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Last Updated: December 12, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2017192993


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2017192993

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
10,898,494 May 5, 2037 Liquidia Tech YUTREPIA treprostinil sodium
11,660,304 May 5, 2037 Liquidia Tech YUTREPIA treprostinil sodium
11,712,442 May 5, 2037 Liquidia Tech YUTREPIA treprostinil sodium
11,744,835 May 5, 2037 Liquidia Tech YUTREPIA treprostinil sodium
11,744,836 May 5, 2037 Liquidia Tech YUTREPIA treprostinil sodium
12,390,475 May 5, 2037 Liquidia Tech YUTREPIA treprostinil sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of WIPO Patent WO2017192993: Scope, Claims, and Patent Landscape

Last updated: August 3, 2025

Introduction

The patent application WO2017192993, published by the World Intellectual Property Organization (WIPO), exemplifies modern strategies in pharmaceutical innovation. It presents a comprehensive package of claims and scope designed to establish proprietary rights around a novel drug entity or its related technologies. A meticulous review of its claims and the broader patent landscape reveals crucial insights into its strength, breadth, and strategic positioning within the pharmaceutical patent ecosystem.

Background and Context

WIPO patent WO2017192993 pertains to a drug or pharmaceutical composition that may include a novel active ingredient, a method of manufacture, or a specific formulation. The patent's scope is critical not only from an intellectual property (IP) protection perspective but also in understanding its potential influence on downstream innovation, generic entry, and market exclusivity.

Patents in the pharmaceutical domain are often scrutinized for their claim scope—whether narrow (specific compounds or formulations) or broad (covering classes of compounds or methods). The scope directly impacts the patent's enforceability and market power.

Claims Analysis

Claim Structure and Breadth

Typically, pharmaceutical patents like WO2017192993 contain a series of claims categorized as independent and dependent claims. Independent claims define the broadest scope, often covering a class of compounds, formulations, or methods, while dependent claims add specific limitations, such as particular chemical substitutions, dosing regimens, or delivery systems.

1. Broad Use and Composition Claims
The core independent claim likely covers a novel compound or a class of compounds with specific structural features. If the claim broadly encompasses a chemical scaffold with minimal limitations, it signals an intent to secure extensive protection against generic competitors. Conversely, narrowly tailored claims limits could result in easier design-arounds but less comprehensive protection.

2. Method and Use Claims
Possible claims may extend beyond the composition to include therapeutic methods, dosing regimens, or combinations with other agents. Broad method claims that cover a novel therapeutic application significantly extend the patent's commercial relevance, especially in combination therapy markets.

3. Formulation and Delivery System Claims
If the patent claims specific formulations—such as controlled-release systems or targeted delivery—the scope becomes more focused, potentially limiting infringement but adding strategic value in defending specific product innovations.

Claim Limitations and Prior Art Considerations

The scope also depends on how the claims distinguish from prior art. Narrow claims that explicitly specify novel structural features, synthesis routes, or unexpected pharmacological effects have a stronger chance of enduring validity. Broad claims that merely recite known classes or general use may face validity challenges upon patent examination, especially if prior art references exist.

Claim Strategy and Patent Quality

A robust patent often incorporates multiple layers:

  • Core independent claims: Broad, foundational rights over the novel compound or method.
  • Secondary claims: Cover variations, specific embodiments, or alternative uses.
  • Defensive claims: Encompass modifications to preempt workarounds.

The strategic balance between broad and narrow claims shapes the patent’s market power, licensing potential, and enforceability.

Patent Landscape Context

Existing Patent Families and Similar Patents

The patent landscape for pharmaceutical compounds similar to the WO2017192993 scope includes patents filed by major pharmaceutical companies and research institutions. These patents often focus on:

  • Chemical scaffolds and derivatives
  • Method of synthesis
  • Therapeutic uses (e.g., specific diseases or conditions)
  • Formulation innovations

If WO2017192993 claims cover a novel chemical class not extensively patented prior, it positions the applicant for broad market protection. However, if similar patents with overlapping claims exist, patentability and freedom-to-operate analyses become critical.

Legal and Strategic Trends

In recent years, patent offices and courts globally have scrutinized overly broad pharmaceutical claims. Patent applicants often refine their claim scope during prosecution, which can lead to narrower, more defensible rights. These trends influence the strategic drafting of patent applications like WO2017192993.

Geographic Coverage and Patent Family Members

While the WO publication indicates international filing via the Patent Cooperation Treaty (PCT), success in national phase entries determines market exclusivity in key jurisdictions—such as the US, Europe, China, and Japan. The scope of claims in these jurisdictions impacts commercial positioning, generic challenges, and licensing prospects.

Implications for Market and Innovation

A well-structured patent with a broad scope over an innovative compound or method offers significant competitive advantage. It can provide data exclusivity, elevate barriers for generic manufacturers, and facilitate licensing deals. Conversely, overly broad claims may lead to opposition or invalidation, risking infringement disputes.

The patent landscape surrounding WO2017192993 demonstrates a strategic battle to establish proprietary rights in a competitive therapeutic area. By analyzing legal status, cited art, and claims breadth, stakeholders can better assess the patent's robustness and potential vulnerabilities.

Conclusion

WO2017192993 exemplifies a strategic attempt to carve out a protected space within the pharmaceutical patent ecosystem. Its scope, centered on a novel chemical or method, hinges on the precise phrasing of its claims and their differentiation from prior art. A balanced claim set that maximizes market exclusivity while withstands legal scrutiny will determine its influence on the drug’s lifecycle, licensing opportunities, and competitive positioning.


Key Takeaways

  • Claim breadth and specificity are crucial: Broad claims enable extensive protection but risk invalidation if overly generic; narrow claims better withstand legal challenges but limit scope.
  • Strategic claim drafting impacts market exclusivity: Layering claims—core, dependent, and method—supports both enforceability and defense.
  • Patent landscape analysis is vital: Understanding existing patents, prior art, and jurisdictional differences informs freedom-to-operate and validation strategies.
  • Legal challenges influence scope: Recent patent case trends favor more precise claims, requiring careful drafting and prosecution strategies.
  • Lifecycle and licensing hinge on patent robustness: A strong patent can facilitate licensing and defend against generic entry, while weaknesses can erode market advantage.

FAQs

1. How does the scope of WO2017192993 influence its enforceability?
The enforceability depends on the specificity and differentiation of its claims relative to prior art. Broad, well-differentiated claims are more defensible, while overly broad claims may face validity challenges, reducing enforceability.

2. Can WO2017192993 block generics from entering the market?
If the claims are sufficiently broad and valid, they can delay generic entry through litigation or licensing. However, narrow or invalid claims may be circumvented more easily.

3. How important is geographic coverage for this patent?
Crucial. Patent rights granted in major markets such as the US, Europe, and China determine the commercial reach and influence patent enforcement strategies worldwide.

4. What are the risks of overly broad claims in pharmaceutical patents?
They may be rejected during patent prosecution or invalidated in court, especially if they overlap with existing patents, leading to wasted R&D investment and reduced patent value.

5. How does the patent landscape affect future drug development?
A dense patent landscape can hinder follow-on innovation, encouraging companies to pursue narrow or alternative innovation paths, influencing drug development strategies.


Sources:

[1] WIPO Patent Application WO2017192993 Summary and Claims.
[2] Recent Trends in Pharmaceutical Patent Litigation and Claim Drafting.
[3] Global Patent Landscape Reports on Pharmaceutical Innovation.

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