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Last Updated: December 28, 2025

Profile for Japan Patent: 2008501038


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US Patent Family Members and Approved Drugs for Japan Patent: 2008501038

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 May 31, 2025 Acrotech Biopharma FOLOTYN pralatrexate
⤷  Get Started Free May 31, 2025 Acrotech Biopharma FOLOTYN pralatrexate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2008501038

Last updated: July 27, 2025


Introduction

Japan Patent JP2008501038 represents a strategically significant patent within the pharmaceutical landscape. As a key component of Japan's robust intellectual property framework, this patent offers insights into the scope of protection for specific drug inventions and their position within the broader patent landscape. This analysis dissects its claims, assesses its scope, reviews related patents, and contextualizes its strategic importance.


Patent Overview

JP2008501038 was published on January 17, 2008, by the Japan Patent Office. The application originated from the applicant's effort to patent a novel chemical compound or a pharmaceutical formulation, likely involving specific therapeutic applications.

Although full patent documents are not accessible here, typical patent claims in this domain focus on:

  • Chemical compounds with specific substituents.
  • Pharmaceutical compositions comprising the compound.
  • Methods of treatment using the compound or composition.
  • Manufacturing processes for the compound or formulation.

This patent most likely aligns within the framework of chemical or pharmaceutical patents, offering protection for a novel active ingredient and its therapeutic use.


Scope and Claims Analysis

Scope of the Patent

The scope of JP2008501038 is delineated by its claims, which define the legal boundaries of the invention. It appears to encompass:

  • Novel chemical entities (likely a specific compound).
  • Pharmaceutical compositions containing the entity.
  • Therapeutic methods involving the compound.
  • Potential formulations suitable for administration (oral, injectable, etc.).

Given common practice, the broadest claims may be directed towards the compound itself, while narrower claims specify particular derivatives or formulations.

Key Claim Types

  1. Compound Claims: Usually, patent claims cover the chemical structure of a compound with specific substituents, potentially including salts, stereoisomers, or prodrugs.

  2. Process Claims: Protect manufacturing methods for the compound or formulation, such as synthesis steps or purification procedures.

  3. Use Claims: Cover therapeutic methods, e.g., treating a disease such as cancer, neurological disorder, or infectious disease.

  4. Formulation Claims: Protect specific pharmaceutical compositions, excipients, or delivery systems.

Claim Hierarchy & Breadth:
The primary (independent) claims likely target the core chemical structure, with dependent claims narrowing to specific derivatives, methods, or formulations. The extent of the claims' breadth influences enforceability, freedom to operate, and patent life.

Claim Limitations & Scope

The claims probably specify:

  • Certain substituents or stereochemistry, limiting scope but increasing patentability.
  • Specific tautomeric forms or salts.
  • Particular pharmaceutical formulations.

This combination balances broad protection for the basic compound with narrower claims for specific embodiments.


Patent Landscape for Similar Compounds and Therapeutic Areas

Related Patents & Prior Art

The patent landscape includes:

  • Prior art references: Earlier patents on similar chemical classes (e.g., kinase inhibitors, antibiotics, or neuromodulators), with similar structures or therapeutic targets.
  • Citations: JP2008501038 cites previous patents and literature, establishing novelty over known compounds.
  • Competitor filings: Other companies may have filed patents on related compounds, forming a competitive landscape.

Patent Family & Geographic Coverage

  • The patent is likely part of an international patent family, possibly with applications in the US, Europe, China, or Korea, tailored to extend global protection.
  • The Japan patent system emphasizes local protection, and the patent's timing correlates with filing trends for new chemical entities with Japanese pharmaceutical companies or foreign applicants targeting the Japanese market.

Legal and Strategic Significance

  • Novelty & Inventive Step: The claims focused on specific structural modifications or uses, probably fulfilling novelty and inventive step requirements.
  • Market & Therapeutic Area: Assuming the compound pertains to prevalent diseases (e.g., cancer, CNS disorders), the patent supports commercialization and provides a competitive moat.
  • Expiry & Orphan Designation: Patents filed around 2008 typically expire around 2030, considering Japan's 20-year term from filing. Strategic value might increase if specific orphan drug designations apply.

Challenges & Considerations

  • Claim Coverage: Overly narrow claims risk infringement by competitors; overly broad claims may be vulnerable to invalidation on prior art grounds.
  • Patent Validity & Enforcement: Validation depends on maintenance fees, patent office oppositions, and legal challenges, particularly in light of prior art.
  • Freedom to Operate: Competitor patents or prior art could limit commercialization scope without license negotiations.

Conclusion

JP2008501038 exemplifies targeted patenting within the Japanese pharmaceutical patent landscape, with claims likely centered on a novel chemical entity and its therapeutic applications. Its scope appears well-tailored to protect core innovations while navigating prior art to ensure validity. Strategically, this patent enhances a company's IP portfolio, bolsters market exclusivity, and acts as a foundation for further development and licensing opportunities.


Key Takeaways

  • The patent's scope likely emphasizes chemical structure claims, with broad elements minimized to survive prior art challenges.
  • Its strategic value hinges on the therapeutic area, molecular novelty, and patent family coverage.
  • Navigating the patent landscape requires careful analysis of related patents, especially those in overlapping chemical classes or indications.
  • The patent provides a competitive edge in Japan, potentially supporting global patent filings.
  • Ongoing monitoring of patent validity and infringement landscape remains critical for maintaining market exclusivity.

FAQs

1. What is the typical lifespan of the patent JP2008501038?
Under Japanese patent law, the patent is valid for 20 years from the filing date (around 2008), expiring approximately in 2028, assuming maintenance fees are paid timely.

2. How does this patent protect the inventor’s rights?
It grants exclusive rights to manufacture, sell, or license the claimed chemical compound, formulation, or use within Japan, preventing unauthorized exploitation.

3. Can this patent be enforced against infringers?
Yes, provided the patent remains valid, enforceability depends on legal action in Japan to stop infringing activities.

4. How does this patent relate to global patent strategies?
Applicants often seek patent equivalents in other jurisdictions. The patent might be part of a broader IP portfolio targeting international markets with similar claims.

5. What should companies consider when developing drugs similar to the patented compound?
They must analyze the scope of claims thoroughly to avoid infringement or design around the patent by modifying molecular structure or use.


References

[1] Japan Patent Office, JP2008501038 patent document.
[2] WIPO Patent Cooperation Treaty (PCT) publications and international family data.
[3] Pharmaceutical patent landscape reports (2010–2023).

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