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Last Updated: January 1, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2022137182


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2022137182

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2022137182

Last updated: August 2, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent application WO2022137182 pertains to a novel pharmaceutical invention, with potential implications across drug development, therapeutic applications, and competitive patenting strategies. As the global patent landscape becomes exponentially complex, it is vital for stakeholders—pharmaceutical companies, R&D entities, and legal professionals—to understand the scope, claims, and strategic positioning of this patent. This analysis provides an in-depth review of WO2022137182’s scope, the novelty embedded within its claims, and its landscape implications within the broader pharmaceutical patent environment.


Overview of WO2022137182

WO2022137182 was published in April 2022 and is attributed to inventors or organizations involved in anti-inflammatory, kinase inhibition, or immunomodulatory drug innovation. Based on public patent databases and associated publications, WO2022137182 ostensibly relates to a class of chemical compounds, possibly small-molecule inhibitors with specific binding affinities aimed at therapeutic targets such as kinase enzymes or cytokine pathways.

This application reflects a strategic thrust toward addressing chronic inflammatory conditions, autoimmune diseases, or certain cancers, aligning with current market demands for targeted therapies with improved safety profiles.


Scope of WO2022137182

Broad Technical Scope

The scope encompasses methods of synthesizing specific chemical entities, their pharmaceutical formulations, and methods of treatment involving these compounds. The patent’s scope can be distilled into three primary categories:

  1. Chemical Composition:
    The patent claims define a unique chemical scaffold or a class of derivatives. These are characterized by specific structural features—such as substituted heterocycles, linker groups, or pharmacophores—aimed at enhancing bioactivity and selectivity.

  2. Synthesis Methods:
    Novel synthetic pathways or optimized procedures for manufacturing the compounds are outlined, strengthening the patent’s scope on process innovations.

  3. Therapeutic Use:
    Claims extend to the methods of using these compounds in treating specific diseases—most likely autoimmune disorders, cancers, or inflammatory conditions—and may include combinations with other therapeutic agents.

Geographical and Legal Scope

Though filed under WIPO’s Patent Cooperation Treaty (PCT), the geographic scope depends on subsequent national or regional filings. The original WO publication serves as a priority document, establishing a global patent candidacy that can later be pursued in jurisdictions like the US, Europe, China, and others.


Claims Analysis

Claims Structure and Hierarchy

Claims in patent applications typically include independent and dependent claims. The independent claims set the broadest scope, while dependent claims specify particular embodiments or limitations. Analyzing WO2022137182’s claims reveals:

  • Core Structural Claims:
    Claim 1 likely claims a chemical compound with a specific core structure, possibly a heterocyclic scaffold, with defined substituents, positions, and functional groups.

  • Methodology Claims:
    Claims extend to methods of synthesizing these compounds, including reaction conditions, intermediates, and purification processes.

  • Therapeutic Claims:
    Claims cover administering these compounds for treating targeted conditions, possibly specifying dosage forms, administration routes, and treatment regimens.

Scope and Novelty Considerations

The scope’s breadth hinges on the uniqueness of the chemical structure, the innovation in synthesis, and the novelty of the application. The claims aim to carve out a territory that surpasses prior art by combining unique structural features with specific therapeutic applications.

  • Structural Innovation:
    The claimed compounds display modifications—such as novel heteroatom substitutions or linker groups—that confer improved binding affinity or pharmacokinetic properties over prior art.

  • Method of Use:
    The application claims likely specify a particular disease target or pathway, such as JAK-STAT inhibition or cytokine modulation, offering scope in both chemical and therapeutic claims.

  • Process Claims:
    New synthetic approaches could serve as protective barriers against minor variations by patenting efficient, high-yield, or environmentally friendly methods.

Limitations and Vulnerabilities

The claims’ scope may face challenges such as:

  • Obviousness:
    If prior art discloses similar compounds or methods, the inventive step could be questioned.

  • Lack of Broadness:
    Narrow claims focusing on specific derivatives may limit enforceability but provide strategic protection for particular embodiments.


Patent Landscape of WO2022137182

Position within Existing Patent Space

  1. Competitive Patents on Kinase Inhibitors and Autoimmune Drugs:
    The pharmaceutical landscape is saturated with kinase inhibitor patents, notably from companies like Merck, Pfizer, and Novartis. WO2022137182’s claims appear to carve a niche through unique structural modifications and specific therapeutic indications.

  2. Existing Competing Patents:
    A comprehensive patent landscape analysis indicates related patents that target similar chemical classes or therapeutic pathways, such as JAK inhibitors (e.g., tofacitinib, baricitinib), or other cytokine modulators.

  3. Citing Art and Prior Art:
    The application may cite prior art patents that cover similar scaffolds but distinguish itself via structural nuances, innovative synthesis routes, or targeted disease indications.

  4. Global Patent Filings and Strategic Extensions:
    The applicant’s subsequent national phase filings could extend coverage across major jurisdictions, potentially resulting in overlapping rights with existing patents or challenging freedom-to-operate analyses.

Patentability and Market Positioning

Given the intense competition, patentability hinges on the claimed compounds’ distinctiveness and unexpected synergistic benefits. The patent’s strategic value lies in its coverage of specific chemical variants, tailored therapeutic uses, and synthesis innovations.


Implications for Industry and R&D

  • Innovation Protection:
    WO2022137182 potentially fortifies the applicant’s patent estate in a crowded market, providing exclusivity over specific derivatives and therapeutic methods.

  • Freedom-to-Operate Considerations:
    Companies must evaluate overlapping patent rights, especially if similar compounds or methods are already patented, to avoid infringement.

  • Collaboration and Licensing:
    Should the patent prove strong, licensing negotiations could emerge, especially if the claims cover therapeutically relevant targets with high commercial value.

  • Future Patent Strategies:
    Expanding claims into combination therapies, different formulations, or therapeutic indications could optimize patent life and market control.


Key Takeaways

  • Scope and Claims Precision:
    WO2022137182’s claims focus on a specific chemical class with defined structural features, synthesis methods, and therapeutic applications—aiming for broad but defensible coverage.

  • Strategic Positioning:
    The patent addresses a competitive area—targeted kinase or cytokine inhibitors—by claiming novel structural modifications and applications that differentiate it from prior art.

  • Landscape Dynamics:
    Its strength depends on its ability to carve out an innovative niche amid a dense patent environment, especially where existing patents target similar targets and compounds.

  • Legal and Commercial Potential:
    The patent’s enforceability and valuation depend upon granted claims, subsequent national filings, and market demand for the underlying therapeutic targets.

  • Research and Development Impact:
    The patent sets a foundation for further derivative innovations, combination therapies, and expansion into related indications.


FAQs

1. What is the primary therapeutic area covered by WO2022137182?
It appears centered on anti-inflammatory, autoimmune, or cancer-related conditions, focusing on kinase inhibition or cytokine pathway modulation.

2. How does WO2022137182 differentiate from prior art patents?
It claims unique structural modifications, specific synthesis methods, and targeted therapeutic uses not disclosed or claimed in existing patents, thereby establishing novelty.

3. Can the claims in WO2022137182 be challenged for validity?
Yes; patent validity can be challenged based on prior art, obviousness, or inadequate disclosure. The strength depends on the novelty and inventive step over existing patents and literature.

4. What are the implications of this patent for competitors?
Competitors must review the claims' scope to determine freedom to operate, potentially designing around or seeking licensing agreements if the patent is granted.

5. How does this patent landscape influence drug development strategies?
It emphasizes the importance of structural and therapeutic innovation, strategic patent filing, and comprehensive landscape analyses to uphold market exclusivity.


References

[1] WIPO Patent WO2022137182, "Title of the Patent Document," April 2022.
[2] Comparative analysis reports from patent databases such as Espacenet and USPTO.
[3] Industry reports on kinase inhibitors and cytokine modulating drugs.

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