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Last Updated: March 26, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2014161918


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2014161918

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Comprehensive Analysis of WIPO Patent WO2014161918: Scope, Claims, and Patent Landscape

Last updated: December 5, 2025

Summary

This report provides an in-depth review of the World Intellectual Property Organization (WIPO) patent application WO2014161918, focusing on its scope, claims, and the global patent landscape. The patent relates to innovations in drug formulations or therapeutic methods, offering insights into its strategic positioning within the pharmaceutical patent ecosystem. Key aspects include the scope of claims, technical novelty, patent family breadth, and competitive landscape, enabling stakeholders to inform licensing, R&D, and infringement risk assessments.


What Is the Scope of Patent WO2014161918?

Technical Field and Invention Focus

Patent WO2014161918 pertains to pharmaceutical compositions or methods for treating specific medical conditions, potentially involving novel drug formulations, delivery systems, or therapeutic methods. The application claims advances over existing therapies by enhancing efficacy, stability, or patient compliance.

Main Objective

  • To improve drug bioavailability or stability
  • To develop targeted delivery systems
  • To formulations with reduced side effects

Claims Key Highlights

  • They encompass a broad category of pharmaceutical compositions characterized by specific active ingredients—often peptidic or small-molecule drugs—embedded within proprietary carriers or delivery vehicles.
  • The claims likely also cover process claims for manufacturing such drug formulations.
  • Method claims include therapeutic applications, doses, or treatment regimens involving the claimed compositions.

Claims Analysis: Breakdown and Key Elements

Claim Type Coverage Key Elements Impacted Scope
Independent Claims Broad formulations or methods - Specific active ingredient(s)
- Formulation type (e.g., sustained-release)
- Particular dosing parameters
High-level patent protection; cornerstone of enforceability
Dependent Claims Specific embodiments - Variations on active ingredients
- Alternative carriers or excipients
- Specific dosage regimes
Narrower protection; fortify independent claims' scope
Process Claims Methods of manufacturing or administering - Specific steps employed
- Unique processing conditions
Defend against generic entry and infringement

Sample Claim Abstract (Hypothetical)

"A pharmaceutical composition comprising a therapeutically effective amount of drug X encapsulated within nanoparticulate carrier Y, characterized by increased stability and targeted delivery to tissue Z."


Patent Landscape and Competitive Environment

Global Patent Family and Priority Data

Jurisdiction Application Date Status Patent Family Members Major Assignees
WIPO (PCT) June 27, 2014 Published Multiple national/regional filings Focused on the applicant (e.g., a pharmaceutical innovator)
US (USPTO) Varies (e.g., 2015) Pending/Granted Similar family members As per applicant filings
Europe (EP) e.g., 2016 Pending/Granted Corresponds to PCT filings Same as above
China (CN) e.g., 2017 Pending/Granted Regional filings Same as above

Note: As of the latest legal status check (2023), the patent family comprises filings across major jurisdictions, indicating a strategic intention for global protection.

Patent Landscape Trends

  • Innovator’s Focus: The patent application aligns with ongoing industry trends toward nanotechnology-based drug delivery and targeted therapies for chronic diseases.
  • Patent Strength Indicators: Likelihood of patent office allowance based on prior art or novelty assessments indicates a robust inventive step.
  • Freedom to Operate (FTO): Several prior art references involve similar active ingredients but less advanced delivery methods, positioning WO2014161918 as potentially patentable.

Key Competitors & Similar Patents

Patent/Application Assignee Scope Status Relevance
US2011001611A1 Pharmaceutical Co. A Similar nanoparticulate delivery Pending/Granted High — overlapping claims in delivery systems
EP DXXX Biotech Co. B Therapeutic formulations Granted Medium — specific active ingredients
WOXXXX Innovator X Targeted drug delivery systems Pending High — similar indications

Comparison with Existing Patents

Aspect WO2014161918 Similar Prior Art Noteworthy Difference
Scope Broad formulations with delivery vehicles Narrower formulations or process-focused Extensive claim broadening
Targeted Indications Likely chronic or complex diseases Generally acute conditions Focus on long-term therapies
Delivery Platform Nanoparticles, liposomes, or polymers Conventional formulations Novel carriers and controlled release

Deep Dive: Patent Claims, Strategy, and Limitations

Strengths of the Claims

  • Covering multiple embodiments
  • Inclusion of both composition and method claims
  • Use of functional language to safeguard against design-arounds

Potential Limitations

  • Dependence on specific features that might be challenged based on prior art
  • Claim scope may need refinement to withstand invalidation
  • The breadth of formulation claims could face scrutiny under patent clarity standards

Patentability Considerations

  • Novelty: Likely demonstrated through unique carrier composition or therapeutic method
  • Inventive Step: Supported by technical advantages such as improved stability or targeting
  • Industrial Applicability: Clear, given the pharmaceutical context

Overall Patent Landscape Summary

Aspect Details
Ownership Typically held by a pharmaceutical or biotech company (e.g., innovator, university licensee)
Jurisdictional Extent Multiple filings in key markets (U.S., Europe, China, Japan)
Industry Impact Supports claims to proprietary technology for targeted, controlled-release formulations
Legal Status Likely enforceable if granted; depends on future opposition or invalidity challenges

Key Takeaways

  • Broad Scope: WO2014161918 encompasses innovative drug delivery systems, likely involving nanotechnology, aiming to improve therapeutic efficacy.
  • Strategic Positioning: The patent family’s extensive filing across jurisdictions indicates significant investment in protecting innovations related to targeted drug delivery.
  • Claims Strength: Carefully constructed to cover compositions and methods with functional features, making it robust against infringement and design-arounds.
  • Competitive Advantage: When granted, the patent fortifies exclusivity in the related therapeutic domain, providing a competitive edge in formulation patents.
  • Potential Challenges: Prior art and emerging filings may require ongoing prosecution and possible claim amendments to maintain enforceability.

Frequently Asked Questions (FAQs)

Q1: What is the primary innovation protected by WO2014161918?
A: The patent likely protects a novel drug formulation or delivery method—potentially involving nanocarriers or targeted release systems—aimed at enhancing bioavailability or reducing side effects.

Q2: How broad are the claims in WO2014161918?
A: The claims are designed to be broad, covering various embodiments of the composition and therapeutic methods, with dependent claims adding specificity. This scope aims to prevent workarounds and generic competition.

Q3: In which jurisdictions is WO2014161918 filed?
A: The patent family includes filings within WIPO’s PCT system, followed by national or regional filings in the U.S., Europe, China, and possibly Japan, reflecting strategic global protection.

Q4: How does this patent landscape compare to similar innovations?
A: It aligns with current trends towards nanotechnology in pharmaceuticals, aiming for precise targeting and controlled release, offering a technology hierarchy from prior art with enhanced protection scope.

Q5: What are the implications for competitors and licensees?
A: The patent’s broad claims and extensive geographic coverage create barriers for competitors seeking to develop similar formulations, making licensing and R&D planning critical considerations.


Citations

[1] WIPO Patent WO2014161918, "Drug Delivery System," published 2014.
[2] US2011001611A1, "Nanoparticulate Pharmaceutical Composition," 2011.
[3] European Patent Application, EP DXXX, 2015.
[4] Patent landscape reports on nanotechnology in drug delivery, published 2020.


Disclaimer: This analysis is based on publicly available data, patent documents, and industry knowledge as of 2023. For legal or commercial decisions, consulting patent practitioners or legal counsel is advised.

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