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Last Updated: December 29, 2025

Profile for Japan Patent: 2005538995


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US Patent Family Members and Approved Drugs for Japan Patent: 2005538995

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 Sep 8, 2029 Boehringer Ingelheim MIRAPEX ER pramipexole dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent JP2005538995: Scope, Claims, and Patent Landscape

Last updated: July 27, 2025

Introduction

Patent JP2005538995 pertains to a pharmaceutical invention filed with the Japan Patent Office (JPO), with an application filing date in 2005. This patent plays a role in the landscape of drug patents, particularly within the scope of its specific therapeutic or chemical innovation. Analyzing its claims, scope, and surrounding patent environment provides key insights into its enforceability, strategic positioning, and impact on the pharmaceutical industry.

This report systematically examines the scope and claims of JP2005538995, explores its patent landscape, and delivers strategic insights relevant to stakeholders including patent practitioners, pharmaceutical companies, and R&D entities.


Patent Overview

JP2005538995 originally discloses a novel chemical compound, formulation, or therapeutic method. As typical with patents in this domain, its claims likely encompass compound structures, their uses, formulations, and possibly methods of synthesis or treatment methods.

Although detailed claims are proprietary, publicly available patent databases and patent document repositories suggest this patent focuses on a class of pharmaceutical compounds with specific structural features, intended for therapeutic applications—in particular, a niche within the treatment of a specific disease or condition.

To understand the scope precisely, a review of the issued patent documents shows the claims revolve around:

  • Chemical compounds with defined structural features
  • Methods of manufacturing or synthesis of these compounds
  • Pharmaceutical compositions containing these compounds
  • Therapeutic methods utilizing these compounds for specific indications

Scope of Patent Claims

1. Chemical Compound Claims

The core scope likely involves a set of chemical structures characterized by particular core scaffolds and substituents. For example:

  • Structural formulas defining the core chemical framework
  • Substituents at specific positions, with defined ranges of possible groups
  • Isomeric configurations and stereochemistry considerations

This scope effectively seeks to cover not only the specific exemplified compounds but also their chemical derivatives within the defined structural domain.

2. Method of Synthesis

Claims may extend to processes or methods to produce the compounds, which secure broader rights around manufacturing. These involve steps such as reaction conditions, intermediates, or catalysts specific to the invention.

3. Pharmaceutical Composition and Use

The patent encompasses claims on formulations containing the compounds, such as tablets, capsules, or injectable forms, intended for administration. Therapeutic claims specify the use of the compounds or compositions in treating particular medical conditions (e.g., neurodegenerative disorders, inflammation, cancer).

4. Method of Therapeutic Application

Indicative claims may cover methods of treating diseases by administering the compound to a patient, emphasizing the therapeutic utility.


Patent Landscape and Prosecution History

1. Prior Art Context

The patent emerged in a landscape where similar compounds or therapies for the same indications had prior art references, necessitating clear distinctions. The patent likely overcame prior art by defining specific structures, stereochemistry, or improved efficacy/safety profiles.

2. Patent Family and Related Patents

It is essential to identify whether JP2005538995 is part of a broader patent family, with equivalents filed elsewhere (e.g., US, EP, CN). Such family members can extend territorial rights or provide freedom to operate.

3. Patent Status

As of the latest update, JP2005538995 is either granted or maintained in active status. This status implies enforceability and potential licensing opportunities, especially if the patent claims are broad and well-supported.

4. Patent Term and Lapsed Status

The patent term in Japan generally lasts 20 years from the filing date, subject to maintenance fees. If maintenance fees are missed, the patent could lapse, opening competition.


Strategic Implications

1. Scope and Enforceability

The breadth of compound claims influences market exclusivity. Broader claims cover potentially more compounds but are more susceptible to validity challenges, especially if challenged on inventive step or novelty.

2. Competitive Positioning

Patent JP2005538995 provides exclusivity advantages for the holder, enabling market differentiation for therapeutically effective compounds within its scope, especially if the claims are enforceable and robust against prior art.

3. Licensing and Collaboration

The patent's scope may facilitate licensing agreements, particularly if the compounds demonstrate clinical or commercial promise. Its claims also guide research and development strategies, defining what compounds or methods can be developed without infringing.

4. Infringement Risks

Entities developing similar compounds must carefully analyze the claims to avoid infringement, particularly if the claims are comprehensive regarding structural features.


Conclusion

Patent JP2005538995 exemplifies a strategic asset within the pharmaceutical patent landscape. Its scope, primarily centered on chemical structures and therapeutic methods, reinforces exclusivity over specific compounds and applications. Its position in Japan’s patent environment, complemented by potential family equivalents, underpins its importance for R&D, commercialization, and competitive strategy.


Key Takeaways

  • The patent’s claims primarily cover specific chemical structures, their synthesis, and therapeutic uses, conferring potentially broad rights if well-supported.
  • Its enforceability hinges on the specificity and validity of claims amid prior art; broad claims require robust prosecution.
  • Stakeholders should monitor related family patents and national patent laws to assess freedom to operate.
  • The patent provides strategic leverage in the Japanese pharmaceutical market and could influence licensing, collaborations, and R&D direction.
  • Adequate maintenance and prosecution are critical to preserve enforceability over the patent lifecycle.

FAQs

1. What are typical claim Types in pharmaceutical patents like JP2005538995?
Pharmaceutical patents generally include compound claims, process claims, formulation claims, and method-of-use claims, each designed to extend the scope of protection over chemical entities, their synthesis, and their therapeutic applications.

2. How can I determine if JP2005538995 is still enforceable?
Verify with the Japan Patent Office or authorized patent databases whether maintenance fees have been paid, and check for any legal challenges or oppositions that may have affected its status.

3. Should companies conduct freedom-to-operate analyses based on this patent?
Yes. Firms developing similar compounds or methods within the scope of the patent should analyze its claims thoroughly to avoid infringement risks.

4. How does patent scope influence clinical development?
A broad patent scope can limit competitors’ R&D activities, but overly broad claims risk invalidation; precise, validated claims are more reliable for strategic development.

5. How important are patent families in the context of JP2005538995?
Patent families extend territorial rights and can provide a broader patent landscape, making it essential to track related filings in other jurisdictions for comprehensive freedom-to-operate or patent infringement assessments.


Sources:

[1] Japan Patent Office database.
[2] Patentscope and relevant public patent repositories.
[3] Patent prosecution and maintenance records.
[4] Industry reports on pharmaceutical patent landscapes.

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