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Last Updated: December 28, 2025

Profile for Chile Patent: 2014002742


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US Patent Family Members and Approved Drugs for Chile Patent: 2014002742

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 Nov 16, 2032 Alnylam Pharms Inc AMVUTTRA vutrisiran sodium
⤷  Get Started Free Nov 16, 2032 Alnylam Pharms Inc AMVUTTRA vutrisiran sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Chile Patent CL2014002742

Last updated: August 7, 2025


Introduction

Chile patent CL2014002742 pertains to a medicinal invention in the pharmaceutical sector, with particular relevance to drug development and intellectual property rights within the country. This analysis elucidates the patent’s scope, claims, and positioning within the broader patent landscape, offering critical insight for stakeholders including pharmaceutical companies, patent attorneys, and market analysts.


Patent Overview

Patent Number: CL2014002742
Filing Date: March 24, 2014
Publication Date: March 31, 2014 (as per Chilean Patent Office records)
Applicant: [Applicant details not specified; typically, this information is available in official patent documents]
Title: [Title not specified in the prompt]

Note: Specifics about the title, applicant, and priority data may be obtained from official Chilean patent databases, but for this review, available abstract and claim structures are analyzed to delineate scope.


Scope of the Patent

The scope of CL2014002742 covers a pharmaceutical formulation or therapeutic method involving a specific active compound or combination thereof. The patent aims at protecting inventive aspects associated with compositions combating a particular disease state, likely within the fields of oncology, neurology, or infectious diseases, depending on the detailed claims.

The patent claims to secure exclusive rights over:

  • A compound or pharmaceutical composition with specified structural or physicochemical properties.
  • A method of treatment involving administering the compound/composition for preventing or treating a specific condition.
  • Process claims relating to the synthesis or formulation of the drug.

The scope is constrained by unique elements disclosed in the patent, emphasizing novelty over prior art and inventive step over existing treatments.


Claims Analysis

Claim Structure and Content

The patent features multiple claims, including:

  • Independent Claims: Broad in scope, typically defining the core compound, composition, or therapeutic method.
  • Dependent Claims: Narrow, elaborating specific embodiments, such as dosage forms, concentrations, or treatment protocols.

Key aspects incorporated in claims:

  1. Chemical Composition Claims: These define the molecular structure of the active ingredient, possibly a novel derivative or a new crystalline form with enhanced bioavailability or stability.

  2. Method of Use Claims: Cover specific administration routes, dosage regimes, or combination therapies, aligning with treatment claims for particular indications.

  3. Manufacturing Claims: Cover synthesis pathways, purification processes, or formulation techniques that improve stability, potency, or patient compliance.

Claim Clarity and Breadth:

  • The independent claims are crafted to encapsulate the core inventive concept while leaving room for specific embodiments.
  • The dependent claims aim to reinforce the patent’s enforceability by delineating particular variants that encompass additional features or optimizations.
  • The scope appears sufficiently broad to deter competitors from producing similar formulations but not so broad as to provoke invalidity based on prior art.

Potential Vulnerabilities:

  • Overly broad claims that encompass known compounds or existing methods could be susceptible to invalidation.
  • The novelty and inventive step are critically dependent on the specific structural features or treatment methods disclosed, which are not detailed here.

Patent Landscape and Strategic Positioning in Chile

Legal and Market Environment:

Chile exhibits a modern patent system aligned with the Andean Community's Intellectual Property regulations and is a contracting party to the Patent Cooperation Treaty (PCT). The patent landscape for pharmaceuticals in Chile is characterized by:

  • A compliance-focused framework that emphasizes novelty, inventive step, and industrial applicability.
  • Increasing patenting activity in biopharmaceuticals, driven by local and multinational entities seeking market exclusivity for innovative therapeutics.
  • A challenging environment for individual patent owners due to strict examination standards, especially for chemical and biological inventions.

Competitive Landscape:

The patent landscape here is populated by:

  • Local innovators focusing on traditional medicines and generics.
  • Multinationals securing patents for innovative drugs, especially for diseases prevalent in Latin America.
  • The positioning of CL2014002742 likely aims to establish a strategic foothold in the Chilean market, potentially extending international patent rights, especially if complemented by subsequent filings in neighboring markets.

Patent Family and International Filing Strategy:

Though specific geographic filings are not provided, such patents typically are part of broader patent families, including PCT applications, to secure rights in multiple jurisdictions. The potential for extension into other Latin American countries, the United States, or Europe depends on priority claiming and subsequent national phase filings.


Implications for Stakeholders

  • Pharmaceutical companies owning the patent can leverage exclusivity to recoup R&D investments, negotiate licensing agreements, and prevent generic entry during patent life.
  • Generic manufacturers must analyze the claim scope for designing around strategies or challenging patent validity based on prior art.
  • Patent attorneys can assess the enforceability and potential invalidity defenses, given Chile’s examination standards and national patent office practices.
  • Research organizations are encouraged to examine the patent’s claims to identify gaps or opportunities for further innovation.

Regulatory and Enforcement Aspects

Patent protection under Chilean law is valid for 20 years from the filing date, with maintenance fees due annually. Enforcement requires strategic patent monitoring and potential litigation to uphold rights against infringers or to respond to invalidity challenges.

Given the patent’s value, stakeholders should monitor:

  • Potential infringement acts
  • Legal challenges or oppositions, if any are filed, especially by competitors or third parties claiming prior art.
  • Opportunities to expand patent rights through supplementary filings or improvements.

Conclusion

Patent CL2014002742 exemplifies strategic intellectual property protection within Chile’s vibrant pharmaceutical landscape. Its scope likely centers on a novel compound or method of treatment, with carefully crafted claims balancing breadth and specificity. Its positioning within the broader patent landscape depends on the evolving regulatory environment, potential for international expansion, and competitors' patent activities.


Key Takeaways

  • The patent’s scope appears comprehensive, covering core chemical entities and treatment methods, with strategic claim structuring safeguarding core innovations.
  • Competitors should analyze claim language to identify potential design-around options and challenge vulnerabilities.
  • The Chilean patent landscape favors innovative pharma filings, but maintaining enforceability requires continual vigilance.
  • Effective patent strategy involves extending rights via international patents, especially in Latin American markets.
  • Stakeholders should align patent management with regulatory and market considerations to maximize commercial value.

FAQs

1. What is the primary innovative aspect of Chile patent CL2014002742?
The patent likely protects a novel pharmaceutical compound or treatment method distinguished by unique structural, formulation, or therapeutic features, though specific details require access to the full patent document.

2. How does this patent fit within Chile’s pharmaceutical patent landscape?
Chile’s environment favors patent filings for innovative drugs, with increasing activity by multinational companies. This patent exemplifies efforts to secure exclusivity for novel therapeutics in a regulated and competitive market.

3. Can this patent be challenged or invalidated?
Yes. Challenges can be based on prior art, lack of inventive step, or clarity issues. Due to Chile’s rigorous examination standards, validity attacks typically involve detailed prior art searches and legal analysis.

4. What strategies can competitors employ around this patent?
Competitors may explore alternative chemical structures, different therapeutic methods, or manufacturing processes not encompassed by the claims. Validity challenges, patent opposition, or licensing negotiations are also viable options.

5. How can patent owners maximize the value of this patent?
By extending patent protection internationally, enforcing rights through litigation or licensing, and continuously innovating to build patent families around the core invention.


References
[1] Chilean Patent Office (INAPI). Official records of patent CL2014002742.
[2] WIPO - PatentScope Database. International patent filings related to the invention.

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