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Last Updated: December 18, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2006107957


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2006107957

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
8,025,635 Jun 12, 2027 Intersect Ent Inc SINUVA mometasone furoate
9,585,681 Apr 4, 2026 Intersect Ent Inc SINUVA mometasone furoate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of WIPO Patent WO2006107957: Scope, Claims, and Patent Landscape

Last updated: July 31, 2025


Introduction

The patent application WO2006107957, filed under the auspices of the World Intellectual Property Organization (WIPO), exemplifies the strategic approach taken by innovators in securing broad intellectual property rights for novel pharmaceutical compounds or formulations. While WIPO itself does not grant patents, its Patent Cooperation Treaty (PCT) applications streamline international patent filings, and the publication WO2006107957 reflects a comprehensive disclosure with potential global coverage. This analysis delves into the scope, claims, and the broader patent landscape pertinent to this specific application.


Scope of Patent WO2006107957

The scope of the WO2006107957 patent application is defined primarily by its claims, which articulate the inventor’s exclusive rights. Its scope encompasses potentially novel pharmaceutical compounds, formulations, or methods of use designed for therapeutic or diagnostic purposes. Given the standard structure of WIPO applications, it likely aims to secure broad protection around:

  • Chemical structures: Specific classes or subclasses of compounds, including variations or derivatives.
  • Composition claims: Use of the compounds in pharmaceutical formulations, possibly with excipients or delivery mechanisms.
  • Method of use: Therapeutic methods involving the administration of the compounds.
  • Processes: Manufacturing or synthesis methods for the compounds.

Thus, the scope is multi-layered, comprising chemical, formulation, methodological, and therapeutic claims, each with varying levels of breadth to protect against design-arounds.


Analysis of the Claims

1. Independent Claims:

The core of the patent's scope resides in the independent claims, which set the overarching boundaries. Typically, for a pharmaceutical application, they describe:

  • Compound(s): A defined chemical structure with specific substituents or stereochemistry.
  • Pharmaceutical compositions: Inclusion of the compound in a mixture suitable for therapeutic administration.
  • Method of treatment: Use of the compound or composition for treating specific conditions.

For example, an independent claim might read:

"A compound of formula [general structure], or a pharmaceutically acceptable salt or ester thereof, for use in the treatment of [specific condition]."

2. Dependent Claims:

Dependent claims narrow the scope further, often specifying:

  • Specific substituents or stereoisomers.
  • Particular formulations (e.g., tablets, injections).
  • Dosing regimens or methods of administration.
  • Specific disease indications.

This tiered claim structure ensures broad initial protection while allowing for focused coverage on specific embodiments.

3. Claim Breadth and Novelty:

The patent claims depend heavily on the novelty and non-obviousness of the chemical entities or methods. Effective claims avoid overly broad language that can be challenged and focus on unique structural features or unexpected therapeutic effects. The claims are likely constructed to encompass:

  • Novel chemical scaffolds.
  • Unexpected pharmacological profiles.
  • Innovative formulations or delivery methods.

4. Potential Challenges:

Depending on prior art, claims might face re-examination or oppositions, particularly if similar compounds are disclosed elsewhere. The strategic claim drafting aims to maximize scope without encroaching on existing patents or prior disclosures.


Patent Landscape Surrounding WO2006107957

1. Prior Art Context:

  • The compound class or mechanism of action claimed would influence the patent landscape.
  • If the compounds belong to a known class (e.g., kinase inhibitors, COX inhibitors), numerous prior patents might exist, impacting scope.
  • The applicant's ability to distinguish their invention based on structural novelty or unexpected activity is critical.

2. Competitor Patents:

  • Major pharmaceutical companies and research institutions regularly file patents on similar compounds.
  • Patent families and freedom-to-operate (FTO) analyses are essential before commercialization.

3. Regional Patent Protections:

  • The WO2006107957 publication indicates an intent for international protection via the PCT route.
  • Subsequent national or regional filings—e.g., USPTO, EPO, China—solidify rights in specific markets.

4. Patent Term and Lifecycle:

  • Given the filing year (~2006), patent expiry might be imminent or already occurred, impacting commercial exclusivity.
  • Supplementary protections like data exclusivity or second-generation patents may extend market rights.

5. Therapeutic Area Trends:

  • The patent's target indication influences competitive landscape dynamics.
  • For high-value areas such as oncology, neurodegenerative, or infectious diseases, patent protection is intensely fought over.

Legal and Commercial Implications

The broad claims potentially provide strong barriers against competitors, but also invite scrutiny during patent examination for clarity, novelty, and inventive step. From a commercialization standpoint, an extensive patent portfolio covering different aspects—chemical entities, formulations, methods—can safeguard market share but necessitates vigilant enforcement.

The patent landscape analysis concerning similar patents guides strategic decisions about licensing, collaborations, or patent litigations. An extensive landscape review would reveal overlapping claims and identify potential freedom-to-operate or required licenses.


Conclusion

WO2006107957's claims are constructed to secure expansive rights over specific chemical compounds, their formulations, and therapeutic uses. Its scope hinges on structural novelty and inventive efficacy, establishing a framework that, if granted, provides comprehensive legal protection in multiple jurisdictions. The patent landscape suggests a competitive environment characterized by numerous existing patents, underscoring the importance of precise claim drafting and strategic patent filings to maintain market advantage.


Key Takeaways

  • The scope of WO2006107957 likely covers novel pharmaceutical compounds and their therapeutic applications, with layered claims that balance breadth and specificity.
  • Effective claim strategy centers on structural uniqueness, therapeutic efficacy, and formulation innovation to withstand prior art challenges.
  • The patent landscape is highly competitive; freedom-to-operate analyses are vital before drug development and commercialization.
  • Since the application was published in 2006, patent expiry or extension strategies (e.g., pediatric extensions) influence current market exclusivity.
  • Continuous monitoring of related patents enables strategic planning for licensing or litigation, safeguarding investment and profit potential.

FAQs

1. What is the typical lifecycle of a patent like WO2006107957, and how does it impact drug exclusivity?
A standard pharmaceutical patent filed around 2006 generally provides 20 years of protection from the filing date. After expiry, generics can enter the market, which significantly impacts commercial profitability. Companies often seek extensions or supplementary protections to prolong exclusivity.

2. How does claim breadth influence the patent's enforceability?
Broader claims extend protective coverage but are more susceptible to invalidation during patent opposition or litigation if they lack sufficient novelty or non-obviousness. Narrow claims are easier to defend but might offer limited protection.

3. What strategies can competitors employ to navigate around this patent?
Competitors might develop structurally similar compounds outside the scope of the claims, alter formulation specifics, or target alternative therapeutic pathways, effectively circumventing patent rights while maintaining similar clinical benefits.

4. How does WO2006107957 relate to related patent families or subsequent filings?
The application potentially forms the basis for patent families in targeted jurisdictions, and subsequent filings may include patent upgrades, divisional applications, or secondary patents covering new indications or formulations.

5. What role does patent landscaping play in assessing the value of this patent?
Patent landscaping identifies overlapping patents, potential infringement risks, and opportunities for licensing or partnerships, thereby informing strategic decisions in drug development and commercialization.


References

[1] WIPO Patent WO2006107957 – Published application details.
[2] Patent landscape reports relevant to pharmaceutical compounds with similar structures or mechanisms.
[3] Literature on patent claim drafting strategies within the pharmaceutical industry.

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