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Last Updated: December 16, 2025

Profile for Chile Patent: 2013001942


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US Patent Family Members and Approved Drugs for Chile Patent: 2013001942

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Analysis of the Scope, Claims, and Patent Landscape for Chile Patent CL2013001942

Last updated: August 3, 2025


Introduction

Chile Patent CL2013001942 pertains to a pharmaceutical invention, with specific implications for intellectual property rights within Chile’s patent system. This analysis provides a comprehensive review of the patent’s scope, its claims, and the broader patent landscape, informing stakeholders on its strategic importance, potential limitations, and competitive context. As Chile's patent system aligns with international standards, understanding this patent is crucial for pharmaceutical innovators, generic manufacturers, and legal professionals.


Patent Overview and Filing Background

Chile Patent CL2013001942 was filed in 2013, with the patent grant subsequently published in Chile's national patent register. The patent's priority, applicants, and assignees remain integral for contextual understanding. Although full bibliographic data specific to this patent is not publicly available in this overview, patent filings in Chile typically align with patent offices' international standards, allowing detailed analysis of the claims and scope.

Note: For comprehensive, up-to-date data, consulting the Chilean Institute of Industrial Property (INAPI) database is recommended.


Scope of the Patent

The scope of CL2013001942 is primarily defined by its claims, which delineate the legal boundaries of the invention. The scope determines the extent of protection conferred and directly impacts licensing, infringement, and litigation strategies.

In pharmaceutical patents, scope usually revolves around:

  • Chemical Composition: The specific formulation, compound, or molecule.
  • Method of Production: Processes for synthesizing or preparing the active ingredient.
  • Therapeutic Use: Specific indications, delivery methods, or treatment protocols.
  • Formulation and Dosage Forms: Specific delivery systems, such as tablets, injections, or sustained-release formulations.

Analysis indicates that CL2013001942 potentially covers a novel chemical entity or a specific therapeutic combination. The patent claims likely encompass:

  • Main structural formula and its variants.
  • Method of manufacturing the compound.
  • Therapeutic methods for treating a particular disease or condition using the compound.

The comprehensiveness of the claims influences the patent's strength against generic entry and the scope for future innovation.


Claims Analysis

1. Independent Claims

The core innovation is encapsulated in independent claims, which define the broadest scope of protection. For CL2013001942, these may:

  • Cover a novel compound or family of compounds with specific pharmacological properties.
  • Encompass a unique method of synthesis that improves yield, purity, or safety.
  • Protect a specific therapeutic use, such as treatment of a malignant disease or chronic condition.

The precision of these claims determines the enforceability. Broader claims offer stronger market exclusivity but may face challenges during patent examination, especially concerning novelty and inventive step.

2. Dependent Claims

Dependent claims detail specific embodiments, variations, or applications of the independent claims. They often specify:

  • Particular substituents or derivatives of the core compound.
  • Specific pharmaceutical formulations, excipients, or delivery methods.
  • Usage in certain patient populations or with adjunct therapies.

These claims refine the scope, providing fallback positions in infringement disputes and expanding patent coverage.

3. Claim Language and Clarity

Clear, well-structured claims align with global patent standards. Ambiguity or overly broad wording can render claims vulnerable to invalidation. Language elements such as “comprising,” “consisting of,” or “including” influence scope, with “comprising” being inclusive and common in pharmaceutical patents.


Patent Landscape and Competitive Context

The patent landscape for Chilean pharmaceutical inventions is characterized by:

  • Global Patent Families: Companies often file similar patents across jurisdictions; relevance depends on international patent family status. Entities with patents in major markets like the US, Europe, or WIPO PCT applications signal significant R&D investments.

  • Patent Thickets and Overlaps: Multiple patent rights surrounding a core compound can create barriers to entry or license negotiations. In Chile, the presence or absence of overlapping patents impacts market entry timing.

  • Patent Challenges and Litigation: Chile’s relatively efficient patent examination procedures, aligned with international norms, enable timely patent grants. However, validity challenges based on lack of novelty or inventive step are also possible, especially when patent families have prior art disclosures.

  • Related Patent Filings: Other patents in Chile might include improvements (e.g., stable formulations, combination therapies) or diagnostic methods, influencing the scope of freedom to operate.

  • Expired or Lapsed Patents: Patent expiry or lapse due to non-payment of annuities opens opportunities for generics, impacting patent strategies.


Legal and Strategic Considerations

  • Patent Strength: The robustness of CL2013001942 depends on the breadth and clarity of its claims, and whether it successfully overcomes prior art objections during prosecution.
  • Market Exclusivity: Chile's patent law grants 20 years of protection from the filing date, with possible extensions under specific circumstances.
  • Infringement Risks: Given the patent's scope, companies manufacturing similar compounds or therapeutic methods must perform due diligence.
  • Opposition and Litigation: Chilean law permits post-grant opposition, which can challenge the patent’s validity, especially if prior art emerges or if the claims are excessively broad.

Implications for Stakeholders

  • Innovators: Must ensure that claims are sufficiently broad to deter generic competition and encompass potential variations.
  • Generic Manufacturers: Need to map the patent claims carefully; patent expiry or non-infringement paths should be assessed.
  • Legal Professionals: Should monitor oppositions and enforcement actions involving this patent for strategic insights.
  • Research Entities: Can explore patent claims for avenues of further innovation around the protected technology.

Key Takeaways

  • Scope Definition: The patent likely covers a specific chemical entity or therapeutic method with particular formulations or synthesis routes, balancing breadth for market protection with clarity for enforceability.
  • Landscape Positioning: It exists within a competitive patent environment where overlapping rights and potential challenges influence strategic planning.
  • Legal Certainty: Despite Chile’s robust patent system, detailed claim language and ongoing patent maintenance are critical for maintaining enforceability.
  • Patent Strengthening: Broad independent claims complemented by narrow dependent claims improve defensive and offensive patent positions.
  • Future Trends: Watch for potential patent expirations, oppositions, or filings that could influence market dynamics.

FAQs

Q1. What is the significance of the claims language in Chilean pharmaceutical patents?
The claims define the scope of protection and determine enforceability. Clear, precise claims reduce vulnerability to invalidation and ensure competitive advantage.

Q2. How does Chile’s patent law impact the pharmaceutical patent landscape?
Chile offers 20 years of patent protection, with provisions for post-grant opposition. The patent system aligns with international standards, facilitating strategic patent filing and enforcement.

Q3. Can pharmaceutical patents in Chile be challenged post-grant?
Yes. Chile’s law permits third-party opposition within a specific period after patent grant, allowing challenges based on prior art or other grounds.

Q4. What should companies consider regarding patent landscapes in Chile?
They should analyze overlapping patents, expiry statuses, and ongoing patent applications to assess risks and opportunities for market entry and innovation.

Q5. How can understanding this patent inform licensing or infringement strategies?
By analyzing the claims' breadth and territorial scope, stakeholders can evaluate potential infringement risks, negotiate licensing agreements, or prepare defenses against infringing parties.


References

  1. INAPI Chile Patent Database.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. Chilean Patent Law (Decree Law No. 3,610).
  4. Legal analyses and case law from Chile’s Patent Office.
  5. Pharmaceutical patent practices in Latin America.

Further targeted review of the Chilean patent registry and prosecution history is recommended for detailed claim text and legal status.

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