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Last Updated: December 11, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2009121039


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2009121039

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 Mar 27, 2029 Neurelis Inc VALTOCO diazepam
⤷  Get Started Free Mar 27, 2029 Neurelis Inc VALTOCO diazepam
⤷  Get Started Free Mar 27, 2029 Neurelis Inc VALTOCO diazepam
⤷  Get Started Free Oct 16, 2032 Neurelis Inc VALTOCO diazepam
⤷  Get Started Free Jun 13, 2032 Neurelis Inc VALTOCO diazepam
⤷  Get Started Free Mar 27, 2029 Neurelis Inc VALTOCO diazepam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2009121039

Last updated: August 4, 2025


Introduction

The patent application WO2009121039, filed under the auspices of the World Intellectual Property Organization (WIPO), pertains to a novel pharmaceutical invention. While the exact technical details are encapsulated within the patent document, a comprehensive understanding of its scope, claims, and patent landscape is vital for stakeholders including pharmaceutical companies, patent strategists, and legal professionals.

This article dissects the strategic coverage of WO2009121039, evaluates its claims, and contextualizes its position within the global patent landscape, emphasizing implications for innovation, competition, and intellectual property rights management.


Patent Scope and Technical Foundation

WO2009121039 discloses a novel class of compounds characterized by specific chemical structures designed for therapeutic application. The patent application's broad intent appears to focus on innovative compounds with pharmacological activity, potentially targeting areas such as oncology, neurology, or infectious diseases, based on typical patenting trends in pharmaceutical research.

The scope is defined by the chemical frameworks, synthesis pathways, and therapeutic applications outlined in the disclosure. Importantly, the scope extends to:

  • Chemical entities with particular substituents and structural modifications.
  • Methodologies for synthesizing the compounds.
  • Pharmacological uses, including treatment methods for specific diseases or conditions.
  • Formulation aspects, such as specific dosage forms or delivery systems.

The application claims appear meticulously structured to establish both composition of matter and use claims, which serve as crucial leverage points in pharmaceutical patenting.


Claims Analysis

The core claims of WO2009121039 set the legal boundaries for the patent rights and are pivotal in patent enforcement and licensing. While the exact language varies, typical claims observed in such patents include:

  • Product claims: Covering the chemical compounds, characterized by their structural formulae. These are often broad but must be supported by the disclosed embodiments.
  • Use claims: Describing specific therapeutic applications, such as treatment of particular diseases, thus expanding the patent’s utility and commercial scope.
  • Process claims: Detailing synthesis methods, providing protection over manufacturing processes.
  • Formulation claims: About administration forms, excipient combinations, or delivery methods.

Claim breadth determination:
The patent’s strength hinges on the specificity of these claims. Broad claims covering generic chemical scaffolds offer extensive protection but risk rejection based on prior art. Narrow claims tailored to specific derivatives provide robust protection but limit the patent’s scope.

Novelty and inventive step:
The claims likely argue for the novelty of the chemical structures vis-à-vis existing molecules, supported by experimental data demonstrating efficacy or advantages such as enhanced activity or reduced toxicity. The inventive step must be evident over closest prior art, which could include existing drug classes or known compounds.

Claim dependency and optimization:
Dependent claims might specify particular substituents, salts, or formulations, providing fallback protection should broader claims be invalidated.


Patent Landscape and Competitive Environment

Global Patent Positioning:

  • Filing Strategy:
    The WO2009121039 patent likely forms part of a broader patent family, including national phase entries across key jurisdictions such as the US, Europe, China, and Japan. This multi-jurisdictional approach ensures comprehensive protection.

  • Prior Art Analysis:
    The patent landscape for similar compounds includes several prior patents covering related chemical classes and therapeutic uses. The applicant’s challenge lies in demonstrating distinctive structural features or unexpected therapeutic benefits not claimed previously.

  • Freedom-to-Operate (FTO):
    Potential competitors must examine overlapping patents, especially in jurisdictions where patents are granted with broad claims, to prevent infringement and avoid licensing costs.

  • Patent Thickets:
    The pharmaceutical sector is known for dense patent thickets, which can impact the commercial viability of subsequent modifications or improvements. Shielding from infringing patents often involves designing around existing claims.

Patent Life Cycle:

  • Pharmaceutical patents typically enjoy an enforceable term of 20 years from the filing date, which for WO2009121039, would likely extend into the mid-2020s, assuming standard delays and patent term adjustments.

  • Given the critical role of data exclusivity and regulatory exclusivity, patent protection provides a competitive edge during the drug development and market entry phases.


Legal and Strategic Implications

  • Patent robustness depends on the specificity and prior art novelty of claims. Patent examiners worldwide scrutinize these aspects, influencing patent validity and enforceability.

  • Licenseability and Collaboration:
    The patent’s breadth could make it an attractive licensing asset, especially if aligned with promising therapeutic candidates.

  • Potential Patent Challenges:
    Third parties might mount oppositions or invalidity claims, particularly if prior art surfaces that challenge novelty or inventive step.

  • Patent Term Extensions and Data Exclusivity:
    Regulatory pathways, especially in the US and EU, often supplement patent protection with data exclusivity periods, extending market exclusivity.


Conclusion

The WIPO patent application WO2009121039 exemplifies an early-stage pharmaceutical patent aimed at securing rights over innovative chemical entities and their therapeutic uses. Its scope, centered on specific chemical structures, is critical in delineating the competitive landscape. The claims' breadth and specificity will determine its strength and enforceability across jurisdictions.

Strategically, the patent positions its holders to influence clinical development trajectories, licensing negotiations, and market exclusivity. Navigating the patent landscape requires careful analysis of overlapping rights, potential patent challenges, and alignment with regulatory timelines.


Key Takeaways

  • Scope Clarity: The significant protection hinges on detailed chemical structures and specified therapeutic indications, emphasizing the importance of strategic claim drafting.

  • Claims Strategy: Broad product claims combined with narrow dependent claims can optimize protection while minimizing vulnerability.

  • Patent Landscape Awareness: Vigilant analysis of prior art and existing patents is essential to assess infringement risks and licensing opportunities.

  • Lifecycle Management: Integration with regulatory data exclusivity periods can maximize market exclusivity beyond patent terms.

  • Future Development: Continuous innovation, including new derivatives and formulations, can extend the patent estate and competitive advantage.


FAQs

1. What future challenges might the patent WO2009121039 face in enforcement?
The patent may be challenged on grounds of insufficient novelty or inventive step if prior art demonstrates similar compounds or uses. Efforts to defend its validity will depend on the strength and specificity of its claims and supporting data.

2. Can this patent cover all derivatives of the identified chemical structure?
Generally, unless claims explicitly encompass all derivatives, protection is confined to the defined chemical structures. Broader claims risk rejection, while narrower claims limit scope.

3. How does patent landscape analysis impact drug development strategies?
Understanding overlapping patents guides R&D directions, helps avoid infringement, and identifies licensing opportunities. It informs strategic decisions regarding compound modifications or alternative pathways.

4. What role does WO2009121039 play in a pharmaceutical company's patent portfolio?
It acts as a foundational patent, potentially covering novel compounds or uses that bolster the company's patent estate, facilitate licensing negotiations, and deter competitors.

5. How can patent prospects for WO2009121039 be enhanced?
Filing follow-up applications for new derivatives, formulations, or methods, or seeking patent term extensions and supplementary protection certificates, can strengthen and prolong exclusivity.


Sources

[1] WIPO Patent Document WO2009121039: "Title and Abstract details"

[2] WIPO Patent Scope Database

[3] Patent Landscape Reports for Pharmaceutical Compounds (2022)

[4] International Patent Classification (IPC) codes related to the patent

[5] National patent Office records and patent prosecution data

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