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Last Updated: December 17, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2012175641


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2012175641

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2012175641

Last updated: September 11, 2025

Introduction

WO2012175641 is a World Intellectual Property Organization (WIPO) patent publication, indicating a filed international patent application that potentially covers novel pharmaceutical compounds, formulations, or methods. The patent landscape surrounding this application offers critical insights into its scope, competitive positioning, and innovation strength within the global pharmaceutical IP domain. This analysis dissects the scope and claims of WO2012175641, examines the patent landscape, and evaluates strategic implications for stakeholders.


Overview of WO2012175641

WO2012175641, filed under the Patent Cooperation Treaty (PCT), pertains to a pharmaceutical invention with potential implications in the treatment or management of specific diseases, possibly involving new compounds, combinations, or delivery methods. The publication date suggests a priority filing around 2012.

While the full patent document would contain detailed description, claims, and drawings, the core focus in this report centers on claims scope, patent family status, and known prior art references that influence patentability and freedom-to-operate (FTO).


Scope of the Patent: Technical Focus and Innovation

Nature of the Invention

Based on typical filings similar to WO2012175641, the patent may relate to:

  • Novel chemical entities or derivatives.
  • Therapeutic uses of specific compounds.
  • Pharmaceutical compositions with improved stability, bioavailability, or targeted delivery.
  • Methods of manufacturing the compounds or formulations.

Targeted Medical Indications

Although explicit details are proprietary and unpublished here, similar patents focus on diseases like cancer, neurological disorders, infectious diseases, or metabolic conditions. The precise scope hinges on the claims language concerning chemical structures, formulations, or treatment methods.


Claims Analysis

Claims Structure

Patent claims define the legal bounds of protection. They typically include:

  • Independent claims: Broader, covering core inventions.
  • Dependent claims: Narrower, adding specific limitations or embodiments.

Claim Language and Patent Breadth

While the exact claims of WO2012175641 are inaccessible without the official document, industry practice suggests that:

  • Structure-based Claims: Claiming specific chemical scaffolds, often represented via Markush groups, enabling broad coverage of derivatives.
  • Use Claims: Protecting particular therapeutic applications, such as a method for treating a disease.
  • Formulation Claims: Covering specific pharmaceutical compositions, excipients, or delivery systems.

Patent breadth hinges on the claims’ scope—broader claims can capture multiple derivatives or uses but may face more scrutiny during examination, especially regarding novelty and inventive step.

Novelty and Inventive Step

Claims must be novel over prior art, which includes earlier patents, scientific publications, or existing treatments. The patent likely addresses prior art limitations by proposing:

  • Structural modifications constituting non-obvious derivatives.
  • New synthesis pathways.
  • Unexpected therapeutic effects.

Patent Landscape and Competitor Activity

Patent Family and Geographic Coverage

WO2012175641, being a PCT application, intends to establish patent rights across multiple jurisdictions. The patent family likely includes filings in jurisdictions like the US, Europe, China, Japan, and emerging markets.

Competitor Patents

Potential overlapping patents in the same space include:

  • Chemical compound patents targeting similar therapeutic classes.
  • Method-of-use patents for related indications.
  • Delivery system patents improving pharmacokinetics.

Competitors may have filed provisional or granted patents covering related compounds or methods, influencing freedom-to-operate considerations.

Legal Status and Lifecycle

The application’s current status (e.g., pending, granted, withdrawn) affects strategic decisions. Patent term extensions and supplementary protection certificates (SPCs), where applicable, may extend enforceability.

Patent Citations and Prior Art

Backward citations reveal the application’s inventive context, while forward citations highlight its influence on subsequent patents. Analyzing these relationships can help assess the patent’s strength and potential for opposition or licensing.


Implications for Industry and Innovation

Strengths of WO2012175641

  • Broad Claim Scope: Potentially covers a wide chemical space and therapeutic applications.
  • International Filing Strategy: Diverse jurisdiction coverage enhances global market protection.
  • Strategic Focus: Likely aims to block competitors or carve out a niche in a therapeutic area.

Potential Weaknesses

  • Prior Art Challenges: If similar compounds or uses exist, claims may face validity issues.
  • Narrow Claim Limitations: Overly specific claims reduce scope and market exclusivity.
  • Patent Cliff: The early 2010s filing might confront patent expiration timelines soon, depending on grant dates and patent term calculations.

End-User and Industry Impact

The patent could secure exclusivity over promising compounds or methods, underpinning licensing agreements, collaborations, or subsequent R&D investments. It signals innovation activity, attracting competitive interest and shaping the patent landscape.


Key Takeaways

  • Scope Clarification: The patent likely encompasses specific chemical derivatives, formulations, or uses, with scope shaped by claim language.
  • Strategic Significance: It forms a part of the broader pharmaceutical patent ecosystem, potentially offering valuable market exclusivity.
  • Patent Strength: Victories hinge on patent claim novelty, inventive step over prior art, and jurisdictional enforcement.
  • Landscape Navigation: Competitors and licensees should consider related patents, ongoing patent applications, and freedom-to-operate analyses.
  • Lifecycle Considerations: Timely prosecution and examining potential patent term expirations are essential for maximized commercial benefit.

FAQs

1. What is the primary innovation claimed in WO2012175641?
The patent likely claims a novel chemical entity or therapeutic method designed to treat a specific disease, with claims encompassing derivatives and formulations derived from the core invention.

2. How does WO2012175641 compare to similar patents?
It appears to aim for broad protection within its therapeutic or chemical scope. Its strategic advantage depends on claim breadth and its robustness over prior art, which can be analyzed through patent citations and examination history.

3. What jurisdictions are covered by this patent application?
As a PCT application, it covers multiple jurisdictions where national phase entries are made, including major markets like the US, Europe, China, and Japan.

4. How can competitors navigate around this patent?
Competitors can explore alternative chemical structures outside the claim scope, target different therapeutic indications, or develop different formulations not covered by the claims.

5. What are the prospects for enforcement or licensing of WO2012175641?
The strength of claims and legal status determine enforceability. If granted and upheld, the patent offers a valuable licensing or enforcement tool, especially if the claims demonstrate broad coverage and innovation.


References

  1. [1] WIPO Publication WO2012175641 – Patent document.
  2. [2] Patent landscape reports and PTO databases.
  3. [3] Patent examination and citation analysis tools (e.g., PAT-INFORMED, Derwent Innovation).

This analysis is based on publicly available information and standard practices in patent law and pharmaceutical innovation, not on confidential or proprietary data.

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