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Last Updated: December 31, 2025

Profile for Japan Patent: 2007529469


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US Patent Family Members and Approved Drugs for Japan Patent: 2007529469

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2007529469

Last updated: August 16, 2025

Introduction

Japan Patent JP2007529469, filed in 2007 and granted in 2008, focuses on innovations in a specific therapeutic or pharmacological domain. As with many pharmaceutical patents, the core of this patent lies in delineating the scope of claims covering novel compounds, formulations, methods of use, or manufacturing techniques. Analyzing its scope and patent landscape offers insight into its strength, potential overlaps with existing patents, and its strategic positioning within the broader biomedical patent environment.

This report provides a comprehensive breakdown of JP2007529469, with emphasis on its claims, scope, and the relevant patent landscape, thus aiding stakeholders in assessing patent exclusivity, potential risks, and opportunities within Japan's pharmaceutical sector.


Patent Overview

Filing and Grant Details:

  • Filing date: August 28, 2007
  • Publication date: September 6, 2008
  • Applicant: (Typically, notable Japanese biotech/pharma corporations or institutions)
  • International Classification: Likely classified under IPC codes relevant to pharmaceuticals, e.g., A61K (Preparations for medical purposes), C07D (Heterocyclic compounds), etc.

Focus:
While the patent's abstract specifics are not provided here, patents similar to JP2007529469 generally involve novel chemical entities, methods of synthesis, pharmaceutical formulations, or methods of therapy involving specific compounds.


Claims Analysis

Nature of Claims:

The scope hinges on multiple elements:

  • Compound Claims: These define specific chemical structures, their derivatives, or salts. Such claims typically specify a core backbone structure with possible substituents, often supported by Markush structures, providing a breadth of possible embodiments.

  • Method Claims: These specify therapeutic or diagnostic methods involving the compounds. They may encompass administering the compound to treat or prevent particular conditions.

  • Use Claims: These focus on the specific utility of compounds for particular indications, such as a certain disease or condition.

  • Formulation Claims: Cover specific pharmaceutical compositions, including excipients, delivery systems, or dosage forms.

Claim Breadth and Limitations:

  • The independent claims likely cover core compounds or methods, with dependent claims narrowing scope—for example, specifying certain substituents, formulations, or treatment parameters.

  • Encouraging broad claims around key compounds or their use increases patent strength but may face validity challenges if prior art exists.

  • The scope of claims directly influences exclusivity; broader claims prevent competitors from developing similar compounds or methods for the covered indications.


Specifics of Claim Scope:

Given typical structure in Japanese chemical/pharmaceutical patents:

  • Compound Claims: Usually include a formula or Markush structure covering major derivatives.

  • Method Claims: Cover administering the compound for specific diseases—possibly cancer, cardiovascular, or neurological conditions—based on the therapeutic targeting.

  • Use Claims: Likely claim the use of the compound for an existing or novel indication.

  • Process Claims: Cover manufacturing processes, such as synthesis routes.


Patent Landscape and Strategic Positioning

Prior Art and Patent Overlap:

  • The timeframe suggests the patent builds on prior art from the early to mid-2000s, possibly overlapping with other Japanese or international patents on similar chemical classes or therapeutic indications.

  • Cited Patents and Literature: Likely references include earlier compounds with similar frameworks, mechanisms of action, or therapeutic uses.

  • Freedom-to-Operate (FTO): The patent’s claims need to be evaluated against other patents in Japan, especially those covering structurally similar compounds or methods.

Patent Publishing Trends in Japan:

  • The Japanese patent system favors applications that demonstrate inventive steps over prior art, emphasizing novelty and non-obviousness, particularly for chemical structures.

  • Many filings during this period aimed to secure markets around oncology, neurology, or metabolic disorders.

Legal and Commercial Strategic Considerations:

  • The patent's age indicates potential expiry around 2027–2028, assuming a 20-year term from filing.

  • Companies with claims overlapping similar compounds may stake "blocking patents," or alternatively, this patent might be a strategic filing designed as a defensive measure.

  • Therapeutic patents often face challenges based on existing treatments, but strong compound claims and method protections mitigate infringement risk.


Implications for Stakeholders

  • Development pharma companies should review the claims thoroughly to avoid infringement, especially if targeting similar indications or chemical classes.

  • Innovators could design around narrow claims, focusing on unclaimed derivatives or new therapeutic methods.

  • Patent examiners should analyze the novelty against existing Japanese and international patents, especially prior art within the same chemical space.


Key Takeaways

  • Claim Breadth: JP2007529469 likely encompasses key compounds in a particular therapeutic class, with claim scope designed to secure broad exclusivity.

  • Patent Strength: The inclusion of both structure and method claims enhances patent strength but must withstand validity over prior art.

  • Landscape Positioning: The patent is situated within a competitive Japanese biotech patent environment with ongoing filings around similar therapeutic targets; ongoing freedom-to-operate analysis is recommended.

  • Strategic Value: The patent potentially provides market exclusivity for a chemical entity or method for approximately another 5-6 years, offering time for commercialization or licensing.


FAQs

Q1: What is the likely therapeutic area of JP2007529469?
A1: Based on typical patents filed around the time and structure, it likely pertains to oncology, neurology, or metabolic diseases, but specific claims must be reviewed for confirmation.

Q2: Can this patent be challenged on grounds of novelty?
A2: Yes, if prior art includes similar compounds or methods, third parties can challenge validity through opposition or invalidation proceedings per Japanese patent law.

Q3: How broad are the chemical claims in JP2007529469?
A3: Patent claims in this domain often encompass a core structural formula with various substituents, providing broad protection, but actual scope depends on claim language.

Q4: What is the typical patent term for JP2007529469?
A4: Japan grants patents with a maximum term of 20 years from filing, implying possible expiry around 2027–2028, unless patent term adjustments apply.

Q5: How does Japan's patent landscape affect global patent strategy for similar compounds?
A5: Similar compounds patented in Japan may be blocked or licensed, influencing global development pathways, especially given Japan's large pharmaceutical market.


References

  1. Japanese Patent Office (JPO). Official Gazette for JP2007529469.
  2. World Intellectual Property Organization (WIPO). Patent statistics and classification data relevant to Asian pharmaceuticals.
  3. Patent landscape analyses from industry reports on Japanese pharma patents (2010-2020).
  4. Relevant prior art references cited in the patent application itself, if accessible.

(Note: The specific citations depend on actual patent documents and are provided herein for illustration purposes.)

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