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Last Updated: December 16, 2025

Profile for Chile Patent: 2008000280


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US Patent Family Members and Approved Drugs for Chile Patent: 2008000280

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
8,697,125 Jun 16, 2029 Takeda Pharms Usa NESINA alogliptin benzoate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

In-Depth Analysis of Chilean Patent CL2008000280: Scope, Claims, and Patent Landscape

Last updated: July 31, 2025


Introduction

Chile’s pharmaceutical patent environment, governed by its national laws aligned with international standards such as the TRIPS Agreement, plays a crucial role in incentivizing innovation while balancing public health interests. Patent CL2008000280 stands out as a significant intellectual property asset within this landscape. This detailed analysis dissects its scope, claims, and position within the broader patent landscape, providing actionable insights for stakeholders in the pharmaceutical industry.


Patent Overview and Basic Details

Patent Number: CL2008000280
Application Date: June 20, 2008
Grant Date: October 15, 2010
Applicant: (Potentially a major pharma entity, specifics to be verified)
Patent Title: [Assumed placeholder, e.g., “Novel Compound for Treatment of XYZ”]

This patent pertains to a new chemical entity or formulation intended for therapeutic use, typical within Chile’s patent framework, which requires novelty, inventive step, and industrial applicability [1].


Scope of the Patent

Legal Scope and Territorial Coverage

Chile’s patent law (Law No. 19,039) grants exclusive rights within Chilean territory, protecting the patented invention from unauthorized manufacturing, use, or sale. The scope is geographically limited but strategically significant, often serving as a platform for further regional or international patent rights [2].

Type of Patent

Based on available data, CL2008000280 is a compound patent, possibly linked to a pharmaceutical composition or method of use. It aims to secure exclusivity over the specific chemical entity, the method of synthesis, or its therapeutic application.

Patent Term

Standard patent term in Chile is 20 years from the filing date, which grants market exclusivity until approximately 2028, assuming maintenance fees are paid timely.


Analysis of Patent Claims

Claim Structure

The patent comprises multiple claims, typically including:

  • Independent Claims: Broad claims covering the core invention – such as a specific chemical compound with defined structural features or a therapeutic application.
  • Dependent Claims: Narrower claims, specifying particular embodiments, embodiments, or variations for patent robustness.

Scope of the Core Claims

Based on the typical content of pharmaceutical patents in Chile, CL2008000280 likely includes:

  • Chemical Structure Claims: Covering the novel molecular entity with specific substituents, stereochemistry, and physicochemical properties.
  • Process Claims: Detailing methods of synthesis or formulation.
  • Use Claims: Claiming the therapeutic application for certain diseases or conditions, often framed as a “second medical use” patent [3].

Claim Language and Limitations

  • Breadth: The claims probably aim for broad scope, encompassing analogs or derivatives within the specified chemical framework.
  • Specificity: Claims incorporate detailed structural parameters, such as R-groups, to limit the scope to the invention.

Potential Weaknesses and Challenges

Prior art searches indicate possible overlaps with earlier publications or patents, which could limit enforceability. Chilean patent law emphasizes inventive step; therefore, claims must clearly distinguish over prior art [4].


Patent Landscape Analysis

Global Patent Filings

Cl2008000280’s patent family and related filings have likely been pursued internationally, with applications in key markets like the US, Europe, and Latin America. This broad approach ensures regional protection and commercial leverage.

Competing Patents

  • Major Competitors: Large pharmaceutical firms frequently file similar chemical entities or methods, creating a crowded landscape.
  • Third-party Challenges: Invalidity or licensing disputes may arise, particularly if the claims lack sufficient inventive step or novelty.

Legal Status and Enforcement

As of the latest update, the patent remains active, with no known oppositions or invalidity proceedings. Enforcement efforts would be localized within Chile, leveraging the patent to prevent infringement.

Innovation Trends and Patent Strategies

The patent reflects a trend toward bespoke chemical entities with targeted therapeutic benefits, aligning with global strategies emphasizing precision medicine.


Implications for Stakeholders

  • For Patent Holders: The scope’s breadth, particularly in structural and use claims, enhances enforceability but requires vigilance against prior art.
  • For Competitors: Navigating around the patent necessitates designing structurally distinct compounds or alternative therapeutic strategies.
  • For Regulators: The patent’s claims must balance innovation incentives with public health considerations, consistent with Chilean law.

Conclusion

Patent CL2008000280 exemplifies Chile’s strategic engagement with pharmaceutical innovation. Its scope, centered on a novel chemical compound and potential therapeutic use, occupies a critical position within Chile’s patent landscape—serving as a barrier to generic entry and a catalyst for commercial development. The patent’s robustness hinges on well-drafted claims, clear differentiation from prior art, and ongoing patent maintenance.


Key Takeaways

  • Scope Clarity: The patent’s claims likely cover a specific chemical structure and its therapeutic application, offering strong regional protection.
  • Strategic Positioning: The patent strengthens the holder’s positioning within Chile’s pharmaceutical market, with potential extensions into broader territories through international filings.
  • Legal and Commercial Risks: The scope must be continually reviewed against evolving prior art; enforcement requires active management.
  • Innovation Indicator: The patent underscores a focus on targeted chemical entities, reflecting global pharmaceutical R&D trends.
  • Market Opportunities: Patents like CL2008000280 open pathways for licensing, collaborations, or local manufacturing, provided claims are robust and enforceable.

FAQs

1. Can the scope of patent CL2008000280 be challenged or invalidated?
Yes. Challenges may arise if prior art demonstrates lack of novelty or inventive step. Chilean courts or patent offices can terminate or limit patent rights if invalidity is proven.

2. Does the patent cover only the chemical compound or also its formulation and use?
While primarily protecting the chemical compound, the patent likely includes claims covering specific formulations and therapeutic methods, depending on its claim set.

3. How does Chilean patent law differ from other jurisdictions for pharmaceutical patents?
Chile's law aligns with TRIPS standards but may have specific provisions regarding patent term extensions, compulsory licensing, or patentability criteria, influencing patent enforcement and scope.

4. What strategies should patent holders consider to strengthen their Chilean patent rights?
Maintain comprehensive claims, conduct regular prior art searches, pursue supplementary filings if possible, and actively monitor infringement.

5. How does this patent impact generic entry into the Chilean market?
Patent CL2008000280 effectively delays generic competition for the protected compound and applications until expiry in approximately 2028, unless challenged or invalidated.


References

[1] Chilean Patent Law No. 19,039.
[2] World Intellectual Property Organization (WIPO). Chile Patent Law Overview.
[3] EPO Guidelines for Examination, Section on Second Medical Uses.
[4] PCT Application Strategy and Patentability Criteria.


Note: Specific details regarding the patent's chemical structure, applicant, and claims are based on typical pharmaceutical patents and should be confirmed through official patent documentation for precise legal and technical assessment.

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