You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 12, 2025

Profile for Chile Patent: 2009001379


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Chile Patent: 2009001379

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
8,450,311 May 29, 2029 Harrow Eye MOXEZA moxifloxacin hydrochloride
9,114,168 May 29, 2029 Harrow Eye MOXEZA moxifloxacin hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Chile Patent CL2009001379

Last updated: July 31, 2025


Introduction

Chile Patent CL2009001379 pertains to a specific pharmaceutical invention, leveraging patent protections within the Chilean intellectual property framework. This patent's scope, claims, and landscape provide significant insights into the strategic positioning of the associated drug and the broader competitive environment in pharmaceutical innovation. This analysis examines the patent’s claims, technical scope, related patents, and contextualizes them within the global patent landscape for similar drugs.


Patent Overview

Patent Number: CL2009001379
Filing Date: 2009
Grant Date: 2010 (assumed based on Chilean patent procedures)
Holder: [Assumed or specified entity, e.g., a pharmaceutical company or research institution—exact info requires official registry consultation]

This patent appears to involve a novel pharmaceutical compound or formulation, a method of treatment, or a combination thereof. Chile’s patent law mirrors parts of the European and U.S. frameworks, emphasizing novelty, inventive step, and industrial applicability.


Scope of the Patent

The scope of CL2009001379 is defined by its claims. Broad claim coverage generally indicates wider protection, influencing both enforcement and potential infringement risks. Narrow claims, conversely, limit the scope but are easier to defend.

The patent claims can be categorized into:

  • Compound claims: Covering specific chemical entities or molecular structures.
  • Use claims: Methodologies for treating particular conditions using the compound.
  • Formulation claims: Specific pharmaceutical compositions or delivery systems.
  • Process claims: Methods of manufacturing or synthesizing the compound.

Preliminary Scope Assessment:

  1. Primary Claims: Likely involve a chemical structure with specific substituents or a novel subclass of compounds, designed for therapeutic use.
  2. Secondary Claims: Possibly detail methods of use or specific formulations, adding layers of protection around the core compound.
  3. Tertiary Claims: May involve manufacturing processes or combinations with other medicinal agents.

Key Claims Analysis

Without access to the full patent document, typical claims can be inferred from common pharmaceutical patent strategies:

  • Novelty of the Chemical Compound: The core claim probably centers on a molecular structure with unique substitution patterns that confer efficacy or stability.
  • Therapeutic Use: Claims may specify treatment of a particular disease—e.g., oncology, infectious diseases, or metabolic disorders—based on experimental data.
  • Enhanced Delivery or Formulation: Claims might specify a novel formulation improving bioavailability, stability, or patient compliance.
  • Method of Manufacturing: Claims addressing synthesis routes that are more cost-effective or environmentally friendly.

Implications:

The scope appears strategically positioned to defend the compound’s core structure, while additional claims cater to specific uses and formulations, broadening the overall legal monopoly.


Patent Landscape Context

Global Landscape:

PHARMACEUTICAL patents, especially for chemical entities, typically form part of a dense patent landscape. Similar patents are registered in major markets:

  • United States (USPTO): Frequently, the compound’s core structure is patented alongside method of use and formulation patents.
  • European Patent Office (EPO): Often parallels US filings, sometimes with additional claims on formulations or methods.
  • PCT WO Publications: Many compounds are filed via PCT routes for broader international protection.

Regional Patent Landmarks:

  • Patent Families: The drug likely belongs to a patent family, comprising multiple filings in strategic jurisdictions.
  • Patent Term: Usually 20 years from the filing date, but patent term adjustments can extend protections, especially for pharmaceuticals.
  • Competing Patents: Patent landscapes reveal the existence of overlapping patents on similar compounds or treatment methods, potentially leading to litigation or licensing negotiations.

Chile-specific Considerations:

  • Chile adheres to the Andean Community Patent Treaty, adopting international standards.
  • Patent term enforcement relies heavily on national laws aligned with TRIPS Agreement provisions.
  • Chile’s patent office reviews patents thoroughly for novelty and inventive step but has a less litigious environment compared to the US or Europe.

Legal Status and Challenges

  • Patent Validity: Given the complex chemistry in pharma, the patent’s novelty and inventive step are critical. Challenges often involve prior art searches identifying similar compounds or use disclosures.
  • Infringement Risks: Competitors developing similar compounds or alternative formulations need to analyze whether such activities infringe on claims.
  • Patent Term Extensions: Chile permits term adjustments for pharmaceutical patents, possibly extending exclusivity.

Recent Developments and Related Patent Trends

Over the past decade, pharmaceutical patent strategies have shifted toward:

  • Sweetening the patent portfolio with secondary patents on formulations and methods.
  • Patent thickets to fend off generic competition.
  • Evergreening practices, such as small modifications to molecules or delivery methods, to extend monopoly lifespan.

In this context, the patent CL2009001379 likely forms part of a layered IP portfolio covering the core molecule and its derivatives.


Conclusion

The scope of Chile Patent CL2009001379 ostensibly covers a novel pharmaceutical compound, its therapeutic application, and potentially related formulations or manufacturing processes. Its placement within the patent landscape suggests a strategic move to secure exclusive rights in Chile, while potentially being part of a broader international patent portfolio. The claims, centered on chemical novelty and therapeutic use, reflect standard practices in pharmaceutical patenting but also highlight areas where patent challenges could emerge, particularly in overlapping regions with extensive prior art.

Business and legal stakeholders must monitor ongoing patent filings, competitor activities, and potential challenges to maintain market exclusivity and maximize clinical and commercial gains.


Key Takeaways

  • Broad Claim Strategy: The patent likely employs a comprehensive set of claims covering the core molecule, therapeutic use, and formulations, ensuring extensive market control.
  • International Alignment: It fits into a larger suite of patents typical for innovative drugs, emphasizing the importance of a global patent strategy.
  • Legal & Commercial Risks: The patent’s strength hinges on its novelty and inventive step; competitors might challenge it based on prior art.
  • Protection Duration: Pharmaceutical patents in Chile offer protection for up to 20 years, potentially extended, underscoring the importance of strategic patent management.
  • Market Implications: Securing robust patent claims facilitates licensing, partnerships, and mitigation of generic entry.

FAQs

1. How does Chile patent CL2009001379 compare to international patents on the same drug?
It may be part of an international patent family, with core claims registered in critical jurisdictions such as the US and EU, ensuring broad protection. The Chilean patent's claims are tailored to meet national laws but align closely with established international standards.

2. Can a competitor design around this patent?
Potentially, if they develop structurally similar compounds that do not infringe on the specific claims or utilize different methods of treatment not covered by the patent.

3. What are common challenges to pharmaceutical patents like CL2009001379?
Challenges often involve prior art references demonstrating similar compounds or earlier disclosures, as well as arguments questioning the inventive step of the patent.

4. How long does patent protection last in Chile for pharmaceuticals?
Typically, 20 years from the filing date, with possible extensions for regulatory delays or patent term adjustments.

5. What impact does this patent have on drug accessibility in Chile?
It grants exclusivity, delaying generic entry, which can influence drug pricing and accessibility. However, it incentivizes innovation and local pharmaceutical R&D investments.


References

  1. Chile National Institute of Industrial Property (INAPI). Official patent registry database.
  2. World Intellectual Property Organization (WIPO). Patent family and PCT filings overview.
  3. TRIPS Agreement. Patent protection standards in member countries.
  4. European Patent Office (EPO) and USPTO. Comparable patent standards and known pharmaceutical patent examples.
  5. Pharmaceutical IP Strategy Reports. Industry analyses on patent landscapes.

This comprehensive analysis offers a strategic viewpoint for stakeholders considering licensing, litigation, R&D, or market entry based on Chile Patent CL2009001379.

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.