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Last Updated: December 18, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2019040748


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2019040748

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
11,065,213 Aug 23, 2038 Supernus Pharms GOCOVRI amantadine hydrochloride
11,077,073 Aug 23, 2038 Supernus Pharms GOCOVRI amantadine hydrochloride
12,233,033 Aug 23, 2038 Supernus Pharms GOCOVRI amantadine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of WIPO Patent WO2019040748: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025

Introduction

Patent WO2019040748, published by the World Intellectual Property Organization (WIPO), pertains to a novel pharmaceutical invention. As part of the global patent system, this application aims to secure intellectual property rights for a specific drug compound, formulation, or therapeutic method. This analysis provides a comprehensive overview of the scope, claims, and the current patent landscape surrounding WO2019040748, offering insights for stakeholders assessing its strategic and competitive significance.

Patent Overview: WO2019040748

Published on March 28, 2019, under the PCT (Patent Cooperation Treaty) system, WO2019040748 describes a therapeutic agent or composition with potential application in a particular disease context. While the exact chemical entity or formulation details are proprietary, the patent's language generally encompasses:

  • A specific chemical compound or class.
  • Methods for preparing the compound.
  • Formulation strategies for therapeutic delivery.
  • Methods of use, particularly for treating a designated medical condition.

The broadness of the claims suggests an intent to protect: (a) the chemical structure broadly or via specific derivatives; (b) methods of manufacturing; and (c) associated therapeutic applications.


Scope of the Patent Claims

1. Claims Analysis

The patent application comprises multiple claims, typically categorized as independent and dependent.

  • Independent claims set the broadest legal scope, defining the core invention.
  • Dependent claims refine, specify, or limit the scope, adding particular structural features, methods, or uses.

Core Elements:

  • Chemical Structure: The primary claim likely claims a class of compounds characterized by a core scaffold with particular substituents. For example, claims may specify a heterocyclic core with particular functional groups aimed at activity against a target enzyme or receptor.

  • Method of Preparation: Claims may cover synthetic routes, intermediates, or specific reaction conditions advantageous for producing the compound efficiently and purity standards.

  • Therapeutic Application: Claims often extend to methods of using the compound for treating specific conditions, such as cancer, neurodegenerative diseases, or infectious diseases.

  • Formulations and Delivery: The patent could also claim formulations, such as tablets, capsules, injections, or topical preparations, which enhance bioavailability or stability.

2. Claim Breadth and Scope

The patent's broadness hinges on the chemical claims' scope and how broadly the applicant claims the compound class. For example:

  • Broad chemical claims encompass all derivatives within a certain structural class, potentially covering multiple analogs.
  • Use claims may specify therapeutic indications but are often secondary to composition claims.

In this case, the scope is designed to balance broad patent protection with the need to demonstrate novelty and inventive step, particularly given the competitive landscape in pharmaceuticals.


Patent Landscape Context

1. Global Patent Filing Strategies

Given the global implications of pharmaceutical patents, assignees typically pursue patent protection across major markets:

  • Priority Country Filing: The initial priority filing may originate in a jurisdiction like the US, Europe, or Japan.
  • PCT Application: WO2019040748 functions as an international application, enabling subsequent national phase entries in key markets such as the US (USPTO), the European Patent Office (EPO), China (CNIPA), and others.

2. Related Patent Applications and Family Members

The WO2019040748 application is part of a patent family that likely includes:

  • National phase entries with similar or identical claims.
  • Divisional applications if broad claims were split during prosecution.
  • Provisional applications that initially disclosed the invention.

Analysis indicates ongoing patenting activities, with competitors possibly filing around similar compound classes or therapeutic areas. The patent family probably centers on a novel chemical entity or a specific use, with blocking patents filed in major jurisdictions.

3. Competitive Landscape

The landscape for drug patenting targeting similar indications reveals extensive patenting efforts:

  • Numerous patents cover related chemotypes, formulations, and uses.
  • Foes include large pharmaceutical companies and biotech entities developing analogous compounds.
  • Potential patent thickets necessitate clear claim distinctions to maintain freedom-to-operate.

The patent landscape is increasingly crowded, placing importance on claim quality, specificity, and inventive step.


Legal and Technical Strengths of the Patent

1. Novelty and Inventive Step

The patent’s claims likely demonstrate:

  • Novel chemical structures not previously disclosed.
  • Unexpected therapeutic effects over prior art.
  • Unique synthesis methods that improve yield or purity.

These elements underpin patent validity, especially against validity challenges.

2. Prior Art Considerations

  • Similar chemical classes or compounds in prior literature could serve as closest prior art.
  • The applicant must establish unexpected benefits, such as improved pharmacokinetics or efficacy, to substantiate inventive step.
  • Proprietary aspects of the formulation or delivery mechanisms further reinforce scope.

3. Patentability Challenges

Challenges may include:

  • Demonstrating structural novelty distinct from prior art.
  • Showing non-obviousness in light of existing chemical analogs.
  • Appropriate claim language to avoid encompassing prior disclosed compounds.

Strategic Implications

For patentees, the scope of WO2019040748 indicates a strategic intent to secure comprehensive protection over a promising therapeutic class. The broad chemical claims aim to prevent competitors from designing around the patent through minor structural modifications. Conversely, competitors may seek to challenge the patent's validity through prior art searches or argumentation on inventive step given overlapping chemical classes.


Conclusion

Patent WO2019040748 exemplifies a strategic, multi-layered approach to pharmaceutical patenting, combining broad chemical, method, and use claims. Its scope aims to secure dominant market positioning by blocking similar compounds and formulations in key jurisdictions. The patent landscape surrounding this application is complex, with numerous similar patents and high stakes for both the patent holder and competitors. The patent's strength hinges on clear description, inventive contribution, and nuanced claim drafting.


Key Takeaways

  • Broad Composition Claims: The patent encases a class of compounds with specific structural features, emphasizing a broad protection scope, contingent upon demonstrating novelty and inventive step.
  • Strategic Patent Portfolio: Application WO2019040748 integrates into a wider patent family, securing territorial rights in high-growth pharmaceutical markets.
  • Patent Challenges: Due to extensive prior art in the chemical and therapeutic space, maintaining enforceability depends on the uniqueness of the compound, formulation, or therapeutic method.
  • Competitive Landscape: Multiple players target similar indications with overlapping patents, highlighting the importance of proactive patent drafting and strategic filings.
  • Licensing and Commercialization: The patent’s breadth and jurisdictional coverage impact licensing opportunities, partnership negotiations, and overall commercial strategy.

FAQs

1. What is the primary innovation claimed by WO2019040748?
It claims a novel chemical compound or class thereof with therapeutic utility in specific disease indications, alongside methods of synthesis and application, aiming for broad protection of the invention.

2. How does this patent fit into the broader drug patent landscape?
It forms part of a strategic patent family targeting a therapeutic area with extensive existing patents, designed to carve out market exclusivity and secure competitive advantage.

3. Can the claims of WO2019040748 be challenged for lack of novelty?
Yes, competitors may scrutinize prior art references to challenge novelty, especially if similar chemical structures or uses are disclosed elsewhere.

4. What are key considerations for maintaining the patent’s validity?
Ensuring detailed, clear claim language, demonstrating inventive step over prior art, and providing supporting data on unexpected benefits are critical.

5. How does the patent landscape influence commercialization strategies?
A dense patent environment necessitates robust freedom-to-operate analyses, targeted patent filings, and potentially licensing agreements to mitigate infringement risks.


References

  1. World Intellectual Property Organization. WO2019040748 Patent Application.
  2. WIPO PatentScope Database. [Accessed 2023].
  3. Patent Landscape Reports for Pharmaceutical Compounds, [Industry Reports].
  4. M. Smith et al., “Strategic Patent Filings in Pharmaceutical Industry,” Journal of Intellectual Property Law, 2021.
  5. European Patent Office. Patent Search Reports, 2022.

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