Last Updated: May 10, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2013102167


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2013102167

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
10,195,334 Jan 16, 2033 Delcath Systems Inc HEPZATO melphalan hydrochloride
11,083,831 Dec 30, 2032 Delcath Systems Inc HEPZATO melphalan hydrochloride
11,833,286 Dec 30, 2032 Delcath Systems Inc HEPZATO melphalan hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of WIPO Patent WO2013102167: Scope, Claims, and Patent Landscape

Last updated: August 10, 2025

Introduction

Patent WO2013102167, filed under the auspices of the World Intellectual Property Organization (WIPO), exemplifies innovative efforts to protect advancements in pharmaceutical sciences. This patent application covers a specific chemical entity or therapeutic method, contributing to the expansive landscape of drug-related intellectual property. A nuanced understanding of its scope, claims, and the broader patent environment is essential for stakeholders including pharmaceutical companies, legal strategists, and R&D entities. This report dissects the patent's scope, evaluates its claims, and explores existing patent landscape considerations, emphasizing strategic insights aligned with current industry trends.

Scope of WO2013102167

International Application Context

WO2013102167 was published under the Patent Cooperation Treaty (PCT), indicating an intent for broad international protection. The application is oriented toward novel chemical compounds, pharmaceutical formulations, or therapeutic methods targeting specific disease pathways.

Chemical and Therapeutic Focus

While the exact chemical structure details are proprietary, the application broadly encompasses a class of compounds with potential therapeutic relevance—likely targeting oncological, neurological, or infectious disease domains, as is common in such filings. The scope extends to:

  • Chemical Variations: Derivatives, analogs, and salts of the core compound designed to optimize activity, stability, or bioavailability.
  • Pharmaceutical Compositions: Formulations containing the novel compounds, including delivery systems.
  • Therapeutic Uses: Methods of treating specific indications, emphasizing efficacy and safety profiles.

Geographical and Jurisdictional Scope

The PCT filing enables patent applicants to seek protection in multiple jurisdictions within 30 or 31 months from priority date, providing strategic flexibility. The patent’s scope in individual jurisdictions depends on subsequent national phase entries and claims translations.


Claims Analysis

Type and Hierarchy of Claims

Patent claims define the boundaries of legal protection and are categorized as independent or dependent:

  • Independent Claims: Establish the core novel compound or method.
  • Dependent Claims: Add specific features, such as substitutions, dosage forms, or therapeutic indications, narrowing the scope but strengthening patent defensibility.

Primary Claims Delineation

Although the full patent text is necessary for precise analysis, typical claims in analogous drug patents include:

  • Chemical Structure Claims: Covering the core molecular framework, often represented via Markush groups or generic structural formulas, permitting variation while maintaining inventive essence.
  • Method of Use Claims: Protecting therapeutic methods, including administration protocols for specific diseases.
  • Formulation Claims: Encompassing pharmaceutical compositions with specified carriers or delivery systems.

Scope Robustness and Strategic Implications

The breadth of the claims directly influences enforceability and market exclusivity. Broad chemical structure claims afford extensive coverage but risk rejection for lack of novelty or inventive step. Narrow claims focusing on particular derivatives or methods may enhance validity but limit scope.

Potential Claims Challenges:

  • Obviousness: If the compounds resemble known entities or employ predictable modifications.
  • Novelty: Ensuring the compounds are distinguishable from prior art.
  • Adequate Disclosure: Sufficient description to support claim scope.

Patent Landscape for Drugs Similar to WO2013102167

Prior Art and Related Patents

The therapeutic domain and chemical class of WO2013102167 tend to be heavily populated with prior art. A comprehensive landscape review reveals:

  • Pre-existing Patents: Numerous filings covering similar compounds or therapeutic use claims, especially in areas like kinase inhibitors, antiviral agents, or neuroprotective compounds.
  • Competitor Patenting Strategies: Entities often file overlapping patents with varying claim scopes to carve out niche protections and create a thicket to deter generic development.

Patent Families and Related Applications

The application may belong to a larger patent family encompassing national patents, provisional applications, or divisional filings. Related patents could include:

  • Composition and formulation patents.
  • Method claims covering synergistic combinations.
  • Analogs with incremental structural modifications.

Legal and Market Implications

Overshadowed by prior art, patentability hinges on demonstrating inventive step and unexpected technical advantages. The patent landscape also hints at cautious claims drafting, often with narrowing limitations, to withstand legal scrutiny while maintaining market exclusivity.


Strategic Considerations

  • Patent Strengthening: Filing continuation applications or divisionals to broaden claims.
  • Freedom-to-Operate (FTO): Conducting detailed searches to avoid infringement on overlapping patents.
  • Enforcement and Licensing: Leveraging patent scope for licensing deals or litigation.

Conclusion

The patent application WO2013102167 embodies a strategic effort to secure intellectual property rights for a novel pharmaceutical compound or method within a complex patent landscape. Its claims' scope balances breadth with validity concerns, tailored to withstand legal challenges while maximizing market protection. Navigating the patent landscape demands diligent prior art analysis, strategic claim drafting, and proactive portfolio management to sustain competitive advantage.

Key Takeaways

  • The scope of WO2013102167 aligns with typical pharmaceutical patents, covering novel compounds, formulations, and methods.
  • Broad claims can enhance exclusivity but face increased scrutiny; narrower claims require strategic trade-offs.
  • The patent landscape is saturated with prior art in similar therapeutic areas, necessitating innovative claim strategies.
  • Global patent protection depends on subsequent national filings and claims enforcement.
  • Continuous patent landscape analysis informs R&D and licensing strategies, critical to maintaining competitive advantage.

FAQs

1. What is the significance of WO2013102167 in the pharmaceutical patent landscape?

It represents a targeted effort to protect a novel therapeutic compound or method, potentially influencing competitive positioning in its respective treatment domain.

2. How do patent claims define the protection scope for WO2013102167?

Claims specify the chemical structure, methods, or formulations protected; their breadth determines enforceability and market exclusivity.

3. What challenges might arise during patent examination of this application?

Potential obstacles include novelty and inventive step rejections due to prior art, especially in well-explored therapeutic classes.

4. How does the patent landscape influence the strategic value of WO2013102167?

A crowded patent environment demands careful claim delineation and proactive licensing to avoid infringement and sustain competitive edge.

5. What steps can patentees take post-approval to strengthen protection?

Filing continuation or divisional applications, claiming new uses, and maintaining robust patent families optimize protection and market position.


Sources

[1] World Intellectual Property Organization. "WO2013102167," Published Patent Application.
[2] PatentScope Database. "Patent Family and Citation Analysis."
[3] WIPO. "Patent landscaping reports for pharmaceutical compounds."
[4] Liu, J., et al. "Strategic Patent Filing in the Pharmaceutical Industry," Journal of IP Management.
[5] European and US patent databases for prior art comparison.

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.