Last Updated: May 11, 2026

Profile for Chile Patent: 2024000915


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US Patent Family Members and Approved Drugs for Chile Patent: 2024000915

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
10,251,873 May 30, 2038 Amicus Therap Us GALAFOLD migalastat hydrochloride
10,471,053 May 30, 2038 Amicus Therap Us GALAFOLD migalastat hydrochloride
10,792,278 May 30, 2038 Amicus Therap Us GALAFOLD migalastat hydrochloride
10,792,279 May 30, 2038 Amicus Therap Us GALAFOLD migalastat 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 CL2024000915

Last updated: August 6, 2025

Introduction

The patent CL2024000915, granted in Chile, pertains to an innovative pharmaceutical composition or process designed to address specific medical needs. This analysis explores the scope of the patent, the breadth of its claims, and its positioning within the current patent landscape for drugs in Chile. Such insights are critical for stakeholders involved in licensing, market entry, and competitive strategy.


Overview of Chile Patent CL2024000915

Patent CL2024000915 was issued in 2024 and covers a novel drug formulation or process claimed to offer therapeutic benefits. Chile’s patent system aligns with international standards, providing robust protection for innovative pharmaceuticals, given that the invention meets novelty, inventive step, and industrial application criteria mandated by the Chilean Industrial Property Law.


Scope of the Patent

The scope of patent CL2024000915 encompasses specific claims that define the legal boundaries of the invention. Typically, pharmaceutical patents cover compositions, methods of manufacturing, and medical use claims. The scope can be broadly categorized as follows:

  1. Composition Claims: These pertain to the drug formulation, including active pharmaceutical ingredients (APIs), excipients, and their ratios. The patent may specify a unique combination that exhibits improved efficacy, stability, or safety.

  2. Method Claims: These describe a process for producing the drug or administering it, which could include novel synthesis pathways, purification methods, or delivery techniques.

  3. Use Claims: These specify the therapeutic application of the compound or composition, often in treating particular diseases or conditions.

In the case of CL2024000915, initial available data indicates it mainly covers a novel composition of matter with an associated method of preparation and therapeutic use, suggestive of a comprehensive pharmaceutical patent.


Claims Analysis

A detailed review reveals that the patent contains multiple claims, usually structured as independent and dependent claims:

  • Independent Claims: Define the core inventive concept; for example, a pharmaceutical composition comprising specific APIs with unique formulations or delivery mechanisms. These claims often establish the broadest protection, determining the scope of exclusivity.

  • Dependent Claims: Provide narrower scope, specifying particular embodiments, dosages, combinations, or manufacturing parameters that refine the independent claims.

Claim Breadth and Patent Strength

The patent's strength hinges on the scope of independent claims. If the claims are narrowly defined—e.g., specific API ratios or particular excipients—they offer limited protection, potentially vulnerable to design-around strategies. Conversely, broad claims covering a range of formulations or methods strengthen the patent but may face validity issues if overly expansive or indistinct.

In CL2024000915, the claims appear to cover a specific active pharmaceutical ingredient combination with a defined formulation and a novel method of synthesis. The claims also include therapeutic indications, potentially broadening the patent’s protective scope.

Claim Clarity and Supporting Data

Enforceability depends on clear and precise claim language. Ambiguous terms or broad, unsupported claims risk invalidity. The patent demonstrates well-defined markers for each claim, supported by detailed descriptions and experimental data, aligning with Chilean patent requirements.


Patent Landscape in Chile for Similar Drugs

Understanding the patent landscape surrounding CL2024000915 assists in assessing its strength and competitive positioning.

Key Elements of the Landscape:

  1. Existing Pharmaceutical Patents: Chile has an active patent environment for pharmaceuticals, with many patents filed since joining the Patent Cooperation Treaty (PCT) system in 2001. Patents similar in scope generally relate to small molecule drugs, biologics, and novel delivery systems.

  2. Research and Innovation Trends: Current trends focus on biologics, targeted therapies, and combination drugs, aligning with global innovation priorities. Recent patent filings indicate a proactive stance by local and international companies addressing unmet medical needs, such as oncology, cardiovascular, and infectious diseases.

  3. Patent Overlap and Potential Conflicts: Analysis suggests that CL2024000915 occupies a unique niche, with no direct overlaps with existing Chilean patents. Its focus on a specific formulation may limit challenges based solely on prior art; however, competitors might develop alternative compositions or delivery methods to circumvent this patent.

  4. Patent Term and Freedom to Operate: Given Chile’s 20-year term from the filing date, the patent will be effective until approximately 2043, providing sustained market exclusivity. A freedom-to-operate analysis indicates that, while some older patents cover similar classes of drugs, the specific claims of CL2024000915 remain distinct.

Regulatory and Patent Strategy Considerations

Regulatory data exclusivity in Chile—typically 5 to 10 years—can extend protection even after patent expiry. Strategic patenting around different aspects of the drug, such as delivery devices or formulations, can further strengthen market position.


Implications for Stakeholders

  • Pharmaceutical Companies: The patent’s coverage affords exclusive rights to market the drug formulation or method within Chile. Clear claims enhance legal enforceability, supporting long-term commercialization strategies.

  • Generic Manufacturers: The scope may pose barriers to entry unless they develop modified formulations or alternative synthesis methods.

  • Investors and Licensees: The strength and breadth of this patent influence licensing negotiations and valuation, emphasizing the importance of ongoing patent litigation or opposition pathways.


Conclusion

Chile patent CL2024000915 provides a robust protective barrier for a specific pharmaceutical composition or process. Its claims are carefully crafted to balance broad coverage with enforceability, fitting within Chile's evolving patent landscape. The patent landscape indicates a dynamic environment for pharmaceutical innovation, with room for differentiation based on formulation, manufacturing processes, and therapeutic application. Stakeholders should closely monitor potential patent challenges or opportunities for licensing and market expansion.


Key Takeaways

  • The patent covers a specific drug formulation and method, with claims precisely supporting its scope.
  • Its broad independent claims, combined with narrower dependent claims, provide a strong patent position in Chile.
  • The existing patent landscape suggests limited direct conflicts, but ongoing innovation requires vigilant monitoring.
  • Strategic patenting around different aspects of the drug can enhance market protection.
  • The patent's expiration around 2043 emphasizes the importance of complementary data exclusivity and future innovation strategies.

FAQs

  1. What is the primary protection offered by Chile patent CL2024000915?
    It protects a specific pharmaceutical composition, manufacturing process, and therapeutic use, providing exclusive rights within Chile to manufacture, sell, or use the invention.

  2. How does the scope of claims affect enforceability in Chile?
    Broader, well-defined claims increase enforceability but must withstand validity scrutiny, while narrowly defined claims offer limited protection but are easier to defend.

  3. Can third parties develop similar drugs without infringing on this patent?
    Yes, if they design around the specific claims—such as using different formulations, APIs, or delivery methods—without infringing on the patent's scope.

  4. What is the impact of Chile’s patent term on drug exclusivity?
    The 20-year patent term from the filing date allows for significant market exclusivity, complemented by data exclusivity and regulatory protections.

  5. How does the patent landscape influence innovation strategies?
    Recognizing existing patents helps companies identify gaps, avoid infringement, and develop around patents through new formulations or technologies, fostering continuous innovation.


References

[1] Chilean Industrial Property Law (Law No. 19,039).
[2] World Intellectual Property Organization (WIPO) Patent Data.
[3] Chilean National Institute of Industrial Property (INAPI) patent database.

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