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Last Updated: January 1, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2008079339


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2008079339

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
8,318,706 May 1, 2031 Almirall SEYSARA sarecycline hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2008079339

Last updated: August 18, 2025

Introduction

The World Intellectual Property Organization (WIPO) patent application WO2008079339 concerns a novel pharmaceutical invention, the specifics of which encapsulate a unique set of claims designed to protect its innovative features. This analysis provides a comprehensive overview of the patent's scope, claims, and place within the broader patent landscape, offering vital insights for stakeholders involved in drug development, licensing, and competitive intelligence.

Overview of the Patent Application

Patent WO2008079339 was published by the WIPO under the Patent Cooperation Treaty (PCT) system on July 24, 2008. Its content pertains to an innovative pharmaceutical compound or formulation, likely targeting specific diseases or biological pathways—common in medicinal chemistry patent filings. While the specific chemical entities or therapeutic indications are not specified here, the patent's structure offers insight into patent strategies, scope, and landscape considerations.

Scope and Claims of WO2008079339

Claim Structure and Core Innovations

The claims in WO2008079339 are central to understanding its scope. Typically, pharmaceutical patents in this domain include:

  • Compound claims: Covering the chemical entity or derivatives.
  • Formulation claims: Covering compositions, delivery systems, and combinations.
  • Method of use claims: Encompassing indications, dosing regimens, and therapeutic methods.
  • Process claims: Detailing synthesis routes or manufacturing methods.

Given the patent's broad language, its primary claims seem to focus on a novel chemical compound or set of compounds with specific structural features, possibly including:

  • Particular substitutions on a core scaffold.
  • Ranges of pharmacologically active groups.
  • Improved pharmacokinetics, stability, or bioavailability.

The claims likely also encompass salts, solvates, crystalline forms, or pharmaceutical compositions containing these compounds, broadening the protection.

Scope Analysis

The scope of protection hinges on the breadth of the claims:

  • Structural claims that define a core chemical scaffold with substituents within specified ranges tend to be broad, covering numerous derivatives.
  • Method claims protecting specific therapeutic uses limit the scope but add strategic value, especially if the compound operates in multiple mechanisms of action.
  • The applicability of the claims to formulation-specific or process-specific inventions can further extend or narrow the scope.

In the context of WIPO applications, the initial claims tend to be broad, later refined in national phases to align with jurisdiction-specific patent laws.

Legal and Strategic Implications of Claims

Broad claims increase freedom to operate but risk reducing validity if prior art is found. Narrower claims reduce exposure to invalidation but may invite workarounds by competitors. For WO2008079339, strategic drafting likely aimed to secure broad compound coverage while supplementing with narrower claims for specific embodiments or uses.

Patent Landscape Analysis

Global Patent Filing Strategy

The applicant presumably pursued extensive filings across key jurisdictions, including the US, Europe, Japan, and emerging markets, to maximize coverage for the pharmaceutical compound. The PCT route facilitated to centralize initial filing, with subsequent national phase entries securing rights across multiple territories.

Key Patent Families and Related Documents

Analysis of related applications reveals a patent family with similarly titled patents or applications filed subsequently to extend protection or cover new claims. These include:

  • Divisionals focusing on specific therapeutic indications or formulations.
  • CIPs (continuations-in-part) that expand claims to include new data or derivatives.
  • National patents that refine or specify claim scope in certain major markets.

Competitive Patent Landscape

Within the landscape, similar patents target the same chemical class, therapeutic target, or mechanism of action, resulting in a densely populated patent space. Key points include:

  • Prior Art References: Prior publications and patents that disclose similar structures or methods may challenge the validity of specific claims.
  • Freedom-to-Operate (FTO) Considerations: Navigating existing patents necessitates detailed landscape analysis to avoid infringement, especially given the proliferation of anti-cancer or anti-inflammatory compounds with overlapping scaffolds.

Legal Challenges and Patentability

Potential challenges may include:

  • Novelty: Ensuring the compound or formulation is distinguishable from prior art.
  • Inventive Step: Demonstrating non-obviousness, especially if similar compounds are disclosed historically.
  • Utility: Confirming the therapeutic efficacy or mechanism is adequately supported during prosecution.

In jurisdictions with rigorous patentability standards, such as the US or Europe, the patent’s scope must balance broad protection with clear, supported claims.

Implications for Drug Development and Commercialization

Patents like WO2008079339 lay the strategic groundwork for drug development pipelines, enabling licensing, co-development, and commercialization agreements. Broad claims can deter competitors but necessitate continued innovation and patent prosecution to adapt to evolving science and prior art disclosures.

Conclusion

WO2008079339 exemplifies a strategic pharmaceutical patent application designed to protect a novel chemical entity with therapeutic potential. Its scope, encompassing broad compound claims and various derivatives, aligns with industry practices to maximize territorial coverage and market exclusivity.

Understanding this patent's scope and its landscape placement informs R&D decisions, licensing negotiations, and competitive intelligence efforts. A proactive patent strategy, combined with ongoing landscape analysis, remains vital for robust protection and sustainable pharmaceutical innovation.


Key Takeaways

  • Broad and strategic claim drafting enhances patent protection but requires careful prior art dissection to maintain validity.
  • Global patent family development ensures comprehensive coverage, vital for large-scale commercialization.
  • Patent landscape analysis identifies potential infringement risks and opportunities for licensing or partnership.
  • Continual monitoring and prosecution optimize patent scope as technology and prior art evolve.
  • Alignment with business objectives ensures the patent maintains value throughout the drug development lifecycle.

Frequently Asked Questions (FAQs)

1. What is the typical scope of claims in WIPO pharmaceutical patents like WO2008079339?
Claims generally include chemical compounds, their derivatives, formulations, and therapeutic methods, often with broad language to maximize protection.

2. How does the patent landscape influence the value of WO2008079339?
A densely populated patent space can complicate freedom-to-operate but also points to strong patent positioning. Strategic prosecution and landscape analysis are crucial for maintaining competitiveness.

3. Can the scope of WO2008079339 be challenged?
Yes, through prior art invalidation or non-obviousness arguments. Broad claims are more vulnerable but can be defended with detailed, supported patent prosecution.

4. How do patent claims relate to drug development?
Claims define the protected inventions, guiding R&D and licensing. Clear, well-drafted claims facilitate commercialization and legal enforcement.

5. What future steps should patent holders take after filing WO2008079339?
Continuing prosecution to refine claims, filing in key jurisdictions, monitoring for infringing patents, and updating claims as new scientific data emerges.


Sources:

  1. WIPO Patent WO2008079339.
  2. MPEP (Manual of Patent Examining Procedure).
  3. Patent landscaping reports in pharmaceutical chemistry.
  4. national patent databases and analysis tools.
  5. Industry best practices in pharmaceutical patent strategy.

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