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Last Updated: December 16, 2025

Profile for Chile Patent: 2017002456


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US Patent Family Members and Approved Drugs for Chile Patent: 2017002456

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
11,324,734 Mar 31, 2036 Akebia VAFSEO vadadustat
11,844,756 Mar 31, 2036 Akebia VAFSEO vadadustat
>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 CL2017002456

Last updated: August 1, 2025


Introduction

Chile Patent CL2017002456, granted to specified assignees, pertains to a novel pharmaceutical invention. Analyzing this patent involves understanding its scope, claims, and placement within the broader patent landscape. Such an assessment informs stakeholders—from competitors to licensing entities—about innovation boundaries, potential overlaps, and market exclusivity periods.


Patent Overview

Patent Number: CL2017002456
Application Filing Date: (Assuming based on typical timelines) — likely filed in 2017
Grant Date: (Assuming recent, potentially 2018-2019)
Assignee: (Details not specified)
Title: (Typically reflects the pharmaceutical compound, method, or formulation)

While specific details from the official patent document are necessary for exhaustive analysis, standard practice involves examining the claims, description, and prosecution history to determine scope.


Scope of the Patent

The scope defines the protected rights awarded by the patent, articulated through its claims. Typically, pharmaceutical patents include claims covering the compound’s chemical structure, pharmaceutical compositions, methods of use, and manufacturing processes.

Type of Claims in CL2017002456:

  • Compound Claims: Likely encompass a specific chemical entity, possibly a novel molecular structure intended for targeted therapy, e.g., kinase inhibitor, monoclonal antibody, or a similarly innovative molecule.

  • Use Claims: Probably cover therapeutic applications of the compound, including indications, such as oncology, infectious diseases, or metabolic disorders.

  • Formulation Claims: May involve specific formulations, including delivery systems like controlled-release, nanoparticles, or combination therapies.

  • Process Claims: Cover manufacturing methods or synthesis pathways that provide advantages like higher yield or purity.

Scope Interpretation:

  • Narrow claims restrict protection to the exact chemical structure or specific use, allowing competitors to potentially design around.
  • Broad claims might cover a class of compounds (e.g., all heterocyclic derivatives with certain substituents), increasing the patent’s defensive strength but often facing more scrutiny during patentability analysis.

Claims Analysis

Given typical patterns in pharmaceutical patent claims, the CL2017002456 claims likely include:

  1. A chemical compound with a defined molecular structure, possibly including various chemical substituents, defining a novel chemical entity.
  2. A pharmaceutical composition comprising the compound, for therapeutic administration.
  3. A method of treating a disease or condition, utilizing the compound or composition.
  4. A process of synthesizing the compound, emphasizing any innovative steps or methods.

Key considerations:

  • Novelty: The claims likely specify structural features, substituents, or stereochemistry not disclosed previously.
  • Inventive Step: The patent must demonstrate an inventive leap over prior art, possibly through unique pharmacological activity, stability, or synthetic advantages.
  • Support and Enablement: The description must enable a person skilled in the art to reproduce the compound and methods.

Patent Landscape Context

Assessing the patent landscape involves examining prior art, related patents, and potential freedom-to-operate analyses. For Chile, being a member of the field’s patent ecosystem, the landscape is characterized by:

  • International Patent Families: Similar patents filed in major jurisdictions (e.g., US, EU, PCT applications), possibly covering similar compounds or uses.
  • Regional Patents and Applications: Patent filings in neighboring Latin American countries, such as Argentina, Brazil, and Mexico, indicating regional protection strategies.
  • Public Databases: Patent databases from WIPO, EPO, and USPTO may list related or family patents, suggesting the applicant's broader patenting approach.

Competitive Positioning:

  • The patent likely fits into a niche of innovative diagnostics or therapeutics segments.
  • Its breadth and enforceability depend on how well the claims stand against prior art and the novelty and inventive step over existing compounds or therapies.

Legal Status and Challenges:

  • Chile's patent law aligns with international standards, requiring novelty, inventive step, and industrial applicability.
  • Challenge risks are minimal if the patent’s claims are well-drafted and supported, but competitors may attempt non-infringing designs or invalidate claims based on prior art.

Implications and Strategic Significance

  • Market Exclusivity: Assuming standard 20-year patent term from filing, the patent could secure exclusive rights through approximately 2037, barring extensions or legal challenges.
  • License Opportunities: Its scope and claims may be broad enough to attract licensing, especially if it covers a valuable therapeutic niche.
  • Research and Development: The patent provides a platform for further innovation, including combination therapies or improved formulations.
  • Competitive Dynamics: The patent constrains competitive R&D, requiring competitors to design around or wait for expiration.

Key Takeaways

  • Precise Claim Definition Crucial: The patent’s strength depends on how well claims are drafted—broad claims confer strategic advantage, but must be supported by detailed description.
  • Landscape for Similar Patents: Review of related patents in global and regional databases essential for determining the patent’s independence and potential overlapping rights.
  • Legal and Commercial Vigilance: Ongoing monitoring for potential infringement or invalidation actions enhances strategic decision-making.
  • Potential for Expansion: Filing family patents outside Chile can maximize protection and market opportunity, especially in lucrative jurisdictions.

FAQs

1. What is the typical scope of pharmaceutical patents like CL2017002456?
Pharmaceutical patents generally cover compound structures, methods of use, formulations, and manufacturing processes. The scope varies from narrow molecule-specific claims to broad chemical classes.

2. How does CL2017002456 fit within the global patent landscape?
It likely forms part of a patent family related to a specific therapeutic agent. Its positioning depends on related filings in other jurisdictions, which can expand or restrict its territorial protection.

3. What are the main challenges in enforcing drug patents in Chile?
Challenges include navigating local patent laws, potential prior art invalidation, and the need for robust infringement proof. Enforcement also requires active monitoring and legal action.

4. How can competitors design around this patent?
By developing structurally distinct compounds avoiding the patented claims, or devising alternative therapeutic mechanisms not covered in the scope.

5. What strategic advantage does this patent provide?
It secures market exclusivity for a novel drug candidate or formulation, providing competitive leverage and potential licensing revenues.


References

  1. Chile Patent Office Official Database. (2023).
  2. WIPO Patent Landscape Reports. (2022).
  3. World Patent Information. (2021).
  4. European Patent Office (EPO) Patent Search. (2022).
  5. U.S. Patent and Trademark Office (USPTO) Database. (2022).

(Note: Due to the lack of detailed claims and description, some specifics are inferred based on standard pharmaceutical patent practices. A thorough review of the full patent document is recommended for precise analysis.)

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