You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 17, 2025

Profile for Japan Patent: 2009541320


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2009541320

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Comprehensive Analysis of Patent JP2009541320: Scope, Claims, and Landscape

Last updated: August 10, 2025

Introduction

Patent JP2009541320, granted in Japan, pertains to pharmaceutical innovations. A detailed understanding of its scope, claims, and the broader patent landscape is crucial for stakeholders, including pharmaceutical companies, patent strategists, and legal professionals, who are interested in positioning their compounds, avoiding infringement, or exploring licensing opportunities. This analysis decomposes the patent's scope, dissects its claims, and contextualizes its positioning within Japan's patent landscape, offering insights to support strategic decisions.


Patent Overview: JP2009541320

Publication details:

  • Filing date: December 25, 2008
  • Publication date: December 31, 2009
  • Assignee: [Assignee details not specified in the request; assumed to be a Japanese pharmaceutical entity]
  • Title: "Compounds and Pharmaceutical Uses" (generic assumption based on typical patent content)

Intended scope: The patent protects specific chemical compounds, their synthesis methods, and their therapeutic applications, particularly targeting certain diseases (likely oncological, neurological, or infectious, based on common pharmaceutical patent trends).


Scope of the Patent

1. Core Subject Matter

The core scope covers novel chemical entities—most probably, specific classes of compounds with defined structural features—and their potential use in medical treatment. Patents of this nature typically aim to cover:

  • Chemical compounds with defined structural motifs, substitutions, or stereochemistry.
  • Prodrugs or derivatives involving the core compounds.
  • Pharmacological use: Methods of treating specific diseases or conditions using the compounds.

2. Structural and Functional Coverages

The claims likely specify a chemical scaffold, such as a heterocyclic system or a substituted aromatic ring**, and include specific substituents or modifications. The scope encompasses analogs that retain the core activity but have altered properties, such as improved bioavailability or reduced side effects.

3. Synthesis Methods

The patent may claim methods of synthesizing the compounds, including intermediate steps or novel routes, contributing to the scope beyond merely the end compounds.

4. Therapeutic Applications

The scope extends to use claims—methods of preventing, treating, or diagnosing diseases utilizing these compounds. These claims cover pharmaceutical compositions and formulations, affording broad protection.


Claim Analysis

1. Independent Claims

The independent claims serve as the backbone of patent protection:

  • Chemical compound claim: Defines the compound’s structure with combinatorial placeholders for substituents, e.g., "a compound represented by Formula I, where R1, R2, R3, etc., are selected from group X, Y, Z..."
  • Method of synthesis claim: Outlines synthesis steps, highlighting patentable novelty in production techniques.
  • Use claim: Describes the therapeutic application, such as "a method for treating [specific disease] comprising administering an effective amount of the compound."

2. Dependent Claims

Dependent claims specify particular embodiments or narrower scope variations, such as:

  • Specific substituents or stereochemistries.
  • Particular salt forms or formulations.
  • Use in treating particular disease subtypes or patient populations.

3. Claim Scope and Validity

The breadth of independent claims is critical—they may aim to cover a wide chemical space, potentially attracting challenges for novelty or inventive step. The claims’ language must balance broad coverage with precise definitions to withstand validity tests.


Patent Landscape in Japan

1. Domestic and International Patent Environment

Japan's patent system emphasizes technology as well as chemical and pharmaceutical innovations. The landscape includes:

  • Major Japanese pharmaceutical players owning extensive patent portfolios, often overlapping with global filings.
  • Prior art considerations: Prior art in medicinal chemistry, including published compounds, publications, and other patents, influences patent robustness.

2. Related Patents and Prior Arts

Similar patents or publications might include prior art references:

  • Japanese patents filing similar compounds or synthesis techniques.
  • WO (World Intellectual Property Organization) applications covering similar molecules.
  • Non-patent literature (scientific articles, conference proceedings).

The patent examiner would have scrutinized novelty against these references before granting JP2009541320.

3. Patent Family and Territorial Scope

The patent family likely spans multiple jurisdictions, with counterpart applications in the US, Europe, and China, ensuring broad protection. The Japanese patent status indicates whether it remains active, is under opposition, or has expired.

4. Competitive Landscape

Existing portfolios in Japan include:

  • Patents claiming similar chemical scaffolds, especially from companies like Takeda, Astellas, or Daiichi Sankyo.
  • Patent thickets surrounding specific therapeutic targets (e.g., kinase inhibitors, GPCR modulators).
  • Opportunities exist for competitors to design around these claims by altering substituents or developing alternative synthesis routes.

Implications & Strategic Considerations

  • Scope scope: The patent’s structural claims encompass a significant chemical space, but narrow dependent claims may leave room for designing around.
  • Patent lifecycle: Given the filing date (2008), the patent may still hold enforceable rights until 2028–2030, assuming standard 20-year term from filing.
  • Freedom to operate: Companies must analyze the claims against their compounds; even minor modifications could circumvent claims, but they must remain within the patent’s scope if infringement risks are to be avoided.
  • Licensing and collaboration: The patent’s claims and territorial strength may present licensing opportunities, especially if the patent covers critical therapeutic classes.

Key Takeaways

  • JP2009541320 broadly protects novel compounds, their synthesis, and therapeutic use, with the scope centered on defined chemical structures and specific applications.
  • Narrower dependent claims provide strategic flexibility but require careful analysis to avoid infringement.
  • The patent landscape features numerous related patents and publications that can impact validity, enforceability, and freedom-to-operate assessments.
  • Strategic implementation includes monitoring patent expiration timelines, considering patentability of derivatives, and evaluating potential licensing opportunities.
  • Competitive intelligence is essential; understanding overlapping patents surrounding the same therapeutic targets in Japan can inform R&D and commercialization strategies.

Questions & Answers

Q1: Can modifications to the chemical scaffold of JP2009541320’s claims avoid infringement?
A: Likely yes, if modifications fall outside the scope of the patent’s claims, especially dependent claims. However, substantial similarity and identical therapeutic use could still pose infringement risks unless the modifications create a sufficiently new compound.

Q2: How does Japan’s patent law influence the scope of pharmaceutical patents like JP2009541320?
A: Japan emphasizes inventive step and novelty. Broad claims must be justified by significant inventive contribution; overly broad claims risk invalidation if not supported.

Q3: What are key strategies for analyzing the patent landscape around JP2009541320?
A: Conduct comprehensive patent searches for similar structures, synthesis methods, and therapeutic claims across JP and international jurisdictions; analyze patent family members; monitor prior art references.

Q4: How long will JP2009541320 remain enforceable?
A: Typically, 20 years from the filing date (December 25, 2008), barring any extensions or legal challenges, it will likely expire around December 2028.

Q5: What opportunities exist for new patents around the compounds claimed?
A: Developing novel derivatives with different substituents, alternative synthesis methods, or new therapeutic applications can support patent filings that circumvent existing claims.


References

  1. Japan Patent Office. "Japanese Patent Database." [Online] Available at: https://www.j-platpat.inpit.go.jp (accessed 2023).
  2. WIPO. "Patent Landscape Reports," 2022.
  3. MIP Life Sciences. "Strategies for navigating pharmaceutical patent landscapes," 2021.
  4. European Patent Office. “EPO Patent Search,” 2022.
  5. World Intellectual Property Organization. "Patent Cooperation Treaty (PCT) Resources," 2022.

Note: Precise chemical structures, claim language, and legal status details would necessitate direct examination of the patent document JP2009541320, which is beyond the scope of this summary.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.