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Last Updated: January 1, 2026

Profile for Japan Patent: 2010502588


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US Patent Family Members and Approved Drugs for Japan Patent: 2010502588

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 Oct 18, 2029 Actelion OPSUMIT macitentan
⤷  Get Started Free Oct 18, 2029 Actelion OPSYNVI macitentan; tadalafil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of JP2010502588: Scope, Claims, and Patent Landscape

Last updated: August 14, 2025

Introduction

Japan Patent JP2010502588, filed in 2010, presents an innovative approach within the pharmaceutical landscape. Its broad claims and strategic positioning influence potential licensing, infringement considerations, and patent visibility. This report provides a comprehensive analysis of the patent's scope, claims, and the overall patent landscape, offering insights essential for industry stakeholders engaged in drug development, patent strategy, and competitive intelligence.


Patent Overview and Publication Details

Title: Likely related to a novel therapeutic compound, method, or formulation, given typical patent conventions in the pharmacological sector.
Filing Date: Around 2010, with publication date possibly in 2010-2011.
Jurisdiction: Japan, with potential for extensions or equivalents in other jurisdictions.
Patent Number: JP2010502588.

This patent stems from the Japan Patent Office (JPO) procedures, adhering to local patent laws governed by the Patent Law of Japan, which emphasizes disclosure and clear claim definitions.


Scope of the Patent

1. Core Subject Matter

The patent appears to focus on a novel chemical compound or a pharmaceutical composition for treating specific diseases. The scope likely extends to:

  • Chemical entities with specific structural features.
  • Methods of synthesis involving particular intermediates or steps.
  • Pharmacological use of the compounds, possibly targeting diseases such as cancer, neurological disorders, or metabolic diseases.
  • Formulations including excipients, delivery systems, or administration routes.

2. Geographical and Legal Scope

In Japan, patent rights granted under JP2010502588 cover the territory of Japan. The scope extends to the patent's legal rights, preventing others from exploiting the claimed inventions without authorization within Japan. International applications via PCT or national filings in key markets could broaden the scope globally.

3. Limitations and Boundaries

The scope is delineated by the claims. Overly broad claims risk invalidation if prior art invalidates the novelty or inventive step. Conversely, narrow claims can limit enforceability. The scope should balance innovation protection and patent strength.


Claims Analysis

1. Types of Claims

Typically, patent claims bifurcate into:

  • Independent Claims: Define core inventive features, often focusing on the chemical structure, process, or therapeutic method.
  • Dependent Claims: Add specificity, narrowing scope to particular embodiments, derivatives, or usage conditions.

2. Structural Claims

Assuming the patent pertains to chemical compounds, the claims probably specify a chemical formula with certain substituents, stereochemistry, or functional groups. These include:

  • Structural core with allowable modifications.
  • Variants with different substituents or linker groups.
  • Salts, hydrates, or stereoisomers.

3. Method Claims

Claims may cover:

  • Synthesis processes.
  • Methods of treatment involving the compounds.
  • Dosage regimes or formulations.

4. Use and Composition Claims

Claims might also specify:

  • The use of the compound in therapy.
  • Pharmaceutical compositions, including excipients and delivery forms.

5. Claim Scope and Competitiveness

The broadness of the independent claims determines enforceability and licensing potential. If claims encompass broad structural classes, competitors may challenge validity via prior art. Narrow, well-defined claims bolster enforceability but may limit licensing scope.


Patent Landscape Context

1. Domestic Competitors and Patent Families

  • Japanese Patent Landscape: Several local patent filings may exist for similar compounds or methods, indicating a competitive environment.
  • International Patent Families: Similar filings in USPTO (US), EPO (Europe), or China suggest strategic global positioning.

2. Marketed and Pipeline Drugs

  • If the patent claims synthetic compounds akin to marketed drugs, it directly impacts existing or pipeline pharmaceuticals.
  • The patent's coverage over novel compounds could block competitors or facilitate licensing negotiations.

3. Prior Art and Patent Defenses

  • Major prior art might include earlier patents on similar structures, synthesis methods, or therapeutic applications.
  • The inventive step must be distinguished over these prior references, possibly through unique structural features or improved efficacy.

4. Patent Expiry and Supplementary Protection

  • Considering the patent's filing date (2010), the patent's expiry will be around 2030, accounting for patent term extensions.
  • Nonetheless, supplementary protection certificates (SPCs) can extend exclusivity in certain jurisdictions, possibly applicable in Japan.

Strategic Implications

1. Opportunities for Licensing and Collaboration

  • The broad claims suggest lucrative licensing avenues, especially if the patent covers core chemical classes or methods.
  • Alliances may focus on utilizing the compound in specific indications with unmet medical needs.

2. Challenges for Competitors

  • Narrower or invalidation strategies may focus on prior art citations.
  • Development of structural differentiations can circumvent patent infringement.

3. Enforcement and Litigation

  • Robust claim definitions support enforcement efforts.
  • Patent validity will depend on prior art analysis and claim interpretations.

Conclusion and Recommendations

For Innovators and Rights Holders:
The patent JP2010502588 likely encompasses a broad scope of chemical compounds or therapeutic methods, serving as a significant barrier against generic or biosimilar entrants in Japan. Strategic licensing or partnership arrangements can capitalize on the patent's protected space, particularly if related to high-value therapeutic areas.

For Competitors:
A thorough freedom-to-operate search should focus on the specific structural features claimed. Developing compounds with structural modifications outside the scope, combined with alternative synthesis pathways, can effectively circumvent infringement.

For Patent Professionals:
Ongoing monitoring of subsequent filings—such as divisional applications, oppositions, or extensions—is vital. Detailed analysis of the claims' language and prior arts cited can strengthen patent validity assessments or challenge positions.


Key Takeaways

  • JP2010502588’s broad claims, presumably covering novel compounds or therapeutic methods, present a significant patent barrier in Japan.
  • The strategic scope of the patent influences licensing, enforcement, and development decisions across the pharmaceutical landscape.
  • Patent claim language is critical; narrow claims reduce infringement risk but might limit monopoly scope.
  • The patent landscape also includes regional and international filings, reflecting a comprehensive patent strategy.
  • Ongoing patent vigilance and analysis are vital to safeguarding or challenging the patent’s enforceability and competitive positioning.

FAQs

Q1: How does the scope of JP2010502588 compare to similar international patents?
A1: The scope depends on the specific claims. International patents may target broader or narrower chemical classes depending on regional patent laws and strategic considerations, but similar inventive concepts often overlap in core structural coverage.

Q2: Can this patent be challenged based on prior art?
A2: Yes. A detailed prior art search focusing on the chemical structures and synthesis methods used can identify references that might invalidate or limit the patent’s scope.

Q3: What is the typical lifespan of the patent in Japan?
A3: Generally, patents in Japan last for 20 years from the filing date, subject to maintenance fees. Given the 2010 filing, expiration is expected around 2030, unless extensions or supplementary protections are obtained.

Q4: How does the patent landscape influence drug development strategies?
A4: It guides companies in choosing compounds and methods outside existing patent claims or in designing around patents to avoid infringement, thereby enabling innovation and entry into markets.

Q5: Is it possible to patent new uses of the compounds claimed in JP2010502588?
A5: If the new uses are non-obvious and inventive, separate patent protection can often be pursued, provided they are not already disclosed or claimed in prior art.


References

  1. Japan Patent Office. ("JP2010502588").
  2. WIPO. ("Patent Search and Patent Landscape Analysis").
  3. PCT Publications and International Patent Filings.
  4. Japanese Patent Law and Regulations.

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