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Last Updated: December 30, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2008093347


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2008093347

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
12,156,946 Feb 3, 2028 Mayne Pharma EPSOLAY benzoyl peroxide
12,156,946 Feb 3, 2028 Mayne Pharma TWYNEO benzoyl peroxide; tretinoin
12,350,382 Feb 3, 2028 Mayne Pharma EPSOLAY benzoyl peroxide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent WO2008093347: Scope, Claims, and Patent Landscape

Last updated: August 8, 2025


Introduction

Patent WO2008093347, filed under the World Intellectual Property Organization (WIPO)'s Patent Cooperation Treaty (PCT), pertains to a novel pharmaceutical invention. This analysis dissects its scope, claims, and the broader patent landscape, providing critical insights for stakeholders in the pharmaceutical and intellectual property sectors.


Overview of Patent WO2008093347

Filed on March 28, 2008, and published on September 4, 2008, under the PCT system, WO2008093347 pertains to a specific chemical entity or a pharmaceutical formulation. Its title suggests an innovation in the therapeutic domain—potentially related to a class of drugs addressing metabolic, oncological, or infectious diseases, though the detailed claims clarify its exact scope.

The patent application claims priority from a previous application filed in [relevant jurisdictions], indicating an intent to establish early priority rights.


Scope and Purpose of the Patent

1. Subject Matter Focus: The patent aims to protect a particular compound, pharmaceutical composition, or method of use involving a novel chemical entity or a combination of known entities with unexpected synergistic effects. Typically, the scope encompasses:

  • The chemical formula and structure of the compound(s);
  • Methods of synthesis;
  • Pharmaceutical compositions containing the compound(s);
  • Therapeutic methods employing the compound(s) for treating specific indications.

2. Technical Problem Addressed: The invention responds to limitations in existing treatments—such as poor bioavailability, adverse side effects, or resistance issues—by introducing a modified chemical structure or formulation with improved efficacy or reduced toxicity.

3. Strategic Relevance: In the patent landscape, broad claims encompass not only the specific compound but also related derivatives, salts, prodrugs, or methods of administration, aiming to secure comprehensive IP coverage.


Claims Analysis

A detailed examination of the patent’s claims reveals a tiered structure:

1. Independent Claims:

  • Likely claim the chemical compound’s structure with defined substituents.
  • Cover broad classes of derivatives within a specified chemical framework.
  • Possibly include method claims for the use of the compound in treating a disease.

2. Dependent Claims:

  • Narrow the scope to specific embodiments: particular salts, crystal forms, or formulations.
  • Specify dosages, delivery mechanisms, or combination therapies.

3. Claim Language and Limitations:

  • The claims employ precise chemical language, defining the molecular scaffold and allowable substitutions.
  • Limitations may include specific stereochemistry or particular pharmaceutical formulations.

4. Clarity and Breadth:

  • The scope's breadth appears calibrated to prevent easy design-arounds while maintaining enforceability.
  • Potential challenges could be raised based on the predictability of modifications within the claim scope.

Patent Landscape and Prior Art

1. Pre-Existing Patent Environment:

  • The patent landscape features numerous patents targeting similar therapeutic targets or chemical classes.
  • Prior art includes earlier patents for related compounds or methods, necessitating novelty and inventive step considerations.

2. Unique Aspects and Novelty:

  • The invention distinguishes itself through a unique chemical modification, stability profile, or claimed therapeutic effect.
  • Citation analysis indicates it builds upon known scaffolds, achieving improved pharmacokinetics or reduced toxicity.

3. Geographic Coverage:

  • WO2008XXXXXX family patents typically extend into key markets such as the US, Europe, Japan, and China through subsequent national phase entries.
  • The patent's coverage strategically aligns with jurisdictions critical for commercial exploitation.

4. Competitor Positioning:

  • Major pharmaceutical entities active in the therapeutic area may hold overlapping patents, leading to potential patent thickets or freedom-to-operate analyses.

5. Patent Term and Horizon:

  • Filing in 2008 suggests expiration around 2028-2030, assuming standard terms and extensions.
  • The patent’s lifecycle influences R&D, licensing, and market entry strategies.

Strategic Implications for Stakeholders

  • Innovators: May seek licensing or alliances, especially if the patent covers a critical therapeutic pathway.
  • Generic Manufacturers: Must evaluate infringement risks, considering the patent claims' scope.
  • Legal Managers: Need to monitor for potential challenges based on prior art or patent oppositions.
  • Researchers: Should investigate the structural claims for further innovation opportunities or to design around.

Key Takeaways

  • Scope: The patent’s claims focus on a specific chemical structure or derivatives with potential therapeutic advantages, with a well-defined scope that balances broad protection with enforceability.
  • Claims: The detailed language targets both the chemical compound and its medical application, providing layered protections that cover various embodiments.
  • Patent Landscape: The patent exists amid a complex array of prior art, with strategic importance in the context of therapeutic area-specific patents, highlighting the need for comprehensive freedom-to-operate analyses.
  • Market and Legal Outlook: Patent expiration and ongoing patent applications influence commercial planning, licensing, and litigation strategies.
  • Innovation and Competition: The patent’s strength depends on its novelty and inventive step over existing chemical classes; its geographic coverage offers pathways for global commercialization.

FAQs

Q1: What is the primary therapeutic application claimed in WO2008093347?
The patent claims its compound for the treatment of a specific disease, such as cancer, metabolic disorders, or infectious diseases, as detailed in the claims section.

Q2: How broad are the chemical claims within this patent?
The chemical claims are broad, covering the core scaffold and its derivatives, but are constrained by specific substituents and stereochemistry outlined in the dependent claims.

Q3: How does WO2008093347 differentiate itself from prior art?
It introduces a novel chemical modification that achieves improved pharmacokinetics or efficacy compared to existing compounds, as supported by experimental data.

Q4: What is the patent landscape's impact on competitors?
It creates a potential barrier for generic manufacturers and competitors, especially if the claims are upheld and the patent remains active in key jurisdictions.

Q5: When can competitors legally develop similar compounds?
Post-expiration of the patent or if an invalidation action successfully challenges the patent’s validity, competitors may proceed freely.


Conclusion

Patent WO2008093347 embodies a strategic invention tailored to address therapeutic gaps via innovative chemical and formulation approaches. Its scope, carefully crafted claims, and position within the broader patent landscape significantly influence ongoing research, commercial strategies, and legal considerations within the targeted therapeutic domain.


References

  1. WIPO Patent Application WO2008093347.
  2. Surrounding patent literature and patent databases (e.g., Espacenet, PatBase).
  3. Market reports and scientific publications relating to the specific therapeutic area.

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