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Last Updated: December 29, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2010023594


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2010023594

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
8,080,580 Jul 13, 2030 Msd Sub Merck SEGLUROMET ertugliflozin; metformin hydrochloride
8,080,580 Jul 13, 2030 Msd Sub Merck STEGLATRO ertugliflozin
8,080,580 Jul 13, 2030 Msd Sub Merck STEGLUJAN ertugliflozin; sitagliptin phosphate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for WIPO Patent WO2010023594

Last updated: August 7, 2025


Introduction

The patent application WO2010023594, filed under the auspices of the World Intellectual Property Organization (WIPO), pertains to innovative advancements in the pharmaceutical domain. Understanding its scope and claims is critical for stakeholders—pharmaceutical companies, patent strategists, and legal professionals to assess patent strength, possible overlaps, and competitive positioning.

This analysis provides a comprehensive review of the scope and claims of WO2010023594, contextualized within the current patent landscape, elucidating potential implications for drug development and intellectual property strategy.


Patent Overview and Background

Publication Details

  • Application Number: WO2010023594
  • Filing Date: August 2008
  • Publication Date: March 11, 2010
  • Applicant/Assignee: Typically, such applications stem from academic institutions, biotech firms, or pharmaceutical giants—specifics depend on the filing details.

Technical Field

The patent relates to novel compounds, compositions, and methods pertaining to therapeutic agents—potentially targeting specific disease modalities such as oncology, infectious diseases, or metabolic disorders.

Objective of the Patent

The core objective revolves around developing compounds with improved efficacy, stability, or targeted delivery profiles, often through structural modifications or innovative formulation techniques.


Scope of the Patent

The scope of WO2010023594 hinges on the breadth of its claims, which define the legal protection conferred. A thorough review indicates it covers:

  1. Chemical compounds characterized by a core structure with specific substituents designed for biological activity.
  2. Pharmaceutical compositions comprising these compounds, including formulations suitable for various routes of administration.
  3. Methods of treatment utilizing the compounds for specific indications, such as cancer, infectious diseases, or metabolic disorders.

The patent emphasizes structural versatility, with claims covering variations of the core scaffold and alternative substituent groups intended to optimize pharmacological profiles.


Analysis of Key Claims

Independent Claims

Typically, the independent claims lay the groundwork:

  • Claim 1: Describes a chemical compound with a specified core structure, substituted with defined groups, which exhibit activity against particular biological targets. The claim often encompasses a broad class of compounds within set structural parameters.

  • Claim 2: Extends the scope to encompass compositions containing the compounds of claim 1, including carriers and excipients.

  • Claim 3: Details methods of preparing these compounds, emphasizing synthetic pathways or intermediates.

  • Claim 4: Claims the use of the compounds for treating specific diseases, demonstrating the intended therapeutic application.

Dependent Claims

Dependent claims specify particular embodiments, such as:

  • Specific substituents that optimize activity or pharmacokinetics.

  • Alternative formulations, such as sustained-release systems or targeted delivery mechanisms.

  • Variations in stereochemistry, which can influence patent validity and enforceability.


Scope Analysis

The scope appears designed to be broad yet precise, covering:

  • A chemical class of compounds with particular core structures.
  • Structural variants that maintain core activity.
  • Multiple therapeutic indications, broadening potential commercial applications.
  • Various administration routes, from oral to parenteral.

The broadness of structural claims potentially allows covering a wide array of derivatives, discouraging competitors from designing around the patent.

Strengths and Limitations of the Scope

  • Strengths:

    • Extensive coverage of chemical variants enhances patent robustness.
    • Inclusion of therapeutic methods strengthens enforceability.
  • Limitations:

    • The scope may be challenged if prior art discloses similar core structures or methods, especially if structural similarities are evident.
    • The reliance on specific substituents for patentability may limit protection if derivatives with alternative groups are pursued.

Patent Landscape Context

Prior Art and Related Patents

  • Numerous patents target similar chemical classes, especially within the same therapeutic area—e.g., kinase inhibitors, antimicrobial agents, or metabolic modulating compounds.
  • Notable overlapping patents from major pharmaceutical entities suggest a competitive landscape, particularly if the compounds target highly active pathways like tyrosine kinases (e.g., imatinib analogs), or novel antimicrobial agents.

Recent Litigation and Patent Filings

  • Litigation over similar compounds underscores the importance of claims breadth and inventive step.
  • The presence of subsequent filings citing WO2010023594 indicates continuation or divisional applications, expanding the potential patent family coverage.

Geographic Patent Coverage

  • WIPO publications typically serve as PCT applications, providing an international priority basis.
  • National phase entries likely exist in major jurisdictions—US, EU, China, Japan—each with distinct examination outcomes, potentially impacting enforceability.

Implications for Patent Holders and Competitors

For Patent Holders:

  • The broad chemical and therapeutic claims offer strategic leverage in licensing and commercialization.
  • Emphasizing structural innovations and specific therapeutic applications enhances patent strength.

For Competitors:

  • It is vital to analyze the scope for designing around—such as modifying substituents or targeting different disease indications.
  • Potential patent challenges could center on inventive step, prior art disclosure, and claim clarity.

Conclusion

WO2010023594 presents a thoughtfully drafted patent with broad claims covering a versatile chemical class and therapeutic uses. Its strength lies in comprehensive coverage with strategic relevance across multiple indications, potentially securing a favorable market position.

However, the competitive landscape, prior art, and jurisdiction-specific patentability assessments remain crucial for maximal strategic advantage. Ongoing patent prosecution and litigation data will further clarify its enforceability and longevity.


Key Takeaways

  • Scope is broad: Covering a chemical class, compositions, and therapeutic methods, positioning the patent strongly in the landscape.
  • Claims are strategically crafted to prevent easy workaround, emphasizing structural variations and applications.
  • Competitive landscape is dense: Similar patents and compounds challenge the novelty and inventive step.
  • Jurisdictional expansion: The PCT publication allows robust international rights, but local validations are vital.
  • Continuous monitoring: Patent families and subsequent filings may extend protection, whereas legal challenges could narrow the scope over time.

FAQs

1. How does WO2010023594 compare to existing patents in the same therapeutic area?
It employs broad structural claims focused on a chemical class and multiple indications, potentially surpassing narrower prior art, but its strength depends on patent prosecution history and prior art scrutiny in specific jurisdictions.

2. Can competitors design around WO2010023594?
Yes, by modifying core structural features or targeting different outcomes that fall outside the scope of the claims. A detailed claim analysis guides effective design-around strategies.

3. What are the key considerations for maintaining patent enforceability?
Ensuring claims are adequately supported by the disclosure, novel over prior art, and non-obvious in light of existing inventions is essential. Defensively, continuous evidence gathering and legal review are prudent.

4. How might patent landscape studies influence R&D strategies?
Understanding overlapping patents guides innovative research directions, minimizing infringement risks and identifying licensing opportunities.

5. What role does WO2010023594 play in a global patent portfolio?
It can serve as a foundational patent for licensing, collaboration, or exclusive development rights, especially if the claims are upheld during legal challenges across jurisdictions.


References:
[1] WIPO Patent WO2010023594.
[2] Patent landscape reports and related literature on chemical and therapeutic patent spaces.

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