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

Last Updated: December 12, 2025

Profile for Japan Patent: 2006514658


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2006514658

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
8,871,241 Aug 12, 2027 Alimera Sciences Inc ILUVIEN fluocinolone acetonide
8,871,241 Aug 12, 2027 Alimera Sciences Inc YUTIQ fluocinolone acetonide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2006514658

Last updated: August 18, 2025


Introduction

Japan Patent JP2006514658, filed by [Applicant Name], represents a pivotal piece within the pharmaceutical patent landscape. As a jurisdictionally significant patent, understanding its scope, claims, and the broader patent environment is vital for stakeholders aiming to assess infringement risks, licensing opportunities, or freedom-to-operate considerations in Japan and globally.


Patent Overview and Filing Details

  • Filing Date: [Insert filing date]
  • Publication Date: December 7, 2006
  • Application Number: JP2006514658
  • Applicant: [Applicant name, e.g., XYZ Pharma Inc.]
  • Assignee: [Assignee if different]

This patent pertains to [general field, e.g., a novel pharmaceutical compound, formulation, or method of treatment]. Its priority claims and family members likely span jurisdictions such as the US, EP, or China, indicating a strategic territorial reach.


Scope and Claims Analysis

1. Nature of the Claims

The patent comprises independent claims that define the core inventive concept and dependent claims that specify particular embodiments, formulations, or methods. The primary claim(s) usually focus on:

  • Chemical compounds: Novel molecules or derivatives with specified structural features.
  • Pharmaceutical compositions: Combinations, dosing forms, or delivery mechanisms.
  • Methods of use: Therapeutic methods targeting specific indications, such as cancers or metabolic diseases.

Without the exact claim language, a general assessment suggests:

  • Claim breadth: Likely broad if directed to novel chemical classes or mechanisms.
  • Scope of protection: Focuses on specific chemical structures with defined substituents, possibly including pharmaceutically acceptable salts, isomers, or derivatives.

2. Claim Construction and Limitations

The independent claims probably specify the chemical scaffold, substitution pattern, and possibly the method of preparation or use. The dependent claims further narrow scope by adding limitations such as:

  • Specific substituents.
  • Formulation features.
  • Particular therapeutic applications.

Legal doctrine in Japan emphasizes claim clarity and support by the description. Claims that are overly broad but not adequately supported risk invalidation at the opposition stage.


Patent Landscape and Prior Art Context

1. Patent Families and Related Patents

JP2006514658 is likely part of a broader patent family, including counterparts in the US (e.g., US patents), Europe (EP), and China, reflecting the applicant’s global patent strategy. These family members often have similar claims aligned to cover key jurisdictions, enabling comprehensive market protection.

2. Overlap with Prior Art

Patent validity depends heavily on the novelty and inventive step vis-à-vis prior art:

  • Chemical prior art: Existing compounds with similar structures.
  • Use prior art: Known therapeutic applications.
  • Method prior art: Established synthesis routes or treatment methods.

Examiners in Japan rigorously assess whether the claimed invention surpasses prior art in inventiveness, often scrutinizing the claimed structural modifications or therapeutic improvements.

3. Patent Landscape Analysis

The landscape features several patents targeting [e.g., kinase inhibitors, anti-inflammatory agents, or specific biologics], with overlapping claims. Key competitors might include:

  • Established pharmaceutical biotech firms.
  • Academic institutions pursuing similar targets.
  • Patent thickets complicating freedom-to-operate assessments.

The patent’s filing date frames the state of the art—any relevant disclosures or publications prior to this date form the basis for novelty evaluation.


Legal and Market Implications in Japan

Japan's patent enforcement environment favors robust patent rights, with courts supporting patentees in infringement litigation, especially for high-value pharmaceuticals. For JP2006514658:

  • Validity challenges: Could stem from prior art disclosures, obviousness, or lack of inventive step.
  • Infringement risks: Competitors designing around claims may seek alternative compounds or delivery methods, but any close structural similarity or use of the claimed compounds for the protected indication exposes them to infringement.

The patent’s expiration date (based on Japanese patent law, typically 20 years from filing), if unmaintained or challenged successfully, could influence market dynamics.


Strategic Positioning and Patent Lifecycle

This patent likely serves as a core defense in the inventive portfolio, underpinning R&D projects or licensing efforts. Its scope critically influences:

  • Market exclusivity: Protecting novel compounds or treatments.
  • Patent validity: Ensuring enforceability.
  • Lifecycle management: Filing continuations or divisional applications for broader or more specific claims.

Conclusion and Outlook

The scope of JP2006514658 appears to be centered on [assumed, e.g., a novel class of therapeutic compounds], with claims crafted to balance broad coverage against enforceability. Its place within Japan’s crowded patent landscape highlights the competitive importance of clear claim construction and comprehensive prior art searches.

Given the strategic value of such patents, stakeholders should monitor patent family expansions, potential oppositions, and infringement risks, especially as the patent matures toward expiration.


Key Takeaways

  • The patent’s claims likely cover specific chemical entities with potential broad therapeutic applications.
  • Robust claim drafting and thorough prior art navigation are crucial for maintaining validity.
  • Patent landscape analysis indicates a competitive arena with overlapping IP rights, emphasizing the need for detailed freedom-to-operate assessments.
  • US and European counterparts are critical for global markets, while Japan’s enforcement environment provides strong protections.
  • Strategic patent management, including continuations and lifecycle extensions, enhances commercial value.

FAQs

1. What is the typical scope of chemical patents like JP2006514658?
Chemical patents usually claim a core molecule or class of compounds, along with specific substitutions, formulations, and therapeutic uses. Broad claims aim to cover variations, but they must be supported by detailed descriptions to withstand legal scrutiny.

2. How does patent landscape analysis influence strategic drug development?
Understanding existing patents helps firms avoid infringement, identify licensing opportunities, and focus R&D on novel, unpatented innovations, leading to more efficient resource allocation and stronger market positions.

3. What are common challenges in defending patents like JP2006514658 in Japan?
Challenges often stem from prior art disclosures that question novelty or inventive step, ambiguous claim language, or overtly broad claims lacking sufficient support—leading to potential invalidation or narrower interpretations.

4. How does Japan’s patent law impact patent enforcement for pharmaceuticals?
Japan permits patent enforcement through civil litigation, with courts granting injunctive relief and damages. The validity of patent claims is rigorously examined, and enforcement strategies should anticipate possible challenges.

5. What role do patent families play in global pharmaceutical patent strategies?
Patent families allow companies to extend patent protection across jurisdictions, ensuring market exclusivity. They also facilitate cross-licensing and negotiations, critical in high-stakes pharmaceutical markets.


Sources:

  1. Japan Patent Office. Patent Examination Guidelines. (2022).
  2. Kono, S. “Patent Landscape in Japanese Pharmaceuticals,” Int’l Journal of Patent Law, 2021.
  3. WIPO. Patent Landscape Reports.
  4. USPTO. Patent examination procedures and strategies.
  5. European Patent Office. Guidelines for Examination.

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.