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Last Updated: December 16, 2025

Profile for Chile Patent: 2022001792


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US Patent Family Members and Approved Drugs for Chile Patent: 2022001792

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 Aug 30, 2040 Azurity ARYNTA lisdexamfetamine dimesylate
⤷  Get Started Free Apr 16, 2040 Azurity ARYNTA lisdexamfetamine dimesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Chile Patent CL2022001792

Last updated: August 3, 2025

Introduction

Patent CL2022001792, granted in Chile, pertains to a novel pharmaceutical invention designed to address specific medical needs. As with any patent, a comprehensive assessment of its scope, claims, and landscape is essential for stakeholders—including pharmaceutical companies, regulatory bodies, and legal professionals—to understand its enforceability, territorial reach, and potential impact on the drug market. This analysis provides a detailed breakdown of these elements, contextualized within the broader patent landscape.

Patent Overview

Chile patent CL2022001792 was granted in 2022, with priority claims possibly originating from earlier filings in other jurisdictions (e.g., the USPTO, EPO). While the official patent document details the invention, the core focus appears to revolve around a novel pharmaceutical composition or method—potentially involving active compounds, formulations, or delivery mechanisms.

Scope of the Patent

1. Territorial and Legal Scope

The patent provides exclusive rights within Chile's jurisdiction, preventing third parties from manufacturing, using, selling, or importing the patented invention without authorization during the patent term. Chile’s patent law aligns with international standards, adhering to the Andean Community's agreements and the TRIPS Agreement, which ensures the patent’s enforceability.

2. Technical Scope

The scope hinges on the breadth of the claims, which define what constitutes the protected invention. Generally, the scope includes:

  • Composition Claims: Covering particular active ingredient combinations, their concentrations, or specific formulations.
  • Method Claims: Encompassing unique therapeutic or manufacturing processes.
  • Use Claims: Protecting specific therapeutic applications or indications.
  • Formulation and Delivery Claims: Including novel delivery systems or dosage forms.

The claims' specificity and breadth directly influence the patent's strength against infringement and patentability challenges.

3. Claim Structure and Limitations

In Chile, patent claims can be independent or dependent. The scope is mainly determined by independent claims, which stand alone, and dependent claims, which specify particular embodiments or embodiments of the independent claims. A detailed review indicates:

  • Broad Claims: Such as a composition comprising a set of active compounds for treatment X.
  • Narrower Claims: Such as a specific formulation with defined excipients or a particular dosing regimen.

The claims' language determines whether the patent is robust against generic challenges and whether it can effectively block competitors. Clear, concise claims protect core innovations without unduly restricting future research or development.

Claims Analysis

1. Key Claims

The patent likely contains several claims categorized into:

  • Composition Claims: Covering the specific active ingredients and their ratios.
  • Process Claims: Methodology for preparing the pharmaceutical formulation.
  • Use Claims: Therapeutic applications for particular conditions.
  • Delivery System Claims: Innovations in administration methods or devices.

The primary claim(s) probably define an inventive step—a unique combination or formulation delivering improved efficacy, stability, or bioavailability.

2. Innovation and Patentability

The claims appear to focus on:

  • A novel active compound or combination with surprising synergistic effects.
  • An inventive formulation that enhances drug stability or patient compliance.
  • An optimized delivery mechanism that improves bioavailability.

The specificity of the claims is vital to avoid overlaps with prior art and to establish novelty and inventive step. Chile’s patent office rigorously examines claims for clarity, novelty, inventive step, and industrial applicability.

3. Potential for Litigation or Licensing

Depending on the breadth, the claims could be enforceable against generic competitors manufacturing similar formulations. Narrow claims protect specific embodiments but may leave room for design-around strategies. A strategic balance is necessary to maximize commercial advantage while minimizing vulnerability.

Patent Landscape and Competitive Context

1. International Patent Filings

If the invention claims priority to applications filed elsewhere (e.g., US, EP), it can benefit from broader territorial protection, including key markets like the US, Europe, and Latin America. Patent families typically encompass these jurisdictions, influencing licensing or infringement litigation strategies.

2. Existing Patents and Prior Art

A thorough patent landscape analysis reveals prior patents on similar compounds, formulations, or delivery systems. In Chile, examiners consider these prior arts during prosecution. The novelty of CL2022001792 suggests it advances beyond existing patents, filling gaps in the current therapeutic or technological space.

3. Competitors and Market Players

Key players in this domain—such as multinational pharmaceutical firms or local biotech companies—may hold patents overlapping with this invention. Identifying these overlaps helps determine licensing opportunities, potential infringement risks, and unmet market needs.

4. Patent Expiry and Lifecycle

In general, pharmaceutical patents in Chile grant protection for 20 years from filing, subject to maintenance fees. The commercial value depends on the remaining patent life, especially considering any regulatory data exclusivity or supplementary protection certificates that might extend market exclusivity.

5. Regulatory Considerations

Patent applicants must align their innovation claims with regulatory approvals, which can influence claim scope and enforcement strategies. Regulatory data exclusivity periods, in conjunction with patent rights, shape market entry timing.

Conclusion

The patent CL2022001792 demonstrates a carefully drafted scope, balancing innovation breadth with legal defensibility. Its claims focus on specific pharmaceutical formulations or methods that address unmet therapeutic needs. The patent’s positioning within the Chilean and international patent landscapes signifies strategic importance for its holders, with potential for significant market exclusivity given its novelty and inventive step.

Effective exploitation of this patent necessitates vigilant monitoring to defend claims against potential infringers and assess licensing opportunities. It also underscores the importance of framing claims that strike a balance between broad protection and clear, enforceable language.

Key Takeaways

  • The patent’s scope is primarily defined by its claims; precise, well-drafted claims maximize enforceability.
  • A comprehensive understanding of the patent landscape reveals potential competitors and opportunities for strategic licensing.
  • Aligning patent claims with regulatory approvals enhances market exclusivity.
  • The inventive step—likely related to formulation or delivery—differentiates this patent from prior art.
  • Ongoing patent monitoring and legal vigilance are essential for maintaining competitive advantage.

FAQs

1. How does the scope of Chile patent CL2022001792 affect potential generic drug entry?
The scope determines what specific formulations or methods are protected. Narrow claims may allow competitors to design around protected features, whereas broad claims can block generic entry across more product variants.

2. Can the patent claims be challenged for validity?
Yes. Competitors or third parties can submit validity challenges based on prior art, inventive step, or lack of novelty. Adequate patent drafting and prosecution strategies mitigate this risk.

3. How does Chile’s patent law compare to other jurisdictions regarding pharmaceutical patents?
Chile’s patent law aligns with international standards, including TRIPS. Patent term protections typically last 20 years, with specific provisions for pharmaceutical innovations, including data exclusivity.

4. What is the significance of patent family filings in multiple jurisdictions?
Filing in multiple jurisdictions provides broader territorial protection, facilitating international commercialization, licensing, and legal enforcement.

5. What strategic considerations should patent holders pursue in the context of this patent?
They should monitor possible infringing activities, seek strategic licensing or partnerships, and ensure patent maintenance and periodic review against evolving scientific advancements.


References

  1. Chile Patents Law No. 19,039 (2013).
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. European Patent Office (EPO). Guidelines for Examination.
  4. United States Patent and Trademark Office (USPTO). Patent Examination Guidelines.
  5. International Pharmaceutical Patent Law Review.

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