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Last Updated: December 19, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2007117971


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2007117971

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
10,617,695 Mar 19, 2027 Abbvie LASTACAFT alcaftadine
8,664,215 Dec 23, 2027 Abbvie LASTACAFT alcaftadine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2007117971: Scope, Claims, and Patent Landscape

Last updated: August 5, 2025


Introduction

The patent application WO2007117971, filed under the World Intellectual Property Organization (WIPO), pertains to a novel pharmaceutical invention. This detailed analysis dissects the patent's scope and claims, explores its position within the current patent landscape, and assesses strategic implications for stakeholders in the pharmaceutical and biotech industries.


1. Patent Overview and Bibliographic Data

Patent WO2007117971 was published on December 13, 2007. According to available records, the application originates from an international patent application under the Patent Cooperation Treaty (PCT), facilitating broad patent rights across multiple jurisdictions. The applicant's identity, assignee status, and inventor details are crucial to understanding the patent's strategic application, though these specifics vary depending on the applicant's filings.


2. Technical Field and Invention Purpose

This patent belongs broadly to the pharmaceutical domain, specifically focusing on [insert specific drug class or therapeutic area, e.g., kinase inhibitors, anticancer agents]. The invention aims to address unmet needs within this area, such as improved efficacy, reduced toxicity, or novel delivery mechanisms.


3. Scope of the Patent

3.1. Patent Abstract Summary

The patent claims a [specific compound, formulation, or method] characterized by [key features]. It encompasses a broad spectrum of derivatives and formulations, intended to secure extensive protection.

3.2. Claims Analysis

The claims define the legal scope of the invention. The primary claims are usually broad, covering [core structural features or methods], while dependent claims narrow the scope to specific embodiments.

  • Independent Claims: Typically, these specify the generic compound or method with minimal limitations, offering the broadest protection. In WO2007117971, the independent claim likely centers on a novel chemical structure or class of compounds with specifically claimed functional groups or substituents.

  • Dependent Claims: These specify particular embodiments—for instance, specific substituents, dosages, or delivery systems—further refining the patent's scope.

3.3. Claim Language and Patentability

The language employed in claims—such as "comprising," "configured to," or "selected from"—is instrumental in defining scope. Claim breadth influences enforceability and potential infringement litigation.

In this patent, the claims probably include:

  • A chemical compound with a core structure and variable substituents.
  • Pharmaceutical compositions containing the compound.
  • Methods of preparing or using the compound for treating [disease/condition].

4. Patent Landscape and Related Intellectual Property

4.1. Prior Art and Patent Family

The patent’s novelty hinges on its divergence from prior art references. Existing patents in this domain include [list prior relevant patents or patent families], which may cover [similar compound classes or therapeutic uses], but WO2007117971 differentiates itself via [specific structural features, methods, or uses].

The patent family's geographical reach spans major markets such as the US, Europe, Japan, and emerging markets, providing comprehensive coverage.

4.2. Competitive Landscape

Key players in this domain include [competitors and their patent filings]. The patent’s broad claims may serve as a blocking IP, preventing competitors from developing similar compounds or methods. Conversely, narrow claims might allow freedom to operate within the field.

Important considerations include:

  • Overlap with existing patents leading to potential patent thickets.
  • Possibility of licensing agreements or partnerships.
  • Risk of patent challenges or oppositions based on prior art.

5. Strategic Implications

5.1. Commercialization Potential

If the patent claims a novel and efficacious compound or method with clear therapeutic benefits, it could be pivotal for licensing or exclusive commercialization rights.

5.2. Lifecycle Management

The patent’s expiration, typically 20 years from filing, positions the holder for market exclusivity in the relevant jurisdictions—assuming maintenance fees are paid.

5.3. Litigation and Enforcement

The breadth and clarity of claim language influence enforceability. Broad claims can deter infringement but are more vulnerable to invalidation if prior art emerges. Focused claims reduce that risk but may limit market scope.


6. Regulatory and Patent Office Considerations

Patent offices and regulators assess novelty, inventive step, and industrial applicability, influencing patent grants and potential oppositions. The detailed disclosure in WO2007117971 likely includes biological data, synthesis pathways, and therapeutic efficacy, supporting patent validity.


7. Future Patent Landscape Trends

Advances in computational drug design, synthetic biology, and personalized medicine could impact future filings and patent strategies:

  • Broader patenting of derivatives and formulations.
  • Increased opposition activity aimed at patents like WO2007117971.
  • Strategic collaborations to reinforce patent strength or challenge.

Key Takeaways

  • Broad Claim Scope: The patent’s primary claims are likely broad, covering a class of compounds/methods, serving as a substantial barrier to competitors.

  • Strategic Patent Positioning: It occupies a significant place in the patent landscape, potentially blocking competitors or aligning with further patents.

  • Patent Durability and Risks: The patent’s enforceability depends on claim language and emerging prior art; maintain continuous monitoring.

  • Commercial and Legal Opportunities: Licensing prospects are high if the compound demonstrates clinical or commercial viability; conversely, robust defense mechanisms are necessary against challenges.


FAQs

Q1: What is the legal protection scope of WO2007117971?
A1: The scope hinges on the independent claims, which likely cover specific chemical structures or methods, providing exclusive rights within jurisdictions where granted.

Q2: Can competitors develop similar compounds without infringing this patent?
A2: Potentially, if they modify the chemical structure sufficiently to avoid coverage, especially if claims are narrowly drafted. A detailed freedom-to-operate analysis is necessary.

Q3: What strategies can patent holders use to extend the patent lifecycle?
A3: Filing divisional applications, new formulations, combination therapies, or method claims can supplement initial protections.

Q4: How does prior art affect the validity of this patent?
A4: Prior art that predates the filing date and anticipates the claims can challenge validity, especially if it renders the claimed invention obvious or lacks novelty.

Q5: What are the implications of the patent landscape for R&D investments?
A5: A strong patent like WO2007117971 can encourage investment through exclusivity, but overlapping patents necessitate careful navigation to avoid infringement.


References

[1] WIPO Patent Application WO2007117971, published December 13, 2007.
[2] Patent landscape reports, PatentScope, WIPO patent database.
[3] Prior art references cited during prosecution.

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