Last Updated: May 11, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2017214470


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2017214470

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
⤷  Start Trial Jun 9, 2037 Progenics Pharms Inc PYLARIFY piflufolastat f-18
⤷  Start Trial Jun 9, 2037 Aphelion PYLARIFY TRUVU piflufolastat f-18
⤷  Start Trial Jun 9, 2037 Progenics Pharms Inc PYLARIFY piflufolastat f-18
⤷  Start Trial Jun 9, 2037 Aphelion PYLARIFY TRUVU piflufolastat f-18
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2017214470: Scope, Claims, and Patent Landscape

Last updated: August 5, 2025

Introduction

Patent WO2017214470, published under the World Intellectual Property Organization (WIPO) Patent Cooperation Treaty (PCT), pertains to innovative advancements in pharmaceutical compositions. This patent exemplifies the global push toward novel drug development, emphasizing the importance of robust patent protection to secure competitive advantages and foster innovation.

This report provides a comprehensive analysis of the scope, claims, and the patent landscape surrounding WO2017214470, equipping stakeholders with insights necessary for strategic decision-making in the pharmaceutical sector.


Patent Overview and Technical Field

WO2017214470 relates to a novel pharmaceutical compound or composition. The patent's primary focus is on a specific chemical entity, potential therapeutic applications, and related formulations. The patent delineates innovative structural features addressing unmet medical needs, e.g., enhanced efficacy, reduced side effects, or improved bioavailability.

The technical field primarily encompasses medicinal chemistry, pharmacology, and drug delivery systems, with likely applications in areas such as oncology, neurology, or infectious diseases, depending on the detailed chemical structures disclosed.


Scope of the Patent

1. Chemical Entities and Variability

The scope encompasses chemical compounds with specific structural motifs, often represented via a core scaffold with variable substituents. The scope is defined by:

  • The core structure with permissible modifications
  • Specific combinations of substituents and functional groups
  • Stereochemistry considerations
  • Novelty over prior art

By defining a chemical family, the patent aims to cover not only the primary compound but also a broad class of derivatives, thereby extending the patent's breadth.

2. Therapeutic and Formulation Aspects

The patent extends to:

  • Pharmaceutical compositions incorporating the compounds
  • Methods of treatment for particular diseases or conditions
  • Delivery mechanisms—such as sustained-release formulations or targeted delivery systems

The therapeutic claims are tailored to specific indications, possibly involving diseases with significant clinical unmet needs.

3. Patent Claims—Structure and Focus

Patent claims are carefully crafted to balance breadth and specificity, typically categorized into:

  • Composition claims: Covering the chemical compounds and their variants
  • Method claims: Encompassing methods of synthesizing the compounds or administering them for specific indications
  • Use claims: Patents claiming the use of these compounds in particular therapeutic contexts

Claim Scope Analysis:

  • Independent claims likely cover the core chemical structure with broad coverage over substitutes.
  • Dependent claims specify particular embodiments, such as specific substituents, stereochemistry, or formulation techniques, narrowing the scope but adding defensibility.

The scope mitigates risks of invalidation by prior art while widening potential coverage for derivatives.


Claims Analysis

1. Composition Claims

Claims typically define the compound by structural formula, e.g., a general formula with variable groups:

  • Core scaffold with R1, R2, R3 substituents
  • Specific heteroatoms or functional groups

These claims aim to cover a family of compounds sharing key structural features, maximizing market exclusivity.

2. Method of Synthesis

Claims in this category detail specific synthetic routes, potentially involving novel intermediates or reaction conditions, giving the patent a further layer of protective scope.

3. Therapeutic Use Claims

These claims extend protection to the use of the compound in methods of treating particular diseases. They are instrumental in pharmaceutical patent strategies, especially in jurisdictions favoring method claims.

4. Formulation and Delivery Claims

When included, these claims specify particular formulations, such as nanoparticles, sustained-release matrices, or targeted delivery systems, broadening the patent protection into drug-device combinations.


Patent Landscape and Prior Art Consideration

1. Related Patents and Patent Families

WO2017214470 belongs to a landscape comprising:

  • Existing chemical classes with similar scaffolds
  • Previous patents focusing on related therapeutic areas
  • Innovative differentiation in substituents or delivery methods

A patent landscape analysis indicates that the patent attempts to carve out a distinctive niche by combining certain structural features with specific therapeutic claims.

2. Key Competitors and Patent Holders

Major pharmaceutical entities with active R&D pipelines in the relevant therapeutic areas may hold competing patents. Their filings potentially encompass similar compounds, requiring strategic navigation to avoid infringement.

3. Patentability and Freedom-to-Operate

The patent's claims appear to be grounded on inventive step due to specific structural modifications and therapeutic application claims, assuming prior art lacks comparable compounds with identical pharmacological profiles.

Freedom-to-operate analyses must consider patent overlaps in chemical space and therapeutic indications, especially in jurisdictions like Europe, the US, and China.


Legal Status and Geographic Coverage

  • Jurisdictional reach generally extends to international patent applications via PCT, with national phase entries in key markets.
  • Legal status evaluations should verify granted versus pending claims, potential oppositions, or litigations, which influence commercialization timelines.

Implications for Industry and Innovation

  • The patent expands the chemical space protected, incentivizing further development of derivatives.
  • Strategic patent portfolio management requires ongoing monitoring of related patents and potential licensing opportunities.
  • The broad claims reinforce the patent's position, possibly deterring entry by competitors in the specified therapeutic class.

Key Takeaways

  • WO2017214470 secures patent protection over innovative chemical entities with potential therapeutic applications, emphasizing structural modifications to existing compounds.
  • The scope combines compound claims, methods of synthesis, use in specific diseases, and formulation strategies, offering comprehensive shielding.
  • The patent landscape indicates active competition, with similar compounds and indications explored by multiple players.
  • Robust patent claims, if upheld, can significantly block market entry and enable exclusive commercialization.
  • Continuous monitoring of patent status, infringements, and subsequent filings is crucial to sustain competitive advantage.

FAQs

1. What makes WO2017214470 unique in the pharmaceutical patent landscape?
Its broad structural coverage, combined with specific therapeutic use claims and innovative synthetic methods, differentiates it from prior art, especially if it incorporates unique substituents that enhance pharmacological profiles.

2. How can competitors navigate around this patent?
By designing compounds outside the claimed structural scope—particularly altering core motifs or substituent patterns—while maintaining therapeutic efficacy, competitors can attempt to develop non-infringing alternatives.

3. What strategic value does this patent provide to a pharmaceutical company?
It secures exclusivity over a promising class of compounds, facilitates development within protected territory, and supports licensing or partnership opportunities.

4. How does claim language influence the strength and enforceability of this patent?
Precisely drafted claims that balance breadth with novelty enhance enforceability. Excessively broad claims risk invalidation, while overly narrow claims limit the scope.

5. What should stakeholders monitor regarding this patent’s future?
Legal status in key markets, ongoing patent prosecutions, potential oppositions, and related patent filings or litigations globally are critical factors affecting commercial strategy.


References

[1] WIPO Patent WO2017214470. (2017). "Title of the Patent." World Intellectual Property Organization.
[2] Patent landscape reports and patent databases, such as Derwent Innovation and Espacenet, for related chemical and therapeutic patents.
[3] World Patent Index, for jurisdictional statuses and patent family analysis.

(Note: Due to the nature of the task, specific structural and claim details would typically require review of the actual patent document for precise analysis.)

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