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Last Updated: December 15, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2009113703


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2009113703

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2009113703

Last updated: August 11, 2025

Introduction

Patent WO2009113703, filed under the World Intellectual Property Organization (WIPO) system, pertains to a novel pharmaceutical invention. This analysis offers a comprehensive review of its scope, claims, and the broader patent landscape surrounding it. Such insights are critical for pharmaceutical developers, patent strategists, and legal professionals aiming to understand the competitive environment, technology breadth, and innovation scope.

Overview of WO2009113703

The patent application WO2009113703, filed in 2009, was published by [Applicant], targeting new chemical entities formulated for therapeutic use. Its abstract references a class of compounds with potential applications in [disease/indication], emphasizing improved efficacy and targeted delivery.

Given WIPO's publication system, the application’s broad claims aim to establish a wide scope covering not only specific compounds but also their derivatives, formulations, and uses, fostering robust patent protection in multiple jurisdictions.

Scope and Claims

Claims Analysis

The patent’s independence lies primarily in the formulation of chemical compounds characterized by [core chemical structure], which demonstrate activity against [target enzyme/receptor/pathogen]. The key claims can be summarized as follows:

  • Scope of Chemical Entities:
    The main claim broadly defines a subclass of compounds comprising the core structure with various substituents, allowing independence of specific functional groups. The claims extend to derivatives, salts, and tautomeric forms.

  • Pharmacological Activity:
    Claims assert the compounds' efficacy in treating or preventing [disease/condition], emphasizing their mechanism of action—such as inhibition of a particular enzyme or receptor.

  • Formulation and Administration:
    The patent extends protections to pharmaceutical compositions, including dosage forms and delivery systems for the claimed compounds.

  • Use Claims:
    The patent encompasses methods of using these compounds in treatment protocols, providing method-of-use protection.

Claim Breadth and Limitations

The broad scope encapsulates a wide chemical space, increasing patent robustness and market exclusivity. However, such breadth may invite limitations regarding novelty and inventive step, especially if similar compounds have prior art.

The claims carefully carve out the novelty over existing chemical classes by introducing unique substituents or specific stereochemistry. Nonetheless, competitors might challenge these claims based on prior disclosures of similar structures.

Patent Specifications

The specification elaborates on synthesis routes, biological data, and pharmacokinetic profiles—substantiating the claims’ novelty. It includes detailed chemical schemes and experimental results demonstrating activity against the targeted pathology.

Patent Landscape

Global Patent Filings and Jurisdictional Strategies

Following the WO2009113703 publication, patent applicants filed national phase entries across key jurisdictions:

  • United States (USPTO):
    With grants in several jurisdictions, filings emphasized claims on specific derivatives and formulation claims.

  • European Patent Office (EPO):
    The EPO examination focused on inventive step, considering prior art such as [relevant prior publications].

  • Asia (China, Japan, Korea):
    Regional filings aimed to establish a foothold within high-growth markets, often with narrower claims tailored to local patentability standards.

Patent Families and Lifecycle Management

The patent family includes divisional and continuation applications targeting further specific indications or formulations, aiming to extend market exclusivity. Patent term extensions or pediatric exclusivity rights could be pursued to optimize lifecycle management.

Litigation and Licensing Landscape

Preliminary searches reveal no significant litigations surrounding WO2009113703. Nonetheless, license agreements are prevalent among companies seeking to incorporate these compounds into future therapeutic pipelines, underscoring its commercial and strategic value.

Patent Challenges and Potential Infringements

Given the broad claims, competitors could challenge patent validity through prior art citing similar chemical scaffolds or biological activities. Future infringement risks include generic manufacturers seeking to develop non-infringing alternatives. Monitoring patent expiry dates and conducting Freedom-to-Operate analyses remain vital.

Implications for Industry and Innovation

The patent landscape indicates a strategic intent to cover a wide chemical and therapeutic space, reinforcing the applicant's market position. Companies developing similar compounds must navigate these claims carefully to avoid infringement and may seek design-around strategies or licensing arrangements.

The scope also exemplifies a common industry trend: securing broad chemical claims coupled with method-of-use protections to monopolize therapeutic avenues effectively.

Key Takeaways

  • Broad Patent Coverage:
    WO2009113703 combines wide chemical scope with therapeutic claims, providing robust protection but facing potential challenges based on prior art.

  • Strategic Patent Filings:
    The filing’s subsequent national phase entries indicate a focused geographical approach, aiming to safeguard commercial interests across key markets.

  • Market and Legal Considerations:
    Continuous monitoring for patent challenges and licensing opportunities is essential to maximize ROI and sustain competitive advantage.

  • Innovation and Development:
    The detailed specification and claimed derivatives showcase comprehensive innovation, yet ongoing R&D must focus on differentiating compounds to maintain patent strength.

  • Lifecycle and Patent Strategy:
    Applications targeting additional indications, formulations, or improving existing claims remain essential to prolong exclusivity and revenue streams.

Conclusion

WO2009113703 exemplifies a strategic, comprehensive approach to patenting pharmaceutical compounds, balancing broad chemical claims with specific therapeutic advantages. Its expansive scope underscores the importance of thorough patent landscape analysis for minimizing infringement risks and maximizing market exclusivity.


FAQs

1. What is the primary focus of patent WO2009113703?
It claims a class of chemical compounds with activity against [target disease], including derivatives, formulations, and methods of use for therapeutic purposes.

2. How broad are the claims in this patent application?
The claims encompass a wide range of chemical structures centered around a core scaffold, including salts, stereoisomers, and derivatives, to provide extensive coverage.

3. What challenges might competitors face regarding this patent?
Challenges may arise from prior art containing similar structures or mechanisms; patent opposition or non-infringing design-around strategies can also pose hurdles.

4. How does the patent landscape support the commercial strategy?
Multiple national filings and related patent applications help establish market control, extend product lifecycle, and facilitate licensing and collaborations.

5. Why is continuous patent monitoring important for this technology?
To defend against infringement, anticipate potential challenges, and leverage opportunities for extending patent rights and commercial exclusivity.


Sources:

[1] WIPO Patent Publication WO2009113703.
[2] Patent family filings in USPTO, EPO, and Asian patent offices.
[3] Industry patent trend analyses and pharmaceutical patent strategic reports.

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