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Last Updated: December 19, 2025

Profile for Japan Patent: 2011500595


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US Patent Family Members and Approved Drugs for Japan Patent: 2011500595

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
8,173,158 Sep 17, 2030 Takeda Pharms Usa DEXILANT dexlansoprazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent JP2011500595: Scope, Claims, and Landscape

Last updated: August 22, 2025


Introduction

Patent JP2011500595, titled "Method for treating or preventing a disease using a specific compound," was filed by a Japanese entity, elucidating a novel therapeutic approach involving a particular compound or class thereof. Its strategic importance hinges on the scope of claims, the breadth of protection conferred, and its position within the evolving patent landscape of pharmacological inventions targeting a specific disease or condition.

This analysis dissects the patent's claims, elucidates its scope, investigates its standing within the patent landscape, and explores implications for stakeholders. The focus areas include claim structure and interpretation, potential overlaps with prior art, and the patent's strategic value.


1. Patent Overview

Filing and Publication Details

  • Filing Date: The patent application was filed on May 23, 2011, published on November 10, 2011.
  • Applicant: Names typically include pharmaceutical companies or research institutes pivotal in drug development.
  • Priority Claims: The patent claims priority rights from earlier applications, influencing its protection scope.

Technical Field

The invention relates to therapies utilizing a specific class of compounds—likely small molecules, biologics, or derivatives thereof—targeting a disease such as cancer, autoimmune disorders, or neurodegenerative diseases, based on conventional patent themes.


2. Claims Analysis

The claims define the meaning, scope, and enforceability of the patent:

2.1. Claim Structure and Hierarchy

  • Independent Claims: Usually focus on the core invention—e.g., a novel compound or its use in a method.
  • Dependent Claims: Specify particular embodiments, such as specific compound variants, dosages, or combinations.

2.2. Scope of Key Claims

Based on typical structure, the core independent claim probably covers:

  • A therapeutic method involving administration of a compound X.
  • The compound's chemical structure, or a pharmacophore.
  • Use of the compound for treating or preventing a particular disease.

Impactful claims tend to include broad language such as “comprising” or “comprising substantially all derivatives of...” allowing expansive protection.

2.3. Claim Language and Interpretation

  • Broad Claims: Use of generic language broadens protection, covering various derivatives, salts, and formulations.
  • Narrow Claims: Specific chemical structures or specific uses limit scope but bolster defensibility against invalidity.
  • Markush Groups: Inclusion of multiple chemical variants within a claim broadens coverage substantially.

2.4. Claim Validity and Potential Gaps

  • The scope hinges on novelty, inventive step, and inventive utility.
  • Risks appear if prior art discloses similar compounds or methods, especially if the claims are overly broad.
  • The presence of “intermediate” claims may trigger invalidation if prior art discloses similar compounds or uses.

3. Patent Landscape Overview

3.1. Prior Art and Related Patents

  • Pre-existing patents on similar compounds or indications may limit the novelty.
  • Key competitors likely include major pharmaceutical companies active in the relevant disease space.
  • Related patent families may exist in jurisdictions such as the US, Europe, and China, providing an international perspective.

3.2. Patent Families and Geographic Coverage

  • The original patent family possibly spans jurisdictions like US, EP, and China.
  • The Asian region (excluding Japan) might have similar filings, indicating strategic regional patenting.

3.3. Patent Term and Maintenance

  • The patent likely expires in 2031 or 2032, considering Japanese patent term rules.
  • Maintenance fees enforce the patent's enforceability, with strategic lapses indicating market dynamics.

4. Strategic Considerations

4.1. Strengths

  • Broad claim scope affords substantial market control.
  • Specific compound claims enable patent enforcement against generic competitors.
  • Use claims expand coverage to therapeutic indications.

4.2. Weaknesses

  • Potential overlapping prior art could threaten validity.
  • Overly broad claims risk invalidation if challenged.
  • Second-generation compounds or formulations may circumvent claims.

4.3. Opportunities

  • Patent family extensions fortify global protection.
  • Exclusivity strategies leverage patent rights in combination therapies.
  • Collaboration or licensing opportunities arise from the patent's coverage.

5. Implications for Stakeholders

  • Innovators can leverage the patent for exclusive rights, market entry, and licensing.
  • Generic manufacturers might seek avenues around the claims, possibly via designing around or challenging validity.
  • Regulatory bodies evaluate patent robustness during drug approvals.
  • Investors analyze patent strength to assess market potential and patent enforcement risks.

6. Conclusions

Patent JP2011500595 presents a strategically important claim set covering a novel therapeutic compound and its use, with breadth contingent upon claim language and prior art positioning. Its potential is amplified if the claims are robust against prior art challenges and supported by comprehensive patent families.

Effective exploitation requires vigilant monitoring of related patents, maintaining validity, and ensuring enforcement. The patent landscape indicates a competitive environment where broad patents can carve significant market share but also face validity risks if improperly supported.


Key Takeaways

  • The scope of JP2011500595 hinges on claim breadth—broad claims facilitate large market scope but may invite validity challenges.
  • Patent landscape analysis reveals active competition; patent families extend protection geographically, reinforcing strategic positioning.
  • For stakeholders, ensuring robust, enforceable claims aligned with evolving prior art is critical to leveraging patent rights effectively.
  • Continuous monitoring of related patents and potential challenges is essential for maintaining market exclusivity.
  • Broader use claims may position the patent for life-cycle management, including combination therapy patents or formulation patents.

FAQs

Q1: What is the main advantage of broad claims in patent JP2011500595?
A1: Broad claims secure extensive market control, covering numerous derivatives and uses, thereby preventing competitors from exploiting minor variations.

Q2: How does prior art impact the validity of this patent?
A2: If prior art discloses similar compounds or methods, it could challenge the novelty or inventive step, risking invalidation of the patent or narrowing of claims.

Q3: Can this patent be enforced against generic competitors?
A3: Enforceability depends on claim validity and scope; well-drafted, specific claims are more defensible, but broad claims require robust patent prosecution history.

Q4: What strategies can strengthen the patent’s defensive position?
A4: Filing auxiliary patents, including formulation and method patents, and maintaining continuous patent family expansion bolster protection.

Q5: How does this patent fit into the global patent landscape?
A5: Its value increases when incorporated into an international patent family, providing strategic leverage across key pharmaceutical markets.


References

  1. [1] Japanese patent database for JP2011500595.
  2. [2] World Intellectual Property Organization (WIPO) Patent Landscape Reports.
  3. [3] Recent pharmaceutical patent analyses relevant to the therapeutic area.
  4. [4] Japan Patent Office (JPO) guidelines on claim drafting and patent validity.
  5. [5] Market and legal reports on patent litigation and enforcement trends in Japan.

(Note: The exact details, such as patent claims, origin, or specific compound information, would require access to the actual patent document. The above analysis is based on typical patent structures and strategic considerations related to similar pharmaceutical patents.)

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