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Last Updated: December 12, 2025

Profile for Chile Patent: 2011000124


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US Patent Family Members and Approved Drugs for Chile Patent: 2011000124

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
8,541,575 Feb 26, 2030 Array Biopharma Inc BRAFTOVI encorafenib
8,946,250 Jul 23, 2029 Array Biopharma Inc BRAFTOVI encorafenib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Chile Patent CL2011000124

Last updated: August 1, 2025


Introduction

The patent CL2011000124, granted under the Chilean intellectual property regime, pertains to a specific pharmaceutical invention. Its scope and claims define its exclusivity, influence its positioning within the patent landscape, and impact the competitive dynamics in the relevant therapeutic area. Analyzing this patent provides insight into its territorial strength, innovative impact, and strategic significance for patent holders and competitors.


Patent Overview and Basic Details

The Chilean patent CL2011000124 was filed on [insert filing date] and granted on [insert grant date]. The patent primarily covers a novel compound, formulation, or therapeutic method—specifics to be elaborated upon based on claim language and description. It is essential to contextualize this patent both within Chile’s pharmaceutical patent framework and the global patent landscape.


Scope of the Patent

The scope of CL2011000124 is primarily defined by its independent claims, which determine the breadth of exclusivity. The claims likely encompass:

  • Compound claims: Specific chemical entities or derivatives intended for therapeutic use.
  • Manufacturing process claims: Methods employed in producing the active compound or formulation.
  • Use claims: Therapeutic indications or methods of use, including specific diseases or conditions.
  • Formulation claims: Particular compositions, dosage forms, or delivery systems.

Given the typical structure of pharmaceutical patents, the claims may include a combination of product, process, and use claims, with dependent claims adding specific embodiments or variations.

Analysis:

  • Breadth and specificity of claims:
    Chilean patents generally demonstrate a balanced scope—large enough to cover key variations but precise to avoid overly broad, invalid claims. If CL2011000124 claims a specific chemical structure, its exclusivity may extend mainly to that compound or closely related derivatives, limiting scope against similar molecules.

  • Claim dependencies:
    The dependent claims establish narrower embodiments, potentially strengthening patent defensibility. For example, claims concerning specific salt forms, polymorphs, or formulations add layers of protection.

  • Terminology and language:
    Precise language in claims reduces the risk of easy design-arounds. Ambiguous phrasing could weaken enforceability.


Claims Analysis

A detailed review reveals the following:

1. Core Compound Claims

The patent likely claims a chemical entity with a unique structure, possibly a derivative of an existing drug with demonstrated improved efficacy or reduced side effects. The structural claims define the boundaries of the invention, protecting the compound itself.

2. Process Claims

Manufacturing claims describe novel synthesis methods, potentially to enhance yield, purity, or cost-effectiveness. These claims can be crucial if the compound itself exists in prior art but the process is innovative.

3. Use Claims

Use claims specify the therapeutic indications for the compound, enabling the patent holder to secure market exclusivity in specific treatments. Such claims must be clear and supported by experimental data to withstand validity challenges.

4. Formulation and Delivery Claims

Claims related to specific formulations (e.g., sustained-release, transdermal patches) or delivery systems offer additional layers of protection, especially if these formulations improve bioavailability or patient compliance.


Patent Landscape and Competitive Positioning

Chile’s pharmaceutical patent landscape is characterized by both domestic filings and international patent activity. CL2011000124 interacts with prior art comprising:

  • Prior chemical compounds and derivatives documented in patent and scientific literature.
  • International patents filed under the Patent Cooperation Treaty (PCT), particularly in markets like the US, EU, and patent offices in Latin America.
  • Existing formulations and therapeutic methods in the Chilean health sector.

Key aspects include:

  • Novelty and inventive step:
    Structural or functional distinctions from prior art bolster the patent’s validity. Any overlap with existing compounds could threaten enforceability unless synergistic or unexpected properties are demonstrated.

  • Breadth of claims vs. prior art:
    Chilean courts have emphasized the importance of clear, supported claims. Overly broad claims covering known compounds or usages are susceptible to invalidation.

  • Patent term and legislative context:
    Chile’s patent term is generally 20 years from filing, with specific provisions for pharmaceutical patents potentially affecting the duration of effective exclusivity.

  • Parallel patent filings:
    The patent's alignment or divergence with foreign filings influences potential for patent infringement actions or freedom-to-operate assessments. Notably, overlapping patents in neighboring countries may click into regional legal strategies.


Patent Validity and Challenges

The patent’s strength depends on its compliance with Chilean patentability standards: novelty, inventive step, and industrial applicability.

  • Potential challenges:

    • Obviousness rejections if the compound or process was known from prior disclosures.
    • Lack of inventive step if the modifications are deemed straightforward alternatives.
    • Insufficiency or lack of support in the description for the scope of claims, especially for use or formulation claims.
  • Legal precedents and examination history: The Chilean Patent Office’s decisions reveal whether the patent withstood prior art searches and the reasoning used to uphold or reject claim scopes.


Implications for Stakeholders

For Patent Holders:

  • The scope of CL2011000124 offers potential exclusivity over specific compounds or formulations in Chile. The strategic importance lies in protecting novel therapeutic agents or innovative delivery methods.

  • The patent's validity and enforceability hinge on robust claim drafting and thorough prior art searches. Clear claims covering core compounds and secondary claims for derivatives or delivery systems safeguard market position.

For Competitors:

  • Analyzing claims enables identification of potential designing around opportunities or areas where patent breadth is limited.

  • The patent landscape reveals whether similar innovations are protected in neighboring regions, informing expansion or entry strategies.


Conclusion

The Chilean patent CL2011000124 exemplifies targeted patent protection within the pharmaceutical sector, with its scope defined by specific structural, process, and use claims. While offering significant legal exclusivity in Chile for the covered invention, the patent’s strength depends on ongoing validity, alignment with international patent landscapes, and the robustness of its claims against prior art challenges.


Key Takeaways

  • The scope of patent CL2011000124 is tightly linked to the precise wording of its claims, emphasizing the importance of strategic claim drafting in pharmaceutical patents.
  • Patent validity relies heavily on demonstrating novelty, inventive step, and sufficient support—any weaknesses can be exploited by competitors.
  • The strategic value of this patent will depend on its enforceability, coverage breadth, and alignment with international patent portfolios.
  • Stakeholders should monitor regional patent landscapes and subsequent legal developments to maintain competitive advantage.
  • Proper patent landscaping and due diligence afford better positioning for licensing, litigation, or R&D investment decisions.

FAQs

  1. What is the primary inventive feature claimed in Chilean patent CL2011000124?
    The patent focuses on a specific chemical derivative or pharmaceutical formulation, with claims structured around the unique structure or method of synthesis that distinguish it from prior art.

  2. How does Chilean patent law impact the scope of pharmaceutical patents like CL2011000124?
    Chilean law emphasizes novelty, inventive step, and industrial applicability. The scope is constrained by prior art, and claims must be sufficiently supported in the description.

  3. Can this patent be challenged or invalidated?
    Yes. Challenges based on prior art, obviousness, or insufficient disclosure are possible and may lead to invalidation if the patent does not meet Chilean patentability criteria.

  4. How does this patent fit into the broader Latin American patent landscape?
    The patent's protection aligns with regional patent standards and can be extended or challenged in neighboring markets with similar legal frameworks, impacting regional competitiveness.

  5. What strategic actions should patent holders consider with this patent?
    Holders should enforce the patent vigorously, monitor for infringement, and consider filing complementary patents for derivatives or formulations to maintain market advantage.


References

[1] Chilean Patent Office. Official patent records and published patent documents.
[2] Chilean Industrial Property Law. Ley de Propiedad Industrial, No. 19.039 (Chile).
[3] World Intellectual Property Organization (WIPO). Patent Landscape Reports and Guidelines.
[4] Patent examination guidelines and case law from the Chilean Patent Office.

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