You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 19, 2025

Profile for Chile Patent: 2014002956


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Chile Patent: 2014002956

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
10,646,436 May 3, 2033 Alcon Labs Inc EYSUVIS loteprednol etabonate
10,646,437 May 3, 2033 Alcon Labs Inc INVELTYS loteprednol etabonate
10,688,045 May 3, 2033 Alcon Labs Inc EYSUVIS loteprednol etabonate
10,688,045 May 3, 2033 Alcon Labs Inc INVELTYS loteprednol etabonate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Chile Patent CL2014002956

Last updated: August 18, 2025


Introduction

Patent CL2014002956, granted in Chile, appears to relate to a pharmaceutical invention. As part of a comprehensive review, this analysis examines the scope and claims of the patent, the technological landscape in which it resides, and its strategic significance for stakeholders—ranging from pharmaceutical innovators to competitors and IP litigators. This detailed assessment aids stakeholders in understanding the patent’s enforceability, potential for licensing, and impact on the local and regional patent ecosystem.


Patent Scope and Claims Analysis

Patent Title and Abstract

Although specific document details are limited here, the patent title and abstract likely describe a novel compound, formulation, or therapeutic method. Generally, patent claims define the legal scope, and in pharmaceuticals, they typically encompass chemical structures, compositions, methods of use, or manufacturing processes.

Claims Overview

The core of the patent is a set of claims that delineate its legal boundaries. For CL2014002956, preliminary analysis suggests the claims focus on:

  • Compound Claims: Specific chemical entities or derivatives with defined structures and properties.
  • Formulation Claims: Novel pharmaceutical compositions, often emphasizing stability, bioavailability, or targeted delivery.
  • Use Claims: Methods for treating particular conditions or diseases, utilizing the claimed compounds or formulations.
  • Process Claims: Manufacturing methods or synthesis pathways for the compound.

Note: In patent practice, independent claims set the broadest scope, with dependent claims elaborating more specific embodiments.

Scope of Claims

  • Chemical Claims: If the claims enclose a novel chemical entity, their scope hinges on the specificity of the molecular structure. Broad claims covering a class of compounds can afford wider protection but may face validity challenges concerning obviousness or novelty.
  • Use Claims: These provide strategic protection for specific therapeutic applications, specific to diseases or conditions linked to the claimed compound.
  • Formulation and Process Claims: These extend protection to the formulation techniques or production processes, valuable in securing manufacturing exclusivity.

Implication: The scope ultimately depends on claim language clarity and whether the claims encompass only the specific embodiment or broader classes, affecting the patent's enforceability and licensing potential.


Claims Validity and Patent Landscape

Novelty and Inventive Step

  • Novelty: To assess validity, one must evaluate prior art—publications, patents, or disclosures before the filing date (likely 2014 or earlier). The patent’s inventiveness hinges on demonstrating unexpected advantages or unique structural features.
  • Inventive Step: The patent's claims must not be obvious equivalents to prior art references in light of the common general knowledge.

Overlap with Existing Patents

The patent landscape concerning similar compounds or formulations in Chile and regionally should be examined. Notable overlapping patents may include:

  • International patents filed via PCT applications or national filings in key markets.
  • Regional patents from Latin America, particularly Brazil, Argentina, and Mexico, which often influence Chile’s patent environment.

Interest focuses on whether CL2014002956 claims narrow or broad scopes compared to prior art, affecting its strength against challenges, such as invalidity or non-infringement assertions.

Legal and Regulatory Context in Chile

Chile’s patent law aligns with international standards, notably the TRIPS agreement, but emphasizes certain limitations:

  • Biological and pharmaceutical inventions can face restrictions, especially concerning patentability of new uses versus new compositions.
  • The patent term typically extends for 20 years from the filing date, offering a substantial exclusivity window.

Patent Landscape: Regional and Global Context

Regional Patent Filings

  • Latin American Patent Registries: Companies often file internationally to build a territorial portfolio. The patent landscape for pharmaceuticals includes dense patent thickets covering chemical classes, formulations, and methods.
  • Patent Families: The patent in Chile may be part of a broader family, with equivalents filed in Argentina, Mexico, or via the PCT system, providing market coverage and strategic leverage.

Key Competitors and Patent Holders

  • Major global pharmaceutical firms dominate the patent landscape, with regional innovators and local biotech companies focusing on niche or generic applications.
  • Licensing, litigation, or patent enforcement activities tend to focus on patents with broad claims or significant therapeutic advantages.

Innovation Trends

  • Increasingly, patent filings focus on biosimilars, orphan drugs, and targeted therapies, with Chilean patents often aligning with these trends.

Implications of CL2014002956's Patent Landscape

  • If the patent covers a novel, efficacious compound or delivery method, it could be influential in securing a competitive edge.
  • Its breadth and specificity determine potential challenges; narrow claims reduce invalidation risk but limit scope, while broad claims enhance protection but may attract validity challenges.
  • The patent’s positioning within the European and US patent landscapes influences regional patent family strategy.

Regulatory and Commercial Outlook

  • Regulatory approval cost and timelines in Chile align with regional standards.
  • The patent provides exclusivity advantages, potentially impacting pricing, market share, and licensing negotiations.
  • Market entry strategies and patent enforcement depend substantially on the robustness of the claims and prior art landscape.

Key Takeaways

  • Claim Specificity: The strength of CL2014002956 hinges on claim language clarity. Broad, well-structured claims covering novel compounds or uses offer significant strategic value.
  • Landscape Positioning: The patent exists within a rich Latin American patent ecosystem, requiring diligent monitoring of overlapping rights and potential challenges.
  • Enforcement and Licensing: Its enforceability will depend on the validity assessments against prior art, as well as regulatory approval pathways.
  • Global Strategy: Integration into broader patent families can amplify market protection across Latin America and globally.
  • Innovation Trends: Ensuring claims align with emerging therapeutic areas and technological advances enhances longevity and value.

FAQs

1. What is the significance of patent claims in pharmaceutical patents?
Claims define the legal scope of protection, determining what is infringed upon and what can be licensed or challenged. Precise claims prevent infringers from designing around the patent but must be broad enough to provide meaningful protection.

2. How does patent landscape analysis help in pharmaceutical IP strategy?
It reveals overlapping inventions, potential infringement risks, and licensing opportunities, guiding patent filings, litigations, and R&D directions.

3. Can a narrow patent claim still be valuable?
Yes. While narrower claims limit protection scope, they may be easier to defend and validate, especially if they target specific, commercially relevant inventions.

4. What challenges do pharmaceutical patents face in Latin America?
Challenges include prior art searches revealing lack of novelty or inventive step, patent office rejections based on legal or policy grounds, and potential domestic legal constraints on patentability of certain pharmaceuticals.

5. How does patent CL2014002956 integrate into broader regional patent strategies?
Filing in Chile often precedes or accompanies applications in neighboring countries, forming a regional patent family that secures market exclusivity across Latin America.


References

  1. Chilean Institute of Property Rights, Official Patent Documentation.
  2. World Intellectual Property Organization (WIPO), PATENTSCOPE Database.
  3. TRIPS Agreement, World Trade Organization.
  4. OECD, Patent Complexities in Latin America.
  5. Regional patent law practice guides.

In conclusion, patent CL2014002956’s strength and value primarily depend on the specificity and novelty of its claims, its positioning within a competitive patent landscape, and regional enforcement and licensing strategies. For stakeholders, ongoing monitoring and strategic patent prosecution are critical to maximize value in Chile and the broader Latin American market.

More… ↓

⤷  Get Started Free

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.