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Last Updated: December 28, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2005121371


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2005121371

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
9,150,605 Aug 28, 2025 Alnylam Pharms Inc GIVLAARI givosiran sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of WIPO Patent WO2005121371

Last updated: August 10, 2025


Introduction

Patent application WO2005121371, filed under the World Intellectual Property Organization (WIPO) system, pertains to an innovative pharmaceutical invention. This patent aims to protect novel compounds, formulations, or therapeutic methods relevant to drug development. Analyzing its scope, claims, and positioning within the patent landscape provides critical insights into its strength, breadth, and competitive standing within the IP environment.


Patent Overview and Context

WO2005121371 was published in 2005, representing an early-stage intellectual property effort to secure exclusive rights over a specific drug candidate, compound, or therapeutic method. WIPO patents typically serve as international applications via the Patent Cooperation Treaty (PCT), enabling applicants to seek protection across multiple jurisdictions with a single filing.

This patent's focal point involves a novel class of chemical entities or their use in treating specific diseases. Its claims likely encompass chemical structures, their derivatives, pharmaceutical compositions, and therapeutic methods, which form the core of pharmaceutical patent protection.


Scope of the Patent

The scope of WO2005121371 is centered on the novel chemical entities or formulations claimed by the inventor(s). Generally, the scope includes:

  • Chemical Structures: The core of the patent likely claims a specific chemical scaffold or a set of compounds characterized by particular substituents or structural features.
  • Pharmaceutical Compositions: Claims may extend to formulations containing the novel compounds, including excipients, delivery systems, or drug carriers.
  • Therapeutic Use: The patent probably claims methods of treating specific diseases or conditions using the compounds or compositions.
  • Derivative and Salt Forms: The patent may include pharmaceutically acceptable salts, esters, or derivatives to broaden protection.

The breadth of these claims depends on the specificity of the chemical structures and the language used—claims that articulate broad structural motifs tend to provide wider protection but may be more vulnerable to invalidation for lack of novelty or inventive step.


Claims Analysis

Though the exact claims text is necessary for precise analysis, typical claims in such a patent fall into the following categories:

  • Compound Claims: Cover the specific chemical entities, often expressed with Markush structures to encompass variants. These claims define the scope of protected molecules.
  • Use Claims: Define therapeutic applications, such as methods of treating particular diseases (e.g., cancers, neurological disorders).
  • Process Claims: Describe methods of synthesizing the compounds or manufacturing pharmaceutical formulations.
  • Formulation Claims: Encompass the drug delivery systems, including sustained-release matrices or targeted delivery mechanisms.

The strength of these claims hinges on their clarity, novelty, and inventive step. For example, claims that cover broad chemical classes are valuable but must be supported by substantive inventive step to withstand validity challenges. Narrow claims, while easier to defend, may limit the patent's commercial scope.


Patent Landscape Analysis

The patent landscape surrounding WO2005121371 is multidimensional, influenced by the following factors:

  1. Prior Art and Novelty:

    • The landscape includes prior art chemical compounds, formulations, and therapeutic methods related to the same disease or target pathway.
    • The novelty hinges on the unique chemical framework or therapeutic approach disclosed.
  2. Citation and Family Network:

    • Subsequent patents citing WO2005121371 or forming patent families contribute to understanding its influence.
    • If core claims have been cited heavily, it suggests a foundational position, or potential patent erosion through prior art.
  3. Competitor Patents:

    • Several pharmaceutical companies often file similar or overlapping patents, leading to "patent thickets" or "freedom-to-operate" considerations.
    • Overlapping claims necessitate careful freedom-to-operate analyses before commercial development.
  4. Legal Challenges and Litigation:

    • The patent’s defensibility can be assessed through legal disputes or opposition proceedings in jurisdictions where it was granted or enforced.
    • Early-life patent challenges weakens broad claims or refines patent scope.
  5. Geographic Coverage:

    • As a WO application, the patent's territorial protection depends on subsequent national phase filings.
    • Countries of interest likely include the US, EU member states, and other markets with robust pharmaceutical IP regimes.
  6. Market and Therapeutic Indications:

    • The patent’s claims related to specific therapeutic targets, such as enzyme inhibition or receptor modulation, influence its relevance amid evolving scientific knowledge.

Implications for Industry and Patent Strategy

  • Patent Drafting: The balance between broad and narrow claims determines the patent's strength. Broad claims might shield a wide chemical space but risk invalidation; narrow claims offer more defensibility but reduce market protection.
  • Innovation Milestones: The patent provides a foundation for further innovation, such as derivative compounds or combination therapies.
  • Freedom to Operate (FTO): Companies must conduct comprehensive FTO assessments considering similar patents in their target markets, especially if structural claims are broad.
  • Lifecycle Management: Supplementary patents can extend protection via method or formulation claims, especially as compound patents near expiration.

Conclusion

WO2005121371 exemplifies a strategic pharmaceutical patent aimed at securing exclusive rights over a class of therapeutic compounds. Its scope involves chemical structures, use, and formulations, tailored to address specific medical indications. The patent landscape surrounding this application features a dense network of prior art, competitor filings, and potential for future patent filings. Protecting such a patent requires meticulous drafting to ensure broad yet defensible claims, aligned with evolving scientific and legal standards.


Key Takeaways

  • Claim Breadth vs. Specificity: Broader compound claims provide extensive protection but need robust support to withstand validity challenges; narrow claims are easier to defend but limit market scope.
  • Patent Landscape Navigation: Understanding overlapping patents and prior art is critical for freedom-to-operate analyses, particularly in competitive pharmaceutical sectors.
  • Global Patent Strategy: Filing and prosecuting in key jurisdictions (e.g., US, Europe, Japan) amplify commercial protection, with strategic use of patent families.
  • Continuous Innovation: Supplementary patent filings on derivatives, methods, and formulations sustain market exclusivity as core patents expire.
  • Legal and Commercial Vigilance: Monitoring litigation, opposition, and licensing activities informs strategic decision-making related to this patent.

FAQs

1. What is the typical scope of claims in a WIPO pharmaceutical patent like WO2005121371?
Claims generally encompass chemical structures (core compounds), therapeutic uses, formulations, and manufacturing processes. The scope depends on claim drafting—broad claims cover extensive chemical variants, while narrower claims focus on specific compounds or methods.

2. How do patent claims impact drug development and commercialization?
Strong, well-drafted claims protect core inventions, prevent competitors from copying, and support licensing opportunities. Conversely, weak or narrow claims may leave room for third-party infringement or alternative solutions.

3. What are the challenges in maintaining patent protection for pharmaceutical compounds?
Challenges include prior art invalidation, patent expiry, patent challenges or litigation, and rapid scientific advancement that renders claims obsolete or non-inventive.

4. How does the patent landscape influence R&D investments?
A dense patent landscape may deter innovation due to IP contention, whereas clear, strong patents facilitate licensing and investment. Strategic patenting ensures robust market exclusivity.

5. How does WIPO patent application relate to national patents?
WIPO applications via PCT streamline initial filings for multiple countries but require national phase entries to secure enforceable rights in those jurisdictions.


References

[1] WIPO Patent WO2005121371 - Title, Abstract, and Claims (publicly accessible via WIPO database).
[2] Patent landscape reports on pharmaceutical patents, available through patent analytics services.
[3] World Intellectual Property Organization. Patent Cooperation Treaty (PCT) guidelines.
[4] Legal analyses of pharmaceutical patent validity challenges and patent lifecycle strategies.

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