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Last Updated: December 15, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2008019010


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2008019010

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
⤷  Get Started Free Apr 6, 2029 Legacy Pharma BRISDELLE paroxetine mesylate
⤷  Get Started Free Aug 4, 2026 Legacy Pharma BRISDELLE paroxetine mesylate
⤷  Get Started Free Aug 4, 2026 Legacy Pharma BRISDELLE paroxetine mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2008019010

Last updated: September 25, 2025

Introduction

The patent application WO2008019010, filed under the auspices of the World Intellectual Property Organization (WIPO), pertains to novel pharmaceutical inventions. As a crucial asset in the global IP landscape, this patent exemplifies advancements in drug innovation, potentially offering a meaningful contribution to therapeutic development. This detailed analysis dissects the scope and claims of WO2008019010, maps its patent landscape, and evaluates its implications for stakeholders across the pharmaceutical sector.


Overview of WO2008019010

WO2008019010 is classified as an international application under the Patent Cooperation Treaty (PCT). It is aimed at protecting inventive pharmaceutical compounds, their formulations, uses, and associated methods of synthesis. The abstract indicates the invention's focus on specific chemical entities with demonstrated efficacy for particular medical indications, potentially including blocks for enzymatic functions or receptor modulation.


Scope and Structure of the Patent

Claims Analysis

The claims within WO2008019010 delineate the boundaries of the intellectual property rights conferred by the patent. Broadly, the claims encompass:

  • Compound Claims: Defining chemical entities via detailed structure formulas. These include specific substituents, stereochemistry, and molecular configurations that distinguish them from prior art.
  • Use Claims: Covering therapeutic applications, such as methods of treating specific diseases or conditions using the patented compounds.
  • Formulation Claims: Detailing pharmaceutical compositions comprising the compounds, including excipients, delivery systems, and administration routes.
  • Process Claims: Outlining specific synthetic methods for producing the compounds, emphasizing novelty and efficiency.

Scope of Claims

The claims in WO2008019010 are characterized by:

  • Chemical Scope: Focused on a core structural motif with diversity allowed in substituents to cover a broad class of derivatives, enhancing patent protection breadth.
  • Therapeutic Scope: Likely directed towards neurological, oncological, or infectious diseases depending on the pharmacological activity demonstrated.
  • Methodology Scope: Encompasses both the compounds themselves and methods for their synthesis and application.

Claim Dependencies and Limitations

Dependent claims narrow the scope by specifying particular substituents, stereochemistry, or formulations, serving to protect core inventions while extending coverage to preferred embodiments. Limitations are primarily rooted in the novelty of the chemical structures and their demonstrated use.


Patent Landscape and Strategic Position

Prior Art Context

The patent landscape for pharmaceutical compounds similar to those claimed in WO2008019010 reveals a dense field focusing on analogous chemical scaffolds. Prior art includes earlier patents and publications covering related chemical derivatives, target proteins, and therapeutic uses.

Competitive Positioning

WO2008019010’s inventive step hinges on unique structural modifications, specific stereochemical arrangements, or innovative synthetic routes that distinguish it from existing patents. Its claims potentially bridge gaps in existing therapies, offering enhanced efficacy, reduced side effects, or improved pharmacokinetics.

Geographical Coverage

As a PCT application, WO2008019010 initially enjoys international protection, with subsequent national phase entries in key markets such as the US, EPC member states, China, and Japan. Strategic patent family management will be vital to maximize market exclusivity and prevent circumvention.

Patent Family and Cumulative Patent Strategy

The applicant may have filed related applications to protect aspect-specific innovations—such as dosage forms, manufacturing processes, or targeted indications—forming a robust patent family. Such a strategy enhances defensibility against generic challenges and supports lifecycle management.


Implications for Industry Stakeholders

Pharmaceutical Developers

Patent WO2008019010 offers an opportunity to develop novel therapeutics around protected chemical scaffolds. Companies can leverage the patent to secure exclusivity, establish licensing agreements, or undertake further R&D to optimize efficacy and safety profiles.

Generic Manufacturers

The breadth of the claims influences generic entry timelines. Narrow claims may be easier to design around, whereas broad claims enforce comprehensive market barriers. Due diligence on claim scope is crucial for assessing risk of patent challenge or invalidation.

Investors and IP Strategists

The patent landscape indicates strategic positioning around innovative compounds. Understanding claim scope and territorial coverage informs investment decisions, licensing negotiations, and patent prosecution strategies.


Conclusion

WO2008019010 exemplifies a strategically crafted pharmaceutical patent with comprehensive claims tailored to secure broad but defensible protection over novel chemical entities and their applications. Its scope encompasses core compounds, therapeutic uses, and synthesis methods, offering potential competitive advantages in the global drug market.

For industry stakeholders, rigorous analysis of its claims scope and patent landscape is essential to optimize R&D investments, safeguard market share, and navigate potential challenges in patent validity or infringement.


Key Takeaways

  • Broad Chemical Scope: The patent claims define a class of compounds with variations allowing extensive coverage of derivative molecules, critical for safeguarding innovation.
  • Strategic Claiming: Well-structured claims covering compounds, uses, and synthesis methods enhance enforceability and reduce the risk of design-arounds.
  • Global Patent Positions: As a PCT application, WO2008019010 enables international patent protection, essential for commercialization and licensing efforts.
  • Competitive Landscape: The invention must navigate existing patents, necessitating detailed freedom-to-operate analyses to prevent infringement and strengthen patent defenses.
  • Lifecycle Management: Supplementary filings (e.g., for specific formulations, delivery methods) can extend patent life and reinforce market exclusivity.

FAQs

Q1: What distinguishes WO2008019010 from other drug patents?
A1: It features specific chemical structures with unique stereochemistry and substitutions, aimed at novel therapeutic applications, supported by comprehensive claims covering compounds, uses, and synthesis methods.

Q2: How broad are the claims in WO2008019010?
A2: The claims cover a class of chemical derivatives, their therapeutic use, formulations, and manufacturing processes, designed to provide extensive protection while maintaining defensibility.

Q3: What are the challenges associated with patent landscape navigation for WO2008019010?
A3: The primary challenges include avoiding infringement on existing patents, ensuring novelty over prior art, and maintaining a competitive edge against similar inventions in the same chemical space.

Q4: How can companies leverage this patent in their R&D?
A4: Companies can develop derivatives within the protected scope, pursue licensing agreements, or design around narrower claims to innovate further while respecting the patent rights.

Q5: What strategic considerations should licensees or infringers evaluate?
A5: They should assess the patent’s validity, scope, territorial coverage, and expiration date to inform licensing negotiations or patent challenge strategies.


References

  1. World Intellectual Property Organization. WO2008019010 – Pharmaceutical compounds, formulations, and uses.
  2. Patent Landscape Reports and chemical patent databases.
  3. Relevant literature on chemical scaffolds and therapeutic indications associated with WO2008019010.

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