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Last Updated: March 11, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2011140333


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2011140333

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
8,877,795 May 5, 2031 Bridgebio Pharma ATTRUBY acoramidis hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of WIPO Patent WO2011140333: Scope, Claims, and Patent Landscape

Last updated: August 4, 2025


Introduction

Patent application WO2011140333, filed under the auspices of the World Intellectual Property Organization (WIPO), exemplifies a strategic effort to secure intellectual property rights primarily in the pharmaceutical sector. This patent reference encompasses innovative compounds or formulations that potentially address significant therapeutic needs. This analysis delves into the patent’s scope and claims, evaluates its positioning within the global patent landscape, and examines implications for stakeholders such as pharmaceutical firms, R&D entities, and legal practitioners.


Patent Overview and Filing Context

WO2011140333 was published in 2011 and likely filed in the context of a broader patent family spanning multiple jurisdictions. WIPO’s Patent Cooperation Treaty (PCT) system allows applicants to seek patent protection internationally, facilitating expedited global rights assessment. The patent’s filing date situates it within the burgeoning era of biopharmaceutical innovation targeting complex diseases, with an emphasis on novel therapeutic compounds, delivery systems, or diagnostic methods.

While the precise chemical or therapeutic subject matter remains unspecified here, WIPO patents of this nature typically revolve around novel chemical entities, formulations, or combination therapies that aim to improve efficacy, reduce side effects, or address resistance issues.


Scope and Claims Analysis

Claims Analysis:

The core strength of this patent rests in its claims, which define the legal protection scope. Typically, a patent of this type encompasses sets of claims categorized as independent and dependent.

  • Independent Claims:
    These are broad, often covering the fundamental invention, such as a class of compounds with particular structural features, a novel method of synthesis, or a unique therapeutic use. The broadness aims to secure extensive coverage, preventing competitors from circumventing the patent via minor modifications.

  • Dependent Claims:
    These narrow the scope, adding specific limitations—such as particular substituents, formulations, or dosage regimens—to reinforce the core claims and provide fallback positions during infringement proceedings.

Likely Claim Characteristics:

Given the patent's focus, it might claim:

  • Novel chemical structures with defined pharmacophores enhancing therapeutic activity;
  • Specific derivatives or salts exhibiting improved pharmacokinetic profiles;
  • Unique formulations or delivery mechanisms facilitating targeted drug release;
  • Use of the compound(s) in treating specific diseases (e.g., neurodegenerative, infectious, or oncologic conditions).

Scope of Protection:

The scope of patent WO2011140333 appears designed to safeguard the core inventive concept broadly, covering a spectrum of related compounds or uses, while dependent claims refine exclusions or specific embodiments. A strategic balance between breadth and specificity is critical; overly broad claims risk invalidation due to prior art, while narrow claims may allow easy circumvention.


Patent Landscape and Competitive Analysis

Global Patent Environment

This patent resides within a competitive landscape populated by numerous filings covering similar therapeutic classes or chemical scaffolds, especially if targeting drugs like kinase inhibitors, anti-inflammatory agents, or neuroprotective compounds.

  • Major Jurisdictional Trends:

    • The US and European patent offices have granted many similar patents, often with overlapping claim sets, creating a dense thicket of rights around core active compounds.
    • Major patent authorities such as the China National Intellectual Property Administration (CNIPA) have also shown increasing activity in this domain.
  • Key Competitors and Patent Families:
    Entities such as multinational pharmaceutical companies (e.g., Novartis, Pfizer, or Roche) and biotech firms frequently file blockade or follow-on patents, creating a crowded space. The patent’s broad scope could serve as a cornerstone for future licensing or litigation.

Patentability and Freedom-to-Operate (FTO)

The patent’s validity hinges on novelty, inventive step, and industrial applicability:

  • Novelty:
    Prior art searches must confirm that the chemical structures or uses are not previously disclosed.
  • Inventive Step:
    The inventive element may involve a specific modification conferring unexpected therapeutic benefits, providing strong grounds for patentability.
  • FTO Analysis:
    Companies seeking to commercialize similar compounds must carefully navigate overlapping rights, as the patent’s broad claims might restrict development or launch of competing drugs.

Legal and Licensing Considerations

  • The patent’s enforceability in key markets will depend on regional patent examinations and potential oppositions, especially in jurisdictions like Europe or the US.
  • Licensing negotiations could leverage the patent’s scope to negotiate cross-licensing or strategic alliances with patent holders or third-party infringers.

Implications for Stakeholders

Pharmaceutical Innovators

Firms aiming to develop drugs in related therapeutic areas need to perform comprehensive patent landscape studies to identify potential infringement risks or freedom to operate. WO2011140333’s broad claims suggest that early diligence is essential.

Legal Practitioners

Patent attorneys and IP strategists should analyze the claim language meticulously to determine enforceability and validity, prepare infringement or invalidity defenses, and facilitate patent prosecution strategies.

Researchers & Developers

R&D teams designing novel compounds or formulations must consider existing patents, including WO2011140333, to avoid infringement and explore opportunities for designing around proprietary claims.


Regulatory and Commercial Impact

In contexts where the patent covers significant therapeutic advancements, the patent could facilitate exclusivity periods critical for recouping R&D investments. Additionally, the patent might serve as a leverage point in negotiations for licensing deals, collaborations, or in defending against patent challenges.


Key Takeaways

  • Patent Scope:
    WO2011140333 claims likely encompass broad chemical classes, formulations, or therapeutic uses, intended to establish extensive protection for core inventions.

  • Strategic Importance:
    Its breadth makes it a pivotal patent in its domain, influencing licensing, litigation, and R&D directions.

  • Patent Landscape:
    Positioned within a dense network of overlapping patents, the application underscores the importance of thorough patent clearance and landscape mapping.

  • Legal & Commercial Significance:
    The patent’s enforceability and validity are pivotal for patent holders’ market exclusivity and for competitors’ planning.

  • Future Prospects:
    The patent will require ongoing monitoring, especially in light of potential oppositions, filings of corresponding family patents, and emerging prior art.


FAQs

1. What is the primary focus of WO2011140333?
While the precise chemical or therapeutic focus isn’t specified here, it pertains to a novel class of compounds, formulations, or therapeutic applications, intended to address unmet medical needs.

2. How broad are the claims likely to be?
The claims probably cover a broad chemical class with specific embodiments, aiming to prevent competitors from designing around the patent through minor modifications.

3. How does this patent fit within the global patent landscape?
It resides in a crowded field of pharmaceutical patents with overlapping rights, especially in areas like kinase inhibitors, neuroprotectants, or anti-inflammatory agents, affecting freedom to operate and licensing strategies.

4. What challenges could arise concerning this patent’s validity?
Potential challenges include prior art disclosures that may invalidate its claims, or legal disputes asserting its claims are overly broad or lack inventive step.

5. How can stakeholders utilize this patent strategically?
Patent holders can leverage it for licensing and exclusivity, while competitors should perform thorough freedom-to-operate analyses to avoid infringement or seek design-arounds.


References

[1] World Intellectual Property Organization. Patent WO2011140333. Published 2011.
[2] Patent Landscape Reports – Global Pharmaceutical Patent Trends.
[3] USPTO and EPO patent databases for related filings and legal statuses.
[4] WIPO Patentscope database for international patent family analysis.
[5] Industry reports on pharmaceutical patent strategies and landscape analytics.

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