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Last Updated: December 12, 2025

Profile for Chile Patent: 2018001199


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US Patent Family Members and Approved Drugs for Chile Patent: 2018001199

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
10,548,846 Nov 8, 2036 Gilead Sciences Inc BIKTARVY bictegravir sodium; emtricitabine; tenofovir alafenamide fumarate
11,744,802 Nov 8, 2036 Gilead Sciences Inc BIKTARVY bictegravir sodium; emtricitabine; tenofovir alafenamide fumarate
>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 CL2018001199

Last updated: August 3, 2025


Introduction

Patent CL2018001199, granted by the Chilean Patent Office, pertains to a pharmaceutical invention aimed at securing exclusive rights over a specific drug formulation or method. The scope of this patent, including its claims, significantly influences the competitive landscape in Chilean pharmaceutical markets. Analyzing this patent’s claims and its position within the broader patent landscape is essential for stakeholders looking to assess potential patent rights, infringement risks, and opportunities for innovation or licensing.


Patent Overview and Context

Chile’s patent system, aligned with the Patent Cooperation Treaty (PCT), grants enforceable rights to inventors over novel, non-obvious, and industrially applicable inventions. Pharmaceutical patents typically cover active compounds, formulations, methods of manufacture, or specific therapeutic uses.

Patent CL2018001199 was filed to protect a specific drug or formulation, with its priority date likely in or around 2018. These patents usually seek to extend exclusivity over innovative medicinal products, often related to novel compounds, optimized delivery systems, or therapeutic indications.


Claims Analysis

The claims of CL2018001199 define the scope of the patent’s protection. Detailed evaluation involves assessing their breadth, specificity, and potential overlaps with existing patents.

1. Independent Claims:
Most pharmaceutical patents possess one or more independent claims, establishing the core inventive concept protected. For CL2018001199, the independent claim(s) likely delineate the key active ingredient(s) or formulation parameters, such as:

  • A particular chemical compound or its salt form.
  • A specific dosage form (e.g., sustained-release tablet).
  • A combination of active ingredients with synergistic effects.

Example:
"A pharmaceutical composition comprising [active compound], characterized by [specific excipients], wherein said composition exhibits [specific release profile]."

This claim would broadly cover the patented invention, with dependent claims narrowing the scope (e.g., specific concentrations, manufacturing parameters).

2. Dependent Claims:
These specify particular embodiments or optimized features, providing fallback positions but also narrowing scope due to their specificity. They can specify:

  • Dosage ranges
  • Methods of preparation
  • Therapeutic indications

The strength of these claims depends on their granularity and how distinct they are over known art.

3. Claim Breadth and Validity:
The broader the claims, the higher the potential enforceability but also the increased risk of invalidation based on prior art. In pharmaceuticals, overly broad claims covering generic classes are often challenged, whereas narrowly tailored claims tend to be more robust.


Scope of Patent CL2018001199

Given typical patent drafting strategies, this patent likely aims to:

  • Cover a novel active compound or a surprising formulation feature.
  • Encompass specific dosage regimens or delivery mechanisms.
  • Provide therapeutic coverage over a particular medical condition.

The scope's actual breadth depends on how expansively the claims are drafted, balancing innovation protection with defensibility against invalidation and ease of design-around.


Patent Landscape in Chile and International Context

1. Chile’s Patent Environment for Pharmaceuticals:
Chile recognizes pharmaceutical patents as security for innovative active compounds and new formulations, subject to patentability criteria such as novelty, inventive step, and industrial applicability. However, Chile is not a pharmaceutical manufacturing hub; thus, patent enforcement balances international standards and local patent practice.

2. Patent Families and International Filings:
The patent in question is likely part of a global patent family, with filings in major jurisdictions such as the US, Europe, or PCT applications, ensuring broader protection. Tracking these related filings provides insights into the patent’s strength and value.

3. Overlap with Other Patents:
Patent landscapes reveal overlapping claims by innovator companies or generic manufacturers. In this context, CL2018001199 might intersect with patents covering similar compounds or formulations, creating potential freedom-to-operate or infringement considerations.

4. Litigation and Market Entry:
In Chile, patent enforcement depends on judicial actions, with pharmaceutical patents sometimes facing invalidation or opposition challenges. The scope and claims influence whether competitors can manufacture generic equivalents or whether patent holders can enforce exclusivity.

5. Patent Expiry and Licensing Opportunities:
Given filing timelines, the patent’s expiration could be around 2038, assuming 20-year terms from priority. Before expiry, licensing negotiations or strategic patent litigations are critical.


Legal and Commercial Implications

  • Protection of Innovation: The scope of CL2018001199 appears geared toward securing exclusive rights over a specific formulation or compound, deterring generic entry during its enforceable lifetime.
  • Potential Infringement Risks: Competitors must carefully analyze the claims to avoid infringement, especially if their products resemble features claimed in the patent.
  • Research and Development (R&D): The patent landscape influences R&D investments, especially around designing around claims or developing second-generation formulations.
  • Freedom to Operate (FTO): Enterprises should conduct thorough FTO analyses, considering both CL2018001199 and allied patents, to mitigate legal risks.

Conclusion

Patent CL2018001199 exemplifies a strategic effort to protect a pharmaceutical invention within the Chilean market, with its scope primarily defined by its claims, covering specific formulations, compounds, or methods. Its position within a complex patent landscape necessitates detailed due diligence concerning overlapping rights and potential for infringement or licensing. The evolving landscape underscores the importance of harmonized global patent strategies in pharmaceuticals, especially in markets like Chile that serve as regional hubs.


Key Takeaways

  • The scope of Chilean patent CL2018001199 hinges on its independent claims, which likely cover specific drug formulations or compounds, with dependent claims narrowing protection.
  • Broad claims enhance territorial exclusivity but face greater invalidation risks; precise drafting aligns with stronger enforcement.
  • The patent landscape for pharmaceuticals in Chile is matured but competitive, with overlap and potential patent thickets requiring rigorous FTO analysis.
  • Stakeholders should monitor related international patent filings to understand broader protection strategies.
  • Timing of patent expiry offers commercial opportunities; until then, licensing, litigation, and strategic planning are vital.

FAQs

1. How does Chilean patent law affect pharmaceutical patent enforcement?
Chile recognizes pharmaceutical patents subject to global patentability criteria. Enforcement requires judicial action, and patent validity can be challenged, necessitating robust claim drafting and patent strategy.

2. What are the typical components of claims in pharmaceutical patents like CL2018001199?
Claims usually specify active ingredients, formulations, manufacturing methods, or therapeutic uses. Broad independent claims cover core inventions, with dependent claims detailing specific embodiments.

3. Can patents like CL2018001199 be challenged or invalidated?
Yes. Challenges can be based on prior art, lack of inventive step, or insufficient disclosure. Validity assessments are common during litigation or opposition proceedings.

4. How important is the patent landscape beyond Chile for drugs filed in Chile?
Highly significant. Global patent portfolios, patent family overlaps, and similar claims influence Chilean patent validity, infringement risks, and licensing possibilities.

5. When does a pharmaceutical patent in Chile typically expire?
Generally, 20 years from the filing date, with possible extensions for patent term adjustments or later filings in related jurisdictions.


References

  1. Chilean Patent and Trademark Office (INAPI). Patent Regulations and Guidelines.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. European Patent Office (EPO). Guidelines for Examination of Pharmaceutical Patents.
  4. "Pharmaceutical Patent Law in Chile," IPR Legal Insights, 2022.
  5. Global Patent Databases (e.g., Patentscope, Espacenet).

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