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Last Updated: January 1, 2026

Profile for Uruguay Patent: 33311


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US Patent Family Members and Approved Drugs for Uruguay Patent: 33311

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
8,618,076 Jun 11, 2031 Gilead Sciences Inc EPCLUSA sofosbuvir; velpatasvir
8,618,076 Jun 11, 2031 Gilead Sciences Inc HARVONI ledipasvir; sofosbuvir
8,618,076 Jun 11, 2031 Gilead Sciences Inc SOVALDI sofosbuvir
8,618,076 Jun 11, 2031 Gilead Sciences Inc VOSEVI sofosbuvir; velpatasvir; voxilaprevir
8,633,309 Sep 26, 2029 Gilead Sciences Inc EPCLUSA sofosbuvir; velpatasvir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for Uruguay Drug Patent UY33311

Last updated: July 29, 2025

Introduction

Patent UY33311, registered in Uruguay, represents a strategically significant intellectual property (IP) asset within the pharmaceutical landscape. This analysis examines its scope, claims, and the broader patent environment, providing insights critical for stakeholders including pharmaceutical companies, generic manufacturers, and legal practitioners. As Uruguay is a member of the Patent Cooperation Treaty (PCT), the patent's development offers a window into regional patenting strategies and competitive positioning.

Overview of Patent UY33311

Uruguay Patent UY33311 was filed with the National Directorate of Intellectual Property (DNPI) and published in accordance with national procedures, reflecting Uruguay's adherence to international patent standards. Based on available data, the patent pertains to a novel pharmaceutical compound or formulation with potential applications in specific therapeutic areas, possibly involving any of the following:

  • A new chemical entity (NCE)
  • A novel polymorph or salt form
  • An innovative delivery or formulation method
  • A new therapeutic use of an existing compound

The patent's filing date, priority date, and initial publication date (assumed for analysis) are vital to understanding its patent life cycle and potential for licensing or litigation.

Scope and Claims Analysis

Claims Structure and Breadth

The scope of UY33311 is primarily defined by its claims, which delineate the boundaries of patent protection. These claims typically encompass:

  • Independent Claims: Broadly cover the main invention, such as a chemical compound structure, method of synthesis, or therapeutic application.
  • Dependent Claims: Specify particular embodiments, such as specific substituents, dosage forms, or manufacturing methods.

A high-level analysis suggests the claims likely focus on a specific chemical compound or class with claimed therapeutic benefits or delivery mechanisms. The claims may also extend to pharmaceutical compositions and methods of treatment.

Claim Specificity and Exclusivity

  • Narrow Claims: Offer limited protection but reduce infringement risk from competitors. Pure compound claims with specific structural formulas are often considered narrow.
  • Broad Claims: Encompass a wider scope, including genus claims covering a family of related compounds, or methods of use, providing a competitive edge against generic entrants.

In Uruguay, patent law allows for both types, but examiners scrutinize the novelty and inventive step, affecting the validity and enforceability of broad claims.

Novelty and Inventive Step

For UY33311 to be granted, the claims must demonstrate:

  • Novelty: No prior art discloses the exact compound/formulation/method.
  • Inventive Step: The invention must not be obvious to a person skilled in the art, considering existing datasets.

Given Uruguay's rigorous examination standards, the patent likely survived thorough novelty and inventive step assessments, though regional prior art searches may reveal existing disclosures.

Potential Challenges

  • Prior Art Opposition: Competitors or third parties may challenge the patent's validity, especially if similar compounds or formulations exist elsewhere.
  • Patent Term and Maintenance: The patent's enforceability depends on maintenance fees and timely disclosures, which must be monitored for potential lapses.

Patent Landscape in Uruguay and Regional Context

Local and Regional Patent Trends

Uruguay's pharmaceutical patent landscape aligns with Latin American innovation trends, characterized by:

  • Focus on Novel Chemical Entities: Countries favoring innovation to protect exclusive market rights.
  • Regulatory Requirements: National laws implementing TRIPS compliance, with some national exceptions.
  • Patent Term Extensions: Typically 20 years from filing, but regional differences can arise in enforcement and utility.

Key Competitors and Patent Filings

The patent landscape reveals a concentration of filings by multinational pharmaceutical firms aiming to secure regional exclusivity. These filings often include:

  • Composition of matter patents for innovative compounds.
  • Method-of-use patents covering new therapeutic indications.
  • Formulation patents for improved drug delivery.

In the context of Uruguay, recent filings indicate a focus on oncology, neurology, and infectious diseases, aligning with global trends.

International Patent Strategies

Stakeholders often pursue foreign patent applications through PCT routes, subsequently nationalizing patents like UY33311 to protect commercial interests. This approach allows for:

  • Broader territorial coverage.
  • Flexibility to adapt patent claims to local laws.
  • Strategic licensing and partnering opportunities.

Regional Patent Overlap and Compatibility

Uruguay's legal framework recognizes patents granted through PCT routes and offers a harmonized environment aligned with regional treaties, but differences in patentable subject matter and examination standards can influence the patent landscape.

Implications for Stakeholders

  • Innovators: UY33311's narrow or broad claims impact the drug's market exclusivity.
  • Generic Manufacturers: Patents covering core compounds threaten generic entry; however, challenges based on prior art or inventive step can erode validity.
  • Investors: Patent strength influences valuation and licensing negotiations.
  • Legal Practitioners: Need to monitor patent prosecution, opposition proceedings, and potential infringements carefully.

Key Takeaways

  • UY33311's claims' scope likely addresses a specific chemical structure or therapeutic use, with broad claims offering extensive protection, subject to regional patent laws.
  • The patent landscape in Uruguay reflects a strategic emphasis on chemical innovation, with regional adaptations for Latin American markets.
  • Ongoing patent challenges, including prior art and legal disputes, require vigilance.
  • Effective regional patent prosecution and strategic claim drafting are essential to maximize exclusivity and market leverage.
  • Renewals and enforcement mechanisms are crucial for maintaining patent value throughout its lifecycle.

FAQs

Q1: How does Uruguay's patent law influence the scope of pharmaceutical patents like UY33311?
Uruguay's patent law adheres to TRIPS standards, requiring patents to cover new, inventive, and industrially applicable inventions. The law permits both product compounds and methods but emphasizes thorough examination to ensure claims are novel and non-obvious. This influences patent scope, necessitating carefully drafted claims to balance broad protection with legal validity.

Q2: Can competitors challenge the validity of UY33311?
Yes. Third parties can file submitted prior art or opposition during the patent granting or post-grant periods. Challenges focus on novelty, inventive step, and industrial applicability, particularly if earlier disclosures exist that undermine the patent's claims.

Q3: What is the significance of regional patent strategies for pharmaceutical companies owning UY33311?
Regional strategies enable companies to extend patent protections across Latin America via PCT filings—protecting market share, deterring generic competition, and enabling licensing. Understanding regional legal nuances ensures robust patent enforcement and strategic patent portfolio management.

Q4: How does patent term in Uruguay affect pharmaceutical innovation?
Typically, patents last 20 years from the filing date, providing a period of market exclusivity. However, extensions or patent term adjustments for regulatory delays are not standard, making timely filing and maintenance critical to maximizing patent life.

Q5: What are the common pitfalls in drafting patents like UY33311?
Vague claims, narrow claim language, inadequate disclosure, or failure to consider regional patent standards can compromise patent protection. Comprehensive claims drafting aligned with emerging scientific disclosures is vital for enforceability and competitive advantage.


References

  1. Uruguay Patent Law, Ley No. 17.611.
  2. World Intellectual Property Organization. "Patent Cooperation Treaty (PCT)." https://www.wipo.int/pct/en/
  3. Regional patent trends in Latin America, WIPO IP Statistics Data.
  4. National Directorate of Intellectual Property (Uruguay). Patent search and public records.
  5. Patent Examination Guidelines, Uruguay DNPI.

(Note: Specific technical details of UY33311, such as chemical structure or claims wording, are proprietary or not publicly disclosed; this analysis is based on typical patent features and regional practice.)

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