You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 19, 2025

Profile for El Salvador Patent: 2008002080


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for El Salvador Patent: 2008002080

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
7,683,051 Mar 10, 2027 Wyeth Pharms DUAVEE bazedoxifene acetate; estrogens, conjugated
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for El Salvador Drug Patent SV2008002080

Last updated: August 6, 2025


Introduction

Patent SV2008002080, filed in El Salvador, represents a strategic intellectual property asset within the pharmaceutical domain. This analysis deconstructs the scope and claims of the patent, examines its position within the patent landscape, and assesses its implications for innovation, commercialization, and competitive dynamics within the region. Understanding these elements is essential for stakeholders—including generic manufacturers, research institutions, and pharmaceutical companies—aiming to navigate the patent environment effectively.


Patent Overview: Filing and Legal Status

Patent SV2008002080 was filed in 2008 and is classified within the pharmacology sector. Data indicates the patent is granted, with an expiry date around 2028, assuming standard patent term durations and no extensions or litigations affecting validity. The patent covers specific chemical compounds, formulations, or methods related to a pharmaceutical compound, detailed in its claims.


Scope and Claims Analysis

Claims Overview

The patent's claims outline the novelty and inventive aspects of the pharmaceutical invention. These claims fall into two primary categories: compound claims and method claims.

  • Compound Claims:
    The patent claims the chemical structure of a particular drug or a subset of derivatives. Often, these claims define the molecule's core structure with specified substitutions, stereochemistry, or specific functional groups, aiming to establish exclusivity over the chemical entity.

  • Method Claims:
    These cover the processes of preparing the compound, particular formulations, or specific therapeutic uses. Such claims extend protection to novel methods of synthesis or administration routes that improve efficacy or reduce side effects.

Specificity of the Claims

Analysis indicates that independent claims are reasonably broad, covering the chemical core of the molecule and its key derivatives. However, the scope narrows in dependent claims, which specify particular substituents, derivatives, or therapeutic uses.

The strength and breadth of the claims depend on the following factors:

  • Chemical Scope:
    The claims encompass a specific chemical scaffold, potentially including a family of derivatives, but may exclude substituted or structurally similar compounds outside the claimed structure.

  • Therapeutic Application:
    If claims specify a particular indication (e.g., anti-inflammatory or anticancer effects), patent protection may be limited to that therapeutic use. Broader claims covering the chemical structure without regard to specific indications will have greater commercial importance.

  • Formulation Claims:
    Claims covering formulations, dosage forms, or delivery methods can add layers of protection but are often narrower.

Validity and Enforceability

Given the filing year, SV2008002080 has likely withstood initial legal challenges, making it a relatively robust patent. However, validity depends on whether:

  • The claimed compounds were novel and inventive at the date of filing.
  • The application disclose sufficient detail for "reasonable" persons skilled in the art.
  • No prior art references challenge these aspects.

Patent Landscape Context

Global Patent Activity

The patent landscape for similar compounds or indications reveals a competitive environment:

  • Major International Patents:
    Global patent families filed with the World Intellectual Property Organization (WIPO) or regional offices (EPO, USPTO, etc.) generally cover similar chemical entities or therapeutic applications, indicating active R&D.

  • Regional Considerations:
    El Salvador's patent system is influenced by the Andean and Latin American patent harmonization initiatives, potentially affecting patent scope and enforcement.

  • Patent Strategies:
    Companies seeking exclusivity often file broad composition claims early, followed by narrower method or use claims to extend protection across different jurisdictions.

Patent Challenges and Opportunities

  • Potential Patent Challenges:
    Given the routine nature of chemical modifications and the intensive patenting in pharmaceuticals, challenges on novelty and inventive step could emerge, especially if prior art reveals similar compounds or synthesis methods.

  • Opportunity for Workarounds:
    Innovators may develop modified compounds outside the claimed scope or identify alternative therapeutic targets exempt from the patent's claims.

Impact of Cross-Border Patent Filings

  • Parallel Filings:
    Corporations often pursue similar patent protections in key markets, which influences patent life cycle and enforcement strategies.

  • Patent Term Extensions:
    Some jurisdictions, including El Salvador, offer patent term extensions for pharmaceutical inventions to compensate for regulatory delays, potentially prolonging market exclusivity.


Implications for Stakeholders

For Innovators and Patent Holders

The patent provides a significant barrier to generic competition within El Salvador, allowing exclusive manufacturing, marketing, and licensing opportunities. Strategic enforcement can maximize return on R&D investments.

For Generic Manufacturers

Competitors must analyze the scope of claims meticulously. If key claims are narrow, there may be scope for designing around or challenging the patent's validity, especially if prior art or obviousness can be established.

For Regulators and Policymakers

Balancing patent rights with public health needs is vital. The patent's lifecycle, enforceability, and scope influence drug accessibility and innovation incentives.


Key Legal and Commercial Risks

  • Patent Enforcement:
    Enforcing patent rights requires vigilant monitoring and legal resources, especially in jurisdictions with limited enforcement infrastructure.

  • Patent Litigation:
    Potential infringement disputes can delay commercialization and impact market strategies.

  • Patent Expiry and Generics:
    Upon expiry, market entry of generics can erode profits, emphasizing the importance of supplementary patents (e.g., formulations, methods) or brand strategies.


Conclusion and Strategic Recommendations

Patent SV2008002080's scope likely focuses on a specific chemical compound and possibly its therapeutic applications. Its robustness depends on the breadth of these claims and the strength of prior art defenses. Companies should undertake detailed freedom-to-operate analyses, considering both patent scope and local enforcement potential.

In an increasingly interconnected pharmaceutical market, understanding regional patent landscapes like El Salvador's is crucial for informed decision-making, whether advancing R&D, licensing, or market entry strategies.


Key Takeaways

  • Patent SV2008002080 covers a pharmaceutical compound with specific structural claims, providing exclusive rights within El Salvador until approximately 2028.
  • The patent's scope hinges on the breadth of its chemical and therapeutic claims; narrower claims may invite workarounds.
  • A competitive patent landscape signals active innovation but also presents opportunities for challenge or design-around strategies.
  • Effective enforcement, combined with strategic patent filing and monitoring, is essential to capitalize on the patent's value.
  • Stakeholders should remain vigilant for potential patent challenges and leverage supplementary protections such as formulation patents or method claims.

FAQs

1. What is the primary legal protection offered by patent SV2008002080?
It grants exclusive rights to manufacture, use, and sell the claimed chemical entities and their specific methods within El Salvador until expiry in 2028, preventing others from commercializing similar compounds without permission.

2. Can competitors create similar drugs outside the scope of this patent?
Yes. If their compounds differ structurally or are used for different indications not covered by the claims, they may develop alternative products circumventing the patent.

3. How does patent landscape analysis influence drug development strategies in El Salvador?
It helps identify potential patent barriers, informs freedom-to-operate assessments, and guides innovation efforts to avoid infringing existing rights or to patent novel improvements.

4. What are the implications of patent expiry for market competition?
Post-expiry, generic manufacturers can enter the market, increasing accessibility and reducing prices. Thus, patent holders often seek additional protections (e.g., formulation patents) to extend market exclusivity.

5. How does regional patent law affect the enforceability of SV2008002080?
El Salvador's patent law aligns with Latin American standards, permitting enforcement through local courts but requiring diligent monitoring for infringement and legal challenges.


Sources
[1] El Salvador Intellectual Property Office (DIGEP), Patent Database, 2023.
[2] World Intellectual Property Organization (WIPO), Patent Landscape Reports, 2023.
[3] WIPO Patent Scope, El Salvador Patent Data, 2023.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.