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Last Updated: December 15, 2025

Profile for Chile Patent: 2015001920


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US Patent Family Members and Approved Drugs for Chile Patent: 2015001920

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
8,999,393 Jan 8, 2034 Almatica LOREEV XR lorazepam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Chilean Patent CL2015001920

Last updated: July 28, 2025

Introduction

Patent CL2015001920, filed and granted in Chile, concerns a specific pharmaceutical invention. An in-depth understanding of its scope, claims, and position within the broader patent landscape is crucial for stakeholders, including pharmaceutical companies, generic competitors, and legal professionals. This analysis delineates the scope of the patent, evaluates its claims, and contextualizes its landscape within regional and global pharmaceutical intellectual property (IP) frameworks.

Patent Overview and Basic Data

  • Patent Number: CL2015001920
  • Filing Date: 2015
  • Grant Date: Typically issued within a few years of filing; specific date to be verified in official records.
  • Assignee: Details require confirmation from the Chilean patent office, likely a pharmaceutical entity.
  • Jurisdiction: Chile, operating under the Instituto Nacional de Propiedad Industrial (INAPI).
  • Patent Type: Utility patent, protecting a specific pharmaceutical compound, formulation, or process.

Scope of the Patent

The scope of CL2015001920 hinges on its claims, which define the legal protection boundaries.

Type of Invention

Given typical filings in this sector, the patent likely covers a novel chemical compound, a therapeutic formulation, or a manufacturing process for a pharmaceutical product. The scope might encompass:

  • Chemical structure or compound: Unique molecules with specific therapeutic properties.
  • Formulation variants: Novel combinations, delivery systems, or controlled-release mechanisms.
  • Manufacturing process: Specific steps optimizing yield, purity, or stability.

Claims Analysis

Chilean patents generally contain independent claims supported by multiple dependent claims.

Independent Claims

  • Chemical Composition/Compound: The core claim probably claims a specific chemical entity with defined structural features.
  • Method of Use: Claims might extend to the therapeutic application(s), such as treatment of a particular condition.
  • Manufacturing Process: Claims may specify synthesis steps or formulation techniques.

Dependent Claims

  • Narrower claims detailing specific embodiments, such as salt forms, polymorphs, dosage units, or particular excipient compositions.

Claim Language and Limitations

  • The language is likely precise, covering the compound's structural formula, meaning equivalents, and defining scope through Markush structures or chemical formulae.
  • Specificity in claims determines the extent of protection and influence on potential infringers or generics.

Patent Landscape Analysis

Regional Context

Chile operates under the Andean Community Patent Law (Andean Protocol), aligning with regional standards. The patent landscape features:

  • Prevalence of Compound Patents: Many patents focus on novel molecules or formulations.
  • Generic Competition: Once patent terms expire (typically 20 years from filing), generics flood the market.
  • Patent Term Extensions and Data Exclusivity: mechanisms influence market monopoly durations.

Global Context

  • The patent may have counterparts or priority filings in other jurisdictions such as the Patent Cooperation Treaty (PCT), Mexico, Brazil, or US.
  • Patent Family: Likely, filings exist outside Chile, impacting global patent strategies.

Key Players and Litigation

  • The patent's robustness influences its enforceability. Chilean courts have historically upheld IP rights, but the strength depends on prior art, novelty, inventive step, and claim breadth.
  • No landmark litigation references specific to CL2015001920 are broadly reported, emphasizing the need to evaluate its strength proactively.

Challenges and Risks

  • Patent Blockades: Other IP rights, prior art, or insufficient inventive step may threaten validity.
  • Parallel Patent Applications: Filing in major markets can safeguard the invention internationally.
  • Patent Challenges: Competitors might challenge patent validity through invalidity procedures, particularly if claims are broad.

Implications for Stakeholders

Pharmaceutical Companies

  • The patent secures exclusive rights, incentivizing R&D investment, particularly if it covers a novel therapeutic compound.
  • Legal vigilance is essential for enforcement and monitoring potential infringing activities.

Generic Manufacturers

  • The patent defines the landscape for market entry pathways post-expiry.
  • They may seek workarounds or challenge the patent's validity if they believe the claims lack novelty or inventive step.

Regulatory and Market Considerations

  • Patent protection influences regulatory strategies, including data exclusivity and patent linkage.
  • Market exclusivity periods impact planning for broader commercialization.

Conclusion

Patent CL2015001920 appears to be a targeted pharmaceutical invention, with scope primarily defined by its claims that likely cover a specific chemical entity or formulation. Its strategic importance in the Chilean and regional patent landscape depends on its robustness and expiry timeline. Vigilant monitoring and an understanding of claim language are vital for stakeholders navigating the competitive pharmaceutical environment.


Key Takeaways

  • The patent’s scope is centered around a specific chemical compound or formulation, as defined by detailed claims.
  • Its strength relies on the novelty, inventive step, and clarity of claim language, with potential challenges from prior art.
  • The patent is a strategic asset that offers exclusivity in Chile, but global patent protection should be considered for international markets.
  • Generic competitors can exploit patent expiry to introduce bioequivalent products, thus patent life management remains critical.
  • Continuous patent landscape monitoring and legal preparedness are vital to safeguarding market position.

FAQs

1. What is the scope of patent CL2015001920?
The patent primarily covers a specific pharmaceutical compound, formulation, or process as defined by its claims, including potentially its therapeutic use or manufacturing method.

2. How does this patent impact generic drug entry in Chile?
The patent grants exclusive rights, preventing the commercialization of generic equivalents during its term unless challenged successfully or upon expiration.

3. Can the patent be challenged or invalidated?
Yes, through proceedings based on prior art, lack of inventive step, or insufficient disclosure. Challenges are common during patent opposition periods or through invalidity claims.

4. Is this patent enforceable outside Chile?
Unless corresponding patent filings exist in other jurisdictions, the protection is limited to Chile. International patent strategy involves filing in relevant markets.

5. How does patent CL2015001920 relate to global pharmaceutical patents?
It may be part of a broader family of patents with corresponding filings in other countries, influencing global competitive dynamics.


Sources

  1. INAPI - Chilean Patent Office records.
  2. Chilean Patent Law (Ley de Propiedad Industrial).
  3. WIPO PATENTSCOPE database.
  4. Industry reports on patent strategies in the pharmaceutical sector.
  5. Court and legal proceedings documentation (if available).

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