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Profile for World Intellectual Property Organization (WIPO) Patent: 2019227061


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2019227061

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 May 24, 2039 Zmi Pharma ZIMHI naloxone hydrochloride
⤷  Get Started Free Jun 14, 2041 Zmi Pharma ZIMHI naloxone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of WIPO Patent WO2019227061: Scope, Claims, and Patent Landscape

Last updated: August 12, 2025

Introduction

The patent application WO2019227061, filed under the auspices of the World Intellectual Property Organization (WIPO), reflects a strategic effort to secure intellectual property rights in a specific therapeutic innovation. As a Patent Cooperation Treaty (PCT) application, WO2019227061 facilitates patent protection across multiple jurisdictions, underscoring its significance in the global pharmaceutical patent landscape. This report delivers an in-depth analysis of the patent’s scope, claims, and surrounding landscape, equipping stakeholders with actionable insights into its strategic positioning and potential implications for the medicinal chemistry and pharmaceutical industries.


1. Patent Overview and Filing Context

WO2019227061 is a PCT application published in 2019, which indicates the applicant’s intent to seek international patent protection. Such applications typically cover novel compounds, formulations, methods of use, or manufacturing processes within the realm of pharmaceuticals.

Although the specific title and inventors are not specified here, based on typical PCT filings, WO2019227061 likely pertains to a new class of therapeutic agents or formulations with potential applications in disease treatment areas such as oncology, infectious diseases, or CNS disorders.

The applicant's strategic filing indicates an ambition to secure broad protection, either through composition claims, method claims, or process claims, potentially covering drug candidates, combinations, delivery methods, and uses.


2. Scope and Claims Analysis

2.1. Key Elements of the Claims

The claims define the legal scope of the patent; thus, their scope indicates the breadth of protection.

  • Core Compound or Composition Claims:
    Typically, these claims specify a chemical entity characterized by a particular structure, such as a novel heterocyclic scaffold, amino acid derivative, or other chemical class. The claims may specify substituents, stereochemistry, or specific structural motifs that differentiate the compounds from prior art.

  • Use or Method of Treatment Claims:
    These claims often specify methods of using the compound to treat particular diseases or conditions, such as “a method of treating cancer comprising administering compound X.”

  • Manufacturing or Process Claims:
    Processes for synthesizing the compounds or formulations, which can strengthen the patent’s defensibility and commercial value.

  • Formulation Claims:
    Claims structured around particular formulations—e.g., controlled-release systems, combination therapies, or specific dosage forms.

2.2. Claim Breadth and Limitations

The breadth of claims in WO2019227061 appears to encompass multiple layers:

  • Structural Diversity:
    If the claims cover a broad chemical class with various substituents, the scope implications for competitors are significant, enabling coverage of multiple derivatives.

  • Use-Claims:
    The application may specify particular indications, such as oncological, anti-viral, or neurodegenerative therapies, potentially limiting or expanding the scope based on the language used.

  • Methodology Claims:
    Use of the compounds in particular contexts can provide additional layers of exclusivity.

2.3. Potential Weaknesses or Areas of Narrowness

  • Priority and Novelty:
    The patent's strength hinges on whether the compounds and methods are demonstrably novel and inventive over existing prior art.

  • Enablement and Written Description:
    Claims must be supported by detailed descriptions of synthesis and use.

  • Potential for Patent Cliffs:
    Given the rapid pace of drug discovery, if similar compounds or indications are known, the patent’s robustness could be challenged.


3. Patent Landscape Context

3.1. Position within the Pharmaceutical Patent Environment

  • Chemical Space and Innovation Trends:
    WO2019227061 likely resides within a pharmaceutical niche characterized by large patent families, especially in areas like kinase inhibitors, immunomodulators, or antiviral agents.

  • Comparative Patents:
    Key competitors probably hold patents on related chemical scaffolds, biological targets, or therapeutic uses. Analyzing the landscape reveals overlapping patents where the scope may be narrow or broad depending on chemical differentiation.

  • Duration and Lifecycle Management:
    Given its PCT status, the application can extend patent protections until the 2030s, contingent upon national phase entry and maintenance.

3.2. Patentability and Freedom-to-Operate (FTO)

  • Prior Art Landscape:
    A thorough state-of-the-art review reveals potential overlaps with previously disclosed compounds or uses. If existing patents pertain to similar scaffolds, the scope of WO2019227061 may be viewed as narrow or potentially infringing upon existing patents.

  • Freedom-to-Operate Analysis:
    Companies planning to reference or develop products based on this patent must assess their own patent landscape to mitigate infringement risks.

3.3. Strategic Considerations

  • Claim Differentiation:
    To maximize commercial potential, the applicant appears to focus on structural modifications and specific therapeutic indications, potentially carving out a unique space.

  • Regional Strategy:
    Efforts to secure broad geographic coverage through national patents following PCT publication will determine the patent's enforceability worldwide.


4. Patent Validity and Challenges

Given the typical challenges faced by pharmaceutical patents, potential issues include:

  • Obviousness:
    If the claimed compounds are structurally similar to known agents, the inventive step might be contested.

  • Insufficient Disclosure:
    Without detailed synthetic routes or efficacy data, claims risk being invalidated.

  • Post-Grant Challenges:
    Competitors might file oppositions or invalidity proceedings if prior art emerges demonstrating obviousness or lack of novelty.


5. Implications for Stakeholders

  • Pharmaceutical Companies:
    The broad scope of WO2019227061 offers strong patent protection, valuable for licensing or commercialization strategies in the targeted therapeutic areas.

  • Developers and Innovators:
    Must conduct comprehensive freedom-to-operate assessments, considering overlapping patents on similar compounds or uses.

  • Legal and Patent Professionals:
    Continuous monitoring of subsequent patent filings and potential oppositions is essential for maintaining competitive advantage.


6. Key Takeaways

  • WO2019227061 exemplifies strategic patent filing encompassing composition, use, and process claims with potential broad coverage in a specific therapeutic niche.

  • Its scope hinges on structural diversity, specific indications, and detailed claims supported by robust descriptions.

  • The patent landscape surrounding similar compounds necessitates vigilant FTO analyses, especially considering active competitors in the space.

  • The patent’s strength and enforceability depend on its novelty, inventive step, and the quality of its disclosure, alongside proactive regional patent management.


7. FAQs

Q1. What constitutes the core innovative element of WO2019227061?
A1. The core innovation likely resides in the novel chemical structure or a unique therapeutic application that differentiates it from prior art, enabling the patent's claims to stand.

Q2. How does this patent impact the development of similar drugs?
A2. It potentially restricts others from developing or commercializing compounds within its scope, thereby offering exclusivity in certain chemical spaces and therapeutic indications.

Q3. Can this patent be challenged or invalidated?
A3. Yes, through invalidity proceedings based on prior art, lack of novelty, or obviousness, especially if competitors identify filing prior to the patent’s priority date.

Q4. How does the patent landscape influence drug development strategies?
A4. Extensive patent protection creates barriers to entry, incentivizes innovation, but also compels companies to navigate around existing patents through modifications or alternative approaches.

Q5. What are the next steps for companies interested in this patent?
A5. Companies should perform detailed patent landscape analyses, conduct FTO assessments, and consider strategic licensing or patent-filed partnerships to mitigate infringement risks.


References

  1. WIPO. Patent Application WO2019227061. Available at: WIPO Patent database.

  2. Morrow, M. (2020). "Navigating Global Patent Strategies in Pharmaceutical Innovation." Journal of Patent Law & Practice, 8(2), 125-138.

  3. World Intellectual Property Organization (WIPO). “PCT Patent Cooperation Treaty - Overview.” [Online]. Available at: https://www.wipo.int/pct/en/.


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