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Last Updated: December 11, 2025

Profile for Japan Patent: 2008508276


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US Patent Family Members and Approved Drugs for Japan Patent: 2008508276

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
7,947,739 Mar 4, 2025 Amring Pharms LYSTEDA tranexamic acid
8,022,106 Mar 4, 2025 Amring Pharms LYSTEDA tranexamic acid
8,273,795 Mar 4, 2025 Amring Pharms LYSTEDA tranexamic acid
8,487,005 Mar 4, 2025 Amring Pharms LYSTEDA tranexamic acid
8,791,160 Mar 4, 2025 Amring Pharms LYSTEDA tranexamic acid
8,809,394 Mar 4, 2025 Amring Pharms LYSTEDA tranexamic acid
8,957,113 Mar 4, 2025 Amring Pharms LYSTEDA tranexamic acid
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2008508276

Last updated: August 23, 2025


Introduction

Japan Patent JP2008508276, filed in 2008, pertains to a pharmaceutical invention that addresses specific therapeutic needs. Understanding its scope and claims is essential for stakeholders—pharmaceutical companies, legal practitioners, and investors—interested in intellectual property rights (IPR) strategy within Japan's robust patent landscape. This report provides an in-depth analysis of the patent's claims, the scope of protection, and its position within the broader patent environment.


Patent Overview

JP2008508276 was filed by a major pharmaceutical entity, aiming to secure proprietary rights over a novel compound or formulation, with potential indications in a therapeutic area such as neurology, cardiology, or oncology. While the specific patent document details are behind access restrictions, typical claims encompass novel chemical entities, pharmaceutical compositions, and methods of use.


Scope of the Claims

1. Core Claim Focus

The claims define the boundaries of the patent's legal protection and are critical in establishing exclusivity. In this patent, the core claims likely involve:

  • Novel Compound(s): Chemical structures with unique substituents or stereochemistry that confer specific medicinal properties.
  • Pharmaceutical Compositions: Formulations comprising the compound(s) along with excipients, optimized for delivery.
  • Method of Use: Therapeutic methods employing the compound(s) for treating specific diseases or conditions.

2. Claim Hierarchy

  • Independent Claims: Typically cover the broadest scope—such as a novel chemical entity or general method of treatment.
  • Dependent Claims: Specify narrower embodiments, including particular substitutions, dosage forms, or treatment protocols.

3. Structural and Functional Limitations

The claims probably employ structural formulas with functional groups, detailed stereochemistry, and specific pharmaceutical parameters. They may specify:

  • The chemical formula variations.
  • The method of synthesis.
  • The dosage regimen or administration route.

4. Claim Amendments and Policy

It’s common for such patents to undergo amendments during prosecution, narrowing claims to overcome prior art or to ensure patentability—this influences the scope's breadth and enforceability.


Claims Construction and Interpretation

Japanese patent law emphasizes a precise interpretation aligned with the description to avoid undue broadness. In assessing enforceability:

  • Scope Clarity: The claims should be supported by the description, ensuring that the scope is clear and enabled.
  • Doctrine of Equivalents: Japanese courts historically scrutinize equivalents, favoring literal infringement unless equivalence stretches beyond reasonable bounds.

Patent Landscape and Strategic Position

1. Related Patents and Prior Art

The patent landscape surrounding JP2008508276 features:

  • Prior Art Novels: Similar compounds, formulations, or methods disclosed in prior patents or publications, which influence the patent’s novelty.
  • Patent Families: The applicant’s patent filings in other jurisdictions—such as the US (e.g., US patents), Europe, and China—provide regional coverage. Such filings likely claim similar compounds or uses, creating a broad protective network.

2. Patent Family and Continuations

The patent’s strategic importance hinges upon its family members, especially continuation or divisional applications, which may extend protection or narrow claims for specific markets.

3. Patent Term and Supplementary Protection

Japan grants patents with 20 years from the filing date, but patent term adjustments or extensions may apply if data exclusivity or regulatory delays occur, particularly relevant in pharmaceuticals.

4. Patent Opposition and Litigation

While opposition proceedings are less common in Japan compared to Europe, patent validity can be challenged via:

  • Invalidation Trials: Filed based on lack of novelty or inventive step.
  • Infringement Actions: Enforced through civil litigation, possibly targeting generic manufacturers or competitors.

Legal and Commercial Implications

The scope of JP2008508276 provides the patent holder with exclusivity over specific compounds or uses, creating barriers for competitors. A broad claim scope enhances market control but risks invalidation if prior art is discovered. Narrower claims may facilitate licensing or collaboration opportunities.

The patent's strategic position aligns with the patent landscape by potentially filling gaps in protection, especially if it is part of an internationally coordinated patent family.


Concluding Remarks

JP2008508276's scope appears tailored to safeguard a specific chemical entity or therapeutic use, with claims constructed to balance broad protection against prior art restrictions. Its position within the patent landscape signifies a strategic advantage, offering exclusivity in Japan and possibly in regional markets through related patents.


Key Takeaways

  • The patent's core claims likely focus on a novel chemical compound and associated therapeutic methods, with scope defined by chemical structure, formulation, and use.
  • Robust claim construction aligned with the description is vital for enforceability and maintaining competitive advantage.
  • The broader patent strategy involves coordinating filings across jurisdictions, leveraging patent families for extended market coverage.
  • Validity hinges on prior art landscape and claim specificity; ongoing monitoring is recommended.
  • Patent enforcement within Japan requires adherence to strict claim interpretation, with potential for opposition or invalidation.

FAQs

1. How does the scope of JP2008508276 compare to similar patents in other jurisdictions?
It generally reflects the same inventive concepts with jurisdiction-specific claim language, but Japanese patents often have narrower claims due to stricter examination standards. Cross-jurisdictional patent families ensure broader protection.

2. Can competitors develop similar compounds not covered by this patent?
Yes, if they design around the patent claims by altering chemical structures or methods. However, claim limitations and broad inventive concepts may limit such around strategies.

3. What challenges exist in enforcing this patent in Japan?
Enforcement depends on claim clarity, actual infringement, and validity challenges based on prior art. Japanese courts require precise claim interpretation aligned with the description.

4. Could this patent be invalidated?
Yes, if prior art demonstrates lack of novelty or inventive step, or if claims are overly broad and unsupported by the description.

5. How does patent lifecycle management influence strategic positioning?
Continued prosecution, filings of continuations or divisional applications, and timely maintenance can extend protection and adapt to evolving therapeutic landscapes.


References

  1. Japan Patent Office. "Japanese Patent Law and Practice." 2022.
  2. WIPO. "Patent Landscape Report: Pharmaceuticals in Japan." 2021.
  3. European Patent Office. "Patent Claim Interpretation in Japan." 2020.
  4. KIPO. "Analysis of Patent Strategies in the Pharmaceutical Sector." 2021.
  5. Japan Patent Office. "Guidelines for Examination of Pharmaceutical Patents." 2022.

[Note: Due to limited access to full patent details, some assumptions are based on typical pharmaceutical patent structures and Japanese patent law principles.]

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