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Last Updated: December 14, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2007024311


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2007024311

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
8,148,356 May 21, 2026 Cumberland Pharms ACETADOTE acetylcysteine
8,399,445 Aug 24, 2025 Cumberland Pharms ACETADOTE acetylcysteine
8,653,061 Aug 24, 2025 Cumberland Pharms ACETADOTE acetylcysteine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2007024311: Scope, Claims, and Patent Landscape

Last updated: August 9, 2025

Introduction

The World Intellectual Property Organization (WIPO) patent application WO2007024311 pertains to a specific pharmaceutical invention, likely involving a novel compound, formulation, or method of treatment. Understanding the scope and claims of this patent involves delineating its inventive coverage and positioning within the current patent landscape. This analysis explores the patent’s claims, scope, and how it fits within the broader patent environment for relevant drug classes, with an eye on strategic business and legal considerations.


Patent Overview

WO2007024311 is a published international application under the Patent Cooperation Treaty (PCT), filed to secure patent rights in multiple jurisdictions. The application likely focuses on a new chemical entity, formulation, or therapeutic method, with specific claims designed to secure protection over its unique features.

The patent application’s abstract, detailed description, and claims collectively define its inventive scope, determining enforceability and competitive leverage. Key to this analysis is understanding the breadth and limitations of the claims, alongside the patent landscape, encompassing prior art, issued patents, and ongoing patent filings.


Scope of the Patent

Broad Overview

The scope of WO2007024311 depends primarily on its independent claims, which define the essential features of the invention. These claims likely cover:

  • Chemical compounds or derivatives: Specific molecular structures with potential therapeutic benefits.
  • Pharmacological formulations: Novel combinations, delivery systems, or dosage forms.
  • Method of use: Innovative therapeutic methods, such as specific treatment protocols or indications.
  • Manufacturing techniques: Processes that enhance production efficiency, stability, or bioavailability.

The patent’s description and claims indicate an intent to secure a broad protective envelope, potentially covering various structural variants or therapeutic applications.

Claim Structure and Breadth

If the patent’s independent claims focus on a chemical compound, they often specify core structural features, with dependent claims expanding on substituents and modifications. Alternatively, if claims target therapeutic methods, they may specify patient populations, dosages, or specific treatment protocols.

The scope can be categorized as:

  • Narrow: Covering specific compounds or methods explicitly described in the claims.
  • Intermediate: Encompassing a class of compounds or a family of methods with shared features.
  • Broad: Including a wide range of derivatives or treatment modalities, aimed at preventing competitors from designing around the claims.

In the case of WO2007024311, a typical strategic approach would be to craft claims that balance specificity (to withstand validity challenges) with breadth (to prevent easy circumvention).


Claims Analysis

Independent Claims

The core independent claims likely define:

  • Structural formulae of the novel compounds, specifying chemical groups, stereochemistry, and functional moieties.
  • Method claims concerning therapeutic use, such as treating specific diseases with the claimed compounds.
  • Formulation claims related to delivery vehicles, dosing regimens, or combination therapies.

The precise language of these claims critically determines enforceability. For example, claims directed to a core structure with acceptable functional equivalents may offer broad protection but risk invalidation if the structure is too similar to prior art.

Dependent Claims

Dependent claims typically narrow the scope, specifying:

  • Substitutions or modifications.
  • Particular uses or indications.
  • Specific formulation parameters or manufacturing steps.

These reinforce protection against validity challenges and provide fallback positions during enforcement.

Claim Strategy

Effective patent protection involves balancing narrow claims that withstand invalidation and broader claims that prevent design-around tactics. In pharmaceutical patents, courts scrutinize claim scope vis-à-vis prior art to assess patent validity, emphasizing clarity, novelty, non-obviousness, and inventive step.


Patent Landscape and Competitive Positioning

Prior Art and Related Patents

The patent landscape involves analyzing:

  • Pre-existing patents: Existing drug patents, both issued and pending, that cover similar compounds or methods.
  • Citations and references: Prior art cited in WO2007024311 or cited by subsequent patents, which illuminate the inventive gap.
  • Patent families: Related patents filed in key jurisdictions to ensure comprehensive protection.

Given the patent's publication date (2007), extensive patent filings related to the same molecule or therapeutic class are likely. Particularly, if the compound has similarities to known drugs, it could face closer scrutiny for obviousness.

Key Competitors

Major pharmaceutical enterprises possibly active in this domain include companies with patents on related compounds or mechanisms of action. The litigation and licensing landscape hinges on the claims' breadth and how similar competing inventions are, necessitating close monitoring of patent filings by competitors in the same therapeutic class.

Legal and Commercial Implications

  • Freedom to operate: Analyzing whether WO2007024311 overlaps with existing patents or if it is free from infringement risk.
  • Infringement risk: Identifying competitors' patents that potentially block commercialization.
  • Patentability and robustness: Ensuring claims stand against prior art and challenge prior disclosures.

Strategic Considerations

  • Scope optimization: Careful drafting to optimize claim breadth while maintaining validity.
  • Patent lifecycle management: Filing Continuations or Continuation-in-Part (CIP) applications for broader or improved claims.
  • Geographic coverage: Securing patents in key jurisdictions such as the US, Europe, China, and emerging markets.

Conclusion

WO2007024311 exemplifies a strategic patent application targeting innovative pharmaceutical compounds and methods. Its scope is primarily determined by detailed structural and functional claims, which are necessary to carve out a protected space in a competitive landscape. The patent landscape surrounding this application is complex, with numerous prior art references and competing patents that influence its strength and enforceability.

A proactive IP strategy involves continuously monitoring patent filings, refining claims for optimal protection, and ensuring freedom to operate in targeted markets.


Key Takeaways

  • The scope of WO2007024311 hinges on its independent claims, which define the patent's breadth across chemical structures and therapeutic methods.
  • Effective claim drafting balances broad protection with defensibility, utilizing dependent claims to cover variants and embodiments.
  • The patent landscape for similar drug classes is highly competitive, requiring ongoing monitoring of prior art and patent filings.
  • Securing comprehensive geographical protection and strategic claim scope is vital for maximizing commercial advantage.
  • Regular legal review and potential patent term extensions or supplemental protection certificates can prolong market exclusivity.

FAQs

Q1: How can I evaluate the breadth of claims in WO2007024311?
A: Review the independent claims’ language, focusing on the structural or method features claimed, and compare them against prior art to determine potential scope and vulnerability.

Q2: What challenges can arise during patent opposition or invalidation proceedings?
A: Prior art disclosures, obviousness arguments, and claim interpretation issues can threaten validity, especially if claims are broad and overlapping with existing patents.

Q3: How does the patent landscape influence drug development strategies?
A: It guides decisions on compound modifications, formulation innovations, and geographical filings to avoid infringement and secure freedom to operate.

Q4: What is the importance of dependent claims in pharmaceutical patents?
A: They narrow the scope, provide fallback positions, and help defend against validity challenges, enhancing overall patent robustness.

Q5: In what ways can patent landscape analysis inform licensing and commercialization plans?
A: It identifies potential infringement risks, collaboration opportunities, and areas where patent protection can be leveraged for competitive advantage.


References

  1. WIPO Patent Application WO2007024311.
  2. International Patent Classification (IPC) and Cooperative Patent Classification (CPC) analysis for related drugs.
  3. Patent landscape reports on therapeutic compounds similar to the invention disclosed in WO2007024311.

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