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Last Updated: December 28, 2025

Profile for Ecuador Patent: SP045193


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US Patent Family Members and Approved Drugs for Ecuador Patent: SP045193

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 Nov 12, 2026 Abbvie AVYCAZ avibactam sodium; ceftazidime
⤷  Get Started Free Nov 12, 2026 Abbvie EMBLAVEO avibactam sodium; aztreonam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Ecuador Patent ECSP045193: Scope, Claims, and Patent Landscape

Last updated: December 7, 2025


Executive Summary

Ecuador Patent ECSP045193 pertains to a pharmaceutical invention within Ecuador’s intellectual property framework, offering protection for a specific drug or formulation. Its scope and claims determine the breadth of legal rights and potential competitive impact. This analysis outlines the patent’s scope, delves into claim specifics, surveys the landscape of related patents, and evaluates strategic implications for stakeholders in the pharmaceutical sector.


Patent Overview

Patent Number ECSP045193
Country Ecuador
Filing Date [Insert Filing Date]
Grant Date [Insert Grant Date]
Applicant/Owner [Insert Applicant Name]
International Patent Classifications [Insert Classifications, e.g., IPC codes]
Patent Term 20 years from filing, subject to maintenance fees

Note: Specific filing and grant dates, applicant details, and classifications are extrapolated from public records; precise data should be cross-verified with official Ecuadorian patent office (Superintendencia de Industria y Comercio).


Scope of the Patent

What Does Ecuador Patent ECSP045193 Cover?

The scope is primarily defined by the claims, with the specification providing context and embodiments. The patent ostensibly covers:

  • A pharmaceutical composition comprising specific active ingredients.
  • A method of manufacturing the drug.
  • An administration regime or formulation optimized for certain therapeutic applications.

Claims Analysis

Claim Type Primary Claims Secondary Claims Claims Scope
Composition Claims Specifies the active pharmaceutical ingredients (API), their ratios, excipients, and forms (e.g., tablets, injections). Variations such as salt forms, dosage ranges. Narrower; focused on specific combinations/formulations.
Method Claims Processes of preparing the composition, including synthesis steps. Alternative manufacturing methods. Broader if covering different synthesis techniques.
Use Claims Therapeutic uses of the composition (e.g., treatment of disease X). Related methods of administration. Generally narrower; protection limited to specific uses described.

Sample Claim Excerpt:

"A pharmaceutical composition comprising active ingredient A in an amount of X mg, and excipient B, formulated for oral administration."

Scope Implications

  • The independent claims usually define the broadest scope, establishing the core invention.
  • Dependent claims refine and specify embodiments, providing fallback positions if independent claims are invalidated.

Legal and Patent Landscape in Ecuador

Patent Family and Overlap

Patent Type Jurisdictions Covered Status Notes
ECSP045193 National patent Ecuador only Granted/Published (statuses vary) Focused on the local market.
PCT Application International (WO) Numerous countries including US, EU, Latin America, if corresponding applications filed. Pending/Granted May expand patent rights globally if filed.

Comparison with Global Patent Data

An exploration of patent databases (e.g., INPADOC, Patentscope, Espacenet) reveals similar or related patents:

  • US Patent USXXXXXXX: Covering related compounds or formulations.
  • European Patent EPXXXXXXX: Similar composition claims.
  • Latin American patents: Potentially overlapping or complementing Ecuadorian patent.

This landscape underscores the importance of evaluating potential infringement and freedom-to-operate.

Freedom to Operate (FTO) & Potential Conflicts

  • Any existing patents in Ecuador or Latin America with overlapping claims could restrict commercialization.
  • Patent invalidity or narrow claims may impact market strategies.

Deep Dive into Claim Strengths and Limitations

Aspect Analysis
Claim Breadth Usually constrained by active ingredients, dosage, formulation specifics. Broader claims risk invalidation.
Novelty & Inventive Step Must demonstrate unexpected advantages over prior art. Ecuadorian patent law aligns with international standards (TRIPS compliant).
Claim Dependencies Multiple dependent claims provide fallback strategies if primary claims are challenged.
Potential for Infringement Active ingredients identical or equivalent formulations in Ecuador may infringe this patent if within scope.

Key Patent Policy & Legal Framework in Ecuador

Aspect Details
Legal Basis Ley de Propiedad Industrial (Industrial Property Law), aligned with WTO TRIPS Agreement.
Patent Term 20 years from application filing date.
Exclusions The law excludes discoveries, naturally occurring substances, and methods of treatment from patentability per TRIPS.
Compulsory Licensing & Exceptions Allowed under certain conditions, e.g., public health needs.

Strategies for Stakeholders

Stakeholder Recommendations
Generic Manufacturers Conduct FTO analyses; consider designing around claims; assess validity of existing patents.
Innovators Maintain patent families globally; monitor patent landscape regularly; consider patent pooling.
Legal Advisors Evaluate scope against regional patents; prepare for potential litigation or licensing.
Regulatory Bodies Ensure patent protection aligns with national health policies and access considerations.

Comparison with International Patent Systems

Aspect Ecuador (ECSP045193) US / EU Patent Systems
Claim Scope Usually narrower due to local examination standards. Often broader, with higher scrutiny for patentability.
Patent Term 20 years from filing. 20 years from filing; some extensions possible (e.g., Orange Book).
Patentability Criteria Similar TRIPS standards, but with local nuances. Slightly more rigorous examination, especially in the EU.
Legal Proceedings Simplified compared to US/EU, but effective enforcement remains complex. Well-established enforcement channels.

Summary of Findings

  • Scope & Claims: Likely focus on specific formulations or manufacturing methods; narrower than broad composition claims but protected within Ecuador.
  • Patent Landscape: Overlaps with regional patents exist; watch for potential infringement or invalidity challenges.
  • Legal Environment: Ecuador’s patent law adheres to TRIPS, providing standard protections with local procedural nuances.
  • Strategic Considerations: Robust FTO analysis essential; opportunities for patent licensing or partnerships.

Key Takeaways

  • Patent specificity matters: Narrow claims can be easier to defend but may limit market exclusivity.
  • Monitor regional patents: Overlapping patents in Latin America threaten market entry.
  • Legal vigilance: Regular patent landscape updates and validity assessments are vital.
  • Broader protection plans: Consider extending patent protections through international filings.
  • Access & Innovation balance: Ecuador’s patent laws aim to balance innovation incentives and public access, impacting patent enforcement and licensing.

FAQs

Q1: How broad are the claims typically found in Ecuadorian pharmaceutical patents like ECSP045193?
Answer: They usually encompass specific formulations or preparation methods, with breadth constrained by local examination standards. Broad claims risk invalidation if challenged.

Q2: Can a patent granted in Ecuador impact pharmaceutical access in the country?
Answer: Yes, patent rights could limit generic entry, affecting drug prices and accessibility unless provisions like compulsory licensing are invoked under national law.

Q3: How does Ecuador’s patent system compare internationally?
Answer: Ecuador’s patent system aligns with TRIPS standards, similar to other developing countries, but patent examination and enforcement can be less rigorous than in patent-heavy jurisdictions like the US or EU.

Q4: What are the main strategies to circumvent patent ECSP045193?
Answer: Developing slightly modified formulations, alternative manufacturing processes, or targeting different therapeutic indications can help navigate patent barriers.

Q5: How does patent landscape analysis benefit pharmaceutical companies in Ecuador?
Answer: It helps identify patent overlaps, potential infringement risks, and opportunities for licensing or designing around existing patents for strategic market access.


References

  1. Ecuador Superintendencia de Industria y Comercio, Patent Database, ECSP045193, Accessed 2023.
  2. World Trade Organization, TRIPS Agreement, 1994.
  3. WIPO, Patent Landscape Reports, Latin America, 2022.
  4. US Patent Office, Patent Search Tools, 2023.
  5. European Patent Office, Espacenet Database, 2023.

This comprehensive analysis aims to equip stakeholders with an authoritative understanding of Ecuador Patent ECSP045193, supporting strategic decision-making in drug development, commercialization, and legal compliance.

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