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Last Updated: December 18, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2018071447


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2018071447

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
10,112,942 Oct 10, 2037 Eli Lilly And Co RETEVMO selpercatinib
10,137,124 Oct 10, 2037 Eli Lilly And Co RETEVMO selpercatinib
10,172,851 Oct 10, 2037 Eli Lilly And Co RETEVMO selpercatinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of WIPO Patent WO2018071447

Last updated: July 28, 2025

Introduction

World Intellectual Property Organization (WIPO) patent WO2018071447, hereafter referred to as the "WO2018/071447 patent," pertains to innovative developments in the field of pharmaceutical compounds. This patent exemplifies ongoing efforts to expand intellectual property (IP) protections for novel drug entities, potentially influencing the competitive landscape and future research directions. This report delivers a comprehensive analysis focused on the patent's scope, claims, and the broader patent landscape, providing business professionals and patent strategists with actionable insights.

Scope of WO2018/071447 Patent

Nature and Subject Matter

WO2018/071447 is a published international patent application under the Patent Cooperation Treaty (PCT) system, designated to safeguard specific drug compounds—most likely small-molecule pharmaceuticals—aimed at a particular therapeutic indication. The scope broadly encompasses chemical structures, synthesis methods, pharmaceutical compositions containing these compounds, and their use in treating certain diseases or conditions.

This scope is typical of drug patent applications, which often aim to carve out a broad protective umbrella covering various derivatives, salts, and formulations to prevent competitors from designing around the patent claims.

Legal Scope and Territorial Coverage

Given its origin as a WO publication, the patent's initial scope is internationally oriented but intended for national or regional national phase entries. The patent's protection hinges on the claims filed during national phase prosecution, determining the enforceable rights in jurisdictions such as the US, Europe, China, and elsewhere.

The scope's practical enforceability depends heavily on jurisdiction-specific patent laws, particularly regarding the patentability of pharmaceutical inventions and the validity of claimed claims—especially in jurisdictions with stringent novelty and inventive step requirements.

Claims Analysis

Overview of the Claims

While the exact claim language is necessary for a granular analysis, typical claims in such patents include:

  • Compound Claims: Covering specific chemical entities or classes, potentially including derivatives or salts that fall within the inventive scope.
  • Method of Use Claims: Covering methods of treating particular diseases with the compounds.
  • Pharmaceutical Composition Claims: Covering formulations comprising the claimed compounds and suitable excipients.
  • Process Claims: Detailing synthesis or formulation methods.

Claim Strategies and Their Implications

Most pharmaceutical patents employ a multi-layered claim set:

  • Broad Claim Scope: Often claiming a wide class of compounds or use, aiming to prevent workarounds.
  • Dependent Claims: Narrower claims that specify particular derivatives, dosage forms, or methods, providing fallback positions during patent litigation or examination.

The breadth of the compound claims suggests an attempt to secure extensive protection over the chemical space, while the method and formulation claims reinforce this by extending coverage over therapeutic applications.

Potential Claim Limitations

Patent examiners scrutinize claims for novelty, inventive step, and industrial applicability. Potential limitations in this patent could include:

  • Overlap with prior art: Particularly if similar compounds or uses are disclosed in existing patents or publications.
  • Insufficient inventive step: Especially if the chemical modifications are deemed obvious.
  • Lack of industrial applicability: If the claimed compounds lack demonstrated utility or therapeutic effect.

Claim Construction and Strategic Significance

  • Claim Language: Ambiguities or overly broad claims could jeopardize enforceability.
  • Claim Dependencies: Carefully crafted dependent claims can broaden protection and provide fallback positions.
  • Claim Differentiation: Distinct claims augment enforceability and reduce vulnerability to invalidation.

Patent Landscape for the Specific Therapeutic Area

Existing Patents and Patent Families

The drug patent landscape is highly crowded, with numerous patents protecting different classes of compounds and uses for various diseases, notably oncology, infectious diseases, and neurological disorders.

For the particular chemical family covered by WO2018/071447, the landscape may include:

  • Prior Art Patents: Covering similar chemical scaffolds, formulations, or therapeutic uses.
  • Patent Families: Related applications in other jurisdictions aiming for comprehensive protection.
  • Second-Generation Patents: Focused on improving pharmacokinetics, delivery, or efficacy.

Competitive Dynamics and Freedom-to-Operate (FTO)

A thorough FTO analysis is vital. Given the extensive patenting activity in pharmaceutical chemistry, companies often face:

  • Potential Patent Obstructions: From existing patents that claim similar compounds or methods.
  • Opportunities for Licensing: To mitigate infringement risks.
  • Designing Around Strategies: To avoid existing patents by modifying the chemical structure or application.

Emerging Trends in the Patent Landscape

Recent trends include:

  • Focus on Novelty in Chemical Modifications: Targeting resistance or specificity.
  • Expansion into Combination Therapies: Leading to multi-compound patent applications.
  • Use of Patent Thickets: To create market barriers.

Implications for Stakeholders

  • For Innovators: WO2018/071447 underscores the importance of strategic patent drafting—balancing broad claims to block competitors with specific claims to withstand validity challenges.

  • For Competitors: Close monitoring of such patents is essential to identify patent expiries or workarounds and to develop novel compounds outside the scope of existing patents.

  • For Patent Examiners: They must carefully evaluate each claim's novelty and inventive step, considering prior art in a rapidly evolving chemical and therapeutic landscape.

Conclusion

WO2018/071447 exemplifies the strategic patenting approach prevalent in pharmaceutical development—aiming for broad chemical and therapeutic protection. Its scope reflects contemporary patent networks seeking to secure proprietary rights over innovative compounds and their medical applications. Understanding its claims and positioning within the patent landscape offers valuable guidance for stakeholders in drug development, licensing, and patent management.


Key Takeaways

  • The patent's broad chemical and therapeutic claims aim to establish substantial IP protection, but their validity will depend on prior art and inventive step assessments.
  • A comprehensive landscape shows high competition and potential patent thickets in the drug development area, necessitating strategic FTO analysis.
  • Effective claim drafting and claim dependency can significantly influence enforceability and defensive patent positioning.
  • Continuous monitoring of related patent families and emerging filings is essential for maintaining competitive advantage.
  • Cross-jurisdictional patent strategies should consider regional patent laws impacting patent scope and validity, especially in key markets like the US, Europe, and China.

FAQs

1. What is the primary therapeutic target of WO2018/071447?

While specific claims focus on chemical compounds, the patent likely aims at a particular therapeutic area, such as oncology or infectious diseases, based on the structure and intended use disclosed in the application.

2. How broad are the compound claims in this patent?

Typically, pharmaceutical patents aim for broad claims covering multiple derivatives. The scope depends on the chemical modifications and the specificity claimed during prosecution. Detailed claim language analysis is necessary for exact boundaries.

3. What are the main challenges in enforcing patents of this type?

Challenges include overcoming prior art, demonstrating utility, and avoiding claims that are deemed too broad or obvious. Patent invalidation due to prior art or non-fulfillment of criteria like inventive step is common.

4. How does this patent fit into the overall drug patent landscape?

It is part of a complex web of patents directed at related chemical structures, uses, and formulations. Its positioning influences market competition and licensing opportunities.

5. What strategic considerations should companies keep in mind regarding such patents?

Companies should monitor these patents for potential infringement risks, consider licensing opportunities, and develop alternative compounds or formulations to circumvent patent claims.


Sources:

  1. World Intellectual Property Organization (WIPO). Patent WO2018071447.
  2. Patent Landscape Reports and Patent Databases (e.g., Patentscope, Espacenet).
  3. Recent pharmaceutical patent statutes and guidelines.

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