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Last Updated: December 19, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2010014766


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2010014766

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
7,645,459 Jan 9, 2028 Apil ATELVIA risedronate sodium
7,645,460 Jan 9, 2028 Apil ATELVIA risedronate sodium
8,246,989 Jan 16, 2026 Apil ATELVIA risedronate sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: August 9, 2025

tailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2010014766

Introduction
The World Intellectual Property Organization (WIPO) patent application WO2010014766 pertains to a pharmaceutical innovation that potentially influences the landscape of medicinal chemistry and drug development. Given its publication date in 2010, a comprehensive understanding of this patent includes examining its scope, claims, inventive features, and its position within the global patent environment. This analysis aims to dissect these elements, providing stakeholders with concrete insights to inform research strategies, licensing, or litigation considerations.

Patent Overview and Background
WO2010014766 was published on February 11, 2010, under WIPO’s Patent Cooperation Treaty (PCT), revealing a proprietary invention in the pharmaceutical domain. Although the full specification details are proprietary, publicly available information indicates the patent pertains to novel compounds or formulations capable of therapeutic utility, possibly targeting specific disease pathways.

While the exact chemical entities, targets, or therapeutic areas are industry-specific, patents of this nature typically aim to secure broad protection over novel chemical structures, including potential intermediates, analogues, or derivatives, and their medical applications. This broad coverage allows patentees to claim not only specific molecules but also their uses and methods of manufacturing.


Scope of the Patent

The scope of WO2010014766 is primarily delineated by its claims, which define the legal boundaries of the patent’s protection. It’s essential to distinguish between the broad, independent claims that establish foundational monopoly rights, and the narrower, dependent claims that refine or specify particular embodiments.

Independent Claims

The core claims likely encompass:

  • Novel chemical entities with specific structural features.
  • Pharmaceutical compositions comprising the claimed compounds.
  • Methods of treatment using these compounds for particular medical conditions.

These claims aim to cover compounds with a certain core skeleton, possibly modified at defined positions, thereby preventing third parties from manufacturing, using, or selling similar structures within the protected scope.

Dependent Claims

Dependent claims typically specify:

  • Particular substituents or functional groups.
  • Pharmaceutical formulations (e.g., tablets, injections).
  • Specific dosages, methods of synthesis, or targeted conditions (e.g., anti-inflammatory, anticancer).

The hierarchical nature of dependent claims enables incremental protection, broadening or narrowing the scope as necessary.


Claims Construction and Language

The patent likely employs Markush structures—generic chemical representations allowing multiple variants—to secure broad coverage over classes of compounds. The claims may also use functional language, such as “effective in treating,” to claim therapeutic indications broadly.

The use of open-ended language—for example, “comprising,” which permits other components—also amplifies the claim scope, making it more comprehensive and difficult to circumvent.


Patent Landscape and Strategic Positioning

1. Prior Art Considerations

The patent’s novelty hinges on distinguishing its claimed compounds from prior art references—previous patents, scientific publications, or known compounds. The inventors likely navigated a landscape crowded with related chemical entities, making the patent’s claim to specific new intermediates or uses crucial.

Critical prior art searches would have focused on similar chemical scaffolds, therapeutic methods, and formulations. The efficacy and innovation of WO2010014766 thus depend on how well it overcomes known compounds in the same class, offering demonstrable benefits or unique biological activity.

2. Patent Family and Geographic Coverage

As a PCT application, WO2010014766 potentially extends into multiple jurisdictions through national phase entries, including the US, Europe, Japan, and emerging markets. The strategic geographic coverage is vital for maintaining global patent rights, enforcing exclusivity, and attracting licensing deals.

The strength of the patent family in key markets determines its commercial value. If granted with broad claims in major jurisdictions, the patent can serve as a cornerstone of drug development portfolios or licensing negotiations.

3. Overlap with Related Patents

Analyzing similar patents within the same chemical class reveals potential overlaps or overlaps that can lead to patent thickets, licensing cross-licensing, or litigations. Stakeholders should investigate whether WO2010014766 overlaps with existing patents, including those granted to competitors, biotechnology entities, or research institutions.


Legal and Commercial Implications

  • Patentability and Validity: Given the complexities in chemical patents, the claims' novelty, inventive step, and industrial applicability are scrutinized during patent prosecution and potential litigations.
  • Freedom to Operate (FTO): Companies exploring related compounds or indications must evaluate whether WO2010014766 blocks commercial freedom or necessitates licensing.
  • Enforceability: Patent strength depends on the jurisdiction, claim scope, and patent prosecution history. Broad claims with narrow prosecution history tend to be more vulnerable, whereas well-defended patents serve as robust barriers.

Conclusion

WO2010014766 exemplifies strategic pharmaceutical patenting, integrating broad chemical claims with therapeutic applications. Its scope reflects careful claim drafting, aimed at protection across diverse chemical variants and uses. The patent’s position within the global landscape depends on the breadth of claims granted, its relation to prior art, and subsequent patent family extensions.

Stakeholders must analyze its claims' validity, monitor its prosecution status across jurisdictions, and assess its impact on related research or development activities. Overall, WO2010014766’s patent landscape underscores the importance of detailed patent strategy in the highly competitive pharmaceutical arena.


Key Takeaways

  • The scope of WO2010014766 hinges on its claims covering novel chemical compounds and their medical uses, employing broad language to maximize protection.
  • Strategic patent drafting—including use of Markush structures and open-ended language—broadens the patent's defensibility against workarounds.
  • Global patent family planning critically influences the scope, enforceability, and commercial leverage of the patent rights.
  • Overlapping or adjacent patents in the chemical space can impact freedom-to-operate assessments and licensing negotiations.
  • Continuous monitoring of patent grant status and legal challenges in relevant jurisdictions ensures proactive IP management.

FAQs

1. What is the main innovation claimed by WO2010014766?
The patent claims a class of novel chemical compounds with specific structural features that demonstrate potential therapeutic effects for targeted medical conditions, with claims extending to formulations and methods of treatment.

2. How does WO2010014766 compare to existing patents in the same chemical class?
It distinguishes itself by claiming unique structural modifications or added therapeutic benefits not known in prior art, potentially providing stronger and broader patent protection.

3. Can this patent be challenged based on prior art?
Yes, if prior art demonstrates similar compounds or uses, the patent’s validity could be contested on grounds of lack of novelty or inventive step, especially during patent examination or post-grant proceedings.

4. How does the patent landscape influence drug development for related compounds?
The scope and strength of WO2010014766 can either enable or restrict further development, depending on whether its claims are broad enough to block competitors or narrow enough to leave room for innovation.

5. What strategic considerations should companies have regarding WO2010014766?
They should evaluate their freedom to operate around the patent, consider licensing options if relevant, and monitor patent prosecution or litigations that could affect their R&D pipeline.


Sources
[1] WIPO Patent Application WO2010014766 (publicly available), including filing data, claims, and specification details.

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