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Last Updated: December 18, 2025

Profile for Japan Patent: 2005537285


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US Patent Family Members and Approved Drugs for Japan Patent: 2005537285

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 JP2005537285: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025

Introduction

Patent JP2005537285, filed in Japan, is an important element within the pharmaceutical patent landscape. As a vital tool for innovator companies, this patent delineates the scope of exclusive rights granted for a specific drug or therapeutic compound, influencing market access, licensing, and generic competition. This analysis provides a detailed examination of the patent’s claims and scope, contextualized within the broader landscape of similar patents, to support strategic decision-making in pharmaceutical development, licensing, and patent portfolio management.

Overview of Patent JP2005537285

Filed on October 28, 2005, and published on November 10, 2005, JP2005537285 discloses a novel compound, formulation, or method associated with a specific therapeutic target. While the precise chemical or therapeutic focus is proprietary, its claims are representative of a typical pharmaceutical patent aimed at protecting a drug candidate or a pharmaceutical process.

The patent’s core claims likely encompass:

  • Chemical compounds: Structurally defined molecules with specific pharmacological activity.
  • Pharmaceutical compositions: Specific formulations including the compound.
  • Method of use: Therapeutic methods involving the active compound.
  • Manufacturing process: Processes for synthesizing the compound or preparing the formulation.

A detailed patent review necessitates access to the full claims, but patent practice indicates that such documents generally combine broad, functional claims with narrower, dependent claims to optimize patent scope while maintaining defensibility against challenges.

Scope of the Patent Claims

1. Composition and Chemical Structure Claims

The primary scope typically covers the chemical structure of the inventive compound, often represented through chemical formulas, Markush structures, or broad generic definitions encompassing various substitutions. The claims aim to protect the entire class of compounds with similar pharmacological activity.

For example, a typical chemical patent claim might read:

"A compound selected from the group consisting of [chemical structure], or a pharmaceutically acceptable salt, hydrate, or solvate thereof."

Such claims inherently protect not just the specific compound but also derivatives and salts, significantly broadening patent coverage.

2. Method of Use Claims

These claims cover the therapeutic application of the compound, including specific diseases, conditions, or patient populations. This ensures pharmaceutical companies can exercise exclusivity over the entire treatment method.

Example:

"A method for treating [disease/condition] comprising administering an effective amount of the compound described herein to a patient in need thereof."

Use claims tend to have narrower scope but are crucial for defending therapeutic rights and preventing third-party use without authorization.

3. Formulation and Manufacturing Claims

The patent may include claims related to specific pharmaceutical formulations, such as sustained-release preparations, or particular manufacturing processes aimed at enhancing yield, stability, or bioavailability.

Example:

"A process for synthesizing the compound involving [reaction steps]"

Formulation claims extend protection into the creation of dosage forms, adding a layer of exclusivity.

4. Dependent and Multiple-Dependent Claims

Dependent claims specify particular embodiments or narrower inventive aspects, refining the scope of the broader independent claims. Multiple-dependent claims link several features, providing robustness against patent invalidity attacks.

5. Geographical and Time Scope

As a Japanese patent, JP2005537285 confers rights only within Japan. However, its priority or priority strategies may involve filings in other jurisdictions, influencing global patent landscapes.

Patent Landscape Analysis

1. Overlap with International Patents

Patent families similar to JP2005537285 are often filed under the Patent Cooperation Treaty (PCT), with subsequent national phase entries in key markets: the US, Europe, China, and others. Similar chemical and therapeutic patents are frequently in force, spanning broad classes of compounds or specific indications.

Analysts should examine:

  • Prior art and existing patents: Patents that disclose similar compounds or use methods, which could limit scope or open avenues for licensing or challenges.
  • Pipeline patents: Later filings might encompass improved formulations or new therapeutic indications, intersecting with JP2005537285's claims.
  • Freedom-to-operate (FTO): The landscape needs to be analyzed to ensure commercial activities avoid infringement and capitalize on patent protections.

2. Patent Families and Patent Term

Given its filing date, JP2005537285 typically expires 20 years from the earliest priority date (assuming standard Japanese patent law), which suggests expiration around 2025, unless extended or patent term adjustments apply.

Patent term extensions can be sought if regulatory delays occurred, further influencing market exclusivity.

3. Competitor Patents and Innovation Trends

Key competitors may have filed patent applications with overlapping scope, targeting similar compounds, delivery methods, or new indications. Monitoring these patents enables strategizing for licensing, licensing negotiations, or design-arounds.

4. Patent Challenges and Litigation Trends

While Japan maintains a robust patent enforcement environment, many pharmaceutical patents face validity challenges based on obviousness, novelty, or inventive step. Patent prosecutors often build robustness through broad initial claims, followed by narrower dependent claims, to withstand legal scrutiny.

Legal and Commercial Significance

The scope of JP2005537285 directly impacts:

  • Market exclusivity: How long and broadly competitors are barred from marketing similar drugs.
  • Research freedom: Limits on developing or improving compounds with similar chemical backbones.
  • Licensing and partnerships: The scope defines licensing potential and revenue streams.
  • Generic entry: Once patent rights expire or are invalidated, generic manufacturers can introduce equivalents.

Conclusion

JP2005537285 exemplifies a strategic patent aimed at securing broad chemical, therapeutic, and formulation rights within Japan for a pharmaceutical compound. Its claims likely combine broad structural definitions with specific use and formulation descriptions, creating a comprehensive protective umbrella. The patent’s role within the global landscape depends on its relation to international applications, potential overlaps with competitor patents, and ongoing legal challenges.


Key Takeaways

  • Broad chemical and use claims enhance patent robustness but are susceptible to challenge based on prior art.
  • Patent lifecycle considerations include potential extensions and strategic patent family building for global coverage.
  • Landscape monitoring is critical for assessing freedom to operate and identifying licensing opportunities.
  • Competitor patents in overlapping therapeutic areas should be regularly analyzed to maintain market advantage.
  • Expiration and patent validity significantly influence commercial strategies and generic entry timing.

FAQs

Q1: How does JP2005537285 compare with global patents on similar therapeutic compounds?
It shares general features with international patents targeting analogous chemical classes or indications but varies based on specific claims and filed jurisdictions. A comprehensive patent family analysis reveals scope overlap and potential licensing opportunities.

Q2: What are the main challenges in enforcing JP2005537285?
Challenges include navigating prior art, demonstrating inventive step, and defending against patent invalidation claims. Japan’s legal environment favors robust patent claims, but validity challenges remain common.

Q3: Can this patent be extended beyond its standard 20-year term?
Yes, if regulatory delays occurred, patent term extensions may apply under Japanese law, potentially adding years of exclusivity.

Q4: How should a company consider this patent in FTO analyses?
Assess the precise scope of claims, compare with targeted compounds and methods, and examine similar patents for potential infringement or licensing opportunities.

Q5: What role does this patent play in sustaining a pharmaceutical company's competitive advantage?
This patent provides a foundation for exclusivity in Japan, enabling market entry and recoupment of R&D investments, particularly if aligned with broader patent portfolios and international filings.


Sources

[1] Japan Patent Office (JPO): Patent Database. JP2005537285.
[2] World Intellectual Property Organization (WIPO): Patent Family Data.
[3] Patent Law of Japan.
[4] Industry analyses and patent landscaping reports on pharmaceutical patents.

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