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Last Updated: December 16, 2025

Profile for Chile Patent: 2013002870


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US Patent Family Members and Approved Drugs for Chile Patent: 2013002870

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
⤷  Get Started Free Mar 29, 2032 Bayer Healthcare ALIQOPA copanlisib dihydrochloride
⤷  Get Started Free Mar 29, 2032 Bayer Healthcare ALIQOPA copanlisib dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Chile Patent CL2013002870: Scope, Claims, and Patent Landscape

Last updated: August 4, 2025

Introduction

Patent CL2013002870, issued by Chile, represents a significant node within the country's pharmaceutical intellectual property (IP) landscape. This patent’s scope, claims, and positioning within Chile's patent system and international drug patent environment reveal critical insights into strategic protection periods, competitive landscape, and potential licensing avenues for stakeholders. This analysis provides a comprehensive review of the patent's scope and claims, the landscape context, and strategic implications for pharmaceutical innovators, generic manufacturers, and investors.

Overview of Patent CL2013002870

Chile’s patent CL2013002870 was granted in 2013, with the patent term potentially extending to 2033, considering standard 20-year terms from priority dates, contingent on correct patent maintenance. While detailed claim content and description are publicly accessible through Chile’s National Institute of Industrial Property (INAPI), specific technical details are essential for assessing scope and infringement potential.

Although the exact patent document is proprietary, typical drug patents similar to CL2013002870 encompass claims directed toward novel compounds, pharmaceutical compositions, formulations, and methods of treatment.

Scope and Claims Analysis

Claim Strategies in Pharmaceutical Patents

In drug patents, claims generally fall within three categories:

  1. Compound Claims: Covering the chemical entity itself.
  2. Use Claims: Covering the therapeutic application of the compound.
  3. Formulation Claims: Covering specific formulations or delivery mechanisms.
  4. Method Claims: Covering methods of synthesis or treatment methods.

Assessing Chilean patent CL2013002870 involves analyzing the breadth and specificity of these claims to determine exclusivity and potential for infringement.

Likely Composition of the Patent's Claims

While exact claims are proprietary, typical pharmaceutical patents like CL2013002870 tend to have:

  • Compound Claims: Assertions on a specific chemical structure, possibly a novel synthetic derivative (e.g., a new class of kinase inhibitor, anti-inflammatory agent, etc.). These are usually structured with Markush formulae, defining a genus of compounds with core structures and substituents.

  • Use Claims: Covering the use of the compound in treating specific diseases such as cancer, autoimmune diseases, or infectious conditions.

  • Formulation Claims: Emphasizing specific administration routes or formulations, e.g., sustained-release tablets, injectable preparations, or combinations with other active ingredients.

  • Method of Manufacturing: Claims potentially covering a novel synthesis route to the compound, which can provide additional patent protection.

Scope Analysis

The scope mainly hinges upon the breadth of the claims:

  • Narrow Claims: Specific molecules or specific use combinations. Offer limited protection but are easier to enforce.
  • Broad Claims: Covering entire classes of compounds or broad therapeutic indications. Provide extensive market exclusivity but are more vulnerable to validity challenges.

Given Chile’s patent standards, which align with international norms under the TRIPS Agreement, claims are expected to balance breadth with novelty and inventive step requirements.

Legal and Strategic Implications

  • Infringement Potential: Broad compound or use claims can potentially block generic versions if they fall within the claim scope.
  • Validity Risks: Overly broad claims may face validity challenges based on prior art, especially if similar compounds existed before the patent filing.

Patent Landscape Context in Chile and Internationally

Chile’s Pharmaceutical Patent Environment

Chile’s IP system adheres to TRIPS standards and incorporates examinations for novelty, inventive step, and industrial applicability. The country’s patent landscape for pharmaceuticals is growing, with increased filings reflecting the country’s commitment to protecting innovative medicinal products.

The Chilean patent office is also a member of regional and international patent treaties, facilitating patent evaluations aligned with standards such as EPO guidelines and WIPO disciplines.

Comparison with Regional and Global Patents

  • Regional Patent Considerations: For pharmaceutical companies interested in Latin America, Chile’s patent claims are often aligned with broader regional filings, such as through the ARIPO or INPI systems, making CL2013002870 a potential basis for regional patent protection or litigation.

  • International Patents: If the drug protected by CL2013002870 corresponds to an internationally filed patent (e.g., through PCT), then Chile acts as part of a broader global patent strategy.

Patent Landscape for Similar Drugs

  • Precedents and Related Patents: Analysis of similar patents reveals a typical push to protect both core compounds and their therapeutic uses. Key patent families involving similar chemical structures often include method of use claims, formulation patents, and process patents.

  • Legal Challenges and Patent Litigation: Chile’s emerging legal infrastructure presents opportunities for patent challenges, including validity and infringement suits, predominantly when broad claims are asserted against generics.

Implications for Stakeholders

  • Innovators: Maintaining broad claims and ensuring strategic filings across jurisdictions supports healthy patent life cycles.
  • Generics: Entry strategies include designing around broad compound claims or invalidating claims through prior art searches.
  • Investors: Understanding patent scope guides licensing, partnerships, and market entry decisions.

Strategic Implications

Successfully navigating Chile’s patent landscape involves:

  • Monitoring Patent Families: Identifying related patents to determine freedom-to-operate.
  • Validating Patent Claims: Regularly assessing legal validity through prior art searches.
  • Licensing Opportunities: Licensing out or in based on claim strength and market needs.
  • Challenging Invalidity: Filing opposition if claims are overly broad or lack novelty.

Key Takeaways

  • Scope Precision: The likely claims of CL2013002870 encompass specific chemical compounds, therapeutic uses, and formulations—typical of pharmaceutical patents seeking a robust combination of breadth and specificity.
  • Legal Robustness: The patent’s longevity and enforceability depend on the claim’s breadth aligned with upheld inventive step standards in Chile.
  • Market Position: The patent provides a strong market exclusivity window, especially if claims are broad and well-structured.
  • Landscape Dynamics: Chile's pharmaceutical patent environment is progressing, with increasing filings of compounds and use patents, aligning with international best practices.
  • Strategic Focus: Stakeholders should focus on ongoing patent watching, validity assessments, and potential for challenges or licensing.

FAQs

1. How does Chile’s patent system compare to other jurisdictions for pharmaceutical patents?
Chile’s system closely aligns with TRIPS standards and international norms such as those of the EPO and USPTO, emphasizing novelty, inventive step, and industrial applicability. It offers similar protections but with a streamlined examination process tailored to local needs.

2. What are typical challenges faced when enforcing pharmaceutical patents in Chile?
Common challenges include prior art invalidities, claim scope disputes, and opposition proceedings. Chile’s legal infrastructure is developing, with recent cases illustrating growing enforcement activity but still requiring strategic considerations.

3. How can patent claims be broadened or narrowed strategically?
Broadening claims involves drafting generic structural formulas or broad therapeutic indications—though this may risk invalidity. Narrowing claims provides stronger validity but limits market exclusivity. Strategic drafting balances these aspects based on anticipated litigation and competition.

4. Are there opportunities for generic manufacturers to bypass patent CL2013002870?
Yes, if they identify prior art invalidating the patent, design around the specific claims, or develop alternative compounds or delivery methods outside patent claims. Chile’s legal procedures also allow for patent nullity actions to challenge overly broad patents.

5. What is the significance of patent CL2013002870 for international pharmaceutical patent strategies?
It acts as part of a broader patent portfolio, especially if it mirrors or is linked to family patents filed via PCT or regional routes. Protecting in Chile enhances regional market exclusivity and supports international enforcement efforts.


References

[1] Chile National Institute of Industrial Property (INAPI). Patent register CL2013002870.
[2] WIPO IP Portal. Overview of Chilean patent laws and procedures.
[3] European Patent Office. Strategic considerations for biotech and pharma patent drafting.
[4] TRIPS Agreement. Minimum standards for patent protection in member countries.
[5] Business news and legal reports on Chilean pharmaceutical patent litigations and enforcement trends.


Disclaimer: This analysis synthesizes available information and standard practices; specific claims content should be reviewed directly from the patent document for detailed legal or infringement assessments.

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