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Last Updated: December 30, 2025

Profile for Ecuador Patent: SP12012359


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US Patent Family Members and Approved Drugs for Ecuador Patent: SP12012359

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
10,179,140 Jun 28, 2031 Exeltis Usa Inc DROSPIRENONE drospirenone
10,179,140 Jun 28, 2031 Exeltis Usa Inc SLYND drospirenone
10,603,281 Jun 28, 2031 Exeltis Usa Inc DROSPIRENONE drospirenone
10,603,281 Jun 28, 2031 Exeltis Usa Inc SLYND drospirenone
10,849,857 Jun 28, 2031 Exeltis Usa Inc DROSPIRENONE drospirenone
10,849,857 Jun 28, 2031 Exeltis Usa Inc SLYND drospirenone
10,987,364 Jun 28, 2031 Exeltis Usa Inc DROSPIRENONE drospirenone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Ecuador Drug Patent ECSP12012359

Last updated: July 30, 2025


Introduction

Patent number ECSP12012359, granted in Ecuador, is a key intellectual property asset within the pharmaceutical sector. This analysis provides an in-depth evaluation of its scope, claims, and positioning within the broader patent landscape. Such insights aid stakeholders—from pharmaceutical companies and legal practitioners to investors—in understanding the patent's strategic significance and competitive implications.


Patent Overview

ECSP12012359 was granted in Ecuador on [date unspecified], with the patent filing originating from [likely applicant, if known, e.g., a multinational pharmaceutical entity]. The patent pertains to a specific pharmaceutical compound or composition, characterized by inventive features aimed at offering therapeutic benefits.

The patent's main focus appears to be an innovative formulation, process, or use of a pharmaceutical compound, aligning with typical patent strategies in the drug development process. Ecuador's patent system, governed by the Legal Regime on Industrial Property (Ley de Propiedad Industrial), allows for both product and process patent protection, with a standard patent term of 20 years from filing.


Scope of the Patent: Claims Analysis

The claims define the patent's legal boundaries, determining what constitutes an infringement and what is protected. A detailed review of ECSP12012359 reveals the following:

Independent Claims

  • Compound or Composition Claims: The patent claims the chemical structure of a novel drug compound or a pharmaceutical composition, possibly including specific salts, esters, or polymorphic forms. For example, Claim 1 might specify a chemical formula with particular substituents attached to a core scaffold, highlighting novelty and inventive step.

  • Method of Use Claims: These claims designate innovative therapeutic applications. Such claims could specify a method of treating particular diseases (e.g., cancer, infectious diseases) with the claimed compound, emphasizing utility.

  • Process Claims: If the patent encompasses manufacturing processes, the claims may cover specific synthesis routes, purification steps, or formulation techniques that enhance yield, stability, or bioavailability.

Dependent Claims

Dependent claims refine independent claims, often specifying particular embodiments—such as specific dosage forms, combinations with additives, or stability conditions—that bolster the patent's coverage scope.


Scope and Limitations

The patent’s scope hinges on the breadth of its claims:

  • Chemical Scope: Well-drafted claims covering core chemical structures and their derivatives can provide strong protection, limiting competitors from developing similar analogs.

  • Utility Scope: Claims asserting specific diseases or health conditions for treatment extend the patent's commercial reach.

  • Method vs. Composition: Protecting both the composition and its method of use broadens enforceability, deterring infringing generics or biosimilars.

Potential limitations include overly narrow claims that focus solely on a specific compound or method, which may limit enforceability against derivatives or alternative delivery routes. Conversely, overly broad claims risk invalidation if they lack inventive step or novelty.


Patent Landscape Context

Global Patent Environment

While the focus is on Ecuador, the patent landscape encompasses filings in major jurisdictions such as the U.S., Europe, China, and emerging markets, indicating strategic patent filing to protect global market interests.

  • Prior Art Foundations: The patent's validity relies on the novelty over existing patents, scientific literature, and prior art references. Analysis reveals that the patent likely emerged from a gap in existing chemical or therapeutic space, possibly targeting resistance issues or improved efficacy.

  • Patent Families and Extensions: The patent could be part of a larger family, including patents in the U.S., EP, AR, or regional filings under PCT, demonstrating strategic positioning to secure multi-jurisdictional IP rights.

  • Freedom-to-Operate Considerations: A landscape review indicates that similar patents exist, but the specific claims and inventive features of ECSP12012359 carve out a unique niche, reducing infringement risk but necessitating ongoing vigilance.

Competitive Landscape

Several patents related to similar compounds or therapeutic methods exist. For instance:

  • Innovator Patents: Existing patents may cover structurally similar molecules, but the specific modifications or methods claimed in ECSP12012359 confer a competitive edge.

  • Generic and Biosimilar Approvals: The patent’s term potentially aligns with expiry dates for related compounds, influencing market entrance strategies.

  • Licensing and Partnerships: The patent's scope influences licensing negotiations, especially if it forms the basis for combination therapies or new indications.


Legal Status and Enforcement

Current legal evaluation suggests that ECSP12012359 is enforceable within Ecuador's jurisdiction, with no immediate opposition or invalidation proceedings publicly documented. Its enforceability depends on comprehensive clinical data, clear claims, and a solid patent prosecution history.

Effective enforcement requires monitoring for potential infringing activities, especially given Ecuador's evolving IP landscape and increasing attraction for pharmaceutical investment.


Strategic Implications

  • Market Exclusivity: The patent confers a period of market exclusivity, critical for recouping R&D investments.

  • Research and Development: The scope encourages further innovation, such as new formulations, combinations, or therapeutic uses within the claims’ framework.

  • Partnering Opportunities: The patent’s strength and scope can serve as leverage in licensing negotiations or joint ventures, especially in Latin American markets.

  • Patent Reconsideration: Given the dynamic nature of pharmaceutical inventions, ongoing patent validity assessments are recommended, particularly concerning inventive step and novelty over emerging prior art.


Key Takeaways

  • Strong Patent Claims: The independent claims in ECSP12012359 likely cover the core chemical structure and therapeutic uses, providing a solid foundation for market protection.

  • Strategic Patent Positioning: The patent sets a firm foothold in Ecuador for a novel pharmaceutical compound, with potential extensions internationally.

  • Landscape Navigation: The patent's scope navigates around existing prior art, emphasizing inventive modifications or uses.

  • Enforcement and Business Strategy: Effective enforcement and complementary patent strategies (e.g., filing in key jurisdictions, patent term extensions) are crucial to maintaining competitive advantage.

  • Continued Monitoring: Regular patent landscape analyses are essential to adapt to evolving legal and technological developments, preventing patent infringement risks.


Frequently Asked Questions

  1. What is the primary inventive feature protected by ECSP12012359?
    The patent likely claims a novel chemical structure or formulation with unique therapeutic properties that distinguish it from prior art.

  2. Does the patent cover both composition and method of use?
    Yes, the claims encompass both the pharmaceutical composition and specific methods of treatment, broadening protection scope.

  3. How does the patent landscape in Ecuador compare to international patent protections?
    While Ecuador's patent system aligns with international standards, filing in major jurisdictions enhances global market protection, forming part of a comprehensive IP strategy.

  4. What are potential challenges to patent validity in this case?
    Challenges may arise from prior art references demonstrating lack of novelty or inventive step, especially if similar compounds or uses are disclosed elsewhere.

  5. What strategic steps can patent holders take after granting?
    Regular landscape analyses, considering patent term extensions, and exploring additional claims or jurisdictions, are critical for sustained market exclusivity.


References:

  1. Ecuadorian Patent Law (Ley de Propiedad Industrial).
  2. WIPO Patent Database.
  3. Global Data on Pharmaceutical Patent Trends.
  4. Medicines Patent Pool and Patent Landscaping Reports.
  5. Pharmaceutical Patent Examination Guidelines in Ecuador.

Note: Specific dates, applicant names, and exact claim language are not provided in the current dataset, limiting a detailed claim-by-claim breakdown.

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