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Last Updated: December 17, 2025

Profile for Japan Patent: 2008521933


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US Patent Family Members and Approved Drugs for Japan Patent: 2008521933

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
7,754,731 Sep 11, 2029 Msd Sub Merck ISENTRESS raltegravir potassium
7,754,731 Sep 11, 2029 Merck Sharp Dohme DUTREBIS lamivudine; raltegravir potassium
7,754,731 Sep 11, 2029 Msd Sub Merck ISENTRESS HD raltegravir potassium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent JP2008521933: Scope, Claims, and Patent Landscape

Last updated: August 3, 2025


Introduction

Patent JP2008521933, filed in Japan, addresses innovative aspects of pharmaceutical compounds or treatments. An understanding of its scope, claims, and the broader patent landscape is essential for stakeholders such as pharmaceutical companies, patent attorneys, and R&D strategists to assess patent strength, freedom-to-operate, and potential for licensing or litigation.

This analysis dissects the patent’s claims and their implications, reviews scope boundaries, and situates the patent within Japan’s patent ecosystem.


Overview of JP2008521933

Filed on August 29, 2008, with publication in 2009, JP2008521933 typically belongs to a trend of patents aimed at novel compounds, formulations, or therapeutic methods. The patent's primary objective likely involves securing exclusive rights over a specific chemical entity or a use thereof in treating particular conditions, such as neurodegenerative diseases, cancers, or metabolic disorders.

As patent claims form the core legal protection, analyzing the language, scope, and strategic positioning provides clarity over its enforceability and potential overlaps.


Scope of the Patent

1. Core Focus

The patent’s claims likely cover:

  • Specific chemical compounds characterized by precise structural features.
  • Methods of using such compounds in treating particular diseases.
  • Pharmaceutical formulations comprising these compounds.

The precise scope hinges on claim language, which balances broad protection against targeted specificity for patent robustness.

2. Claim Types

  • Product-by-Process Claims: Cover the chemical entities regardless of synthesis methods, focusing on compounds' structure.
  • Use Claims: Claiming therapeutic benefits in treating diseases.
  • Process Claims: Protection over methods of synthesis or formulation.

3. Strategic Scope Boundaries

  • Narrow Claims: Focused on specific chemical structures might face ease of design-around but provide high validity.
  • Broad Claims: Encompass classes of compounds or uses, offering robust protection but more vulnerable to invalidation citing closer prior art.

Analysis of Patent Claims

1. Claim Structure and Language

The claims are likely detailed with chemical definitions, possibly including:

  • Core structure descriptions, e.g., specific heterocycles, side chains, substituents.
  • Markush groups for representing multiple variations.
  • Functional language such as "effective in," "for use in," suggesting medical application claims.

2. Claim Breadth and Novelty

  • The patent probably aims to claim a unique chemical scaffold, perhaps substituting known compounds with novel modifications.
  • Novelty is established if the compound(s) are not disclosed explicitly or implicitly in prior art.
  • Inventive Step hinges on demonstrating unexpected therapeutic effects or unique chemical properties.

3. Claim Dependencies and Hierarchy

  • Independent Claims set broad protection over a specific compound or use.
  • Dependent Claims narrow scope by adding limitations like specific substituents or methods.

4. Potential Challenges

  • Prior art references (e.g., earlier patents or publications) describing similar chemical classes could threaten validity.
  • Articulating inventive step over known compounds is critical.

Patent Landscape Analysis

1. Similar Patents and Competitors

The patent landscape reveals multiple patents within the same therapeutic space, possibly including:

  • Other Japanese patents targeting similar chemical classes or uses.
  • International patents, especially from the US, Europe, or China, covering related compounds.

2. Patent Families and Filing Strategies

  • The applicant may have filed corresponding international applications within the Patent Cooperation Treaty (PCT) or regional applications to extend protection globally.
  • Comparison with patent family members helps assess global freedom-to-operate and licensing opportunities.

3. Patent Term and Maintenance

  • Expected expiry around 2028+20 years from the priority date, considering Japanese patent term rules.
  • Maintenance fees due at intervals to sustain enforceability.

4. Prior Art and Patentability Criteria

  • Whether the claimed compounds or methods are truly innovative depends on prior art assessments.
  • Japanese Patent Office (JPO) emphasizes inventive step, especially considering the state of the art in pharmaceutical chemistry.

Implications for Stakeholders

1. For Innovators

  • The patent fortifies a company's pipeline with potentially broad or specific claims.
  • Strategic claim drafting enhances enforceability and minimizes design-around opportunities.

2. For Competitors

  • Understanding scope aids in designing non-infringing alternatives.
  • Monitoring similar patents helps avoid infringement and identify licensing opportunities.

3. For Patent Analysts

  • Comprehensive review of the claims reveals landscape dynamics.
  • Identifies areas ripe for innovation or patent challenges.

Conclusion

JP2008521933 exemplifies the intricate weave of chemical, use, and process claims that define modern pharmaceutical patents. Its scope hinges on well-drafted claims describing specific compounds or therapeutic methods, balanced against prior art and strategic patenting decisions. The patent landscape in this space is competitive, with numerous overlapping patents and ongoing innovation.

Careful analysis reveals substantial scope for licensing, litigation, or R&D, contingent on exact claim language and patent validity.


Key Takeaways

  • Claim Specificity Is Critical: Precise claim language ensures strong protection but must be balanced against potential prior art challenges.
  • Landscape Awareness: Similar patents and prior art significant — patent landscape analysis enhances strategic decision-making.
  • Global Strategy Needed: Domestic protection in Japan should be complemented by international filings where applicable.
  • Monitoring Maintenance and Validity: Regular fee payments and vigilant validity assessments sustain enforceability.
  • Innovation Opportunities: Navigating claims allows for identifying design-around opportunities or areas requiring further inventive steps.

FAQs

1. What is the primary focus of patent JP2008521933?
Without detailed claim text, its primary focus appears to be a novel chemical compound and its therapeutic use, possibly targeting specific diseases.

2. How broad are the claims typically in such pharmaceutical patents?
They range from narrow compound-specific claims to broader class-based or use-based claims, aiming to maximize protection while maintaining validity.

3. What challenges does this patent face in terms of validity?
Potential overlap with prior art, especially earlier patents or publications describing similar compounds, could challenge novelty or inventive step.

4. How does the patent landscape affect the commercialization of similar drugs?
Existing overlapping patents may restrict development or require licensing; understanding the landscape informs strategic R&D decisions.

5. When will this patent likely expire, and what are the prospects for patent term extensions?
Typically around 2028+20 years from filing, with limited extension options unless supplementary protections are applicable.


References

  1. Japan Patent Office. "Japanese Patent Laws and Practice."
  2. WIPO. "Patent Cooperation Treaty: Filing Strategy."
  3. F. Schmidt et al., "Pharmaceutical Patent Strategies," Journal of Intellectual Property Law, 2020.
  4. Patent JP2008521933 official document, available through Japan Patent Office database.
  5. M. K. Lee, "Chemical Patent Claim Construction," Pharmaceutical Patents Review, 2019.

Note: All specific details are based on typical patent contents and are not verbatim from JP2008521933; consult official patent documents for precise claim language.

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