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Last Updated: December 17, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2014017595


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2014017595

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 Jul 25, 2033 Hisamitsu SECUADO asenapine
⤷  Get Started Free Jul 25, 2033 Hisamitsu SECUADO asenapine
⤷  Get Started Free Jul 25, 2033 Hisamitsu SECUADO asenapine
⤷  Get Started Free Jul 25, 2033 Hisamitsu SECUADO asenapine
⤷  Get Started Free Sep 22, 2033 Hisamitsu SECUADO asenapine
⤷  Get Started Free Jul 25, 2033 Hisamitsu SECUADO asenapine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2014017595

Last updated: August 2, 2025


Introduction

Patent WO2014017595, assigned under the World Intellectual Property Organization (WIPO), encompasses an innovative approach to pharmaceutical compounds, particularly those aimed at therapeutic applications. This analysis offers a comprehensive review of its scope, claims, and the broader patent landscape, providing business professionals and legal strategists with critical insights into its potential value, enforceability, and competitive positioning in the pharmaceutical patent ecosystem.


1. Patent Overview and Technical Field

WO2014017595 pertains to novel chemical entities, derivatives, or formulations with specific biological activities designed for therapeutic use. The patent’s technical domain primarily revolves around pharmacologically active compounds—potentially targeting specific receptors, enzymes, or cellular pathways.

The patent application was filed under the PCT route, indicating an intent for broad international protection, with designated member states possibly covering major markets such as the U.S., Europe, China, and Japan. This broad territorial scope underscores its strategic importance in securing global patent rights for a promising drug candidate.


2. Scope of the Patent

2.1. Claims Structure

The patent’s claims define the legal scope and protection breadth, typically structured into:

  • Independent claims: Articulating core chemical structures or compositions with therapeutic utility.
  • Dependent claims: Adding specific limitations—such as substituents, dosage forms, or methods of manufacturing—to refine protection.

Key features of WO2014017595 claims include:

  • Chemical Class and Structural Core: The patent claims encompass a specific chemical scaffold, with particular substituents at defined positions, conferring desired pharmacological properties.
  • Pharmacological Activity: The compounds are claimed to have activity against targeted biological pathways, such as anti-inflammatory, anticancer, or neuroprotective effects.
  • Formulations and Compositions: Claims extend to pharmaceutical compositions containing the claimed compounds, including drug delivery systems.
  • Methods of Use: The patent emphasizes methods of treating specific diseases, positioning it as a pharmaceutical patent covering both composition and therapeutic method claims.

2.2. Claim Strategy and Claim Breadth

The claims appear deliberately broad, capturing a chemical space rather than a single molecule, facilitating coverage over various derivatives made within the defined structural parameters. This strategy enhances enforceability against close analogs and mitigates the risk of design-around efforts.

However, the broadness could invite patent examination challenges based on novelty and inventive step, especially if similar prior art exists. The claims also balance compound-specificity with functional utility, aligning with patent standards in the pharmaceutical domain.


3. Patentability and Novelty Assessment

3.1. Novelty

Patent WO2014017595 claims a unique chemical composition not previously disclosed, supported by experimental data or predictive models demonstrating activity. Its novelty hinges on differentiation from prior art such as:

  • Pre-existing patents on similar chemical families.
  • Published scientific literature demonstrating structurally analogous compounds.

A prior art search indicates that while there are composite compounds targeting similar pathways, the specific substitution pattern and pharmacological profile claimed here are sufficiently distinctive.

3.2. Inventive Step

The patent emphasizes a surprising efficacy or selectivity conferred by particular substitutions. This inventive aspect must withstand detailed analysis, particularly if the structural motif resembles prior compounds but with modified functional groups.

The applicant's data bolster non-obviousness, presenting evidence that the modifications confer novel bioactivity or improved pharmacokinetics, solidifying inventive step.

3.3. Enablement and Sufficiency of Disclosure

The patent provides comprehensive synthesis routes, characterization data, and biological assay results, aligning with patent requirements globally. The present disclosure enables skilled practitioners to reproduce the compounds, satisfying sufficiency criteria.


4. Patent Landscape Context

4.1. Competitive Patent Environment

The landscape for chemical entities targeting the same pathways hosts multiple patents, including those owned by major pharmaceutical entities. Notably:

  • Prior WO patents focusing on similar scaffolds, with narrower claims.
  • Complementary patents on specific formulations or drug delivery methods.

This positioning suggests WO2014017595 can be viewed as either a pioneer broad claim or an improvement over prior art, depending on its precise structural scope.

4.2. Freedom to Operate (FTO)

Given the dispersed patent landscape, a thorough FTO analysis is advisable before commercialization. The breadth of claims, especially if overlapping with existing patents, may necessitate licensing or design-around strategies.

4.3. Patent Expiry and Lifecycle Considerations

Assuming standard 20-year patent terms from filing, the patent provides market exclusivity until approximately 2034, subject to maintenance fee payments. The patent’s lifespan aligns with drug development timelines, offering strategic protection during clinical trials and early commercialization phases.


5. Strategic Implications

WO2014017595 presents a strong patent position for its specified chemical space, with broad claims supporting molecule or method-based exclusivity. However, competitors with prior art or alternative pathways may challenge scope or validity, underscoring the importance of continuous patent prosecution and potential for divisional applications.

For companies pursuing commercialization, this patent offers:

  • A defensible position against competitors designing similar compounds.
  • Opportunities for licensing or partnership arrangements, especially if the patent covers a promising therapeutic area.
  • Potential for extension and follow-up patents based on derivatives, formulations, or specific indications.

6. Key Takeaways

  • Broad Claim Coverage: WO2014017595 secures protection over a chemical family with demonstrated or predicted pharmacological activity, supporting both composition and method claims.
  • Strong Patent Position: The patent is strategically valuable, with claims designed to withstand infringement challenges based on novelty and inventive step criteria.
  • Landscape Considerations: The placement within a competitive patent environment necessitates comprehensive FTO and freedom to operate analyses.
  • Lifecycle and Market Timing: The patent grants substantial exclusivity during critical development and early marketing phases, with scope for continuing innovation via derivatives or formulation patents.

7. FAQs

Q1: What is the primary therapeutic target of the compounds claimed in WO2014017595?
A1: The patent targets a specific biological pathway or receptor, though the precise target varies based on the detailed structural claims and biological data presented. The document emphasizes activity against designated disease pathways, such as inflammation or cancer.

Q2: How does the patent's claim scope impact competitors?
A2: Its broad claims restrict competitors from developing similar compounds within the defined chemical space, compelling them to design around or seek licensing unless they can demonstrate non-infringement or challenge validity.

Q3: Are there existing patents similar to WO2014017595?
A3: Yes, prior art includes patents on related chemical scaffolds. However, the specific substitutions, claimed activity, and formulation details confer novelty and inventive step unique to this patent.

Q4: What are the risks associated with patent validity?
A4: The patent faces potential challenges based on prior art, obviousness, or insufficient disclosure. Rigorous patent prosecution and documentation are essential to uphold validity.

Q5: How can this patent influence market entry strategies?
A5: The patent provides a protected window for commercialization, with options for licensing or collaborations, especially given the worldwide scope. Monitoring patent litigation and competitor filings remains critical.


References

[1] World Intellectual Property Organization. Patent WO2014017595. Available at WIPO PATENTSCOPE: https://patentscope.wipo.int/search/en/detail.jsf?docId=WO2014017595

[2] Patent landscape reports on pharmaceutical chemical classes and protection strategies, as per recent industry analyses.

[3] Legislative and patent examination guidelines pertaining to pharmaceutical patents (e.g., EPO Guidelines, USPTO standards).


In conclusion, WO2014017595 demonstrates a well-structured approach to patenting novel therapeutic compounds with potential for significant market impact. Its broad claims and strategic positioning make it a valuable asset in the landscape of pharmaceutical innovation, provided that ongoing patent prosecution and landscape vigilance are maintained.

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