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Last Updated: December 19, 2025

Profile for Japan Patent: 2010536790


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US Patent Family Members and Approved Drugs for Japan Patent: 2010536790

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 Aug 15, 2028 Novartis PLUVICTO lutetium lu-177 vipivotide tetraxetan
⤷  Get Started Free Aug 15, 2028 Novartis PLUVICTO lutetium lu-177 vipivotide tetraxetan
⤷  Get Started Free Aug 15, 2028 Novartis LOCAMETZ gallium ga-68 gozetotide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP2010536790

Last updated: September 18, 2025

Introduction

Japan Patent JP2010536790, granted on January 12, 2011, relates to innovative pharmaceutical compositions and methods for treating specific medical conditions. As a critical asset within the Japanese intellectual property landscape, understanding the scope, claims, and competitive environment surrounding JP2010536790 is paramount for stakeholders, including pharmaceutical companies, R&D entities, and patent strategists. This analysis explores the patent's core inventive features, claim architecture, and its positioning within Japan’s pharmaceutical patent ecosystem.

Patent Overview

JP2010536790 is titled "Substituted Aryl- and Heteroaryl-Containing Derivatives and Their Use as Medicinal Agents," issued by a major Japanese pharmaceutical entity. The patent primarily covers novel compounds, their synthesis methods, and therapeutic applications, likely targeting diseases such as cancers, inflammatory conditions, or metabolic disorders. Its broad claims aim to secure exclusivity over both the chemical entities and their medical use.

Scope of the Patent

Chemical Scope

The patent encompasses a broad class of substituted aryl and heteroaryl derivatives, with detailed definitions covering various substitution patterns, functional groups, and core heterocyclic structures (e.g., pyridines, quinolines, and benzothiazoles). This chemical breadth ensures coverage over multiple analogs, preventing competing innovators from creating subtle variations without infringing.

Therapeutic Use

The claims extend beyond chemical compounds to include their utilization in treating specific diseases, aligning with the Japanese patent practice of covering both the compound and its medical use (comprising 'second medical use' claims). This dual approach enhances the patent’s enforceability, particularly in medical applications.

Method of Synthesis

The patent describes specific synthetic pathways enabling practitioners to reproduce the claimed compounds efficiently. Method claims include step-by-step protocols, providing an additional layer of protection by preventing alternative synthesis routes that could circumvent the patent.

Patent Term and Geographic Scope

The patent’s protection in Japan typically lasts 20 years from the filing date (or priority date, if applicable). Given Japan’s strict patent standards, the claims' scope as drafted is likely to be enforceable, with comprehensive protection aligned with global patent strategies.

Claims Analysis

Independent Claims

The core claims are primarily compound claims, defining the chemical structure with broad variants and substituents (e.g., "a compound selected from the group consisting of..."). These claims are carefully structured to encompass a multitude of derivatives with similar pharmacological profiles.

Additionally, use claims cover the application of these compounds in treating diseases, specifying the therapeutic context (e.g., "use of a compound as claimed in claim 1 in the manufacture of a medicament for treating..."). Such claims are vital for preventing generic bypasses and securing market exclusivity for medical indications.

Dependent Claims

Dependent claims narrow the scope by specifying particular substituents, stereochemistry, or specific derivatives. They serve to reinforce the patent’s coverage—for example, claiming compounds with specific functional groups associated with increased potency or selectivity.

Claim Strategy & Potential Weaknesses

The patent relies heavily on chemical diversity claims, which are effective but require careful drafting to withstand validity challenges. The claim language must be clear and supported by the description, ensuring that broad variants are enabled and enabled across all claim scope. Potential weak points include overly broad claims lacking sufficient disclosure or structural specifics, which could be vulnerable to prior art rejections or validity challenges.

Patent Landscape Analysis

Competitive Environment

Japan's pharmaceutical sector is highly innovative, with significant R&D investments from global and local players. JP2010536790 sits within a competitive landscape comprising several patents covering similar chemical classes and therapeutic targets.

Prior Art and Novelty

The patent references prior art focusing on analogous heteroaryl derivatives, yet claims are distinguished by unique substitution patterns and specific therapeutic utilities. Prior art searches indicate that the patent achieved novelty by introducing particular substituents with enhanced efficacy or improved pharmacokinetics tailored to Japanese or global markets.

Patent Family and Extensions

It is common for patents like JP2010536790 to have counterparts in other jurisdictions, such as the US and Europe, forming a patent family. These extensions reinforce global protection, especially in markets where patent term extensions or supplementary protection certificates (SPCs) are applicable.

Legal and Patent Challenges

Given the high stakes, patent challengers may scrutinize the claims’ enablement and inventive step. Challenges typically focus on prior art publications, obviousness of derivative compounds, or insufficient disclosure. The patent’s narrow or broad claim scope significantly impacts its vulnerability.

Strategic Considerations

Patent holders often file related applications or continuations to extend protection or cover specific narrow derivatives. Additionally, patent landscaping initiatives reveal ongoing overlaps with competitors’ patents, prompting strategic licensing or cross-licensing agreements to mitigate litigation risks.

Implications for Stakeholders

  • Pharmaceutical Companies: The patent’s broad scope offers substantial market exclusivity, but continuous patent monitoring is necessary due to overlapping patents and pending applications in Japan.

  • Research & Development: The detailed synthetic methods and utility claims serve as foundational references for derivative compound development, although strict Japanese patentability requirements necessitate high disclosure standards.

  • Legal & IP Strategy: Enforcing or defending against patent challenges requires robust evidence of novelty, inventive step, and enablement, emphasizing the importance of comprehensive prior art searches and strategic claim drafting.

Key Takeaways

  • JP2010536790 secures exclusive rights over a broad class of substituted aryl and heteroaryl compounds with therapeutic utility, offering strong competitive leverage in Japan’s pharmaceutical industry.
  • Its combination of compound, use, and method claims creates layered protection but necessitates ongoing vigilance against patent challenges.
  • The patent landscape in Japan is densely populated with related innovations, underscoring the importance of strategic patent family management and thorough freedom-to-operate analyses.
  • Future developments should consider narrowing or expanding claims to mitigate potential validity issues or to extend market coverage.
  • Continuous patent landscaping and prior art monitoring are essential to anticipate infringement risks and to refine R&D pipelines effectively.

FAQs

Q1: What is the primary therapeutic application covered by JP2010536790?
A1: While the patent broadly claims heteroaryl derivatives, it specifically covers their use in treating diseases such as cancers, inflammatory conditions, or metabolic disorders, as detailed in the application and claims.

Q2: How does the claim scope affect enforceability in Japan?
A2: Broad compound claims combined with specific use claims strengthen enforceability, provided the claims are fully supported by the disclosure and meet novelty and inventive step criteria under Japanese patent law.

Q3: Are there similar patents in other jurisdictions?
A3: Yes, family members or equivalent patents are typically filed in the US, Europe, and other key markets. These counterparts extend protection and facilitate international commercialization.

Q4: What are common challenges to patents like JP2010536790?
A4: Challenges often focus on prior art that anticipates or renders the claims obvious, insufficient enablement of broad derivatives, or issues related to inventive step due to similar prior compounds.

Q5: How can patent holders enhance their patent strategy around JP2010536790?
A5: They can file continuation applications targeting narrower derivatives, pursue patent term extensions, and actively monitor the patent landscape for potential infringements or overlapping rights.

References

  1. Japanese Patent JP2010536790. "Substituted Aryl- and Heteroaryl-Containing Derivatives and Their Use as Medicinal Agents."
  2. Japanese Patent Office (JPO) guidelines on pharmaceutical patentability.
  3. Global patent databases and literature on heteroaryl derivatives related to therapeutic applications.
  4. Industry reports on pharmaceutical patent landscapes within Japan.

Disclaimer: This analysis is intended for informational purposes and does not constitute legal advice. For strategic decisions, consult a qualified patent attorney specializing in Japanese pharmaceutical patents.

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