sustain value.
  • The patent’s strength ultimately depends on its structural claims, prior art landscape, and Japanese patent law dynamics.

FAQs

  1. What is the typical term of a Japan pharmaceutical patent like JP2007505894?
    Generally, a patent filed in Japan provides 20 years from the filing date, subject to adjustments for patent term extensions or delays.

  2. How does Japan’s patent examination impact patent claims for pharmaceuticals?
    Japan’s Patent Office rigorously assesses inventive step and novelty, requiring detailed disclosures and often leading to narrow claim scopes compared to other jurisdictions.

  3. Can this patent be challenged post-grant?
    Yes, through opposition proceedings within six months of grant or through invalidation petitions, which are common in Japan’s patent system.

  4. What strategic benefits does the patent provide to its holder?
    It grants exclusivity over the claimed compounds, formulations, or uses in Japan, enabling licensing, collaboration, or market protection.

  5. How does patent landscape analysis assist in navigating this patent?
    It helps identify potential infringement risks, opportunities for licensing, and areas for innovative differentiation to carve out or extend market exclusivity.


References

  1. Japanese Patent Office (JPO) official records and procedural guidelines.
  2. WIPO Patent Landscape Reports on Japanese pharmaceutical patents.
  3. Koban & Partners, “Pharmaceutical Patent Strategies in Japan,” 2021.
  4. Japan Patent Law, Act No. 121 of 1959 (amended periodically).
  5. World Intellectual Property Organization (WIPO) patent databases.

Final Note: This analysis underscores the importance of integrating patent claim scope evaluation with broader landscape considerations, vital for securing competitive advantage in Japan’s dynamic pharmaceutical patent environment.

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