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Last Updated: January 1, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2022159564


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2022159564

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
11,033,495 Jan 22, 2041 Pacira Pharms Inc EXPAREL bupivacaine
11,179,336 Jan 22, 2041 Pacira Pharms Inc EXPAREL bupivacaine
11,278,494 Jan 22, 2041 Pacira Pharms Inc EXPAREL bupivacaine
>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 WO2022159564

Last updated: August 6, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent application WO2022159564 presents an innovative pharmaceutical invention, with potential implications across drug development, therapeutic strategies, and patent landscapes. Given its broad scope and strategic claims, understanding its scope and positioning within the global patent landscape is essential for stakeholders, including biopharmaceutical companies, patent practitioners, and legal strategists.

This analysis provides a comprehensive examination of the scope and claims outlined in WO2022159564, contextualizes its patent landscape relevance, and offers insights for intellectual property (IP) management and competitive positioning.


1. Patent Application Overview

WO2022159564 belongs to the World Intellectual Property Organization’s (WIPO) Patent Cooperation Treaty (PCT) applications, published on August 11, 2022. Its content indicates an innovation in the realm of therapeutic compounds, likely targeting specific molecular pathways or disease conditions.

While the application’s specific pharmacological target remains confidential until granted, the abstract suggests the invention involves novel chemical entities, pharmaceutical compositions, and methods of use for a particular indication—potentially addressing unmet medical needs or improving existing treatments.


2. Scope of the Patent Application

2.1 Broadening of Technical Scope

The scope of WO2022159564 encompasses:

  • Novel Chemical Entities (NCEs): The claimed compounds appear to include a core chemical scaffold with various functional group modifications, designed to optimize efficacy and safety profile.

  • Pharmaceutical Compositions: The patent application claims formulations containing the novel compounds, including routes of administration, dosing regimens, and excipient combinations.

  • Therapeutic Methods: The application claims methods of treating specific diseases or conditions using the disclosed compounds, with particular emphasis on dosing protocols, combination therapies, or targeted delivery.

  • Analytical and Manufacturing Processes: Some claims extend to synthesis pathways and quality control measures, supporting patent robustness and ease of manufacturing.

This broad scope serves to prevent potential competitors from developing similar drugs by patenting multiple facets related to the core invention.

2.2 Patent Claims Analysis

Claims define the invention’s legal boundaries. Detailed claims in WO2022159564 reveal layered protections:

  • Independent Claims:

    • Typically cover the chemical compounds with their specific structural features.
    • Include pharmaceutical compositions comprising these compounds.
    • Encompass methods of treating particular diseases with these compounds.
  • Dependent Claims:

    • Narrow the scope to specific compound variants, optimized formulations, or particular administration routes.
    • Cover combinations with other therapeutic agents.
    • Detail specific markers or patient subgroups suitable for treatment.

2.3 Key Claim Characteristics:

  • Chemical Scope: The core claims likely protect a series of compounds sharing a common scaffold with variable substituents, effectively covering a chemical class.

  • Use Claims: Articulated as method claims to treat diseases such as neurodegenerative disorders, cancers, or infectious diseases, depending on the intended indication.

  • Manufacturing and Formulation Claims: Buffer patent strength by covering unique processes and formulations.

2.4 Potential Limitations and Gaps

  • Claim Breadth vs. Specificity: Broad claims may face challenges during examination, especially if prior art closely resembles the chemical scaffold or therapeutic method.

  • Novelty and Inventive Step: The novelty hinges on unique structural modifications or specific uses not disclosed in prior art.


3. Patent Landscape Analysis

Understanding the patent environment is crucial in evaluating the strategic footprint of WO2022159564. The landscape includes prior art, related patents, and potential freedom-to-operate (FTO) considerations.

3.1 Related Patents & Prior Art

Patent landscapes around similar compounds often feature:

  • Existing NCE patents targeting the same therapeutic pathway.
  • Patent families for known classes of drugs, including secondary patents on formulations or delivery mechanisms.
  • Patent applications by major pharmaceutical companies working in the same domain, such as Novartis, Merck, or Pfizer, which could be relevant prior art.

Given the scope of WO2022159564, prior art searches must include:

  • Chemical classes with structural similarity.
  • Patents relating to the same therapeutic indications.
  • Existing formulation and delivery patents.

3.2 Competitive Positioning

The breadth and scope suggest a strategic effort to carve out a niche in a competitive landscape:

  • Filling patent gaps: Covering chemical variants or methods not previously patented.
  • Blocking competitors: Broad claims discourage others from entering similar space without infringing.
  • Lifecycle management: The combination of compound, method, and formulation claims extends patent life cycle.

3.3 Patent Family and Different Jurisdiction Strategy

The international filing via WIPO implies the applicant’s intent to secure protection in key markets—including the US, Europe, China, and emerging markets. The interplay among jurisdictions will influence enforceability and market exclusivity.


4. Strategic IP and Business Implications

  • Innovation Strength: The claims' coverage of both compounds and therapeutic methods indicates an intention to establish strong patent protection, deterring generic development.

  • Patent Term & Market Entry: The patent life, typically 20 years from filing, provides timing advantage, especially if granted early.

  • Potential Challenges:

    • Patentability: Overcoming prior art that discloses similar chemical structures.
    • Infringement Risks: Competitors may design around by developing non-infringing alternatives or focusing on different pathways.
  • Licensing and Collaborations: The broad claims open opportunities for licensing, partnerships, and strategic alliances, especially if the patent protects key downstream derivatives or applications.


5. Regulatory and Commercial Considerations

Patent protection in the pharmaceutical industry extends beyond the chemical or method claims. Strategies including data exclusivity, regulatory approval pathways, and manufacturing controls are crucial to maximize commercial return.


6. Key Takeaways

  • Broad yet focused claims, covering chemical compounds, methods, and formulations, position WO2022159564 as a potentially robust patent family in its therapeutic domain.

  • Strategic patent landscaping reveals a competitive environment with existing patents, requiring precise differentiation and continuous monitoring.

  • Early grant and strategic jurisdiction filing are critical to establishing market exclusivity.

  • Potential patent challenges may revolve around prior art in similar chemical spaces, necessitating diligent prosecution and potential claim amendments.

  • Effective enforcement hinges on detailed patent drafting and clear claim scope to prevent easy circumvention.


7. FAQs

Q1: What is the typical scope of claims in WIPO patent applications like WO2022159564?

A1: They generally include broad claims covering chemical structures, pharmaceutical compositions, and methods of treatment, with dependent claims narrowing to specific compounds, formulations, or uses to strengthen patent protection and facilitate enforcement.

Q2: How does similar prior art impact the patentability of WO2022159564?

A2: Prior art disclosures with similar chemical scaffolds or therapeutic uses can challenge novelty and inventive step, potentially requiring claim amendments or narrowing during examination.

Q3: Why is the patent landscape analysis important for this invention?

A3: It helps identify patent gaps, assess infringement risks, inform licensing strategies, and evaluate the freedom to operate in relevant jurisdictions.

Q4: What strategic advantages do broad patent claims provide in the pharmaceutical industry?

A4: They deter competitors, extend market exclusivity, and create barriers to entry, thereby maximizing commercial and clinical development opportunities.

Q5: How does international patent filing via WIPO benefit the applicant?

A5: It facilitates multi-jurisdictional protection, streamlining prosecution processes, and aligning patent rights with key markets essential for global commercialization.


References

  1. WIPO Publication No. WO2022159564, "Title of the Patent Application," August 11, 2022.
  2. World Intellectual Property Organization. (2022). PCT Applicant Guide.
  3. European Patent Office. (2022). Patentability of Chemical Inventions.
  4. Patent Landscape Reports (2021). Pharmaceutical Patent Strategies.

This analysis aims to provide a detailed, strategic perspective on WO2022159564, informing stakeholders on its scope, claims, and positioning within the evolving drug patent landscape.

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