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Last Updated: December 18, 2025

Profile for Chile Patent: 2019002239


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US Patent Family Members and Approved Drugs for Chile Patent: 2019002239

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
10,045,991 Apr 4, 2037 Bayer Healthcare VITRAKVI larotrectinib sulfate
10,137,127 Apr 4, 2037 Bayer Healthcare VITRAKVI larotrectinib sulfate
10,668,072 Apr 4, 2037 Bayer Healthcare VITRAKVI larotrectinib sulfate
11,191,766 Apr 4, 2037 Bayer Healthcare VITRAKVI larotrectinib sulfate
11,484,535 Apr 4, 2037 Bayer Healthcare VITRAKVI larotrectinib sulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Chile Drug Patent CL2019002239

Last updated: August 15, 2025

Introduction

The patent CL2019002239, granted in Chile, pertains to a drug or pharmaceutical invention with implications for the healthcare market, patenting strategies, and investment considerations. This detailed analysis examines the scope and claims of the patent, contextualizes its position within the global and regional patent landscape, and evaluates its strategic significance for stakeholders in the pharmaceutical industry.


Overview of Chile Patent CL2019002239

CL2019002239 was assigned by the Chilean National Institute of Industrial Property (INAPI). The patent’s filing date, priority, and grant date establish its lifecycle and potential exclusivity period. As of the latest information, the patent relates primarily to a pharmaceutical compound or formulation designed to treat specific medical conditions, possibly involving innovative delivery mechanisms or novel combinations.


Scope of the Patent

The scope of CL2019002239 defines the extent of legal protection conferred by the patent. Based on standard patent practices, the scope is primarily articulated through the patent’s claims, supported by detailed descriptions.

Claims Overview

The patent comprises independent claims that delineate the core inventive concept, and dependent claims that specify particular embodiments or variations. Although an exact listing of claims requires access to official documentation, typical claims for a pharmaceutical patent of this category include:

  • Compound Claims: Covering a chemical entity, such as a novel active pharmaceutical ingredient (API) or a prodrug.
  • Formulation Claims: Covering specific compositions, including excipients, stabilizers, or delivery systems.
  • Method Claims: Covering methods of manufacturing, administering, or treating with the compound.
  • Use Claims: Covering therapeutic indications or specific medical applications.

Interpretation of Claims

The breadth of the claims influences the patent’s enforceability and market exclusivity:

  • Core compound claims—if broad—can prevent competitors from producing similar molecular structures or derivatives.
  • Use claims—if narrowly tailored—may limit the patent’s scope to specific indications.
  • Method claims—if wide—could cover manufacturing processes or treatment protocols.

A comprehensive claim set typically balances broad coverage with specific embodiments to prevent invalidation and maximize market control.


Patent Landscape in Chile and Latin America

Regional Context

Chile’s patent system aligns with international standards, governed by the Industrial Property Law (Ley de Propiedad Industrial). Patent protection is granted for novel, inventive, and industrially applicable inventions, including pharmaceuticals. The Chilean patent landscape demonstrates:

  • Growing pharmaceutical patent filings driven by innovation and market growth.
  • Alignment with Patent Cooperation Treaty (PCT): Many pharmaceutical companies prioritize international filings to secure regional rights.
  • Generic challenges: As patent life expires, generic manufacturers emerge, impacting market dynamics.

Global Patent Landscape

Pharmaceutical patents are often filed and litigated across multiple jurisdictions. Key observations include:

  • Apple of patent families in global filings related to the same compound or formulation.
  • Patent citations: Chilean patents citing or being cited by patents from U.S., EP, CN, and JP jurisdictions.
  • Patent strategy: Companies pursue broad claims in key markets, with narrower claims in regional jurisdictions like Chile.

Implications for CL2019002239

  • The patent’s protection in Chile complements broader patent families filed in other major jurisdictions.
  • Its validity and enforceability depend on compliance with both Chilean patent laws and international standards.

Analysis of the Patent’s Claims

Novelty and Inventive Step

Key to the patent’s validity are the novelty and inventive step:

  • Novelty: The claimed compound or formulation must not have been disclosed before the filing date.
  • Inventive step: The invention must demonstrate an obvious improvement over prior art.

In the context of pharmaceuticals, demonstrating these criteria often involves showing unexpected properties, improved efficacy, or unique formulations.

Claim Scope and Commercial Potential

  • Broader compound claims increase market exclusivity but are also more vulnerable to invalidation.
  • Narrow use or formulation claims may allow competitors to develop alternative formulations or therapeutic methods.
  • The specificity of claims impacts patent lifecycle, commercialization, and litigation risk.

Potential Limitations

  • Claims that overly encompass known chemical structures or common formulations may face challenges during patent examination or opposition proceedings.
  • Efficacy data, stability, and safety profiles support patent robustness, especially in claims related to therapeutic methods.

Patent Landscape and Competitive Analysis

Filing Strategies

  • Major pharmaceutical firms often file multiple patents around a core compound, including composition, method of use, and manufacturing processes.
  • Patent thickets can extend exclusivity, hinder biosimilar entry, and influence licensing negotiations.

Infringement Risks

  • Due to overlapping claims across jurisdictions, infringing activities could occur if competitors develop similar compounds or formulations.
  • Chilean patent enforcement aligns with international standards, with mechanisms for civil litigation and administrative remedies.

Expiration and Lifecycle Management

  • Enforceable protection typically lasts 20 years from the priority date.
  • Patent term extensions or supplementary protection certificates can sometimes prolong exclusivity, especially for pharmaceuticals with long clinical development phases.

Implications for Stakeholders

  • Pharmaceutical companies: The patent constitutes a significant barrier against generic competition in Chile, vital for recouping R&D investments.
  • Generic manufacturers: Must monitor claim scope to identify potential infringing activities or design around strategies.
  • Regulatory agencies: Patent protections influence pricing and market access strategies.
  • Investors: Patents like CL2019002239 influence valuation, licensing opportunities, and market entry plans.

Key Takeaways

  • Scope of protection hinges on the breadth and specificity of the claims, directly impacting market exclusivity and litigation risk.
  • Claim analysis suggests a balanced approach, with core compound claims and method or use claims optimizing patent strength.
  • Chile’s patent landscape reflects integration into the global framework, with strategic filings in jurisdictions like Chile protecting regional market interests.
  • Patent lifecycle management should include proactive filing of divisional applications, patent maintenance, and monitoring competitors’ filings.
  • Strategic considerations involve leveraging patent protections for licensing, partnership opportunities, and safeguarding against patent challenges.

FAQs

1. How does Chilean patent law affect pharmaceutical patent protection?

Chilean patent law grants 20 years of exclusive rights for pharmaceuticals, requiring novelty, inventive step, and industrial applicability. The law also permits patent term extensions under specific conditions, aligning with international standards.

2. What determines the strength of a pharmaceutical patent claim in Chile?

The claim’s breadth, clarity, and novelty, along with supporting data demonstrating unexpected advantages over prior art, influence the strength and enforceability of the patent.

3. Can the scope of CL2019002239 be challenged or invalidated?

Yes, challengers can file opposition, nullity, or infringement lawsuits if they demonstrate prior art or non-compliance with legal requirements, potentially limiting or invalidating the patent.

4. How does the patent landscape affect generic drug entry in Chile?

Strong patents like CL2019002239 delay generic entry by providing exclusive rights. Once patents expire or are invalidated, generics can market similar drugs, increasing competition and reducing prices.

5. What strategies should patent holders adopt for life-cycle management?

Patent holders should consider filing divisional or continuation applications, monitoring competitors, enforcing rights proactively, and exploring licensing opportunities to maximize the patent’s commercial value.


References

[1] INAPI, Chilean Patent Database, Official Records.
[2] Chilean Industrial Property Law (Ley de Propiedad Industrial).
[3] World Intellectual Property Organization (WIPO), Patent Landscape Reports.
[4] IP5 Patent Offices, Pharmaceutical Patent Trends.
[5] Reuters Pharma, Regional Patent Strategies for Pharmaceuticals.


Note: This analysis is based on publicly available information and standard patent practices. For detailed legal opinions or strategic advice, consulting a patent attorney or IP strategist specialized in Latin American pharmaceuticals is recommended.

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