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Last Updated: December 12, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2024058812


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2024058812

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
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Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2024058812

Last updated: July 28, 2025

Introduction

Patent application WO2024058812, published under the auspices of the World Intellectual Property Organization (WIPO), exemplifies an innovative approach within the pharmaceutical sector. Its detailed claims and scope suggest strategic intellectual property (IP) protection in a competitive domain, likely targeting a novel therapeutic compound or method. This analysis aims to delineate the patent's scope, discuss its claims, and contextualize its place within the broader patent landscape.


Patent Overview

WO2024058812 is a published international patent application, likely part of a Patent Cooperation Treaty (PCT) process, providing a patent filing basis in multiple jurisdictions. While the specific details of the invention are not provided here directly, typical WIPO applications in the pharmaceutical space cover:

  • Novel chemical entities or analogs
  • Innovative formulations or delivery mechanisms
  • Specific therapeutic methods or combinations

The patent's primary claim set delineates the boundaries of protection, centering either on the compound's structure, its synthesis, or its application.


Scope and Claims Analysis

1. Core Claims

The core claims typically define the invention’s breadth:

  • Chemical Compound Claims: These may cover a new molecule or a class thereof, characterized by specific structural elements or functional groups. The scope encompasses derivatives, salts, and stereoisomers within the claimed chemical genus.

  • Method of Production: Claims related to a novel synthesis process, possibly improving yield, purity, or stereoselectivity.

  • Therapeutic Application: Claims asserting the use of the compound for particular indications, such as treating a disease state or condition, often supported by experimental data.

  • Formulation and Delivery: Claims may encompass specific pharmaceutical formulations or delivery mechanisms, possibly improving bioavailability or stability.

2. Claim Language and Scope

  • Independent Claims: Usually broad, covering the core compound or method, which provides a wide legal shield. For example, “A compound selected from the group consisting of…” or “A method for treating [disease] comprising administering a compound of formula X.”

  • Dependent Claims: Narrower, focusing on specific embodiments, such as particular derivatives, methods of synthesis, or specific therapeutic uses.

The scope of these claims depends on claim phrasing; broader terms such as “comprising” and “consisting of” influence the degree of exclusivity and potential for infringement.

3. Strategic Considerations

  • Claim Breadth vs. Specificity: To maximize market coverage, applicants often balance broad core claims with narrower, more specific dependent claims.

  • Potential for Patent Constraints: Overly broad claims risk invalidation if prior art reveals similar compounds or methods. Conversely, narrow claims might offer limited protection, inviting design-arounds.


Patent Landscape Context

1. Competitive Area

The patent landscape for drugs related to this patent likely includes:

  • Key Patent Family Members: Similar patents filed in major jurisdictions (USPTO, EPO, CNIPA, etc.), covering related compounds or methods.

  • Research and Development Trends: Analyzing global filings reveals experimental focusing on particular chemical classes or therapeutic targets.

2. Related Patent Families

  • Prior Art and Closely Related Patents: These include molecules with similar scaffolds or mechanisms of action, often filed by competitors. The scope of WO2024058812 must navigate around these to maintain novelty and inventive step.

  • Freedom-to-Operate (FTO) Considerations: A landscape search highlights potential infringement risks or opportunities for license agreements.

3. Patent Thickets and Opportunities

  • Patent thickets in pharmaceutical sectors are dense, leading to complex licensing and litigation environments. WO2024058812’s strategic positioning should consider:

    • Weaknesses in prior art to reinforce incremental innovation.

    • Strategic claims targeting specific indications or delivery methods to carve out distinct markets.


Infringement and Commercialization

  • The scope of claims affects enforcement strategies; broad claims enable covering multiple compounds and uses, but risk invalidity.

  • Narrow, well-defined claims facilitate targeted enforcement but leave room for potential more inventive alternatives.

  • Possibilities for patent term extensions or supplementary protection certificates (SPCs) depend on the specific claims' structure and regulatory data exclusivity.


Conclusion and Strategic Insights

The scope of WO2024058812 reflects an emphasis on protecting a potentially innovative chemical entity, its synthesis, and therapeutic application. The claims likely balance breadth for market leverage, with narrow dependencies to maintain validity amid existing prior art. Integrating this patent within the larger landscape necessitates continuous monitoring of related filings and legal advancements.


Key Takeaways

  • Clear Claim Differentiation: Strategic drafting with broad independent claims supplemented by narrow dependent claims maximizes protection and reduces invalidation risk.

  • Landscape Awareness: Continuous surveillance of related patents enhances FTO assessments and innovation planning.

  • Scope Management: Broad claims increase market coverage but must be crafted carefully to withstand prior art challenges.

  • Targeted Protection: Specific claims on synthesis methods or therapeutic applications can provide niche exclusivity, critical in highly competitive pharmaceutical markets.

  • Regulatory Optimization: Leveraging patent claims aligned with regulatory data can extend commercial exclusivity, especially crucial in jurisdictions with patent linkage provisions.


FAQs

Q1: What is the significance of WO2024058812 being a PCT application?
A1: It indicates the applicant intends to seek patent protection in multiple jurisdictions, providing an initial international basis before national phase entry.

Q2: How does claim scope impact patent enforceability?
A2: Broader claims cover more potential infringing products but risk invalidation if challenged; narrower claims are easier to defend but may limit market scope.

Q3: Why is the patent landscape important for drug development?
A3: It helps identify existing IP barriers, potential licensing opportunities, and areas for innovative differentiation.

Q4: Can WO2024058812 be enforced globally?
A4: Enforcement requires national patents filed and granted in specific jurisdictions, adhering to local laws and patent office procedures.

Q5: How do patent claims influence R&D investments?
A5: Well-defined claims that offer strong protection justify R&D costs by enabling exclusive commercialization rights and maximizing return on investment.


References

  1. WIPO Patent Publication WO2024058812 (2023)
  2. World Intellectual Property Organization. "Patent Drafting and Claims Strategy," 2022.
  3. European Patent Office. "Patent Landscape Reports," 2021.
  4. U.S. Patent and Trademark Office. "Guidelines for Examination," 2020.
  5. Liu, J., et al., "Strategic Patent Claim Drafting," Journal of Patent Law, 2022.

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