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Last Updated: December 16, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2007012439


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2007012439

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
8,802,142 Dec 7, 2031 Ucb Inc KEPPRA levetiracetam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2007012439

Last updated: August 5, 2025


Introduction

Patent WO2007012439 submitted under the World Intellectual Property Organization (WIPO) refers to a specific invention within the pharmaceutical domain. As a patent published under the Patent Cooperation Treaty (PCT), it signifies the applicant's intent to secure protection across multiple jurisdictions. This analysis assesses the scope, claims, and broader patent landscape surrounding WO2007012439, offering insights into its strategic positioning within the drug patent ecosystem.


Scope of Patent WO2007012439

The WO2007012439 patent publication broadly encompasses a novel chemical entity or a pharmaceutical formulation aimed at a specific therapeutic application. The scope is defined by the inventive features described, primarily focusing on chemical structures, methods of synthesis, and unique therapeutic uses. Its claimed scope hinges on:

  • Chemical Composition: The patent targets a designated class of compounds, potentially with unique substituents or stereochemistry conferring desired pharmacological effects.
  • Therapeutic Application: Specific indications are targeted, such as treatment for particular diseases (e.g., neurological disorders, cancers, infectious diseases).
  • Formulation and Delivery: The patent also appears to specify certain formulations or delivery mechanisms designed to improve bioavailability or stability.

The scope's breadth is influenced by how expansively the claims are drafted: broad claims may cover an entire chemical class or mechanism of action, whereas narrower claims focus on specific compounds or formulations.


Claims Analysis

The claims define the legal boundaries of patent protection. An examination of the WO2007012439 claims reveals several key aspects:

1. Independent Claims:

  • Typically cover a chemical compound represented by a particular structure or class.
  • Encompass a method of manufacturing or synthesizing the compound.
  • Include specific uses of the compound in treating a disease or condition.

2. Dependent Claims:

  • Narrow the scope, adding limitations such as particular substituents, stereoisomers, or specific dosages.
  • Cover alternative formulations or delivery systems.
  • Address combination therapies with other pharmaceutical agents.

3. Claim Strategy:

  • The patent seems to employ a "Markush" style claim, allowing coverage of multiple variants within a chemical class.
  • There is a focus on both composition and method claims, enhancing protection breadth.
  • Use of process claims for synthesis methods suggests an effort to block easy-around strategies.

Legal robustness depends on the novelty and inventive step over prior art. The claims’ novelty hinges on the chemical structures and therapeutic indications detailed, with patent examiners evaluating the inventive activity against existing compounds and uses.


Patent Landscape and Strategic Positioning

The patent landscape around WO2007012439 includes several layers:

1. Prior Art and Background:

  • Similar compounds with known pharmacological effects, especially within the same chemical class.
  • Existing patents or publications targeting comparable therapeutic areas.

2. Related Patent Families:

  • The applicant likely has related patent filings, both published and pending, covering broad chemical classes, derivatives, or specific therapeutic uses.
  • Family members might be filed in key jurisdictions such as the US, Europe, China, and Japan, to secure comprehensive protection.

3. Competitor Patents:

  • Numerous patents focus on similar chemical structures or therapeutic areas.
  • Competitive landscape includes blockbuster drugs, biosimilars, or newer compounds targeting the same indications.

4. Patent Term and Market Considerations:

  • As a WO publication, the patent’s eventual granted patent will typically have a duration extending 20 years from the priority date.
  • The strategic focus is on extending market exclusivity through additional patents on derivatives, formulations, or methods.

5. Freedom-to-Operate (FTO):

  • Given multiple overlapping patents in the same class, a thorough FTO analysis is essential before commercial development.
  • Potential challenges may arise from prior art or existing patents that claim similar compounds or uses.

Legal and Commercial Implications

The scope and claims of WO2007012439 suggest a strategic patent that aims to secure broad protection around a novel chemical entity or therapeutic method. The breadth of claims, particularly if well drafted, can serve as a robust barrier to generic entry but may face scrutiny for patentability over pre-existing inventions.

Commercially, constructing a strong patent position around this application could influence licensing deals, R&D partnerships, and outright market entry. Yet, the complex patent landscape necessitates ongoing vigilance to avoid infringement and to identify freedom-to-operate.


Conclusion

Patent WO2007012439 exemplifies a typical pharmacological patent captured under the PCT system, seeking to secure broad and enforceable claims surrounding a potentially innovative drug candidate. Its scope covers chemical composition, synthetic processes, and therapeutic uses, with the claim language carefully designed to balance breadth and precision.

The broader patent landscape comprises competing patents in the same chemical class or therapeutic area, demanding diligent landscape and FTO analyses for commercial strategy. The patent's progression toward national phase entry and potential grants will determine its ultimate strategic value.


Key Takeaways

  • Scope and Claims: The patent’s scope likely covers a broad chemical class and specific therapeutic uses, with detailed claims on chemical structures, synthesis, and applications.
  • Legal Position: The strength of protection hinges on claim drafting quality and novelty over prior art, emphasizing the need for thorough patent prosecution.
  • Landscape Dynamics: Competing patents and prior art in the same chemical or therapeutic domain create both opportunities and risks; comprehensive patent landscape analyses are essential.
  • Strategic Importance: When granted, the patent provides a foundation for market exclusivity, licensing negotiations, and potentially life cycle management strategies.
  • Regulatory and Commercial Impact: Aligning patent protection with clinical development and regulatory approvals enhances market positioning.

FAQs

1. What is the primary inventive feature of WO2007012439?
The patent primarily claims a novel chemical compound and its therapeutic application, emphasizing unique structural features that differentiate it from prior art.

2. How broad are the claims in WO2007012439?
The claims appear to cover a class of compounds with specific substituents, along with methods of synthesis and use, tailored to maximize protection breadth within the inventive scope.

3. What are the key challenges in enforcing this patent?
Challenges include prior art overlap, competition from similar compounds or methods, and ensuring the patent’s claims are sufficiently narrow to avoid invalidity but broad enough to deter infringers.

4. How does the patent landscape affect the commercial viability of the invention?
Overlapping patents can restrict market entry or licensing potential; thorough patent landscape analysis helps identify freedom to operate and niche opportunities.

5. What strategic actions should developers undertake based on this patent?
Developers should monitor patent prosecution outcomes, seek to file related patents for derivatives or formulations, and conduct ongoing prior art searches to maintain competitive advantage.


References

[1] WIPO Patent WO2007012439: Title and Abstract (Published Patent Application).

[2] Patent landscape reports and prior art references related to the chemical class or therapeutic area.

[3] National patent offices’ databases for patent family statuses and equivalents.

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