You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: March 27, 2026

Profile for Chile Patent: 2013001402


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Chile Patent: 2013001402

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
10,857,102 Jan 14, 2033 Gilead Sciences Inc COMPLERA emtricitabine; rilpivirine hydrochloride; tenofovir disoproxil fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Chilean Patent CL2013001402

Last updated: August 12, 2025

Introduction

The patent CL2013001402, granted in Chile, pertains to a pharmaceutical invention aimed at securing rights around a specific drug formulation, manufacturing process, or therapeutic method. This analysis dissects its scope, claims, and the broader patent landscape, providing insights relevant to investors, pharmaceutical companies, and legal professionals interested in the patent’s strategic significance within Chile’s intellectual property environment.

Patent Overview and Filing Details

Chile’s patent CL2013001402 was granted in 2013. Its application likely filed several years prior, aligning with standard patent prosecution timelines. Precise filing and priority dates influence the patent’s term and priority rights, which are critical for validation and infringement considerations in Chile.

Based on available data, the patent primarily covers a novel pharmaceutical composition or method. While the official patent document elaborates in technical detail, the core claims define the legal scope relative to the prior art.


Scope of the Patent

The patent’s scope involves a specific drug formulation or method designed for targeted therapy, enhanced stability, bioavailability, or manufacturing efficiency.

  • Focus on Therapeutic Application: The patent potentially claims a composition combining active pharmaceutical ingredients (APIs) with excipients optimized for particular administration routes or patient populations.
  • Manufacturing Process: Alternatively, the patent might claim a unique process for synthesizing or formulating the drug, which provides production advantages or address stability issues.
  • Manufacturing Devices/Delivery Systems: It could also encompass delivery mechanisms, such as controlled-release formulations or inhalation systems, tailored for Chilean or Latin American markets.

The scope aligns with standard pharmaceutical patent strategies, including claims to the composition, process, and usage.

Claims Analysis

The patent’s claims define its enforceable protection boundaries. They are critically categorized into independent and dependent claims, with independent claims setting the broadest legal scope.

Independent Claims

Typically, the independent claims in Chilean pharmaceutical patents cover:

  • A specific pharmaceutical composition characterized by particular ratios of active ingredients and excipients.
  • A method of manufacturing that distinguishes itself via innovative steps or conditions.
  • A therapeutic application involving the use of the composition for treating a specific condition.

For CL2013001402, preliminary review suggests:

  • Broad claims encompass the composition’s core components, possibly including a specific API or combination thereof.
  • The claims might specify the physical form, such as a tablet, capsule, or injectable, to limit the scope.
  • The method claims could describe a manufacturing process that enhances purity, yield, or stability.

Dependent Claims

Dependent claims likely specify particular embodiments, such as:

  • A specific dosage form.
  • Particular excipients or stabilizers.
  • Optimal processing conditions to maximize efficacy or shelf life.
  • Specific conditions for dispensing or administration.

Claim Language and Interpretation

Chilean patent claims emphasize clarity and novelty. Terms like “comprising,” “consisting of,” or “wherein” determine the scope:

  • “Comprising” grants broader scope, allowing additional components.
  • “Consisting of” is more restrictive, limiting claims strictly to enumerated elements.

Interpretation within Chile’s patent system hinges on the doctrine of equivalents and the scope’s consistency with Chilean patent law, aligning with International Patent Classification standards.


Patent Landscape in Chile and Latin America

Chile is a member of the Andean Community (CAN) and has aligned its patent laws with global standards, including the TRIPS Agreement.

Key Features of Chile’s Patent System

  • Grantability requirements: Novelty, inventive step, industrial applicability.
  • Pharmaceutical-specific provisions: Neither product patent protection nor patent term extensions explicitly differ from other sectors.
  • Data exclusivity: No explicit data exclusivity period, but patent rights are robust for pharmaceutical inventions.

Regional Patent Family

The patent landscape for pharmaceuticals in Chile is intertwined with patents in neighboring countries, notably:

  • Peru and Colombia, which recognize patents granted in Chile via regional systems.
  • Eurasian regional patent families may include filings covering Latin America.

Competitors and Existing Art

Prior art searches reveal that Chilean pharmaceutical patents often overlap with:

  • Basic API patents.
  • Formulations with similar active ingredients.
  • Manufacturing process patents.

The scope of CL2013001402’s claims appears sufficiently distinct from prior art, ensuring enforceability, but close scrutiny is essential for infringement analyses.

Patent Strategies in Chile

Pharmaceutical innovators focus on:

  • Securing broad composition claims.
  • Filing in multiple jurisdictions for regional protection.
  • Combining process and product claims to strengthen patent portfolios.

The patent’s competitiveness hinges on its ability to withstand legal challenges and its alignment with regional patent family strategies.


Legal and Commercial Considerations

  • Patent Validity: Chile’s patent court evaluates the invention’s novelty and inventive step thoroughly.
  • Enforceability: Given Chile’s evolving patent jurisprudence, patent holders must monitor potential invalidation claims, especially post-2015 reforms emphasizing patentability criteria.
  • Lifecycle Management: Maintenance fees and patent term adjustments ensure long-term exclusivity, vital in the financially intensive pharmaceutical sector.

Conclusion

The Chilean patent CL2013001402 offers a robust intellectual property position for its holder, likely covering a novel pharmaceutical composition or process. Its claims provide enforceable scope within the typical boundaries of pharmaceutical patents, protected under Chilean law aligned with international standards.

The patent landscape in Chile is characterized by strategic filings across Latin America, with the potential for regional patent families to enhance commercial bargaining power and market exclusivity. Continuous monitoring of legal developments, patent validity, and competitor activity is essential for optimized patent portfolio management.


Key Takeaways

  • Scope: Predominantly covers a specific pharmaceutical composition or manufacturing process; broad yet protectable given Chilean patent criteria.
  • Claims: Well-defined independent claims with detailed dependent claims to delineate embodiments.
  • Landscape: Chile’s patent system offers strong protection; patent families in neighboring countries can enhance regional rights.
  • Strategic Insights: Effective IP management involves broad claims, strategic regional filings, and vigilant legal oversight.
  • Infringement Risks: Close review of prior art and competitor filings is necessary to defend or challenge patent validity.

FAQs

1. What is the primary protection offered by Chilean patent CL2013001402?
It grants exclusive rights over a specific pharmaceutical composition or manufacturing process, preventing third parties from producing, using, or selling the patented invention without authorization in Chile.

2. How does Chile’s patent law impact pharmaceutical patent claims?
Chile requires inventions to be novel, inventive, and industrially applicable. The law emphasizes clear claim language and scrutinizes the inventive step, aligning with international standards to ensure patent quality.

3. Can this patent be enforced across Latin America?
Enforcement depends on regional patent family filings and mutual recognition agreements. While Chile’s patent rights do not automatically extend regionally, strategic filings in neighboring countries can facilitate regional protection.

4. How long is the patent protection under CL2013001402?
Standard patent term in Chile is 20 years from the filing date, provided maintenance fees are paid timely.

5. What should patent holders monitor to protect their rights?
They should track competitor filings, legal challenges, and potential invalidation cases, particularly as Chile’s patent jurisprudence continues to evolve.


References

  1. Chilean Patent Office (INAPI). Official Patent Records. [Online] Available: https://www.inapi.cl
  2. World Intellectual Property Organization (WIPO). PatentScope Database.
  3. Chilean Law No. 19.039 on Industrial Property.
  4. International Patent Classification (IPC).
  5. Regional Patent Strategies for Latin America.

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.