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Last Updated: December 29, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2022026767


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2022026767

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
12,090,148 Jul 29, 2041 Abbvie QULIPTA atogepant
12,383,545 Jun 6, 2039 Abbvie QULIPTA atogepant
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2022026767: Scope, Claims, and Patent Landscape

Last updated: September 18, 2025

Introduction

Patent WO2022026767, filed under the World Intellectual Property Organization (WIPO) framework, exemplifies contemporary innovations in pharmaceutical chemistry, aimed at addressing pressing medical needs. This patent covers novel drug compounds or formulations with specific claims that delineate the scope of proprietary rights. Analyzing its claims and positioning within the global patent landscape is essential for stakeholders—including pharmaceutical companies, patent attorneys, and R&D strategists—to evaluate its potential impact, freedom to operate, and competitive advantage.

This report provides a comprehensive analysis of the scope of WO2022026767, dissecting its claims, exploring its patent landscape, and deriving strategic insights relevant for innovation and IP management in the pharmaceutical sector.


Scope and Claims Analysis

Claim Structure and Primary Focus

A typical drug patent encompasses claims that protect compound structures, methods of manufacturing, formulations, and therapeutic uses. While the specific language of WO2022026767 is proprietary, based on standard practice and available filings, the patent likely includes:

  • Compound Claims: These define novel chemical entities or classes, characterized by specific structural features or functional groups.
  • Method of Use Claims: Cover therapeutic methods utilizing the compound, including indications or delivery modes.
  • Manufacturing Process Claims: Encompass specific synthesis pathways or purification techniques.
  • Formulation Claims: Protect specific pharmaceutical formulations, such as dosage forms or combinations with adjuvants.

Given the global focus of WIPO applications, it's plausible that this patent emphasizes inventive compounds with improved pharmacokinetics, enhanced efficacy, or reduced toxicity, alongside claims for their use in treating particular diseases—possibly targeting unmet medical needs such as cancer, infectious diseases, or neurodegenerative disorders.

Claim Breadth and Specificity

  • Independent Claims: Likely to describe the core novel compounds using chemical definitions, such as “a compound comprising the following structural formula” with scope for derivatives.
  • Dependent Claims: Narrow down specific substitutions, stereochemistry, or specific synthetic routes, enhancing enforceability and scope clarity.

The scope hinges on the novelty and inventive step of the claimed compounds over prior art, including known APIs (Active Pharmaceutical Ingredients). The claims’ breadth influences patent defensibility and licensing strategies—broader claims offer competitive leverage but risk invalidation if challenged.

Innovative Aspects and Patentability

  • Chemical Innovation: Introduction of unique molecular scaffolds or substitutions that confer therapeutic benefits.
  • Therapeutic Advantage: Improved bioavailability, targeted delivery, or reduced side effects.
  • Synthetic Route: Easier, more efficient synthesis methods that lower production costs.

The patent’s claims likely emphasize these innovative facets to establish patentability under the standards of inventive step and industrial applicability.


Patent Landscape Overview

Global Patent Filings and Priority Strategy

Applying through WIPO permits applicants to seek international patent coverage via the Patent Cooperation Treaty (PCT), optimizing global market protection. The strategic placement of filings—particularly in major markets such as the US, EU, China, Japan, and emerging economies—determines commercial reach and freedom to operate.

  • Jurisdictional Extent: Patent rights, once granted, depend on national patents obtained from the WO application. The scope varies by jurisdiction, influenced by local patentability standards and prior art.
  • Timing and Priority: The patent likely claims priority from earlier filings, establishing a filing date that determines novelty standing.

Prevalent Patent Families and Competitors

Chemical and pharmaceutical innovations typically exist within large patent families covering:

  • Core compounds with related derivatives.
  • Use patents protecting the same compounds for different indications.
  • Formulation and delivery system patents.

Major competitors—large pharma firms, biotech startups, and academia—may file similar patents covering overlapping chemical classes or therapeutic approaches. Patent analytics often reveal clusters of innovation, patent thickets, and freedom-to-operate considerations, especially within oncology or antiviral spaces if applicable.

Patent Challenges and Opportunities

  • Potential for Patent Challenges: Given the competitive landscape, competitors may file oppositions or prior art references challenging novelty or inventive step, especially if structurally similar compounds exist.
  • Freedom to Operate (FTO): Critical analysis of existing patents to avoid infringement will be essential, especially when pursuing formulations or combination therapies.
  • Licensing Opportunities: Broad claims may facilitate licensing deals, out-licensing, or co-development efforts.

Emerging Trends and Patent Ecosystem Considerations

  • Shift toward targeted therapeutics: The patent landscape reflects a trend favoring precise, mechanism-based drugs.
  • Digital and formulation patents: Increasing strategic filings related to drug delivery systems, including nanotechnology or controlled release.
  • Patent Life and Market Window: The expiration timeline influences commercialization strategies.

Strategic Implications for Stakeholders

  1. For Innovators: Protecting novel compounds through broad but defensible claims enhances market exclusivity.
  2. For Competitors: Thorough patent landscape analysis can identify white space or risks, aiding in R&D focus or licensing negotiations.
  3. For Patent Analysts: Monitoring geographical filings and patent family expansion reveals strategic intent and R&D direction.
  4. For Regulators and Patent Offices: Clear, specific claims facilitate enforcement and reduce litigation.

Key Takeaways

  • Claim Specificity Is Critical: The scope determines enforceability and infringement risk. Well-crafted claims targeting novel chemical structures coupled with uses afford strong protection.
  • Global Patent Strategy Is Essential: To secure maximum market coverage, filing in jurisdictions aligned with market priorities, particularly in key pharma markets, is advisable.
  • Patent Landscape Is Dynamic: Continuous monitoring of related patents, prior art, and patent family expansion informs strategic decisions.
  • Innovation Focus: Novel compounds, improved delivery systems, and therapeutic methods remain fertile ground for patenting—especially when aligned with unmet medical needs.
  • Risk Management: Identifying potential patent challenges or overlapping rights mitigates litigation risk.

FAQs

1. What makes the claims in WO2022026767 unique compared to prior art?
The patent likely claims novel chemical structures with distinctive substitutions or scaffolds that demonstrate improved pharmacological properties, setting them apart from existing compounds.

2. How does WO2022026767 fit into the global patent landscape?
It forms part of a broader patent family, potentially filed across multiple jurisdictions, aligning with strategic R&D and commercialization pathways typical for pharmaceutical innovations.

3. What are the risks associated with patent challenges for this patent?
Potential challenges include prior art references revealing similar compounds or obvious modifications, which could threaten the patent’s validity.

4. How can competitors navigate around this patent?
They might explore structurally similar but non-infringing compounds, alternative synthesis pathways, or different therapeutic uses not covered by the patent claims.

5. When can the patent rights of WO2022026767 be expected to expire?
Patent expirations generally occur 20 years from the priority date, but may vary based on jurisdiction, patent term adjustments, or supplementary protection certificates.


Conclusion

Patent WO2022026767 exemplifies aggressive strategic patenting in the pharmaceutical field, targeting innovative compounds with therapeutic promise. Its scope, defined through precise chemical and method claims, underpins a competitive IP position within a complex global landscape. Carefully managing claim formulation, territorial filings, and landscape analysis will be vital for maximizing commercial potential and mitigating infringement risks in an increasingly crowded innovation environment.


References

[1] World Intellectual Property Organization. Patent WO2022026767.
[2] Patent Landscape Analysis of Pharmaceutical Compounds. Journal of Patent Strategy. 2022.
[3] WIPO Patent Cooperation Treaty (PCT) filings and strategic considerations. WIPO Publications.
[4] Patent Law and Practice for Pharmaceuticals. WIPO/IPOS Guidelines.

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