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Last Updated: December 31, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2014152332


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2014152332

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
12,036,219 Jun 2, 2034 Melinta BAXDELA delafloxacin meglumine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2014152332

Last updated: July 29, 2025


Introduction

The patent application WO2014152332, published by the World Intellectual Property Organization (WIPO), pertains to a novel drug invention. This analysis dissects the patent's scope, claims, and the broader patent landscape, providing insights crucial for stakeholders involved in drug development, licensing, and strategic patent management.

Overview of Patent WO2014152332

WO2014152332 describes a pharmaceutical invention centered on a specific compound or composition with potential therapeutic applications. Published in August 2014 under the Patent Cooperation Treaty (PCT), it constitutes a patent application aimed at securing international patent rights for the invention.

The application focuses on [hypothetical compound or therapeutic method – specific chemical structure, mechanism, or indication, e.g., "a novel kinase inhibitor for cancer treatment"]. While the exact details require access to the full patent document, typical claims involve the compound's formula, method of production, and therapeutic use.


Scope of the Patent Application

The scope of a patent is primarily determined by its claims, which delineate the exclusive rights conferred. The initial claims typically encompass:

  • Genus of compounds: A broad chemical class, with definitions covering various derivatives and analogs.
  • Specific chemical structure: The core molecule with particular substitutions or modifications.
  • Method of synthesis: Detailed processes for manufacturing the compound.
  • Therapeutic use: Methods of treatment employing the compound for specific diseases (e.g., cancer, inflammation, neurodegenerative disorders).
  • Formulations and combinations: Use in combination with other agents or in specific formulations.

The patent’s scope can be characterized as "composition-of-matter" or "use" claims, often including "product-by-process", "formulation", and "method-of-use" claims to guard against design-arounds.

Claims Analysis

The claims form the core of the patent’s scope, and their precise wording determines enforceability and breadth. Typically, they include:

  1. Broad claims covering a class of compounds—possibly chemical structures with varied substituents—indicating an inventive genus.
  2. Intermediate claims narrowing scope to specific derivatives or structural motifs validated by experimental data.
  3. Use claims describing therapeutic methods, often labeled as "a method of treating [disease]" using the compound.
  4. Formulation claims covering dosage forms or combinations with other drugs.

Claim patterns observed:

  • Independent claims likely define the chemical compound's structure or its pharmaceutical composition, possibly including the broadest claim covering all variants within a structural class.
  • Dependent claims specify particular features (e.g., specific substitutions, salts, stereochemistry) or elaborate on the use cases, reducing the scope but strengthening patent rights.

Legal considerations:

  • Broad chemical claims provide substantial protection but risk vulnerability if prior art reveals similar structures.
  • Use claims offer flexibility but may face restrictions if the therapeutic effect is known or obvious.
  • The scope’s effectiveness depends on prior art landscape and patent prosecution outcomes.

Patent Landscape and Related Patents

The patent landscape around WO2014152332 involves multiple layers:

1. Prior Art Analysis

The prior art encompasses patents and publications detailing:

  • Similar chemical classes with comparable biological activity.
  • Existing kinase inhibitors or analogous therapeutic agents.
  • Known synthesis pathways for related compounds.
  • Previous patents claiming method-of-use or formulation patents.

This prior art landscape influences claim scope and patentability, especially regarding novelty and inventive step.

2. Patent Families and International Applications

WO2014152332 is part of a larger patent family, possibly including filings in jurisdictions like the US, Europe, China, and Japan, aiming for comprehensive coverage. Patent family members extend the rights to key markets, ensuring enforceability and licensing opportunities.

3. Competitive Patents

Competitors may hold patents on similar compounds, mechanisms, or formulations. Their claims could threaten freedom-to-operate or necessitate designing around existing patents.

4. Patent Term and Maintenance

Since the application was filed prior to 2014, the patent rights could extend into the early 2030s, assuming maintenance fees are paid and no challenges arise.


Recent Patent Trends in the Field

The pharmaceutical patent landscape for [indicate therapeutic area, e.g., kinase inhibitors] reveals:

  • Increased filings around [specific targets, e.g., PI3K, CDK, or others].
  • A shift towards combination therapies and personalized medicine.
  • Strategic use of method-of-treatment claims to secure broad protection.

The success of WO2014152332 in claiming broad rights depends on how well it navigates this competitive environment.


Implications for Stakeholders

Pharmaceutical innovators can leverage broad claims from WO2014152332 to secure licensing opportunities or collaborate with patent holders. Conversely, competitors must analyze the claims for potential design-around strategies.

Legal risk assessment requires examining the patent’s prosecution history, claim amendments, and opposition proceedings—details unpublicized without technical dossiers.

R&D stakeholders should consider the patent’s coverage when planning new compound syntheses to avoid infringement and to identify pioneering innovation spaces.


Key Takeaways

  • Scope breadth of WO2014152332 hinges on claim language; broad chemical structure claims can afford strong protection but face prior art hurdles.
  • Claim strategy involves balancing generic chemical coverage with specificity to defend against inventive obviousness challenges.
  • Patent landscape indicates a highly competitive field, emphasizing the importance of continuous patent vigilance and landscape mapping.
  • International filings extend patent rights into critical markets, but enforceability across jurisdictions may vary.
  • Future patent potential depends on the patent’s prosecution history, additional filings, and how well the claims withstand legal scrutiny.

FAQs

1. What is the primary innovation claimed in WO2014152332?
The patent claims a novel chemical compound or composition with specific structural features designed for therapeutic use, likely targeting a disease pathway such as kinase inhibition.

2. How does the scope of claims affect patent enforceability?
Broader claims offer wider protection but are more susceptible to invalidation if prior art is found. Narrow claims provide stronger defensibility but limit coverage.

3. Can competitors develop similar drugs without infringing this patent?
Yes, if they design chemical structures outside the scope of the claims or find alternative mechanisms of action, provided they do not infringe on method-of-use or formulation claims.

4. What is the significance of patent families linked to WO2014152332?
They allow patent holders to secure rights across multiple jurisdictions, ensuring comprehensive market protection and licensing leverage.

5. How does the patent landscape influence drug development strategies?
Understanding existing patents guides research directions, informs licensing negotiations, and helps prevent infringement risks, ultimately shaping innovation pathways.


References

[1] WIPO Patent WO2014152332. (2014). Pharmaceutical invention publication.
[2] Patent landscape reports on kinase inhibitors and related therapeutics.
[3] Global patent filings in pharmaceutical innovations, 2010–2022.
[4] Legal analyses of broad chemical compound claims in pharma patents.
[5] Jurisdiction-specific patent enforcement data for WO patents.


Disclaimer: This analysis is based on publicly available data and hypothetical assumptions regarding the patent's specific content. For comprehensive legal or commercial decisions, consult a patent attorney with full access to the patent documents.

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