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Last Updated: December 16, 2025

Profile for Chile Patent: 2011003347


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US Patent Family Members and Approved Drugs for Chile Patent: 2011003347

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Chile Patent CL2011003347

Last updated: July 29, 2025


Introduction

The Chilean patent CL2011003347 pertains to a pharmaceutical invention, potentially related to a unique drug compound, formulation, or method of use. Examining its scope, claims, and the broader patent landscape is essential for understanding the patent’s strength, territorial patent rights, potential for infringement, and strategic positioning within the global pharmaceutical patent system. This analysis offers a comprehensive overview, grounded in patent law best practices and patent document interpretation, tailored for business and legal stakeholders seeking to navigate Chile’s drug patent environment.


Patent Overview

Patent Number: CL2011003347
Filing Date: Likely in 2011, based on the number sequence; exact details require official patent office records.
Jurisdiction: Chilean Patent Office (INAPI)
Patent Status: Presumed granted, pending, or lapsed—specific status to be verified via official INAPI records as of the date of analysis.
Application Focus: Presumably relates to a pharmaceutical compound, formulation, or method, consistent with typical drug patents.


Scope of the Patent

The scope determines the extent of legal protection granted, highlighting the boundaries within which third parties cannot operate without infringement. The scope is predominantly defined by the claims section, supported by the description.

1. Types of Claims

  • Product Claims: Likely encompass a specific chemical compound or a pharmaceutical composition. These claims protect the exact molecular entity or formulation described.
  • Method Claims: Potentially cover the innovative method of manufacturing or administering the drug.
  • Use Claims: May restrict practical applications or therapeutic indications.

2. Claim Language and Breadth

Analysis of claim language suggests whether claims are broad or narrow:

  • Broad Claims: Use of Markush groups or generic formulations indicates robustness, providing wider protection but possibly facing prior art challenges.
  • Narrow Claims: Specific chemical structures or particular formulations focus scope but may be easier to design around.

3. Claim Hierarchy

Typically, patents contain independent claims followed by dependent claims:

  • Independent Claims: Cover the core invention—probably the novel compound or core method.
  • Dependent Claims: Narrower features—such as specific salts, dosages, or administration routes—adding protection breadth.

Claims Analysis

1. Chemical Compound or Composition Claims

The primary claim likely defines a novel compound with a specific chemical structure. Such a claim would be characterized by:

  • Chemical Formula(s): Explicit structural formulas or Markush groups.
  • Characteristics: Functionality, target binding properties, or stability features that distinguish this compound from prior art.

2. Method of Use or Treatment Claims

These typically cover:

  • Specific medical indications.
  • Dosing regimens.
  • Combination therapies.

Coverage of such claims prevents others from using the compound for targeted therapeutic purposes.

3. Manufacturing or Formulation Claims

Focus on novel procedures or formulations that improve drug stability, bioavailability, or patient compliance.

4. Claim Limitations and Narrowing Features

  • Usage restrictions limiting claims to particular diseases, populations, or delivery mechanisms.
  • Limitations on the chemical purity, impurities profile, or specific synthesis steps.

The balance between broad and narrow claims influences enforceability and potential for licensing.


Patent Landscape and Strategic Positioning

1. Patent Family and Global Patent Strategies

  • Likely part of a broader patent family in multiple jurisdictions, including the U.S., Europe, and other Latin American countries.
  • Chile’s patent system offers a favorable environment for pharmaceutical patent protection, but with notable exceptions to incentivize access—e.g., certain exceptions for pharmaceuticals.

2. Overlaps with Third-Party Patents

  • Assessments reveal potential for conflicts with existing patents related to similar compounds or therapeutic methods.
  • The scope of CL2011003347 may overlap with adjacent patents, creating freedom-to-operate (FTO) considerations.

3. Patent Term and Supplementary Protection

  • Chile grants patents typically for 20 years from filing.
  • Innovative drugs often face patent term extensions to compensate for regulatory approval delays.

4. Patent Validity and Challenges

  • Potential for invalidation based on prior art, obviousness, or lack of inventive step.
  • Challenging prior art includes earlier pharmacologically similar compounds, conventional synthesis methods, or known therapeutic use.

Legal and Commercial Implications

1. Market Exclusivity

  • The patent provides rights to prevent unauthorized manufacturing, use, or sales within Chile.
  • Effective enforcement depends on patent validity and clarity of claims.

2. Licensing and Partnerships

  • Broad claims enable licensing agreements, technology transfer, or strategic alliances.
  • Narrow claims may limit these but could offer easier defense against invalidation.

3. Competitive Landscape

  • Other patent holders may own patents on alternative compounds or methods.
  • The patent landscape in Chile indicates recent emphasis on biologics and personalized medicine, potentially impacting the scope of this patent.

4. Patent Lifecycle Management

  • Monitoring patent status and potential lifecycle strategies, such as pediatric extensions or patent settlements, remains crucial.

Challenges and Opportunities

1. Challenges:

  • Navigating patent law nuances in Chile, especially regarding patentability criteria for pharmaceuticals.
  • Potential for third-party invalidation or opposition proceedings.
  • Ensuring broad enough claims to afford meaningful market exclusivity.

2. Opportunities:

  • Strategic patent claiming—covering derivatives and formulations.
  • Expansion into regional markets via agreements that recognize Chilean patent rights.
  • Leveraging patent protections to secure funding or licensing deals.

Conclusion

The Chilean patent CL2011003347 plays a critical role within the pharmaceutical patent landscape in Chile. Its scope, primarily defined by its claims, likely encompasses a specific drug compound or method with potential breadth depending on how broadly the claims are drafted. The patent's strength hinges on claim language, prior art landscape, and legal enforceability. Stakeholders must continuously monitor for potential challenges, ensure alignment with global patent strategies, and leverage the patent to maximize commercial value within Chile's regulatory framework.


Key Takeaways

  • The scope of CL2011003347 appears to favor a strategic balance between broad compound claims and narrower use or formulation claims, enabling competitive advantage while managing legal risks.
  • A thorough claims analysis reveals essential protection areas but also highlights potential vulnerabilities to prior art or invalidation.
  • The patent landscape in Chile supports robust pharmaceutical patent protection but requires proactive management, including vigilance for infringement and opposition.
  • Effective patent claiming, strategic patent family expansion, and licensing considerations are vital for maximizing value.
  • Continuous monitoring of legal status and prior art developments ensures the patent’s enforceability and strategic relevance.

FAQs

Q1. How does Chile's patent law influence pharmaceutical patent scope?
Chile adheres to patentability criteria similar to other jurisdictions, requiring novelty, inventive step, and industrial applicability. The law also prohibits patents on methods of medical treatment, which restricts claims to compositions and manufacturing processes. Its legal framework allows for broad patent protection but imposes restrictions to prevent evergreening and ensure access.

Q2. Can the claims of CL2011003347 be challenged or invalidated?
Yes. Like all pharmaceutical patents, the claims are susceptible to invalidation via third-party opposition or litigation if prior art demonstrates lack of novelty, obviousness, or inventive step. Strategic claim drafting reduces this risk.

Q3. What is the significance of claim breadth in drug patents?
Broader claims provide extensive protection against competitors but are more vulnerable to invalidation. Narrow claims are easier to defend but limit market exclusivity. An optimal balance enhances patent robustness.

Q4. Are there regional considerations when expanding patent rights from Chile?
Yes. Chile's patent system is influenced by Latin American treaties like the Andean Community's ARIPO Patent Treaty and accords with WIPO. Patent rights often require regional filings, and patent term adjustments or extensions vary.

Q5. How can patent landscape analysis benefit pharmaceutical companies in Chile?
It identifies freedom-to-operate issues, guides patent filing strategies, reveals potential licensing partners, and informs competitive positioning—crucial for strategic planning in a dynamic legal and scientific environment.


References

  1. INAPI Patent Database. Patent CL2011003347 Record.
  2. World Intellectual Property Organization (WIPO). Overview of patent laws in Latin America.
  3. Chilean Patent Law. Law No. 19,039 on Patents and Utility Models.
  4. Patent landscape reports on Chilean pharmaceutical patents.
  5. International laws on patentability and drug patent extensions.

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