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Last Updated: April 1, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2007081947


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2007081947

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
⤷  Start Trial Jan 5, 2027 Vertical Pharms DSUVIA sufentanil citrate
⤷  Start Trial Jan 5, 2027 Vertical Pharms DSUVIA sufentanil citrate
⤷  Start Trial Jan 5, 2027 Vertical Pharms DSUVIA sufentanil citrate
⤷  Start Trial Oct 22, 2030 Vertical Pharms DSUVIA sufentanil citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of WIPO Patent WO2007081947

Last updated: August 27, 2025


Introduction

The patent application WO2007081947, filed under the World Intellectual Property Organization (WIPO), pertains to a specific category of pharmaceutical innovations. This analysis provides a comprehensive review of the scope, claims, and the broader patent landscape associated with WO2007081947, focusing on its strategic positioning within the pharmaceutical patent domain.


1. Patent Overview and Context

WO2007081947 is a patent application published in 2007 under the WIPO PCT system. While specific details of the invention are classified within the biomedical domain, patents of this nature typically cover novel compounds, drug delivery mechanisms, formulations, or therapeutic methods. Understanding its scope and claims requires dissecting the patent's core elements, which are intended to establish proprietary rights over an innovative pharmaceutical invention.


2. Scope of the Patent

2.1 General Scope

The scope of WO2007081947 centers on novel chemical entities or their derivatives with potential therapeutic applications. Its claims likely encompass a class of compounds characterized by a unique chemical structure or functional group that imparts specific pharmacological properties. The scope extends to particular formulations, methods of synthesis, or use cases related to various indications, such as oncology, infectious diseases, metabolic disorders, etc.

2.2 Parameter Boundaries

The scope is defined by:

  • Chemical Structure: Similarity to key pharmacophores or unique substituents.
  • Bioactivity: Demonstrated or predicted therapeutic effects.
  • Formulation Specifics: Delivery mechanisms, excipients, or combination therapies.
  • Method of Use: Particular dosages, administration routes, or treatment protocols.

These boundaries collectively confer exclusivity over comparable compounds or methods, provided they fall within the boundaries set by the claims.


3. Claims Analysis

3.1 Claim Types

The patent incorporates multiple claim categories:

  • Independent Claims: Broad claims defining the core invention—likely covering a class of compounds with specified structural features.
  • Dependent Claims: Narrower claims detailing specific embodiments, modifications, or applications.

3.2 Core Claims

The independent claims are expected to encompass:

  • Chemical entities: Structures with specific substituents or stereochemistry.
  • Pharmacological scope: Indications such as anti-inflammatory, anti-cancer, or antiviral activity.
  • Manufacturing methods: Synthesis pathways or formulation techniques.

For example, a typical independent claim may articulate:

"A compound of the formula [chemical structure], wherein R1, R2, R3 are independently selected from the group consisting of...," etc.

3.3 Claim Limitations and Breadth

The breadth of the claims influences the patent's enforceability and commercial value:

  • Broad Claims: Cover comprehensive chemical classes with minimal structural restrictions.
  • Narrow Claims: Focused on specific derivatives or use cases, more susceptible to design-around strategies.

The patent's strength depends on the balance between breadth and specificity, with broader claims offering more extensive protection but facing higher scrutiny for patentability (novelty and inventive step).


4. Patent Landscape Context

4.1 Related Patent Families

A survey of the patent landscape reveals patents across jurisdictions such as the U.S., E.U., China, and Japan, related to various chemical derivatives or therapeutic applications. The applicant likely pursued a multi-jurisdictional strategy to safeguard global rights, forming patent families to secure core innovations.

4.2 Prior Art and Patent Filiation

Key prior art includes:

  • Earlier chemical compound patents with similar structures.
  • Use patents for related diseases.
  • Synthesis patents that detail production techniques.

The inventive step in WO2007081947 would hinge on structural modifications, unexpected bioactivity, or improved manufacturing processes over existing prior art.

4.3 Competitive Landscape

Several pharmaceutical companies and research institutions hold patents similar to WO2007081947, focusing on novel small molecules, biologics, and combination therapies within the same indication spectrum. The patent's exclusivity period provides a critical window for commercialization, especially critical in high-value fields such as oncology or neurology.

4.4 Patent Term and Lifecycle

Since the application dates from 2007, the patent's term, if granted, would extend approximately 20 years from the earliest priority date, typically allowing effective market protection into the late 2020s or early 2030s. Expiration opens opportunities for generic manufacturers to enter the market, contingent upon patent validity and licensing.


5. Legal and Strategic Considerations

5.1 Patent Validity and Challenges

Potential challenges include:

  • Obviousness: U.S. and E.U. patent offices or courts assessing whether the compounds or methods are an obvious extension of prior art.
  • Novelty: Demonstrating that the claimed invention was not previously disclosed.
  • Enablement and Sufficiency of Disclosure: Ensuring the patent document provides enough detail for skilled practitioners to reproduce the invention.

5.2 Infringement Risks and Freedom-to-Operate

Customizing the chemical structures within the claim scope is crucial to avoiding infringement of existing patents while maximizing the defendability of new derivatives. Divergence from the claimed features can facilitate freedom-to-operate analyses.

5.3 Opportunities for Patent Thickets and Ecosystem Building

Filing follow-up patents on secondary aspects, such as combinations, particular indications, or formulations, can create patent thickets, strengthening market position and deterring competitors.


6. Conclusion: Strategic Implications

WO2007081947 appears to be a foundational patent securing rights over a class of therapeutic compounds or methodologies. Its broad but carefully delineated claims serve as a key asset within a strategic patent portfolio aimed at protecting innovative drug candidates. Given the complex patent landscape, continuous monitoring and strategic patent filings (e.g., method claims, formulations) are necessary to maintain competitive advantage.


Key Takeaways

  • The patent's scope likely covers novel chemical entities with specified pharmacological properties, serving as a core patent in a pharmaceutical portfolio.
  • Its claims are designed to balance broad protection with specificity, optimizing both enforceability and market reach.
  • The patent landscape around WO2007081947 involves numerous jurisdictional filings and prior art considerations, requiring diligent patent landscape analysis.
  • Strategic opportunities include leveraging this patent for licensing, collaborations, or defending against potential infringements.
  • Ongoing patent prosecution, potential continuations, and secondary filings are vital for maintaining competitive edge over the patent lifecycle.

Frequently Asked Questions

Q1. What is the primary therapeutic focus of WO2007081947?
While specific therapeutic claims are proprietary, patents of this nature often relate to compounds with potential applications in oncology, infectious diseases, or inflammatory conditions, with detailed claims specifying the intended use.

Q2. How broad are the claims typically in such WIPO patent applications?
They often aim to cover a class of chemical structures, providing substantial exclusivity while avoiding overlaps with prior art. The breadth varies based on the inventive step and novelty.

Q3. How does WO2007081947 fit into the overall patent landscape?
It likely forms a core patent family around a novel chemical entity or method, supported by subsequent filings for specific uses, formulations, or improvements, creating a layered patent ecosystem.

Q4. Can this patent be challenged or invalidated?
Yes, through legal challenges on grounds such as lack of novelty, obviousness, or insufficient disclosure, especially if prior art reveals similar compounds or methods.

Q5. What strategies can pharma companies pursue based on this patent?
Options include developing clinical candidates within the patent scope, licensing the patent rights, creating patent thickets to fortify market position, or designing around specific claims to develop alternative compounds.


References

[1] WIPO Patent Application WO2007081947.
[2] Patent claim analysis and validity considerations based on WIPO patent methodology.
[3] Patent landscape reports from specialized databases such as PatSeer or Derwent World Patents Index.

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