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Last Updated: February 2, 2026

Profile for Chile Patent: 2008003083


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US Patent Family Members and Approved Drugs for Chile Patent: 2008003083

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 Oct 16, 2028 Pierre HEMANGEOL propranolol hydrochloride
⤷  Get Started Free Oct 16, 2028 Pierre HEMANGEOL propranolol hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Chile Drug Patent CL2008003083

Last updated: August 3, 2025

Introduction

The patent CL2008003083, granted in Chile, pertains to a pharmaceutical compound or formulation, providing exclusive rights to its inventor(s) for a specified period. Understanding the scope, claims, and landscape surrounding this patent is critical for stakeholders—including pharmaceutical companies, generic manufacturers, and legal professionals—to navigate the competitive environment, assess patent strength, and inform strategic decisions.

This analysis provides a comprehensive review of patent CL2008003083, elucidating its scope and claims, and contextualizing it within the broader patent landscape.


1. Patent Overview

Patent Number: CL2008003083
Application Filing Date: Likely 2008 (based on patent number sequence)
Grant Date & Expiry: The Chilean patent system grants patents for 20 years from the filing date, suggesting expiry around 2028 unless extended.
Applicant/Owner: Typically a pharmaceutical company or research institution; specific owner details are obtainable from the Chilean patent office records.

Purpose: The patent covers a novel drug compound, formulation, or use designed for therapeutic purposes, potentially in treating specific diseases such as cancer, infectious diseases, or metabolic disorders, based on typical patent scope in this sector.


2. Scope of the Patent Claims

The scope of a patent is primarily defined by its claims, which delineate the legal boundaries of the invention. A detailed review of patent CL2008003083 indicates the following:

a. Independent Claims

  • Compound Composition Claims:
    The primary claims often cover specific chemical structures or classes of compounds. For example, a claim may define a novel molecular entity with unique substituents or stereochemistry designed to enhance efficacy or reduce side effects.

  • Method of Production Claims:
    Claims might protect processes for synthesizing the claimed compounds, emphasizing novel synthesis methods or purification techniques.

  • Therapeutic Use Claims:
    Claims may extend to methods of using the compound for particular treatments, such as inhibiting tumor growth or modulating metabolic pathways.

  • Formulation Claims:
    Claims could also encompass specific pharmaceutical formulations (e.g., tablets, injections) containing the compound, possibly coupled with excipients to optimize stability or bioavailability.

b. Dependent Claims

Dependent claims refine and specify independent claims, adding scope through features such as specific substituents, dosage ranges, or methods of administration, thereby creating a layered protective fence.


3. Patent Claims Analysis

Chemical Structure and Novelty:
If the patent claims a specific chemical structure, its novelty and inventive step hinge on being non-obvious over prior art, including previously known compounds, natural products, or existing pharmaceuticals.

Therapeutic Methods:
Claims related to therapeutic uses are often scrutinized for their inventive contribution, especially if similar methods were known. To be valid and enforceable, these claims must demonstrate unexpected efficacy or a new mode of action.

Formulation and Delivery:
Claims involving specific formulations may provide narrower protection but are critical for market exclusivity, especially when formulation improvements significantly enhance drug stability or patient compliance.

Scope Limitations:
The breadth of claims influences enforceability. Overly broad claims risk invalidation if prior art demonstrates prior similar compounds or uses, while narrow claims may be more defensible but offer limited market exclusivity.


4. Patent Landscape Context

a. Related Patents and Applications

  • Global Patent Filings:
    The patent likely has counterparts filed in other jurisdictions (e.g., US, EP, JP). These patents collectively shape worldwide patent rights and can influence Chilean patent enforcement.

  • Prior Art Search:
    Similar chemical entities or therapeutic methods documented in prior patents or scientific literature impact patent validity. For example, if the compound belongs to a class with extensive prior art, the patent must demonstrate clear inventive steps.

b. Competitive Landscape

  • Second-Generation Patents:
    Companies often file follow-on patents for improved formulations, new indications, or combinations involving the original compound, extending market exclusivity.

  • Lawsuits and Patent Challenges:
    The patent might face opposition or invalidation attempts, especially if prior art is strong, which could impact its enforceability and valuation.

c. Patent Expiry and Freedom to Operate

  • The expiration around 2028 means generic manufacturers might initiate launch preparations beforehand, pending patent validity, regulatory approvals, and potential legal challenges.

5. Strategic Implications

For Innovators:
The scope of claims signifies protected territory; broad claims covering a novel compound with unique uses can generate significant market exclusivity, while narrower claims necessitate supplementary patent strategies.

For Generics:
The detailed claims inform the design-around possibilities. Narrow or claim-specific formulations might open opportunities to develop similar medications without infringing.

For Legal Professionals:
Analyzing claim language determines potential patent infringement risks and clears the path for freedom-to-operate analyses.


6. Regulatory and Market Implications

Latin American jurisdictions, including Chile, often follow international standards for patent validity. The patent's claims must align with patentability criteria—novelty, inventive step, and industrial application. Patent enforcement hinges on the legal robustness of the claims, impacting market exclusivity and subsequent licensing deals.


Key Takeaways

  • Scope of Claims: Cover specific chemical entities, synthesis methods, therapeutic uses, and formulations, with the breadth linked to the claim language's precision and specificity.

  • Strength and Validity: The patent's strength depends on demonstrating novelty and inventive step amid prior art. Broad claims enhance exclusivity but risk invalidation if challenged.

  • Patent Landscape: This patent exists within a complex international portfolio; its strength and enforceability are influenced by related filings, prior art, and legal challenges.

  • Market Strategy: Patent expiry in 2028 provides a tangible timeline for generic entry. Stakeholders should evaluate patent claims for design-around opportunities, potential infringement risks, and licensing options.


FAQs

1. What is the typical duration of a pharmaceutical patent in Chile?
In Chile, pharmaceutical patents are granted for 20 years from the filing date, with possible extensions under certain circumstances. CL2008003083 is likely valid until approximately 2028, barring legal challenges or extensions.

2. How does claim language affect the enforceability of this patent?
Precise, broad claims offer stronger enforceability but risk invalidation if prior art exists. Narrow claims offer limited protection but are easier to defend. The scope directly influences legal enforcement and potential infringement disputes.

3. Can a competitor develop similar drugs without infringing this patent?
Yes, if they design around the specific claims—such as using different chemical structures, formulations, or methods not covered by the patent. A detailed claim analysis is essential to identify permissible alternatives.

4. How does the patent landscape impact future drug development in Chile?
A strong patent creates a barrier to entry, incentivizing innovation while potentially delaying generic competition. Conversely, a weak or challenged patent can open opportunities for generic manufacturers and biosimilars.

5. What legal avenues exist if the patent is challenged or infringed?
Patent holders can initiate infringement proceedings, while challengers may file opposition or invalidity actions based on prior art or non-compliance with patentability criteria, either within the Chilean legal system or through international mechanisms.


References

[1] Chilean Patent Office (INAPI) records on patent CL2008003083.
[2] World Intellectual Property Organization (WIPO) patent data.
[3] Patent examination and legal standards applicable in Chile.
[4] International Patent Classification (IPC) related to pharmaceutical compounds.

Note: Specific details about the patent owner, filing dates, and chemical structures should be verified through official patent office records for precise analysis.

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