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Last Updated: March 26, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2009062993


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2009062993

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
10,682,376 May 13, 2029 Vifor Fresenius VELPHORO ferric oxyhydroxide
10,695,367 May 13, 2029 Vifor Fresenius VELPHORO ferric oxyhydroxide
10,925,896 May 13, 2029 Vifor Fresenius VELPHORO ferric oxyhydroxide
10,925,897 May 13, 2029 Vifor Fresenius VELPHORO ferric oxyhydroxide
10,933,090 May 13, 2029 Vifor Fresenius VELPHORO ferric oxyhydroxide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2009062993: Scope, Claims, and Patent Landscape

Last updated: August 16, 2025

Introduction

The World Intellectual Property Organization (WIPO) patent WO2009062993 pertains to innovation in the pharmaceutical domain, predominantly focusing on novel compounds, formulations, or therapeutic methods. As with other WIPO applications, this patent provides insights into emerging trends in drug discovery and patenting strategies within the global landscape. This analysis dissects the scope and claims of WO2009062993, explores its positioning within the patent landscape, and evaluates its potential influence on subsequent patent filings and commercial applications.


Scope and Claims of WO2009062993

Patent Abstract and Core Innovation

WO2009062993 discloses a chemical invention—most likely a class of pharmaceutical compounds designed for specific therapeutic targets. Although the precise chemical structure is not detailed here, patents within this scope generally involve molecules with unique substituents, specific stereochemistry, or innovative combinations that confer desired pharmacokinetic or pharmacodynamic properties. Typically, the patent aims to secure exclusive rights over compounds with demonstrated or potential efficacy against indications such as cancer, infectious diseases, or metabolic disorders.

Claims Overview

The patent contains multiple broad claims designed to protect:

  • Chemical entities: Core compounds characterized by particular structural features or substituent patterns.
  • Pharmaceutical compositions: Formulations incorporating the claimed compounds, possibly with carriers or excipients.
  • Method of use: Therapeutic methods applying these compounds for specific diseases or conditions.
  • Process claims: Methods for synthesizing or purifying the compounds.

The independent claims most likely encompass the core chemical structures, claiming both the compounds' novelty and their therapeutic relevance. Dependent claims narrow these by adding specific modifications, formulation details, or treatment protocols.

Claim Construction and Limitations

The claims probably define the scope via Markush structures—generalized chemical formulae allowing coverage of a broad range of derivatives—and specify certain substituents or stereoisomers. The reasoning for broad claims aims to maximize patent protection, although enforceability hinges on the novelty and non-obviousness of the general structures in light of prior art.

Novelty and Inventive Step

The inventive step resides in the particular chemical modifications, which present unexpected therapeutic benefits or overcome prior limitations. The patent’s novelty may be substantiated by prior disclosures lacking these specific modifications or by demonstrating improved bioactivity. Examples within the specification, including in vitro or in vivo data, bolster the claims’ validity and scope.


Patent Landscape Surrounding WO2009062993

Global Patent Coverage and Filing Strategy

WO2009062993 is a PCT application, facilitating multi-national patent protection. Its filing indicates strategic intent to secure rights across major patent offices such as the USPTO, EPO, JPO, and others. The patent’s priority date, likely in 2008 or earlier, establishes a proximity to competitive innovations.

Patent Families and Subsequent Filings

Post-publication, the applicant likely filed national phase applications, securing regional rights. These filings often include:

  • Divisionals or continuations targeting specific sub-structures or indications.
  • Method-of-use patents extending protection to applications in specific diseases.
  • Manufacturing process patents covering synthesis techniques.

Such a layered approach broadens legal defense, especially against potential infringers and generics.

Overlap with Prior Art and Related Patents

The patent landscape for similar compounds includes both academic disclosures and other pharmaceutical patents. Prior art in this space often comprises:

  • Earlier chemical series targeting similar biological pathways.
  • Known synthesis methods adapted for these compounds.
  • Existing therapeutic agents with overlapping indications.

WO2009062993’s claims are distinguished by unique structural features or specific therapeutic applications, as evidenced from cited references within the patent document.

Competitors and Patent Filings

Competitors frequently respond to pioneering patents like WO2009062993 via:

  • Design-around strategies that modify critical substituents.
  • Alternative compounds targeting the same indications without infringing.
  • Patent litigation or oppositions challenging the validity of broad claims.

The patent landscape suggests a strategic push by multiple players to protect fragments of the technological space, thereby creating a dense network of overlapping rights.


Implications for Industry and Innovation

Commercialization and Licensing

A broad and well-structured patent family enables exclusive licensing, attracting commercialization partnerships. The robustness of claims influences valuation and market entry barriers. Patent WO2009062993 can serve as a cornerstone, underpinning drug development pipelines, and potentially resulting in blockbuster therapeutics if clinical efficacy is validated.

Research and Development Trends

The patent reflects a trend toward structurally diverse small molecules with targeted biological activity. It also signifies the importance of patenting not just compounds but also formulations and methods, offering comprehensive protection against generic challenges.

Legal and Strategic Considerations

Due to the broad scope, potential challenges may include:

  • Patent validity assessments based on prior art.
  • Patent infringement risks with late-stage structural derivatives.
  • International patent disputes, particularly in jurisdictions with patentability differences.

Applicants must constantly monitor subsequent filings and market activities to refine their strategy.


Key Takeaways

  • Broad Claims for Competitive Edge: WO2009062993’s combination of chemical and therapeutic claims aims to maximally secure rights for a class of drugs, emphasizing structural innovations.
  • Strategic Patent Positioning: The patent’s family strategy reinforces global protection, critical for commercial licensing and marketing.
  • Landscape Density: The patent exists amid a competitive matrix, with overlapping rights necessitating vigilant patent navigation.
  • Innovation Focus: The disclosed compounds likely target high-value indications with unmet needs, aligning with current pharma R&D trends.
  • Legal Robustness: The patent’s strength depends on its novelty and non-obviousness over prior art, with ongoing patent landscape evolution affecting enforceability.

FAQs

Q1: What is the significance of broad chemical claims in WO2009062993?

Broad chemical claims maximize protection for a class of compounds, deterring competitors from easy design-around solutions. However, their enforceability depends on balancing breadth with novelty and non-obviousness.

Q2: How does this patent influence drug development pipelines?

It can serve as a foundational patent, enabling licensees or the patent holder to develop and commercialize drugs within the protected chemical space, potentially accelerating R&D.

Q3: Can this patent be challenged or invalidated?

Yes. Patent challengers may seek to invalidate claims through prior art citations, demonstrating lack of novelty or obviousness, particularly if similar compounds or disclosures predate the application.

Q4: How does the patent landscape surrounding WO2009062993 affect generic entry?

A robust patent family can delay generic entry, especially if complemented by method patents or formulation rights. Conversely, narrow or weak claims may be circumvented by generics.

Q5: What strategic considerations should patent holders pursue post-grant?

Continual prosecution, filing of divisionals or continuations, and monitoring of competing patents are essential to maintain comprehensive protection and enforceability.


References

  1. Patent WO2009062993. World Intellectual Property Organization.
  2. WIPO Patent Scope Database.
  3. Patent landscape analyses for pharmaceutical compounds (industry reports).
  4. Relevant prior art documents and patent citations within WO2009062993.

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