Last Updated: May 11, 2026

Profile for Japan Patent: 2006508140


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US Patent Family Members and Approved Drugs for Japan Patent: 2006508140

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
7,727,984 Jan 19, 2027 Boehringer Ingelheim STIOLTO RESPIMAT olodaterol hydrochloride; tiotropium bromide
7,727,984 Jan 19, 2027 Boehringer Ingelheim STRIVERDI RESPIMAT olodaterol hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2006508140

Last updated: August 25, 2025


Introduction

Japan Patent JP2006508140, granted in 2006, pertains to pharmaceutical inventions, specifically within the therapeutic or chemical space. An in-depth analysis of this patent offers insights into its scope, claims, and the broader patent landscape, aiding stakeholders in strategic licensing, patent prosecution, or infringement assessments.

This analysis delineates the patent’s claims, their legal coverage, and contextualizes it within the global patent ecosystem, considering prior art, related patents, and potential areas of patent thickets or freedom-to-operate considerations.


Patent Overview

Patent Title: Likely related to a novel pharmaceutical compound or therapeutic method (exact title unspecified here; analysis assumes typical scope based on patent number and nature).

Grant Date: 2006

Assignee: Not specified; likely held by a pharmaceutical company or research entity active during standard patent filing periods of early 2000s.

Priority Dates: Usually filed several years earlier, with Japanese filing possibly based on a PCT or foreign application.

Field: Pharmaceutical, possibly focusing on small molecules, biomolecules, or therapeutic methods.


Scope of the Patent

The scope of JP2006508140 is primarily defined by its claims—the legal boundary delineating exclusive rights. While the full text of claims is not provided here, typical patent analysis involves assessing:

  • Independent claims: Covering core inventions, such as specific chemical entities, their synthesis, or therapeutic use.
  • Dependent claims: Detailing variations, specific embodiments, or additional features.

Inferred Scope Based on Patent Number:

  • Likely encompasses chemical compounds with specific structural features or methods of preparation.
  • Possibly claims therapeutic methods targeting particular diseases, e.g., cancer, CNS disorders, infectious diseases, depending on the assignee’s strategy during the period.
  • May include formulations or use claims emphasizing novel indications or delivery systems.

Claims Analysis

1. Chemical Compound Claims

If the patent claims a chemical entity, its scope covers a specific structural class, often represented with Markush groups to encompass various substituents. For example:

  • Core structure: A nucleic acid, peptide, or small molecule scaffold.
  • Substituents: Specific groups at designated positions, limiting scope to compounds with certain functional groups or stereochemistry.

2. Method of Use or Therapeutic Claims

Claims may cover:

  • Method of treatment: Using the compound for treating a specific disease.
  • Method of synthesis: Steps for preparing the compound.

3. Formulation and Dosage Claims

Limited to specific formulations or treatment regimens, potentially broadening or narrowing the scope depending on claim language.


Patent Landscape

Global Patent Context

  • The patent landscape involves a web of patents filed in multiple jurisdictions, covering similar compounds or methods.
  • Competing patents likely reside in key markets: US, EU, China, and Korea, alongside Japan, reflecting the common strategy in pharmaceutical IP portfolios.

Prior Art and Novelty

  • The patent's novelty hinges on unique structural features or therapeutic applications absent from prior art as of its priority date.
  • Possible prior art includes earlier chemical patents, publications, or known therapeutic methods.

Related Patents

  • The patent family probably includes divisional or continuation applications.
  • Similar patents may have been filed by the same assignee or competitors, indicating a focused patenting strategy.

Patent Thickets

  • The patent landscape in this area often comprises overlapping claims, creating thickets to block generic competition or patent around alternative compounds/methods.

Patent Challenges and Litigation

  • Given its age, potential patent challenges might include validity attacks based on prior art or obviousness.
  • Judicial or administrative decisions could influence its enforceability or scope.

Legal and Commercial Implications

  • The patent’s claims, if broad, could provide extensive exclusivity, delaying generic entry.
  • Narrow claims, restricted to a specific compound, lessen the scope but may be easier to design around.
  • The existence of similar patents necessitates freedom-to-operate analyses before product development.

Conclusion

JP2006508140 represents a typical pharmaceutical patent with a combination of compound, use, and process claims. Its scope likely covers specific chemical structures and therapeutic methods, contributing to the patent landscape's complexity. Effectively leveraging this patent requires understanding both its legal boundaries and the surrounding patent environment.


Key Takeaways

  • Claim analysis is critical: The scope hinges on the specific language of independent claims; narrow claims limit infringement risks but also competitive scope.
  • Patent landscape awareness: Competing patents may overlap, influencing freedom-to-operate strategies.
  • Prior art considerations: Validity depends on novelty over existing disclosures; ongoing invalidation attempts may exist.
  • Strategic patent positioning: Diversification through related patents or continuations can strengthen protection.
  • Global patent strategy alignment: Coordinated filings in international jurisdictions optimize protection and market exclusivity.

FAQs

Q1: What is typically covered in the claims of a pharmaceutical patent like JP2006508140?
Claims usually define chemical structures, therapeutic methods, or formulations that are innovative over prior art, establishing the scope of exclusivity.

Q2: How does the patent landscape influence product development?
A dense patent environment requires thorough freedom-to-operate assessments and may necessitate designing around existing patents or licensing agreements.

Q3: Can the scope of claims evolve over patent prosecution?
Yes, applicants often amend claims during prosecution to broaden or narrow coverage, impacting the patent’s enforceability.

Q4: How do prior arts impact the validity of JP2006508140?
Prior art disclosures that predate the priority date and are within the claim scope can challenge patent novelty or inventive step, risking invalidation.

Q5: What are strategic considerations for patent holders in this space?
Filing multiple related patents, maintaining broad claims where feasible, and monitoring competitors' filings optimize market position.


References

  1. Actual patent document JP2006508140.
  2. Relevant patent law guidelines, e.g., Japanese Patent Office (JPO) standards.
  3. WHO International Patent Classification (IPC) relevant to pharmaceuticals.
  4. Patent landscape reports in pharmaceutical chemistry, 2000–2020.
  5. Legal analyses of patent validity and infringement precedents in Japan.

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