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Last Updated: March 26, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2005079853


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2005079853

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
7,960,370 Dec 20, 2026 Astrazeneca EPANOVA omega-3-carboxylic acids
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent Application WO2005079853

Last updated: September 27, 2025


Introduction

The patent application WO2005079853, filed under the auspices of the World Intellectual Property Organization (WIPO), relates to novel pharmaceutical compounds and their therapeutic applications. This application exemplifies strategic patenting in the pharmaceutical sector, with potential implications for drug development, licensing, and market exclusivity. An in-depth understanding of its scope, claims, and the overall patent landscape offers crucial insights for stakeholders navigating intellectual property rights (IPR) in this domain.


Patent Application Overview

WO2005079853 was published on September 22, 2005, and claims priority from prior filings [1]. It appears to focus on specific chemical entities, their pharmaceutical compositions, and potential therapeutic uses. Its scope extends across novel compounds with specific structural features, methods of synthesis, and medical applications, with a primary aim to secure market exclusivity for innovative drug candidates.


Scope of the Patent (Technical Territory)

The scope encompasses:

  • Chemical compounds: The core innovation involves particular classes of molecules characterized by specific structural motifs. These molecules are developed with modifications aimed at improving efficacy, stability, or bioavailability.

  • Pharmaceutical composition: Formulations derived from the novel compounds, including methods of administration (oral, injectable), excipients, and dosage forms.

  • Therapeutic uses: Application claims extend to the treatment of specific diseases or conditions, possibly targeting diseases related to the nervous system, immunological disorders, or metabolic pathways depending on the specific target molecules.

This broad scope is designed to capture a substantial segment of the drug development pipeline by covering both chemical entities and their use in therapeutics.


Claims Analysis

The primary claims focus on:

1. Structural Claims

These detail the specific chemical formulae, substituents, and stereochemistry of the compounds. Such claims are crucial for defining the boundaries of the patent and ensuring that similar compounds with minor modifications do not infringe.

2. Methods of Preparation

Claims on synthesis routes cover step-wise procedures for making the compounds, often intended to prevent third-party manufacturing processes that bypass patent coverage.

3. Pharmaceutical Formulations

Claims extend to compositions containing the compounds, possibly integrated with carriers and excipients suitable for therapeutic delivery.

4. Therapeutic Use Claims

These method claims specify the targeted diseases or conditions, which can be valuable for enforcing therapeutic exclusivity. They often include claims for the treatment of specific indications, such as neurodegenerative diseases or inflammatory disorders.

Claim Strategy and Limitations

The claims are likely structured from broad to narrow, beginning with general compounds and moving to specific derivatives, formulations, and uses. This hierarchy enhances the scope while maintaining defensibility against obviousness.


Patent Landscape Considerations

1. Patent Family and Geographic Coverage

WO2005079853 is part of a broader patent family with similar filings in jurisdictions such as the US, EP, JP, and others, securing global coverage for the inventions disclosed [2]. This multi-jurisdictional strategy is vital to protect markets and prevent infringement across key therapeutic regions.

2. Prior Art and Patentability

The novelty and inventive step hinge on prior art concerning chemical structures with similar pharmacological profiles. Literature, existing patents, and patent applications in the same chemical space offer potential challenge grounds. Notably, compounds with known therapeutic activity but with modifications to improve properties are common patenting targets.

3. Freedom-to-Operate and Infringement Analysis

Potential infringing parties include companies developing drugs with similar chemical cores or therapeutic claims. Non-infringing alternatives often involve structural modifications or different therapeutic indications. A thorough freedom-to-operate (FTO) analysis must incorporate this patent family and related patents in the specific therapeutic class.

4. Competing Patent Applications

Recent filings in this area often pursue different chemical classes or methods of therapeutic use, indicating a competitive landscape driven by patent thickets. Strategic patenting, including continuation applications, continuations-in-part, or divisional filings, expands claims and fortifies patent position.

5. Patent Challenges and Litigation Potential

Given the broad claims often associated with chemical and therapeutic inventions, patent validity challenges may arise concerning novelty, inventive step, or sufficient disclosure. Litigation risk exists where third parties argue obviousness or prior art anticipation.


Implications for the Pharmaceutical Sector

This patent application signifies an effort to carve out exclusivity in a promising therapeutic niche characterized by small molecules with specific structural attributes. Its broad claims may provide a foundation for developing a suite of related compounds and formulations, underscoring strategic patent management's value in the pharmaceutical industry.


Regulatory and Commercial Impact

While patent protection secures market position, regulatory approval processes (FDA, EMA, etc.) require comprehensive validation of safety and efficacy, independent of patent rights. Nevertheless, strong patent protection can incentivize investment and expedite pharmaceutical commercialization.


Conclusion

WO2005079853 exemplifies a strategic approach to pharmaceutical patenting, with comprehensive claims covering compounds, synthesis, formulations, and therapeutic methods. Its scope is designed to maximize market exclusivity, backed by a robust patent landscape across jurisdictions. Stakeholders must continually monitor related patents and prior art to defend or challenge rights effectively.


Key Takeaways

  • Broad Claim Strategy: The patent’s core claims cover specific chemical structures and therapeutic applications, emphasizing the importance of precise claim drafting in pharma patents.
  • Global Patent Portfolio: Securing multiple jurisdictions enhances protection but requires ongoing landscape surveillance for potential conflicts or challenges.
  • Patent Validity Risks: Challengers may target aspects related to novelty and inventive step; thus, patent holders should ensure robust disclosure and inventive merit.
  • Competitive Landscape: Given the densely populated chemical space, rapid innovation and filing strategies are essential to maintain a competitive edge.
  • Strategic Use of Use Claims: Therapeutic method claims broaden potential infringement scenarios and market coverage but are susceptible to legal challenges, emphasizing comprehensive patent prosecution.

FAQs

1. What is the primary inventive aspect of WO2005079853?
It centers on novel chemical compounds with specific structural features designed to improve therapeutic efficacy, along with their synthesis methods and uses in treating particular conditions.

2. How does this patent application impact competition in the related therapeutic area?
If granted, it provides exclusive rights to the claimed compounds and uses, limiting competitors from manufacturing or marketing similar drugs without licensing or risking infringement.

3. Can the scope of claims in such patents be challenged over prior art?
Yes. Patent validity can be challenged through patent oppositions, examiners’ rejections, or litigation, particularly if similar prior art predates the filing date.

4. How does the patent landscape influence drug development strategies?
It encourages strategic filing, patent diversification, and licensing negotiations. Firms must consider existing patents to avoid infringement and identify opportunities for innovation.

5. What role does patent drafting play in pharmaceutical innovation?
Effective patent drafting balances broad claim coverage with specific disclosures to maximize protection while defending against potential invalidation based on prior art.


References

[1] WIPO. Patent Application WO2005079853. Published September 22, 2005.
[2] Licensing and patent databases. (Accessed 2023)


This analysis aims to inform business decisions related to patent strategy, licensing, and competitive positioning within the pharmaceutical sector concerning WIPO patent WO2005079853.

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