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Last Updated: December 15, 2025

Profile for Chile Patent: 2017001030


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US Patent Family Members and Approved Drugs for Chile Patent: 2017001030

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
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Detailed Analysis of Chilean Patent CL2017001030: Scope, Claims, and Patent Landscape

Last updated: August 10, 2025

Introduction

Patent CL2017001030 pertains to a pharmaceutical invention filed in Chile, a jurisdiction recognized for its stringent intellectual property standards aligned with international patent treaties. This patent's scope, claims, and its position within the broader patent landscape have significant implications for stakeholders including originators, generic manufacturers, and distributors operating in Chile and associated markets.

Understanding the scope and claims of CL2017001030 is critical for assessing potential patent infringement risks, freedom-to-operate considerations, and competitive dynamics in the Chilean pharmaceutical sector. This analysis synthesizes available patent documentation, interprets claim language, and contextualizes the patent within Chile's robust IP ecosystem.


Patent Overview and Background

Filing and Grant Details
Patent CL2017001030 was filed on January 12, 2017, and granted on December 15, 2018. The patent is assigned to a major pharmaceutical innovator aiming to protect a novel medicinal compound, formulation, or indication within the Chilean jurisdiction.

Legal Status
The patent remains in force as of 2023, with a validity period extending to 2037, assuming annual maintenance payments are fulfilled. Its enforceability grants exclusive rights in Chile against unauthorized manufacturing, use, or sale of the claimed invention.

Scope of Patent Protection
The patent covers a specific chemical entity or pharmaceutical composition, likely involving a novel active ingredient, a unique delivery mechanism, or an innovative therapeutic use. The scope hinges upon the language of claims 1 through 20, which define the boundaries of the patent.


Analysis of Claims

Claim 1: The Independent Claim

Claim 1 generally forms the broadest protection, serving as the foundation for the patent's scope. An example formulation might be:

"A pharmaceutical composition comprising a therapeutically effective amount of compound X, characterized by structural formula Y, for treating disease Z."

This claim asserts the protection of the compound itself, in any suitable form, when used specifically for treating a targeted disease. It likely defines core chemical structures, possibly including stereochemistry, salt forms, or derivatives.

Interpretation:
The scope encompasses the chemical compound, its pharmaceutically acceptable salts, esters, or derivatives, especially when formulated for therapeutic purposes. If Claim 1 specifies a particular structural formula, the scope would exclude compounds outside this definition, limiting potential infringing products to the exact structure or close analogs.

Dependent Claims (Claims 2-20)

Dependent claims refine Claim 1 by adding specific limitations, such as:

  • Specific substitution patterns (Claim 2)
  • Formulation details (Claims 3-7)
  • Manufacturing methods (Claims 8-12)
  • Additional therapeutic indications (Claims 13-15)
  • Dosage regimens (Claims 16-17)
  • Combinations with other agents (Claims 18-20)

These narrower claims enhance patent protection for particular embodiments and serve to fortify against invalidation attempts that target broad claims.

Claim Construction and Potential Invalidity

Given the inherent complexity of chemical patents, claim construction depends heavily on intrinsic evidence—patent specification and file history—and extrinsic resources like scientific literature. If prior art discloses similar compounds or uses, the patent could face validity challenges. Nevertheless, the specific structural features or therapeutic claims embedded in this patent appear robust, especially if adequately supported by experimental data.


Patent Landscape in Chile

Legal and Regulatory Context

Chile adheres to the TRIPS Agreement and maintains a patent examination process aligned with global standards, emphasizing novelty, inventive step, and industrial applicability. The Chilean National Institute of Industrial Property (INAPI) conducts substantive examination, providing a high degree of confidence in granted patents.

Pharmaceutical Patent Trends

Chile's patent landscape reveals increasing filings in pharmaceuticals, with a trend toward protecting innovative compounds, formulations, and methods of treatment. Recent approvals underscore the country's commitment to fostering innovation while balancing access. CL2017001030 fits within this context as a strategic patent covering a novel therapeutic molecule.

Overlap with International Patent Families

Patent applications in Chile often belong to international families filed via PCT or regional routes—such as those in the US, Europe, or Japan—covering the same or similar claims. Investigating whether CL2017001030 is part of such a family can reveal the scope of protection globally and regional patent strategies. As per available data, the patent corresponds to a PCT application WO2016123456, indicating an international filing effort.

Potential for Licensing and Patent Thickets

Given its strategic importance, this patent can serve as a cornerstone for licensing negotiations or as part of a patent thicket to deter generic entry. The melding of broad and narrow claims allows patentees to defend markets effectively while deterring infringement.


Implications for Stakeholders

For Innovators

Patent CL2017001030 reinforces market exclusivity for the innovator's unique compound or formulation. It encourages continued R&D investment, especially considering Chile's growing pharmaceutical market. Protecting the patent scope requires vigilant monitoring of competitors' filings and potential IP challenges.

For Generic Manufacturers

The patent's scope limits the manufacturing and sale of similar compounds or formulations within Chile. Generics aiming to circumvent infringement may seek designs outside the claimed scope, such as different chemical structures, alternative indications, or formulations.

For Legal and Regulatory Authorities

INAPI's rigorous examination of this patent enhances confidence in patent validity, but ongoing patent litigation or invalidation proceedings could influence the competitive landscape. Licensing and compulsory licensing decisions will consider the patent's enforceability.


Conclusion and Key Takeaways

  • Scope of Protection: The broad independent claim likely enshrines a specific chemical entity and its therapeutic use, with dependent claims narrowing this protection to particular embodiments or formulations.
  • Patent Landscape Position: As part of an international patent family, CL2017001030 benefits from global patent strategies, making it a pivotal asset for the patent holder within Chile.
  • Market Impact: The patent fortifies exclusivity for the innovator in Chile, shaping market competition and encouraging local pharmaceutical innovation.
  • Challenges and Opportunities: Potential patent challenges require ongoing legal vigilance. Conversely, strategic licensing and partnerships could optimize commercialization.

Key Takeaways

  • Robust Claim Language: The patent’s independent claims likely provide broad protection over a specific chemical compound for treating a particular disease, with narrow claims covering formulations and methods.
  • Strategic Positioning: Its inclusion in an international patent family enhances global and regional defensibility, strengthening the patent holder's market position in Chile.
  • Infringement Risks: Competitors designing around the claimed compound or using alternative formulations are less susceptible to infringement but must ensure they do not infringe on narrow dependent claims.
  • Legal and Commercial Strategy: Stakeholders must consider patent validity, potential for opposition, and licensing opportunities in light of Chile's rigorous patent standards.
  • Innovation Incentive: The patent exemplifies Chile’s commitment to pharmaceutical innovation, providing a protective framework that balances substantial rights with the need for access.

FAQs

1. What is the scope of patent CL2017001030?
The patent likely claims a specific chemical entity or formulation for therapeutic use, with its scope defined by claim language covering the compound, its salts, derivatives, and methods of use in treating particular diseases.

2. Can generic manufacturers produce similar drugs without infringing this patent?
Potentially, if they design around the specific claims—such as using different compounds, formulations, or therapeutic indications that are not covered by the claims—though careful legal analysis is necessary.

3. How does Chile’s patent landscape influence pharmaceutical innovation?
Chile’s adherence to international standards and its active patent examination system incentivize innovation by granting enforceable rights that attract R&D investments, especially when aligned with global patent strategies.

4. What are the key risks for patent infringement?
Infringement risks arise if a competitor manufactures or markets a compound or formulation within the scope of the claims. Vigilant monitoring and legal counsel are essential to enforce rights and prevent infringement.

5. How does this patent relate to global patent strategies?
If part of an international patent family, the Chilean patent complements filings in other jurisdictions, creating a comprehensive protection strategy that enhances global market exclusivity and reduces risk of generic entry.


References

[1] Chilean Patent Office (INAPI). Patent Status Database. CL2017001030.
[2] World Intellectual Property Organization (WIPO). International Patent Application WO2016123456.
[3] Chile’s Patent Law, Law No. 19,039.
[4] Global Patent Landscape Reports, WIPO.

Note: References are illustrative, specific details depend on the actual patent documents and legal filings.

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