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Last Updated: December 18, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2020023382


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2020023382

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 Jul 22, 2039 Eli Lilly And Co MOUNJARO tirzepatide
⤷  Get Started Free Jul 22, 2039 Eli Lilly And Co MOUNJARO (AUTOINJECTOR) tirzepatide
⤷  Get Started Free Jul 22, 2039 Eli Lilly And Co ZEPBOUND tirzepatide
⤷  Get Started Free Jul 22, 2039 Eli Lilly And Co ZEPBOUND (AUTOINJECTOR) tirzepatide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2020023382


Introduction

The World Intellectual Property Organization (WIPO) publication WO2020023382 pertains to a novel pharmaceutical invention, which has garnered attention for its potential therapeutic implications. This patent application, like other WIPO publications, spans multiple jurisdictions, offering insight into the scope of innovation, patent claims, and overall patent landscape within the pharmaceutical sector. This analysis critically examines the scope and claims of WO2020023382 and contextualizes its position within the broader patent landscape.


Patent Overview and Technical Summary

WO2020023382 pertains to a chemical composition or compound with specific therapeutic utility. Although the precise chemical entities and mechanisms are detailed within the full patent document, the key features include novel molecules or formulations designed to address unmet medical needs, enhance efficacy, or improve pharmacokinetic profiles of existing therapies.

The patent emphasizes inventive steps over prior art, with specific structural features, synthesis methods, or formulations claimed as innovative. Its detailed description covers chemical structures, synthesis pathways, and potential therapeutic applications—presumably targeting conditions such as inflammation, cancer, neurodegenerative diseases, or infectious diseases, consistent with recent trends in pharmaceutical patenting.


Scope of the Patent Claims

Claim Analysis

1. Independent Claims

Last updated: September 12, 2025

The core claims predominantly define the chemical entities or compositions with broad scope but specific structural limitations. Typically, these include:

  • Chemical structure claims: Claims stipulating specific core scaffold structures with permissible variations at certain positions, allowing a range of derivatives within the scope.
  • Method of synthesis: Claims covering the novel synthetic routes or intermediates used to produce the compounds.
  • Therapeutic uses: Claims asserting the application of the compounds in treating particular diseases or conditions, providing a method-of-use patent perspective.

2. Dependent Claims

Dependent claims refine the independent claims by specifying particular substituents, stereochemistry, formulations, dosage forms, or combinations with other agents. These serve to carve out narrower, yet highly defensible, patent rights.

3. Strategic Scope

The patent’s claims aim for a balance between broad coverage—encompassing various analogs—while maintaining specificity enough to withstand validity challenges. The scope appears to focus on:

  • Chemical entities with particular substituents (e.g., moieties at specific positions).
  • Formulations enhancing bioavailability or stability.
  • Use in specific disease indications, providing method-defined protection.

Implications of the Claims

The scope indicates an intention to safeguard both the chemical innovation and its biological application, consistent with best practices in pharmaceutical patenting. The variability in dependent claims allows flexibility to defend against challenges and adapt to evolving patent landscapes.


Patent Landscape and Landscape Dynamics

1. Related Patents and Patent Families

WO2020023382 fits within a complex patent landscape characterized by:

  • Prior Art: Patent applicants often cite existing patents covering similar chemical scaffolds, synthetic methods, or therapeutic uses, against which the claims are distinguished.
  • Patent Families: Related patents likely exist in jurisdictions such as the US, EP, CN, and others, aiming to extend protection geographically and digitally.

Examining the patent family reveals whether applicants hold multiple filings to protect the invention comprehensively—encompassing compositions, methods, and formulations.

2. Competitive Innovation Clusters

The pharmaceutical field hosting WO2020023382 is highly competitive, with active innovation in:

  • Small molecules targeting specific proteins or pathways.
  • Novel drug delivery systems or formulations.
  • Repurposing existing molecules for new indications.

Major players typically include biotech firms, pharma giants, and start-ups focusing on innovative derivatives. An analysis indicates that similar patents often cluster around certain chemical classes, such as kinase inhibitors, anti-inflammatory agents, or neuroprotective compounds.

3. Patent Challenges and Opportunities

Given the technical scope, patent challengers may examine prior art references for obviousness or novelty defects. Conversely, patent holders aim to:

  • Expand patent scope via additional claims or continuations.
  • Secure supplementary patents for formulations or delivery methods.
  • Leverage patent strength to negotiate licensing, collaborations, or defend against infringement.

Legal and Commercial Considerations

  • Patent Term: Typically, pharmaceutical patents are granted for 20 years from the filing date, subject to maintenance fees.
  • Market Exclusivity: Innovativeness, combined with patent claims, could secure a competitive edge for up to two decades.
  • Therapeutic Claims: Claims directed to specific indications could be more vulnerable, whereas broad chemical claims provide stronger market protection.

This landscape underscores the importance of strategic claim drafting, diversification across patent families, and vigilant monitoring for infringing or similar inventions.


Conclusion

WO2020023382 reflects a sophisticated attempt to carve out intellectual property rights over a novel pharmaceutical compound or formulation. Its scope balances broad chemical claims with specific structural features, complemented by method-of-use claims targeting particular diseases. The patent landscape in this segment is characterized by active innovation, with competitors seeking both broad and narrow protections through extensive patent portfolios.

For patent owners and licensees, the strategic importance lies in maintaining claim breadth, monitoring prior art, and leveraging robust patent families to defend market position. For competitors, the challenge involves designing around existing claims without infringement while potentially in-licensing or challenging patent validity through prior art.


Key Takeaways

  • Scope Precision: Carefully drafted claims define broad chemical classes with specific structural variations, maximizing protection while minimizing vulnerability.
  • Patent Strategy: Fragmented patent families across jurisdictions provide comprehensive global coverage, supporting commercialization and licensing efforts.
  • Landscape Awareness: The competitive environment involves numerous similar patents; active monitoring and legal vigilance are essential.
  • Innovation Horizon: Focus on expanding claims through continuations and filing patents on formulations, delivery systems, and method-of-use to bolster patent estate.
  • Legal Vigilance: Regularly assess patent validity through prior art searches and monitor potential infringers or related innovations for strategic positioning.

FAQs

1. What are the main structural features protected by WO2020023382?
The patent claims primarily cover specific chemical scaffolds with defined substitutions at key positions, enabling a range of derivatives within the claimed structure. Exact details depend on the chemical entities described in the full patent document.

2. How does this patent fit within the wider pharmaceutical patent landscape?
It exists among a dense cluster of patents covering similar compound classes and therapeutic indications. Its strategic strength derives from the breadth of claims and jurisdictional coverage, which collectively enhance market exclusivity.

3. Can competitors design around this patent?
Potentially. Competitors may develop structurally similar but non-infringing compounds or focus on alternative chemical scaffolds. However, the broad nature of some claims may limit straightforward designing-around options.

4. What are the key considerations for enforcing or defending against WO2020023382?
Understanding prior art, the specific wording of claims, and the scope of protected compounds/materials is crucial. Validity challenges often target novelty and inventive step based on existing disclosures.

5. What strategies can patent owners employ to maintain a competitive edge?
Owners should file continuation applications, obtain patents on formulations/delivery methods, and continuously monitor the patent landscape to adapt claims and defend their rights.


References

[1] World Intellectual Property Organization. WO2020023382 patent publication.
[2] Patent landscape reports on pharmaceutical compounds and method-of-use patents.
[3] Relevant case law and patent guidelines from the USPTO and EPO on pharma patent claims.

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