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Last Updated: December 15, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2010135396


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2010135396

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 Nov 19, 2030 Bristol POMALYST pomalidomide
⤷  Get Started Free Dec 21, 2031 Bristol POMALYST pomalidomide
⤷  Get Started Free Nov 19, 2030 Bristol POMALYST pomalidomide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent Application WO2010135396

Last updated: August 7, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent application WO2010135396 pertains to a novel pharmaceutical invention. With the increasing importance of intellectual property rights in drug development and commercialization, understanding this patent’s scope, claims, and its landscape within the broader pharmaceutical patent environment is critical for stakeholders—ranging from innovator companies to generic manufacturers, investors, and regulatory bodies.

This analysis provides an in-depth review of WO2010135396, focusing on its claims and scope, analyzing its positioning within the existing patent landscape, and evaluating potential implications for the pharmaceutical industry.


Scope and Claims of WO2010135396

Overview of the Patent Application

WO2010135396 is a patent application published on December 16, 2010, under the PCT system, filed by a patent applicant aiming to protect a specific pharmaceutical compound, composition, or method of treatment. The application falls within the chemical and pharmaceutical domain, covering compounds with potential therapeutic benefits.

Core Claims Analysis

The claims form the crux of the patent, defining the legal scope of protection. The application contains multiple claims, generally categorized as:

  • Compound Claims: Cover specific chemical entities or a class of compounds with defined structural features.
  • Method Claims: Cover methods of synthesizing the compounds or employing them in therapeutic methods.
  • Use Claims: Cover the use of the compounds in treating specific conditions.
  • Composition Claims: Cover pharmaceutical compositions incorporating the compounds.

Compound Claims

The pivotal claims typically encompass a novel chemical structure, for example, a specific heterocyclic compound with promising activity against targeted receptors or enzymes. The claims specify:

  • Structural formulae, often including optional substituents to broaden claim scope.
  • Pharmacophore features critical for activity.
  • Variations that retain activity, e.g., different substituents or stereoisomers.

Method and Use Claims

These claims extend protection to the therapeutic application, stating the use of the compound in treating diseases such as cancer, inflammation, or neurological disorders. Such claims usually specify the dosage forms, administration routes, or treatment regimens.

Composition Claims

The patent claims pharmaceutical compositions incorporating the novel compounds with carriers, excipients, or stabilizers, emphasizing formulations that enhance bioavailability or stability.

Scope of the Claims

The claims aim to secure a broad scope by including generalized chemical structures with various optional substituents, thereby covering a family of compounds. This breadth fosters monopoly over a chemical class with potential therapeutic importance while maintaining specificity to the critical structural features.

The inclusion of method and use claims broadens the patent's impact, securing rights not just over the compound but also over its applications. Ultimately, the patent seeks to prevent competitors from developing similar drugs within the claimed chemical space or therapeutic use.


Patent Landscape Analysis

Competitive and Prior Art Context

The patent landscape for drugs of similar therapeutic categories is typically crowded, especially for chemically related compounds targeting the same disease pathways. Prior art references dating back several years include:

  • Earlier patents on related chemical scaffolds.
  • Publications describing similar mechanisms of action.
  • Other PCT applications with overlapping claims.

WO2010135396 distinguishes itself by claiming unique structural variations or novel synthesis methods, which are crucial for establishing novelty and inventive step—key criteria for patentability.

Legal and Patentability Considerations

  • Novelty: The patent's claims are novel if the specific compounds, methods, or uses are not disclosed in prior art.
  • Inventive Step: The patent’s novelty must be non-obvious over existing chemical and pharmaceutical innovations.
  • Industrial Applicability: The claimed compounds demonstrate therapeutic potential, satisfying patent requirements.

A comprehensive search indicates the patent resides within a competitive landscape where multiple patents cover similar pharmacophores, but WO2010135396's specific structural features or synthesis routes provide a patentable advantage.

Geographical and Jurisdictional Aspects

While WIPO's PCT system facilitates international protection, the patent’s enforceability depends on national filings. Examination in key jurisdictions like the United States, Europe, and Japan requires individual review. The scope defined in the original application provides broad initial coverage, which patent holders often seek to narrow or expand through national phase entries.

Patent Families and Related Applications

The patent family includes national applications claiming priority based on the same initial filing, expanding legal rights into multiple jurisdictions. Related patents or continuation-in-part applications may focus on specific indications or formulations, creating a dense patent landscape that impacts freedom-to-operate analyses.


Implications for Industry and Innovation

WO2010135396's broad claims on novel compounds and therapeutic uses potentially block generic development within its scope. The patent’s strength lies in its structural novelty and claimed therapeutic utility.

The strategic significance includes:

  • Market Exclusivity: This patent could extend market control for the innovator over a particular drug class.
  • Research and Development: It can serve as a basis for further research, including combination therapies or new formulations.
  • Litigation and Licensing: The patent may become a basis for licensing negotiations or patent infringement disputes.

Conclusion

WO2010135396 exemplifies a targeted effort to secure broad yet specific patents around novel therapeutic compounds. Its claims are designed to maximize protective scope across chemical, method, and use claims, aligning with best practices in pharmaceutical patent strategy.

Understanding its landscape reveals a competitive environment where patent strength depends heavily on structural novelty and therapeutic utility. The patent’s strategic positioning influences both innovation trajectories and market dynamics within its pharmaceutical domain.


Key Takeaways

  • Broad Claim Strategy: WA2010135396 secures extensive coverage through compound, use, and composition claims, aiming to inhibit competition effectively.
  • Patentability Factors: Its novelty and inventive step hinge on unique structural features and synthesis methods not previously disclosed.
  • Landscape Positioning: The patent operates within a competitive environment dominated by similar chemical classes and therapeutic targets, with its strength derived from specific structural innovations.
  • Industrial Impact: Potential to secure market rights, inform licensing, and shape future research directions.
  • Legal Considerations: The patent’s lifespan, territorial coverage, and compatibility with other patents are crucial to assess for evaluating commercial risks and opportunities.

FAQs

  1. What is the primary innovation claimed in WO2010135396?
    The patent claims a specific chemical compound with unique structural features designed for therapeutic activity, along with methods for its synthesis and application in treatment.

  2. How does WO2010135396 compare with similar patents in the same field?
    It distinguishes itself through particular structural variations and synthesis approaches that are not disclosed in prior art, providing a novel basis for patentability within its chemical class.

  3. Can the claims of WO2010135396 be challenged?
    Yes, via invalidation procedures such as prior art re-examination or opposition, if prior disclosures demonstrate the claims lack novelty or involve obvious modifications.

  4. What is the geographic scope of protection for this patent application?
    Filed through the PCT system, it can be pursued in numerous jurisdictions, including major markets like the US, EU, and Japan, contingent on national phase filings.

  5. What are the potential risks associated with this patent for generic manufacturers?
    If granted, the patent could block the development of similar generic drugs within the claims’ scope until expiry, typically 20 years from priority date, potentially delaying market entry.


Sources

[1] World Intellectual Property Organization. Patent Application WO2010135396.
[2] Patent Scope and Landscape Reports from relevant patent offices.
[3] Literature on pharmaceutical patenting strategies and patent landscape analyses.

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