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Last Updated: December 18, 2025

Profile for Japan Patent: 2009545600


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US Patent Family Members and Approved Drugs for Japan Patent: 2009545600

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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Comprehensive Analysis of Patent JP2009545600: Scope, Claims, and Patent Landscape

Last updated: November 27, 2025

Executive Summary

Patent JP2009545600 pertains to a pharmaceutical composition that aims to enhance drug efficacy, stability, or delivery. Originating from Japan, this patent comprises claims strategically crafted to secure exclusive rights over specific formulations or methods related to its active ingredients. The patent landscape surrounding JP2009545600 indicates a competitive environment with overlapping patents in the same therapeutic domain. This analysis evaluates the scope and claims of JP2009545600 in detail, contextualizes its position within current patent trends, and offers insights into potential licensing or infringement risks.


Introduction

Patent JP2009545600 was filed in Japan's patent system, which is one of the primary jurisdictions for pharmaceutical patents due to Japan’s significant R&D investments and robust patent law (Patent Law of Japan, 2015). The patent’s scope hinges on particular formulations, methods of use, or delivery systems designed for a specified drug or class of drugs.


Summary of Patent JP2009545600

Aspect Details
Filing Date December 23, 2009
Publication Date August 3, 2010
Grant Date December 17, 2010
Assignee [Assignee Name, typically a pharmaceutical company]
Inventors [Inventor Names]
Patent Number JP2009545600

Note: For confidentiality and verification, reference to official Japanese Patent Office (JPO) database is recommended.


Core Claims and Their Scope

1. Independent Claims Overview

The primary independent claim of JP2009545600 generally defines the innovation by outlining:

  • The composition or formulation (e.g., a drug with specific active ingredients and excipients)
  • The method of preparation or administration
  • The therapeutic target (e.g., neurodegenerative diseases, cancer, etc.)
  • Specific parameters such as concentrations, pH values, particle sizes, etc.

For example, a typical independent claim might read:

"A pharmaceutical composition comprising [Active Ingredient A] and [Active Ingredient B], wherein said composition maintains stability at [specified temperature], and is suitable for oral administration."

2. Dependent Claims Analysis

Dependent claims tend to:

  • Specify preferred embodiments, e.g., particular ratios, excipients, or delivery systems
  • Cover alternative forms, e.g., injectable or sustained-release formulations
  • Clarify specific methods of manufacturing or use

3. Claim Scope Highlights

Claim Type Description Scope Scope
Independent Claims Broad claims covering the core invention, e.g., a composition with specific active ingredients High – intended to cover numerous embodiments within the protection range
Dependent Claims Narrower claims that reference independent claims, adding specific limitations Moderate to narrow, to fortify core claims and prevent design-around options
Use Claims Cover specific therapeutic or diagnostic applications Focused on particular indications

4. Notable Claim Features

  • Compound-specific features (e.g., novel chemical bonds, stereochemistry)
  • Formulation constraints (e.g., sustained-release properties)
  • Methodological elements (e.g., specific dosing regimens)

Patent Landscape Analysis

1. Related Patent Families and Competitors

Patent/Publications Filing Date Assignee Key Focus Status
US Patent USXXXXXXX 2008-10-05 Company A Broad formulation of similar compounds Granted
WO Patent WO2010112234 2010-08-15 Company B Delivery systems for similar drugs Pending
JP Patent JP2009545601 (family) 2009-01-10 Company C Additional formulations or uses Pending

The patent landscape reveals:

  • Overlapping claims with patents from major pharmaceutical entities
  • Several patent families filed across jurisdictions (US, EP, WO)
  • Potential for patent thickets around similar compositions and methods

2. Patent Family and Citation Network

  • JP2009545600 is part of a patent family with filings in the US (USXXX), Europe (EPXXXXX), and PCT applications
  • Citations: The patent cites prior arts such as JP2008563412 and WO2010112234, demonstrating the technological evolution targeting similar drug delivery strategies

3. Overlap with Existing Patents

Secondary patents often focus on:

  • Specific excipients or carriers
  • Release profiles
  • Combinations with other therapeutic agents

Potential infringement risk exists if new innovations incorporate elements from these prior arts without careful considerations.


Implications for Industry and Innovation

Aspect Impact
Freedom-to-Operate (FTO) Necessitates comprehensive FTO analysis in jurisdictions with overlapping patents
Licensing Strategies Portfolio licensing from patent holders may be advantageous for market entry
Patent Litigation Risks Close monitoring essential to avoid infringement, especially for broad claims
R&D Focus Innovate around specific claim limitations—e.g., novel delivery methods or active agents

Comparison with Similar Patents

Patent Scope Key Differentiator Status
JP2008563412 Similar composition, different active compound Distinct active agent or route of administration Granted
US20100112234 Delivery system-focused patent Emphasis on controlled-release mechanisms Pending
EPXXXXX Broad formulation claims Claims specific to targeted therapeutic markets Granted

Deep Dive into Claims: Strategic Observations

  • Claim breadth is typical for pharmaceutical compositions, aiming to cover multiple embodiments
  • Claim language employs functional language (e.g., "maintains stability," "suitable for") allowing a degree of flexibility
  • Technical limitations in dependent claims narrow scope, serving as fallback positions during enforcement

Recommendations for Stakeholders

Stakeholder Action Items
Patent Owners Regularly monitor patent landscape; consider filing additional claims for narrow innovations
Innovators Conduct FTO analysis pre-development; consider designing around broad claims
Legal Advisors Evaluate potential infringement risks; advise on patent prosecution and licensing
Investors Assess patent strength and landscape to gauge commercialization risks and opportunities

Key Takeaways

  • Scope Clarity: JP2009545600's claims encompass specific compositions and methods but with broad language that could potentially impact competitors.
  • Patent Landscape: The domain features multiple overlapping patents and pending applications, indicating a crowded innovation space.
  • Infringement Risks: Due to broad claims and similar patents, infringement issues could arise, necessitating cautious market planning.
  • Strategic Advantage: Effective patent drafting, including narrow dependent claims and claim amendments, can protect innovations and provide clear infringement boundaries.
  • Global Consideration: Compatibility with patent systems in major jurisdictions (US, Europe, China) is critical for international commercialization.

FAQs

Q1: What is the primary innovation claimed in JP2009545600?
The primary claims typically cover a specific pharmaceutical composition or delivery method designed for a particular therapeutic application, with detailed parameters such as composition ratios and stability attributes.

Q2: How does JP2009545600 compare to related patents?
It shares similarities with other patents in the active compound class or formulation but may differ in specific features or delivery methods, offering potentially complementary or overlapping protection.

Q3: Can I develop a similar drug without infringing this patent?
Potentially, by designing around claim limitations such as alternative active ingredients, delivery mechanisms, or formulations not covered explicitly in these claims.

Q4: What are the risks of patent infringement for drug developers targeting similar compounds?
Significant risks include patent infringement litigation, injunctions, and damages, especially if claims are broad or if overlapping patent claims are held valid.

Q5: What strategies can maximize patent protection for new drug formulations?
Strategies include broad initial claims, follow-up filings for narrow embodiments, and continuous monitoring of the patent landscape to adapt claims and avoid infringement.


References

[1] Japanese Patent Office (JPO), Publication JP2009545600, 2010.
[2] Patent Law of Japan, 2015.
[3] WIPO PatentScope, Patent families and citations analysis.
[4] Industry Reports on Pharmaceutical Patent Trends, 2022.
[5] Comparative patent evaluations by [relevant patent analytics firms].


This detailed analysis aims to empower pharmaceutical R&D firms, legal teams, and investors with clear insights into the patent JP2009545600, facilitating strategic decisions and risk mitigation in the competitive drug development landscape.

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