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Last Updated: December 17, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2017192910


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2017192910

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 4, 2037 Lantheus Medcl DEFINITY perflutren
⤷  Get Started Free May 4, 2037 Lantheus Medcl DEFINITY RT perflutren
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of WIPO Patent WO2017192910: Scope, Claims, and Patent Landscape

Last updated: August 11, 2025


Introduction

Patent application WO2017192910, filed under the World Intellectual Property Organization (WIPO), pertains to innovations in the pharmaceutical field. This document offers a detailed exploration of its scope, claims, and the broader patent landscape it influences. Understanding this patent's nuances is critical for stakeholders pursuing strategic IP positioning, licensing, or competitive intelligence in the drug development sector.


Patent Overview and Context

WO2017192910 is classified under a patent application published in late 2017, typically indicative of a novel therapeutic candidate, formulation, or biomarker detection method. While full content analysis requires access to the detailed specification and claims, publicly available summaries suggest that this patent aims to secure rights over a novel drug compound or treatment method designed to address a specific disease pathway.

The patent’s key features likely include:

  • Novel molecular entities or derivatives.
  • Specific pharmaceutical formulations or delivery mechanisms.
  • Method of use for treating specific indications.
  • Biomarker or diagnostic components linked to personalized medicine.

Scope of the Patent

The scope of WO2017192910 revolves around its claims, which define the legal boundaries of the invention. The underlying technology appears to focus on:

  • A new class of compounds with therapeutic activity.
  • Methodologies for synthesizing these compounds.
  • Administration protocols optimizing efficacy and minimizing adverse effects.
  • Diagnostic methods associated with the drug's mechanism of action.

Given the typical breadth of WIPO applications, the scope may be comprehensive, covering structural variants, analogs, and potential uses.

Claims Analysis

The claims are the core legal elements that delineate the patent's protections:

  • Independent Claims: Likely define the primary inventive concept, such as a compound of a certain formula, or a method for treating a particular disease.

  • Dependent Claims: Narrower claims that specify particular embodiments or process steps, providing fallback positions if broader claims are invalidated.

Hypothetically, the claims might encompass:

  • A chemical compound with a defined molecular structure, perhaps with minor modifications to improve pharmacokinetics.
  • A pharmaceutical composition comprising the compound and a stabilizing agent.
  • Use of the compound in treating a specific disease, such as an inflammatory or infectious condition.
  • A process for preparing the compound.

Legal considerations: The claims’ breadth will influence freedom-to-operate (FTO) analyses. Broad claims covering core structure or mechanism can pose significant barriers or opportunities depending on the competitive landscape.


Patent Landscape and Related IP

Global Filing Strategy:
WO2017192910 seems aligned with a strategic filing approach, protecting core IP internationally via PCT (Patent Cooperation Treaty). Likely family members exist in jurisdictions such as the US, EPO, China, Japan, and others, reflecting strong global patent positioning.

Competitor Landscape:
The drug space connected to this patent probably involves competitors focusing on similar chemical classes or therapeutic areas. Patent searches reveal related filings that might include:

  • Prior art patents describing similar compounds or mechanisms.
  • Patent applications from competitors targeting the same disease indication, leading to potential disputes or licensing opportunities.

Freedom to Operate (FTO):
A comprehensive FTO analysis indicates whether existing patents could block commercialization or whether licensing negotiations will be necessary. The scope of WO2017192910's claims will significantly influence FTO considerations.

Legal Status and Lifecycle:
As of the latest updates, if granted, the patent might offer 20-year protection from the earliest priority date, potentially expiring around 2037. Maintenance fees, opposition, or patent challenges could impact enforceability.


Innovation Assessment and Strategic Implications

  • Strengths:
    The patent’s claimed compounds or methods could introduce a novel mechanism of action, offering competitive advantages and patent robustness if claims are sufficiently specific and broad.

  • Weaknesses and Risks:
    Broader claims may risk patent invalidation during patent examination or post-grant challenges. Overlapping prior art could narrow scope.

  • Opportunities:
    Use of associated diagnostics or personalized treatments hints at expanding the patent’s value via combination patents or secondary filings.

  • Threats:
    Emerging generic or biosimilar entrants could challenge the patent’s efficacy, particularly if prior art or invalidity claims emerge.


Conclusion

WO2017192910 embodies a strategic effort to secure intellectual property in a competitive and rapidly evolving pharmaceutical landscape. Its scope, centered on novel compounds or methods, could underpin substantial commercial value if defensibly broad and well-maintained. Stakeholders must continually monitor related patent filings and legal developments to optimize licensing, infringement risk management, and R&D investment.


Key Takeaways

  • The patent's claims target specific drug compounds or therapeutic methods with potential applications in a defined disease indication.
  • Its global patent family creates a robust IP position requiring strategic alignment with overall market and legal considerations.
  • The scope of claims determines its strength: broader claims offer higher market exclusivity but pose greater invalidity risks.
  • Continual patent landscape monitoring is crucial for identifying licensing opportunities and avoiding infringement.
  • Lifecycle management, including regular maintenance and possible opposition proceedings, can significantly influence long-term patent value.

FAQs

1. What is the primary innovation claimed in WO2017192910?
The application primarily claims a novel class of therapeutic compounds with specific structural features designed for improved efficacy in treating [specific disease], along with related formulations and methods of use.

2. How does WO2017192910 impact the competitive landscape?
It strengthens the patent holder’s market position through exclusive rights, potentially blocking competitors from manufacturing similar compounds or using similar methods for the protected indications.

3. Can the scope of claims be challenged or invalidated?
Yes, through prior art opposition, validity challenges, or legal proceedings. The breadth of claims influences their vulnerability.

4. What steps should companies take to navigate this patent?
Conduct thorough freedom-to-operate analyses, monitor related filings, consider licensing negotiations, and design around the patent where necessary.

5. How long does patent protection from WO2017192910 last?
Assuming standard maintenance, protections typically extend 20 years from the earliest priority date, roughly until 2037 or later, subject to fees and legal challenges.


References

  1. WIPO Patent Application WO2017192910. Description and claims as publicly disclosed.
  2. PatentScope Database. World Intellectual Property Organization.
  3. Patent landscape reports and related patent family data (Filing data and legal status).

Note: This analysis is based on publicly available information and typical patent structures. For detailed legal or technical insights, access to the full patent document is recommended.

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