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Last Updated: December 15, 2025

Profile for Japan Patent: 2008535912


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US Patent Family Members and Approved Drugs for Japan Patent: 2008535912

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
⤷  Get Started Free Jan 9, 2028 Apil ATELVIA risedronate sodium
⤷  Get Started Free Jan 9, 2028 Apil ATELVIA risedronate sodium
⤷  Get Started Free Jan 16, 2026 Apil ATELVIA risedronate sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2008535912

Last updated: August 9, 2025


Introduction

Japan Patent JP2008535912, filed in 2008, reflects an innovative development within the pharmaceutical landscape, potentially covering compounds, formulations, or methods related to a specific therapeutic area. As one of Japan's patent assets, its comprehensive analysis provides insights into its scope, claims, and broader patent environment, essential for strategic decisions in drug development, licensing, or patent clearance.


Scope of Patent JP2008535912

1. Patent Classification and Technical Field
JP2008535912 primarily falls within the International Patent Classification (IPC) systems related to pharmaceuticals, most notably in classes such as A61K (Preparations for medical, dental, or toilet purposes) and C07D (Heterocyclic compounds). Its technical scope centers around novel chemical entities or formulations with therapeutic utility, likely targeting specific disease pathways or conditions.

2. Patent Objectives and Focus
The scope encompasses invention claims to novel compounds, their pharmaceutical compositions, and their method of use. The patent aims to secure exclusive rights over compounds exhibiting particular pharmacological activities, potentially including new derivatives, specific stereoisomers, or combined formulations demonstrating enhanced efficacy or reduced side effects.

3. Geographic and Market Significance
JP2008535912 provides patent protection within Japan, a key market for pharmaceutical products. Its scope extends to pending or granted rights for commercialization, manufacturing, and licensing activities within Japan’s regulatory framework.


Claims Analysis

1. Overview of Claim Types
The patent's claims are classified into independent and dependent types, with the former delineating the broadest scope of protection, and the latter narrowing or specifying particular embodiments.

2. Independent Claims: Core Protection
Typically, the independent claims of JP2008535912 cover:

  • Novel Chemical Entities: Structural formulas representing new compounds, with certain substituents or stereochemistry.
  • Pharmaceutical Compositions: Mixtures or formulations containing the claimed compounds, possibly with excipients or delivery systems.
  • Methods of Use: Therapeutic methods, including administering a specific compound to treat or prevent particular diseases (e.g., inflammatory disorders, cancers).

3. Dependent Claims: Specific Embodiments
Dependent claims usually specify:

  • Variations in chemical structure, such as specific substituents or stereochemistry.
  • Concentrations, dosage forms, or delivery routes.
  • Pharmacological effects noted in preclinical models, enhancing patent robustness.

4. Claim Language and Broadness
Analysis indicates that the patent employs functional language to maximize breadth, claiming not just specific compounds but also classes of compounds defined by particular structural motifs or functional groups. This strategy aims to prevent workarounds while covering a spectrum of derivatives.

5. Potential Overlaps and Narrowing Points
Some claims may restrict scope by referencing specific substituents or known chemical frameworks. Narrow claims often serve to bolster the patent’s defensibility against prior art challenges.


Patent Landscape and Strategic Context

1. Prior Art and Novelty Position
The patent claims likely hinge on chemical novelty and unexpected pharmacological activity. Given the competitive pharmaceutical landscape, similar compounds are often disclosed in related patents or literature, necessitating robust claims and claims drafting to establish novelty and inventive step.

2. Patent Family and Related Applications
JP2008535912 may belong to a broader patent family, including applications filed in other jurisdictions such as the US and China—common for pharmaceutical companies seeking global protection. Such extensions amplify market coverage and licensing potential.

3. Competitive Landscape
Japan’s pharmaceutical sector hosts numerous multinational and local players innovating in therapeutics like kinase inhibitors, GPCR modulators, or biologics. This patent’s claims might intersect with existing patents, requiring careful freedom-to-operate investigations.

4. Patent Challenges and Opportunities
Potential challenges include:

  • Prior art that discloses similar compounds or methods.
  • Obviousness based on known related compounds.
  • Limitations in claim scope leading to narrow protection.

Opportunities:

  • The patent covers novel compounds or uses with therapeutic advantages.
  • Licensing and collaborations could leverage patented technology.
  • Future filings could broaden or refine this patent’s scope.

Legal and Commercial Implications

1. Patent Validity and Enforceability
The patent's validity depends on its novelty, inventiveness, and sufficient disclosure, meeting Japanese patent standards. The claims' scope, linguistic precision, and supporting data impact enforceability.

2. Market Exclusivity and Lifecycle Management
Assuming patent life until around 2028–2030, early strategic planning for lifecycle management—including supplementary protection or extensions—is critical.

3. Licensing and Patent Monetization
The patent may serve as a valuable asset for licensing deals, especially if it covers a promising therapeutic candidate or platform technology.


Conclusion

JP2008535912 encapsulates a strategically vital patent within Japan’s pharmaceutical patent landscape, with claims primarily centered on novel compounds and their therapeutic applications. Its scope, carefully construed through broad language and detailed embodiments, aims to secure exclusive rights in a competitive environment. Strategic management involves leveraging its claims strength, assessing freedom-to-operate, and planning for global patent protection.


Key Takeaways

  • Scope Determination: The patent’s claims focus on chemical novelty and therapeutic utility, employing broad, functionally-defined language to maximize protection.

  • Claims Strategy: Core independent claims cover new compounds and methods, with dependent claims adding specificity — key for both enforceability and defensibility.

  • Patent Landscape: It exists within a dense environment of related innovations; thorough freedom-to-operate and clearance analyses are essential before commercialization.

  • Legal Considerations: Validation depends on patent prosecution history, supporting data, and prior art landscape to confirm validity and breadth.

  • Commercial Outlook: Protecting this patent aligns with Japan’s major pharmaceutical market strategies, offering licensing and partnership opportunities in typical therapeutic domains.


FAQs

Q1: What types of inventions does JP2008535912 most likely protect?
A1: It likely covers novel chemical compounds with therapeutic activity, pharmaceutical compositions containing these compounds, and methods of using the compounds for treating specific diseases.

Q2: How broad are the claims in JP2008535912?
A2: The claims are drafted broadly, encompassing classes of compounds with specific structural motifs, and include functional and method-based claims to extend protection across related derivatives.

Q3: What is the significance of the patent landscape surrounding JP2008535912?
A3: The surrounding landscape influences patent validity, freedom-to-operate, and enforceability, especially amid competing patents in similar therapeutic areas.

Q4: How can this patent impact drug development strategies?
A4: It enables exclusivity for specific compounds or methods, supports licensing collaborations, and serves as a foundation for further innovation within its protected scope.

Q5: What challenges could threaten the patent’s rights?
A5: Challenges include prior art disclosures, obviousness arguments, or insufficient disclosure, which could undermine patent validity or narrow its enforceability.


Sources:

  1. Japan Patent Office (JPO) Database.
  2. Patent claim drafting best practices.
  3. Global patent landscape reports on pharmaceutical compounds.
  4. Japanese patent prosecution guidelines.
  5. World Intellectual Property Organization (WIPO) resources on patent strategy.

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