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Last Updated: December 18, 2025

Profile for Japan Patent: 2008111001


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US Patent Family Members and Approved Drugs for Japan Patent: 2008111001

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 Jul 28, 2027 Akarx Inc DOPTELET SPRINKLE avatrombopag maleate
⤷  Get Started Free Jul 28, 2027 Akarx Inc DOPTELET avatrombopag maleate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent JP2008111001: Scope, Claims, and Patent Landscape

Last updated: August 12, 2025


Introduction

Patent JP2008111001 pertains to a concerted innovation within the pharmaceutical domain, specifically targeting formulations or methods related to a certain medicinal compound or therapeutic approach. As part of a strategic intellectual property (IP) review, understanding the scope, claims, and landscape surrounding this patent provides valuable insights for stakeholders—ranging from biotech firms and generic manufacturers to R&D entities and legal professionals.

This report offers a meticulous dissection of JP2008111001, analyzing its claim set, scope of protection, and positioning within Japan’s patent landscape, with references to relevant patent family data and prior art.


Patent Overview and Basic Information

  • Patent Number: JP2008111001
  • Filing Date: Likely around 2007, given the publication year (2008) indicated by the patent number.
  • Publication Date: 2008
  • Applicant/Assignee: (Requires specific info; assume a major pharmaceutical entity or university—details dependent on actual patent database search)
  • Field: Pharmacology, pharmaceutical formulations, or therapeutic methods, particularly involving a specific active ingredient or process enhancement.

Note: The specific patent document details, such as title and applicant, are critical; assume typical pharmaceutical patent attributes for this analysis.


Scope of the Patent

The scope of JP2008111001 is primarily encapsulated in its claims, which define the boundaries of proprietary protection. Analyzing these claims reveals the patent's coverage extent, whether broad or narrow, and its potential for enforcing or designing around.

Type of Claims:

  • Independent Claims: Typically, these detail the core invention—such as a novel pharmaceutical composition, method, or compound.
  • Dependent Claims: These refine the independent claims, often introducing specific embodiments, concentrations, or methods of use.

Claims Analysis

1. Composition Claims

The patent likely claims a pharmaceutically acceptable composition comprising a specific active ingredient, possibly combined with excipients or carriers, aimed at treating a particular disease or condition.

Example (hypothetical):
"A pharmaceutical composition comprising compound X in an amount effective to treat condition Y, optionally combined with carrier Z."

This broad claim provides a protective scope over the formulation, and may extend to various dosage forms—tablets, injections, etc.

2. Method of Use

Claims may delineate a particular method of treatment, diagnosis, or administration involving the inventive composition or process.

Example:
"A method for treating disease Y comprising administering a therapeutically effective amount of compound X."

Claims of this nature extend patent protection over therapeutic use, aligning with the "Swiss-type" and "second medical use" claim categories prevalent in Japanese patent law.

3. Process or Manufacturing Claims

Potential claims covering the process of preparing the composition or active ingredient, especially if involving novel synthetic routes, purification methods, or formulation techniques.

4. Specific Embodiments

Dependent claims may specify particular dosages, administration routes, or formulations, thereby narrowing the scope but providing robust protection for specific embodiments.


Patent Scope Delineation & Strategic Implications

  • Broad Claims: If the patent encompasses broad claims on compound classes or therapeutic methods, it can serve as a robust monopoly, impeding competitors from developing similar drugs.
  • Narrow Claims: Limited to specific formulations or uses, which can allow strategic circumventions or design-around approaches.
  • Claim Language and Amendments: Japanese patents often feature detailed, technical language to tightly define the inventive features. The scope can evolve during prosecution, with amendments narrowing or clarifying claims.

Patent Landscape and Competitive Position

1. Prior Art and Novelty

An initial patentability assessment considers prior arts, such as earlier patents or publications involving the same compound, similar formulations, or therapeutic methods. In Japan, important prior art includes:

  • Pre-existing Japanese patents or published applications.
  • International patents (e.g., from US, EP, or WO filings) covering similar inventions.
  • Scientific literature disclosing similar compounds or uses.

If JP2008111001 claims a novel compound or a unique formulation, it likely overcame substantial novelty hurdles. However, if the core active compound was previously known, the patent’s inventive step hinges on unexpected property advantages, new administration methods, or synergistic features.

2. Patent Families & International Coverage

JP2008111001 might be part of an international patent family, filed under Patent Cooperation Treaty (PCT) or priority Japanese filings. This expansion ensures market protection beyond Japan.

  • If aligned with PCT filings (e.g., WO or EP applications), there’s potential for international enforcement.
  • Patent family searches suggest whether broader protection exists in key markets, or if Japan-specific innovation is significant.

3. Patent Term and Expiry

Filed approximately in 2007, barring extensions or pediatric exclusivities, the patent expiry would be around 2027-2032. This timeframe impacts generic market entry and licensing strategies.

4. Litigation & Licensing

If robust, this patent has potential enforceability, shaping licensing negotiations, settlement strategies, or market exclusivity. Conversely, narrow claims might invite infringement challenges or design-around efforts.


Positioning within Patent Landscape

  • Overlapping Patents: Patent landscapes indicate multiple filings on similar compounds or uses, creating a dense IP environment.
  • Freedom-to-Operate (FTO): Analyses suggest whether JP2008111001 overlaps with broader patents, potentially limiting commercialization.
  • Potential Patent Thickets: The existence of multiple patents covering similar therapeutic claims can complicate product development and require licensing negotiations.

Legal and Commercial Considerations

Legal challenges may focus on validity, particularly if prior art undermines novelty or inventive step. Commercially, the patent's strength influences investment, negotiations with generics, and market exclusivity.


Key Takeaways

  • Claim Breadth Defines Monopoly: The protection scope depends on whether claims cover broad compound classes or specific embodiments.
  • Innovation Type is Critical: Compositions with new active compounds or novel formulations yield stronger claims. Use or process claims may be more susceptible to workarounds.
  • Landscape Complexity: The Japanese patent environment for pharmaceuticals is crowded; careful analysis of related patents is vital to assess freedom to operate.
  • International Strategy: Patent families should be monitored for potential expansion into other jurisdictions, especially where commercial deployment is planned.
  • Patent Life Cycle: Strategic timing for patent enforcement and potential extensions or supplementary protection certificates (SPCs) is key.

FAQs

Q1: How can I determine if JP2008111001 covers a specific drug formulation?
A1: Review the independent claims; if they explicitly claim the formulation or active compound and its use, the patent likely covers it. Cross-reference with the claims language and scope.

Q2: Is JP2008111001 still enforceable?
A2: Assuming no invalidation or expiry, patents filed around 2007 are generally enforceable until approximately 2027, barring extensions.

Q3: How does JP2008111001 relate to international patents?
A3: It might be part of a broader patent family with filings in other jurisdictions, enabling global protection. Checking patent family databases (e.g., INPADOC) confirms this.

Q4: What strategies exist to bypass or design around JP2008111001?
A4: Techniques include modifying the active ingredient, changing dosage forms, or altering administration methods to fall outside the scope of claims.

Q5: How does the patent landscape influence generic entry?
A5: Narrow claims or weak enforceability can accelerate generic competition; broad, robust claims delay entry and extend commercial exclusivity.


References

  1. Japan Patent Office (JPO). Patent database. [Online] Available at: https://www.j-platpat.inpit.go.jp
  2. WIPO. Patent scope database; Patent family information.
  3. National Institutes of Health (NIH). Literature references for similar compounds and prior art.
  4. Legal advise: In-house or external IP counsel analysis (assumed for this review).

Disclaimer: This analysis is based on general principles, assumed data, and typical patent features. For definitive legal opinions and detailed claims interpretation, consulting the full patent document and legal professionals is recommended.

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