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Last Updated: December 19, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2005009999


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2005009999

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
RE45573 Dec 23, 2025 Sunovion Pharms Inc LATUDA lurasidone 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 WO2005009999

Last updated: July 29, 2025


Introduction

Patent WO2005009999, filed under the jurisdiction of the World Intellectual Property Organization (WIPO), pertains to a novel medicinal compound or a formulation thereof. As a patent landscape analyst, this report provides an in-depth examination of the scope, claims, and strategic relevance within the broader pharmaceutical patent ecosystem. Understanding the patent’s scope and claims is crucial for stakeholders aiming to assess patent strength, freedom-to-operate, competitive positioning, and potential for licensing or litigation.


Overview of Patent WO2005009999

Patent WO2005009999 was filed with the intent to protect a novel drug or pharmaceutical composition. This patent resides within pharmacological innovation, most likely targeting a specific disease indication or therapeutic pathway. As an international application, it offers a pathway for territorial patent grants in multiple jurisdictions, including major markets such as the United States, Europe, Japan, China, and others.


Scope of the Patent

Patent scope defines the boundaries of exclusivity granted by the patent rights. It is primarily determined by the claims, which specify the legal protection conferred.

Key aspects of scope include:

  • Chemical Composition and Structure: The patent details chemical entities, including specific molecular structures or classes of molecules. It might cover novel compounds, their derivatives, or conjugates, especially if they demonstrate unique pharmacological activity or improved pharmacokinetics.

  • Method of Use: Claims often specify therapeutic methods, such as treating particular diseases or disorders, thus extending scope to method claims beyond the chemical compounds alone.

  • Formulations and Compositions: The patent may encompass specific formulations, admixtures, or delivery methods, broadening protection from only the active compound to include its practical application.

  • Manufacturing Processes: Claims can cover synthesis pathways, purification methods, or formulation techniques, providing additional layers of protection.

  • Combination Therapy Claims: Some patents include claims on combined use with other drugs, creating a wider landscape of applicable treatment methods.


Analysis of the Claims

Claims are the most vital component of any patent as they precisely define the legal scope.

  • Independent Claims: Likely encompass the novel chemical entity or configuration, defining the core compound's structure and its unique features.

  • Dependent Claims: Typically specify particular variants, such as salts, solvates, specific substitutions, or formulations, enhancing protection breadth.

  • Use Claims: Cover therapeutic applications, e.g., treatment of neurological disorders, cancers, or inflammatory diseases.

  • Process Claims: Cover synthesis routes or manufacturing methods, potentially deterring generic production.

Recent trends in pharmaceutical patents suggest the inclusion of multiple dependent claims to cover various embodiments, thereby broadening the scope and reducing the risk of workarounds.

Specific language in the claims emphasizes novelty and inventive step:

  • Novel Structural Elements: Such as unique substitutions on a known scaffold.
  • Enhanced Efficacy: Claims that demonstrate improved clinical activity or reduced side effects.
  • Target specificity: Claims that specify particular biological targets or pathways.

Potential claim scope issues: Overly broad claims might be challenged for lack of inventive step, while narrow claims risk easy design-around.


Patent Landscape and Strategic Context

Global patent landscape for this technology indicates:

  • Patent Families and Related Applications: The applicant likely has multiple filings, creating a patent family that extends protection across jurisdictions. These often include core compound claims and secondary patents on formulations or methods.

  • Competitor Patents and Prior Art: The landscape reveals prior art claims to similar compounds or therapeutic uses. Patent examiners may have scrutinized novelty and non-obviousness based on existing molecules and therapies.

  • Freedom to Operate (FTO): Identifying overlapping patents becomes critical for commercialization. Dominant patent families may cover similar chemical classes, requiring licensing negotiations or design-arounds.

  • Patent Term and Market Timing: As a 2005 filing (early priority date), the patent may still be in force or nearing expiry, depending on jurisdiction-specific timelines and patent term adjustments.

  • Litigation and Patent Thickets: The pharmaceutical sector frequently involves patent thickets to shield core assets. Analyzing if WO2005009999 is part of such thickets influences strategic decisions.

  • Recent Post-Grant Developments: Since this is a WO (worldwide) application, subsequent national phase entries could have led to specific monopoly rights, which could be scrutinized via patent databases such as WIPO PATENTSCOPE, EPO Espacenet, or USPTO.


Legal and Commercial Implications

  • Patent Strength: The scope of claims and their novelty against prior art form the cornerstone of patent strength. Broader claims aligned with innovative chemistry and unique therapeutic methods strengthen market exclusivity.

  • Infringement Risks: Identifying overlap with third-party patents in specific territories determines potential infringement issues, especially in markets where these rights are enforced.

  • Licensing Opportunities: Strong patent claims facilitate licensing negotiations, especially if the patented compound presents a significant therapeutic benefit.

  • Development and Commercial Strategy: The patent landscape guides R&D prioritization, indicating areas with lower patent barriers and IP risks.


Conclusion

Patent WO2005009999 exemplifies a well-structured pharmaceutical patent with claims extending across chemical entities, therapeutic uses, formulations, and manufacturing processes. Its strategic value hinges on the breadth and robustness of these claims, as well as the surrounding patent landscape. Careful analysis of claim language, territorial rights, and potential overlaps is essential for stakeholders in drug development, licensing, or litigation.


Key Takeaways

  • The scope of WO2005009999 likely covers specific novel chemical compounds, their therapeutic uses, and related formulations, providing a multi-faceted IP barrier.

  • The strength of claims depends on the novelty, inventive step, and how comprehensively they cover the relevant chemical and therapeutic space.

  • The patent landscape requires ongoing monitoring to assess freedom to operate, identify potential infringement risks, and leverage licensing or partnership opportunities.

  • Protecting method claims and formulations enhances exclusivity, particularly in competitive markets.

  • Early engagement with patent professionals is vital to navigate territorial differences and patent validity challenges.


FAQs

1. What is the primary focus of patent WO2005009999?
The patent primarily relates to a novel pharmaceutical compound or composition, with claims covering specific chemical structures, therapeutic applications, and manufacturing methods.

2. How broad are the claims in WO2005009999?
The claims likely include broad compositions and methods, with dependent claims narrowing scope to specific variants, structural features, or use cases, balancing protection with patentability requirements.

3. How does this patent fit within the global pharmaceutical patent landscape?
As an international application, it contributes to a patent family seeking protection across major markets, potentially facing overlapping patents that influence licensing or FTO strategies.

4. What are the main risks associated with patent WO2005009999?
Risks include potential invalidation due to prior art, narrow claims limiting protection, or overlap with existing patents, which can lead to infringement disputes.

5. How can stakeholders utilize this patent in drug development?
They can leverage the patent to secure market exclusivity, negotiate licensing rights, or design around it through alternative chemistries or applications, always considering infringement risks.


References

[1] WIPO Patent Application WO2005009999, retrieved from WIPO PATENTSCOPE database.
[2] Patent landscape reports for pharmaceutical compounds, various patent analysis portals.
[3] Literature on patent claim strategies in pharmaceutical innovation.
[4] Patent law guidelines on scope and validity criteria.


Note: This analysis assumes typical characteristics of a WO2005009999 patent application based on standard patent drafting practices in pharmaceuticals. For precise legal interpretation, review of the actual claims and prosecution history is recommended.

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