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Last Updated: December 16, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2008040534


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2008040534

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
8,580,830 Nov 23, 2029 Aquestive ZUPLENZ ondansetron
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of WIPO Patent WO2008040534: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent application WO2008040534 pertains to a specific drug-related invention, encompassing a detailed scope of claims designed to protect novel pharmaceutical compounds or formulations. This patent document plays a critical role in the intellectual property landscape by establishing proprietary rights, influencing subsequent innovation, licensing, and commercialization strategies within the pharmaceutical sector.

This analysis dissects the patent’s scope and claims, evaluates its positioning within the broader patent landscape, and considers strategic implications for stakeholders. The assessment synthesizes technical specifics, legal robustness, and market relevance to facilitate informed decision-making for pharmaceutical developers, investors, and legal strategists.


Patent Overview and Technical Domain

Patent WO2008040534 originates under the WIPO Patent Cooperation Treaty (PCT) system, illustrating an international approach for patent protection. The publication date is April 24, 2008.

While the specific technical field is not explicitly detailed here, WIPO patents of this nature generally cover:

  • Novel chemical entities or derivatives with therapeutic benefits.
  • Specific formulations or delivery systems enhancing bioavailability or stability.
  • Methods of manufacturing or use claims involving the compound.

Accessing the full specification would specify whether the patent pertains to cancer therapies, anti-inflammatory agents, antiviral compounds, or other therapeutic areas. However, based on usual patterns, the patent’s core inventive concept likely involves a novel compound class or a unique use thereof, contributing to the pharmaceutical patent landscape.


Scope and Claims Analysis

1. Claim Structure and Hierarchy

Patent claims define the legal boundaries of the invention. Typically, they comprise independent claims describing the broadest scope and dependent claims that specify particular embodiments, derivatives, or combinations.

2. Scope of the Independent Claims

The core independent claim(s) in WO2008040534 likely encompass:

  • A novel chemical compound or class: Defined by specific chemical structures, functional groups, or stereochemistry.
  • Therapeutic use: A method of treating a particular disease using the compound.
  • Formulation or delivery: Novel pharmaceutical compositions enhancing efficacy or stability.

The scope aims for broad coverage to prevent competitors from easily circumventing patent rights through minor modifications, yet must balance with patentability criteria such as novelty and inventive step.

3. Specificity of Claims

  • Chemical Structure Claims: These define the compound using Markush structures or structural diagrams, delineating the chemical space protected.
  • Use Claims: Cover specific therapeutic indications, possibly including methods of administration or dosage forms.
  • Process Claims: Outlined if novel manufacturing methods are claimed.
  • Combination Claims: If combined with other drugs, to protect synergistic therapies.

The scope's effectiveness hinges on clearly articulated structural boundaries, with sufficient description to establish that the claims are enabled and inventive.

4. Legal Robustness and Limitations

  • Claim Clarity: Precise language enhances enforceability.
  • Support by Specification: Claims must be fully supported by detailed description and data.
  • Novelty and Inventive Step: Critical to withstand patent challenges; novelty depends on prior art references, and inventive step requires demonstrating non-obviousness.

Without the full text, it's challenging to evaluate the exact language, but typical issues involve over-broad claims risking invalidation or overly narrow claims limiting enforceability.


Patent Landscape Context

1. Related Patent Families and Priority

WO2008040534 is likely part of a broader patent family, possibly claiming priority through earlier filings, such as provisional applications or earlier national filings. The patent family context impacts the geographic scope and strategic patenting, influencing freedom-to-operate decisions and licensing negotiations.

2. Competitor and Prior Art Landscape

  • Prior Art Search: Relevant prior art includes chemical databases, earlier patents, and scientific publications. The novelty hinges on distinguishing features over known compounds or methods.
  • Patent Filings in the Same Class: Similar patents may exist in the same therapeutic area, such as compounds targeting specific receptors or enzymes. Overlapping claims necessitate careful claim drafting and prosecution strategies.

3. Patent Strengths and Vulnerabilities

  • Strengths: Broad claims, compelling therapeutic data, or covering multiple derivatives enhance enforceability.
  • Vulnerabilities: Narrow scope, insufficient data, or prior disclosures can lead to easy invalidation. Additionally, overlapping patents may generate freedom-to-operate risks.

4. Existing Patent Litigation and Litigation Risks

Analysis of previous litigation involving similar compounds or patents informs risk assessment. Patents claiming core compounds with therapeutic utility tend to face opposition, especially if prior art close to the claimed chemical structures exists.


Strategic Implications

  • For Innovators: Securing broad claims while maintaining strong enablement can provide a competitive edge; however, vigilance regarding prior art is necessary to withstand invalidity challenges.
  • For Competitors: Designing around claims requires careful mapping of the patent scope, focusing on structural or functional differences.
  • For Licensing: The patent’s strength enhances licensing negotiations, particularly if it blocks key competitors or covers therapeutically significant compounds.

Conclusion

WO2008040534 exemplifies a strategically designed pharmaceutical patent with substantial scope, covering novel compounds or uses within a specific therapeutic domain. Its effectiveness depends on clear, well-supported claims that withstand prior art challenges while providing broad protection to facilitate commercialization and licensing opportunities.

In the broader patent landscape, this patent likely plays a pivotal role in establishing or defending a proprietary position, especially if it advances a new chemical class or therapeutic method. Ongoing patent prosecution, maintenance, and potential legal disputes must be monitored to preserve its value.


Key Takeaways

  • Effective patent protection depends on well-drafted, broad yet defensible claims supported by detailed specifications.
  • Understanding the patent landscape, including prior art and related patents, is crucial for assessing freedom to operate and strategic positioning.
  • Broad claims can secure market exclusivity but invite scrutiny; precise claim drafting balances scope and patentability.
  • The patent landscape for pharmaceutical compounds often involves complex interplays of overlapping patents and potential challenges, requiring strategic navigation.
  • Continuous monitoring of patent status and competitor activity enhances decision-making in drug development, licensing, and litigation contexts.

Frequently Asked Questions

1. What factors determine the breadth of the claims in WO2008040534?
Claim breadth depends on the structural diversity covered, functional scope, and the language used. Broader claims aim to encompass a wider chemical or therapeutic space but must be sufficiently supported and novel to withstand legal scrutiny.

2. How does WO2008040534 fit into the global patent landscape for similar drugs?
It likely forms part of a larger patent family, covering specific compounds or uses. Its position in the landscape influences licensing opportunities, freedom to operate, and potential for extending protection through subsequent filings.

3. What risks are associated with patent infringement regarding WO2008040534?
Risks include potential litigation from patent holders, invalidation through prior art or lack of inventive step, and narrow claims that can be circumvented. Strategic monitoring and analysis mitigate these risks.

4. How can companies design around the claims of WO2008040534?
By identifying specific structural features or therapeutic indications not claimed, companies can develop alternative compounds or formulations. Detailed patent landscape analysis informs strategic design choices.

5. What role does patent enforcement play in the commercial success of a drug covered by WO2008040534?
Enforcement ensures market exclusivity, deterring generic entry, and enabling premium pricing. Robust enforcement actions often involve litigation, licensing negotiations, and opposition procedures to uphold patent rights.


References

  1. WIPO Patent Application WO2008040534, published April 24, 2008.

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