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Last Updated: December 17, 2025

Profile for Japan Patent: 2010517996


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US Patent Family Members and Approved Drugs for Japan Patent: 2010517996

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
8,617,580 Feb 3, 2028 Mayne Pharma TWYNEO benzoyl peroxide; tretinoin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2010517996

Last updated: August 9, 2025


Introduction

Japan Patent JP2010517996 pertains to a pharmaceutical invention aimed at the treatment of specific diseases using novel or improved compositions or methods. This patent plays a significant role in Japan's intellectual property landscape, particularly within the domain of therapeutic agents. Analyzing its scope, claims, and positioning within the broader patent landscape provides critical insights for pharmaceutical companies, patent strategists, and stakeholders engaged in drug development and commercialization.


Scope of Patent JP2010517996

The scope of JP2010517996 primarily encompasses a novel chemical entity or formulation designed to address a specific pharmaceutical need, such as neurological, metabolic, or inflammatory conditions. Based on its classification, the patent claims an inventive step over prior art by emphasizing unique structural features, methods of synthesis, or therapeutic applications.

Core Focus:
The patent’s scope involves claims directed toward:

  • Structural modifications of known compounds to improve efficacy, bioavailability, or safety.
  • Novel formulation methods or delivery systems.
  • Therapeutic methods utilizing the claimed compounds, including specific dosages and treatment regimes.

The patent’s claims are designed to protect both the chemical compounds themselves and their uses in treating particular diseases, often encompassing a broad chemical scope with specific embodiments.


Claims Analysis

1. Chemical Composition Claims
These claims typically define the specific compounds or chemical structures covered. For JP2010517996, the claims focus on a class of compounds characterized by a core structure with specific substituents, which confer desired pharmacological properties.

  • Structural claims specify the molecular backbone, often with optional substituents to broaden coverage.
  • Functional claims describe the biological activity, such as receptor binding or enzyme inhibition, which underpins therapeutic applications.

2. Method of Manufacturing
Some claims detail processes for synthesizing the compounds, emphasizing novel or more efficient synthesis routes to establish inventive step and rights over production methods.

3. Therapeutic Use Claims
These claims extend protection to methods of treatment utilizing the compounds, often outlined as methods for treating conditions like depression, neurodegenerative diseases, or metabolic disorders.

  • Such claims reinforce the patent’s commercial scope, covering both the compound and its medical applications.
  • Use claims may specify dosages, formulations, or administration routes.

4. Formulation and Delivery System Claims
If present, these claims cover innovative formulations such as sustained-release preparations, lipid-based carriers, or combination therapies enhancing therapeutic outcomes.

Patent Landscape Context

1. Related Patent Families
JP2010517996 belongs to a broader patent family, likely with counterparts filed in other jurisdictions like US, EP, and China, covering similar compounds or methods.

2. Prior Art and Patent Novelty
Prior art includes earlier patents and publications revolving around similar chemical classes, especially those targeting neurological or metabolic pathways. JP2010517996 differentiates itself through specific structural features or novel synthesis techniques that confer improved pharmacokinetic properties.

3. Competitive Positioning
In the Japanese market, the patent offers exclusivity for a significant period, typically 20 years from their priority date, providing competitive leverage against local or international pharmaceutical firms. The broad claims effectively block competitors from developing or marketing similar compounds or compositions for the targeted indications.

4. Potential Patent Challenges
Given the complex landscape, validity challenges may focus on prior art disclosures related to structurally similar compounds, synthesis methods, or therapeutic use. Patent examiners and competitors might scrutinize the inventive step or whether the claims are sufficiently novel and non-obvious.

5. Filing and Publication Timeline
The patent application’s priority date, likely several years before the publication, influences its standing against subsequent inventions. The publication of JP2010517996 signals its acceptance of the claims and the inventor’s intent to secure rights in Japan.


Conclusion and Strategic Implications

JP2010517996 secures a substantial patent scope rooted in chemical innovation, functional utility, and therapeutic claims. Its broad chemical and use claims aim to establish market exclusivity within Japan and potentially in other jurisdictions via family members. Recognition of its landscape positioning allows stakeholders to anticipate potential patent challenges and carve out pathways for R&D investments and commercial strategies.


Key Takeaways

  • JP2010517996’s scope encompasses a broad class of chemical compounds with therapeutic applications, reinforced by claims on synthesis and methods of use.
  • The patent landscape indicates strong positioning within Japan’s pharmaceutical IP environment, with potential family counterparts expanding its territorial footprint.
  • Strategic considerations include monitoring horizon-scan for prior art challenges, particularly around similar chemical structures, and leveraging the patent for licensing or collaborations.
  • Emergence of generics or biosimilars could threaten market exclusivity; therefore, robust patent prosecution and enforcement are crucial.
  • Companies should evaluate this patent’s claims relative to their pipeline and injunctions to optimize licensing and R&D decisions.

FAQs

1. What is the primary therapeutic application claimed under JP2010517996?
It generally relates to treatment of neurological or metabolic disorders, depending on the specific compounds’ pharmacological profile as detailed in the claims.

2. How does JP2010517996 differ from prior art?
It introduces novel structural modifications or synthesis methods that provide enhanced efficacy, safety, or bioavailability over earlier compounds.

3. Can the scope of this patent be challenged?
Yes, through prior art searches and validity arguments focusing on novelty and inventive step, especially considering similar existing compounds.

4. Are there international equivalents of JP2010517996?
Likely, patent families include counterparts in the US, Europe, and China, which extend the patent’s protective scope and market reach.

5. What should patent stakeholders consider for maximizing value?
Monitoring legal statuses, potential infringing activities, and developing strategic licensing partnerships around the patent’s claims for market dominance.


Sources

[1] Japan Patent Office (JPO). Patent JP2010517996. Publication date: 2010.
[2] Patent analytics reports and drug patent landscape studies.
[3] Pharmaceutical patent law and practice guidelines in Japan.

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