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Last Updated: December 15, 2025

Profile for Japan Patent: 2007533655


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US Patent Family Members and Approved Drugs for Japan Patent: 2007533655

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 Jun 11, 2026 Pf Prism Cv BOSULIF bosutinib monohydrate
⤷  Get Started Free Jun 11, 2026 Pf Prism Cv BOSULIF bosutinib monohydrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2007533655

Last updated: August 11, 2025

Introduction

Japan Patent JP2007533655 pertains to a pharmaceutical invention, notably relating to novel compounds, formulations, or therapeutic methods. Conducting a comprehensive analysis of this patent involves examining the scope of its claims, understanding its position within the patent landscape, and appreciating its strategic relevance for stakeholders such as pharmaceutical companies, investors, and patent attorneys.

This report provides an in-depth evaluation tailored to business professionals seeking to understand the patent's legal scope, technological significance, and competitive environment within Japan's intellectual property framework.

Scope of JP2007533655

Patent Summary

JP2007533655, filed by an unspecified assignee, appears to claim novel chemical entities and their pharmaceutical applications. Based on available data (assuming typical patent content), the invention likely covers:

  • Specific chemical compounds possessing therapeutic activity.
  • Methods of synthesizing these compounds.
  • Pharmaceutical compositions containing the compounds.
  • Methods of treating particular diseases using the claimed compounds.

Claim Structure and Language

In patent law, claims define the boundaries of legal protection. A typical patent in the pharmaceutical domain encompasses independent claims encompassing compound structure, and dependent claims detailing specific embodiments or modifications.

  • Independent Claims: Likely describe the compounds broadly, covering a class of chemical structures or specific molecules with certain functional groups.
  • Dependent Claims: Narrow the scope, specifying particular substituents, formulations, or treatment conditions.

The scope hinges critically on the breadth of the independent claims. If the claims are narrowly drafted—covering only specific molecules—they provide less defensive leverage but may be easier to defend and enforce. Conversely, broader claims protect a wider array of compounds but are more vulnerable to challenges based on obviousness or insufficiency.

Functional Scope and Patentability

The patent likely aims to secure exclusive rights over a new chemical scaffold or a novel application of known compounds. For maximum commercial value, claims must balance breadth with novelty and inventive step criteria under Japanese Patent Law, aligned with the Patent Act [1].

Given the publication date (2007), the claims may have been crafted to encompass broad chemical classes, with possible limitations to specific derivatives or use scenarios.

Claims Landscape

Types of Claims

  • Composition Claims: Covering the chemical compounds in their isolated form or as part of formulations.
  • Method Claims: Detailing the process of synthesizing the compounds or applying them therapeutically.
  • Use Claims: Claiming specific medical indications, such as indications for particular diseases.
  • Formulation Claims: Covering pharmaceutical forms like tablets, injections, or topicals.

Notable Claim Considerations

  • Scope of Chemical Diversity: Whether the claims include extensive structural variants, which expands protection but risks overreach.
  • Therapeutic Claims: Focused on specific diseases or broader therapeutic categories.
  • Method of Use: Claiming novel methods of treatment, which may involve dosing regimens or combination therapies.

Claim Litigation and Free-Running Risks

Japanese patent practice emphasizes clear and supported claims. Overly broad claims risk invalidation if prior art is found or if the claims lack enablement [2].

In the context of pharmaceutical patents, the "first medical use" claims are common but must specify novel applications or compounds to avoid nullity due to lack of inventive step or novelty.

Patent Landscape Analysis

Competitive Environment

Analyzing similar patents filed in Japan reveals the landscape's density:

  • Major Holders: Likely include large pharmaceutical companies or research institutions focusing on chemical therapeutics.
  • Prior Art: The patent intersects with prior Japanese and international patents—necessitating thorough patent landscaping to gauge freedom to operate.

Patent Families and Continuations

Patent families encompassing filings in multiple jurisdictions indicate strategic patenting. Examining continuation or divisional applications related to JP2007533655 could unveil ongoing advancements or defensive strategies.

Innovation Timing and Lifecycle

Given its publication date, JP2007533655’s patent term stretches to 20 years from the filing date, assuming standard maintenance. The patent's lifecycle, including any extensions or litigations, significantly influences commercial exclusivity.

Legal Status and Challenges

  • Maintenances and Oppositions: Japanese law allows for opposition proceedings within six months of grant, potentially impacting enforceability.
  • Licensing and Litigation: The presence of licensing agreements indicates market value; litigation history can reveal enforceability strength.

Strategic Implications for Stakeholders

  • Patent Owners: Can leverage broad claims to secure market exclusivity within Japan.
  • Generic Manufacturers: Must assess claim coverage to design non-infringing products or challenge patent validity.
  • Investors and Collaborators: Should consider patent strength and landscape to evaluate commercial potential and strategic partnerships.

Conclusion

JP2007533655’s scope appears centered on specific chemical compounds with therapeutic utility, with claims likely covering a mixture of composition, process, and use. Its positioning within Japan’s patent landscape hinges on claim breadth, prior art proximity, and ongoing patent strategies by the holder.

Stakeholders must conduct granular prior art searches and freedom-to-operate analyses to navigate licensing, infringement risks, or patent challenges effectively.


Key Takeaways

  • The patent’s strength depends on the breadth and clarity of its claims—broader claims provide more coverage but are more vulnerable.
  • Understanding the competitive landscape requires mapping related patents and patent family members to evaluate patent thicket density and patent lifespan.
  • Strategic patent claim drafting should balance innovation disclosure with infringement risk mitigation.
  • Continuous monitoring for post-grant challenges or oppositions remains critical for maintaining enforceability.
  • Engagement with Japanese patent law specifics—including claim support, inventive step, and recent legal developments—is essential for robust patent portfolio management.

FAQs

Q1: How can I determine whether JP2007533655’s claims cover a specific chemical compound?
A: Cross-reference the compound’s structure with the scope outlined in the independent claims. Patent claims often define the scope through Markush groups or structural formulas, enabling technical comparison.

Q2: What are the typical challenges faced by pharmaceutical patents like JP2007533655 in Japan?
A: Common challenges include prior art invalidation, lack of inventive step, insufficient enablement, and claim interpretation disputes during enforcement or licensing.

Q3: How does the patent landscape influence licensing opportunities for this patent?
A: A dense landscape with overlapping patents can complicate licensing, requiring thorough freedom-to-operate analyses. Conversely, a well-defined niche may attract strategic partners.

Q4: How long does patent protection last in Japan, and can it be extended?
A: Standard patent term is 20 years from the filing date. Extensions are generally limited to certain supplementary protection certificates for pharmaceuticals, subject to Japanese law.

Q5: Should I consider patent litigation or opposition if I believe JP2007533655 unduly restricts market entry?
A: Yes. Conducting a validity assessment and possibly initiating opposition proceedings can challenge the patent’s scope if grounds exist, such as prior art or obviousness.


References
[1] Japanese Patent Act, Law No. 121 of 1959.
[2] Japanese Patent Examination Guidelines, Part IV, Section 2.

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