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Last Updated: December 12, 2025

Profile for Chile Patent: 2017003475


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US Patent Family Members and Approved Drugs for Chile Patent: 2017003475

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
10,590,102 Dec 30, 2036 Genentech Inc COTELLIC cobimetinib fumarate
11,254,649 Dec 30, 2036 Genentech Inc COTELLIC cobimetinib fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Chile Patent CL2017003475

Last updated: July 29, 2025

Introduction

Chile Patent CL2017003475 pertains to a pharmaceutical invention, central to the country’s intellectual property landscape for innovative drugs. As of the filing and grant dates, examining the scope of the claims, their strategic positioning, and the broader patent landscape offers insights critical for stakeholders across the pharmaceutical sector—ranging from patent holders and competitors to regulatory authorities. This analysis delineates these aspects, emphasizing scope, claims specificity, and the surrounding patent environment in Chile for this patent.


Patent Overview and Context

Patent CL2017003475 was filed and granted within the Chilean patent system, aligning with the intellectual property framework governed by the Chilean Industrial Property Law (Decreto Ley N° 4.723 de 1948). Chile, as an active participant in the patent cooperation framework and regional patent alliances such as the Andean Community and potential engagement with the Patent Cooperation Treaty (PCT), fosters a favourable environment for pharmaceutical patent protection.

The patent concerns[1], per the application documents, a novel formulation, method, or therapeutic compound intended for specific medical indications. It is/or was granted in 2017, establishing a 20-year life span from the earliest priority date, likely around 2016 or earlier, reflecting Chile's maintenance policies.


Scope and Claims Analysis

Claim Structure and Language

The patent’s claims define the exclusive rights conferred by the patent grant. They are pivotal—setting the boundary between patent protection and prior art. For CL2017003475, the claims are likely structured into independent and dependent categories, typical for pharmaceutical patents.

  • Independent Claims: Generally focus on the core inventive concept, often encompassing the novel compound, composition, or method.
  • Dependent Claims: Narrow down the independent claims, adding specific embodiments or auxiliary features to strengthen the scope and fallback positions.

Scope of the Patent Claims

The scope hinges on the breadth of independent claims:

  • Compound or Composition Claims: If the primary claim pertains to a specific chemical entity, the scope is confined to that compound or a chemical class defined by structural features.
  • Method of Use Claims: If addressing a therapeutic method, the claims specify particular indications, administration routes, or doses—potentially broadening or narrowing the scope based on language.
  • Formulation Claims: Claims may include specific carriers, excipients, or delivery mechanisms, impacting infringement and patentability.

Analysis indicates that the patent claims are aimed at a specific pharmaceutical compound coupled with a unique formulation for medical indications—potentially including both composition and method claims.

Claim Language Specificity

The claims' clarity directly influences enforceability and scope:

  • If the claims employ broad language such as "comprising" or "including," they potentially cover a wide range of embodiments.
  • Narrow language like "consisting of" or specific chemical structures restricts scope but offers clearer infringement boundaries.
  • The patent likely employs a combination of broad and narrow claims to maximize coverage while providing specificity to withstand clinical and patent prior art challenges.

Novelty and Inventive Step

The patent assertions are based on the novelty of the chemical entity, formulation, or use. Given the competitive pharmaceutical landscape in Chile and globally, the claims' inventive margin must surpass prior art, including existing drugs, patents, or publications.


Patent Landscape in Chile for the Pertinent Drug Class

Regional Patent Trends

Chile’s pharmaceutical patent landscape features:

  • Active Pharmaceutical Ingredient (API) Patents: Chile’s patent law allows for patents on new chemical entities but enforces strict novelty and inventive step criteria.
  • Patent Cooperation and Regional Strategy: Many drug developers prioritize filings under the PCT route, entering regional patent systems such as the Andean Community, which covers Chile, Colombia, Ecuador, and Bolivia.
  • Generic Landscape: Chile has a vibrant generic market subject to patent expirations, with the patent’s enforceability influencing local market dynamics.

Competitive Patent Landscape

Globally, similar compounds or formulations may have patent protection in jurisdictions like the US, Europe, and neighboring Latin American countries. Chile's patent landscape generally reflects this global patenting trend:

  • Prior Art References: The patent examination likely considered prior art similar compounds or formulations.
  • Legal Challenges and Patent Life: Given the pharmaceutical sector's critical nature, legal challenges, including patent oppositions or invalidity claims, can influence the patent's enforceability.

Patent Strategies in Chile

Patent applicants often combine chemical, formulation, and process claims to safeguard their market share. The patent in question appears to follow this approach, expanding protection breadth while reducing vulnerability to invalidity on specific claim grounds.


Implications for Stakeholders

  • Innovators: The patent provides exclusivity for the claimed compound or formulation in Chile, enabling market advantage and recoupment of R&D investments.
  • Generic Manufacturers: Must monitor patent statuses and potential expiry dates to plan market entry or challenges.
  • Regulatory Authorities: Rely on patent data to approve biosimilars or generics, balancing innovation incentives with public health needs.
  • Legal and Business Strategists: Need to evaluate potential infringement risks and opportunities for licensing or collaboration.

Conclusion

Chile Patent CL2017003475 exemplifies strategic patenting in a developing Latin American pharmaceutical environment. Its scope, primarily enclosing specific chemical entities and formulations, reflects a targeted approach balancing breadth with enforceability. The patent landscape in Chile, while aligned with international standards, remains sensitive to prior art and regional patent policies. Protecting such patents supports innovation, but stakeholders must continuously adapt strategies in response to patent expiration timelines, regional patent grants, and evolving legal interpretations.


Key Takeaways

  • The patent’s scope hinges on detailed claim language, balancing broad protection with enforceability.
  • Chile’s patent system offers robust enforcement mechanisms, with a patent term typically spanning 20 years.
  • Similar compounds or formulations may be patented elsewhere, but local patent landscape considerations are critical for market strategy.
  • Patent validity depends on novelty, inventive step, and claims clarity, with regional differences influencing their strength.
  • Continuous monitoring of patent status and regional rights is essential for lifecycle management and strategic planning.

FAQs

1. What generally defines the scope of pharmaceutical patents like CL2017003475?
The scope is primarily determined by the claims’ language—whether they cover a specific chemical compound, formulation, or therapeutic method—and their breadth impacts enforcement and infringement risk.

2. How does Chile's patent system support pharmaceutical innovation?
Chile provides a 20-year patent term from filing, employs examination procedures aligned with international standards (e.g., PCT), and allows patent protection for new chemical entities and formulations.

3. Can similar drugs in other countries impact CL2017003475’s enforceability?
Yes, prior art from other jurisdictions can influence patent validity in Chile, especially if the patent examiner considered such references during examination.

4. What is the significance of claim dependency in this patent?
Dependent claims narrow the scope of independent claims, providing fallback protection, and can strengthen the patent against challenges by specifying particular embodiments.

5. How does patent landscaping influence pharmaceutical R&D in Chile?
It helps identify unmet needs, assess patent barriers, and strategize filing processes, licensing, or patent oppositions as necessary.


References

  1. Chilean Industrial Property Law (Decreto Ley N° 4.723 de 1948).
  2. World Intellectual Property Organization (WIPO). Patent Landscape Report, Latin America.
  3. Chile Patent Search Portal (INAPI).
  4. European Patent Office (EPO). Global patent classification and search tools.
  5. OECD. Innovative Activity and Patent Trends in Latin America.

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