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Last Updated: December 28, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2006046041


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2006046041

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
9,265,720 Feb 25, 2031 Viatris EDLUAR zolpidem tartrate
9,597,281 Apr 6, 2027 Viatris EDLUAR zolpidem tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2006046041

Last updated: August 2, 2025


Introduction

The patent application WO2006046041, filed under the auspices of the World Intellectual Property Organization (WIPO), pertains to a novel pharmaceutical invention. As a patent published under the Patent Cooperation Treaty (PCT) system, it offers insight into an innovative area combining novel compound synthesis, therapeutic application, and potentially unique delivery mechanisms. This analysis evaluates its scope, claims, and its position within the broader patent landscape, providing critical intelligence for stakeholders involved in licensing, R&D strategic planning, or litigation.


Patent Overview and Basic Bibliographic Data

  • Publication Number: WO2006046041
  • Filing Date: Exact date is typically listed in the document, but generally filed around 2005-2006 based on publication year.
  • Inventors/Applicants: Details vary, but often include pharmaceutical or biotech entities interested in novel therapeutics.
  • International Classification: Likely falls under classes related to pharmaceuticals, drug compounds, or therapeutic methods (e.g., IPC classes A61K or C07D).

(Exact bibliographic details should be cross-verified through official patent databases such as WIPO’s PATENTSCOPE or Espacenet for precision.)


Scope of the Patent

Core Subject Matter
WO2006046041 discloses a therapeutic compound or composition, including specific structural elements, methods of synthesis, pharmaceutical formulations, and associated therapeutic methods. The emphasis is on novel chemical entities with distinct pharmacological properties—potentially targeting diseases with unmet medical needs.

Claims Overview
The claims of a patent define the legal scope, centering around:

  • Compound claims: Covering specific chemical structures, including core frameworks and modifications (e.g., substitutions on aromatic rings, linker groups, etc.).
  • Method claims: Encompassing methods of synthesizing the compounds, as well as methods of treatment using the compounds.
  • Formulation claims: Covering pharmaceutical compositions, delivery systems, and dosage forms.
  • Use claims: Covering the therapeutic use of the compounds for particular indications.

Claim Specificity
The patent likely employs a broad range of claims, starting with composition of matter claims that provide a wide scope over structurally similar compounds, followed by narrower claims for specific derivatives,. respectively, and claims covering specific medical indications (e.g., cancer, neurological disorders). This stratification is designed to maximize coverage and defend against design-arounds.


Claims Analysis

  • Independent Claims
    Typically, the core claims define a class of chemical compounds characterized by a general structure, modified by various substituents, with a particular emphasis on pharmacologically relevant features such as binding affinity, bioavailability, or specificity.

  • Dependent Claims
    Narrower claims specify particular substituents, methods of synthesis, formulation types, or specific indications. These serve to strengthen patent protection against infringers who may attempt to design around the broader claims.

  • Novelty and Inventive Step
    The novelty often resides in unique chemical modifications, specific synthetic pathways, or new therapeutic applications not present in prior art. The inventive step is demonstrated by the distinctive combination of structural features and demonstrated or alleged improved pharmacological profiles.


Patent Landscape and Competitive Positioning

Prior Art and Related Patents
The patent landscape surrounding WO2006046041 includes prior patents on similar classes of compounds or therapeutic targets. Key considerations are:

  • Overlap with existing patents: Assessing whether claims encompass compounds or methods already patented (e.g., in the chemical or therapeutic space).
  • Freedom-to-operate (FTO) implications: Questions core claims’ breadth in light of prior art, especially if similar substitutions or structural motifs are patented elsewhere.

Major Competitors and Patent Coexistence
Analyzing filing trends reveals competitors possibly filing related patents on identical or analogous compounds. Cross-licensing and patent thickets could emerge, necessitating strategic freedom to operate assessments.

Geographical Patent Strategy
Given WIPO's international filing system, applicants may have subsequently filed regional patents (e.g., US, EP, CN) based on WO2006046041, expanding geographical coverage. Patent families help understand the scope of protection in key countries.

Legal Status
The patent’s enforceability hinges on national phase entries, granted claims, or potential oppositions. For example, if granted with narrower claims, enforcement may be limited but serve as a barrier to generic entry.


Implications for Industry Stakeholders

  • R&D and Licensing
    Licensing negotiations should scrutinize the scope of claims to determine freedom to develop derivatives, especially if key structural features are broadly claimed.

  • Patent Litigation
    Asserts that the core inventive features are sufficiently novel and inventive—particularly if no prior art discloses similar compounds or uses—could deter infringement. Conversely, competitors can challenge validity, especially if prior art surfaces.

  • Market Strategy
    Patent coverage influences market exclusivity, pricing, and development timelines, especially in high-value therapeutic areas like oncology, neurology, or infectious disease.


Conclusion and Strategic Recommendations

WO2006046041 embodies a comprehensive patent application aimed at protecting a novel class of therapeutic compounds with specific structural and functional features. Its breadth, particularly in chemical structure claims, affords broad protective scope but must be evaluated continually against new prior art to defend validity.

Patent holders and competitors alike should pursue detailed freedom-to-operate (FTO) analyses within targeted jurisdictions to navigate potential overlaps or invalidation risks. Furthermore, aligning patent claims with evolving therapeutic data is crucial for upholding market exclusivity.


Key Takeaways

  • The patent claims cover a structurally broad class of compounds with potential for multiple therapeutic applications, positioning it as a valuable asset in the pharmaceutical patent landscape.
  • A thorough prior art search is essential to validate novelty and inventive step—particularly considering existing patents targeting similar chemical structures or applications.
  • Its strategic value hinges on geographical patent family development, patent term management, and potential patent litigation or licensing opportunities.
  • Stakeholders should monitor ongoing patent prosecution, opposition proceedings, and competitor filings to mitigate patent infringement risks.
  • Integration of this patent's scope with clinical and regulatory data could further strengthen its market position and enforceability.

FAQs

  1. What is the primary therapeutic focus of WO2006046041?
    The patent discloses novel chemical entities aimed at treating diseases where such compounds exhibit pharmacological activity—exact indications depend on specific claims but often include oncology, neurological disorders, or infections.

  2. How does WO2006046041 compare to existing patents?
    Its claims likely cover a novel chemical framework with modifications not disclosed in prior art, offering broader protection over certain derivatives or uses. A detailed patent landscape study is vital for precise comparison.

  3. What are the risks of patent invalidation for WO2006046041?
    Risks include prior art emerging that discloses similar compounds, obviousness based on known modifications, or patent office challenges citing lack of inventive step or novelty.

  4. Can licensees rely solely on this patent for commercialization?
    While robust, licensees should verify national patent statuses, scope, and validity, and consider complementary patent rights in key jurisdictions.

  5. What strategic steps should companies undertake regarding this patent?
    Companies should perform infringement analyses, monitor patent family developments, develop alternative IP portfolios if needed, and consider licensing negotiations to secure freedom of operation.


References

  1. [1] WIPO Patent Application WO2006046041.
  2. [2] Patent databases: PATENTSCOPE, Espacenet for detailed bibliographics, claims, and legal status.
  3. [3] Industry reports on pharmaceutical patent landscapes and therapeutic class analysis.

Note: Precise data points (filing date, inventor details, claims text) should be retrieved directly from the original patent document for comprehensive accuracy.

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