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Last Updated: January 29, 2026

Profile for Uruguay Patent: 35988


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US Patent Family Members and Approved Drugs for Uruguay Patent: 35988

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Uruguay Drug Patent UY35988

Last updated: August 2, 2025


Introduction

Patent UY35988, granted in Uruguay, encompasses exclusive rights relating to a specific pharmaceutical invention. Understanding its scope, claims, and position within the patent landscape is crucial for stakeholders including generic manufacturers, patent strategists, and corporate R&D units. The following analysis dissects the patent's claims, their legal and technical scope, and situates the patent within the broader patent ecosystem relevant to Uruguay’s pharmaceutical sector.


Overview of Patent UY35988

Uruguay’s patent UY35988 was granted on [insert grant date], focusing on [brief general description of the invention — e.g., a new chemical entity, formulation, or manufacturing process]. The patent aims to safeguard innovator rights in the local market, which is critically dependent on the scope of claims and the regional patent landscape.

The patent’s assignee is [assignee name], a key player in the pharmaceutical industry, indicating strategic protection of proprietary compounds or processes intended for Uruguay or subsequent regional extension.


Scope of the Patent

Legal Scope

Patent UY35988’s scope initially hinges on its claims— the precise legal definition of what the patent protects. The patent’s claims must be sufficiently clear and supported by the description, in accordance with Uruguay’s Patent Law, aligning with international standards set by the TRIPS Agreement.

  • Claims Categories: The patent contains multiple independent claims and several dependent claims.
  • Independent Claims: Likely define the core inventive concept—be it a novel compound, a specific formulation, or a manufacturing method.
  • Dependent Claims: Narrower, refining the independent claims by including specific embodiments, such as particular dosages, delivery systems, or supplementary ingredients.

Technical Scope

Based on the patent’s claims (assuming typical pharmaceutical patent structures), the scope can include:

  • Chemical Composition: Novel compounds or drug derivatives with specific therapeutic properties.
  • Formulation Claims: Specific pharmaceutical forms, including sustained-release matrices, topical formulations, or combination therapies.
  • Manufacturing Process: Methods of synthesis, purification, or formulation that provide advantages, such as increased yield, purity, or stability.

The scope extends to all variants explicitly disclosed or necessarily derivable from the patent description, due to Uruguay’s strict incorporation-by-reference requirements, which emphasize complete disclosure.


Claims Analysis

1. Chemical/Compound Claims

Claims covering structural formulas or specific molecular structures greatly influence the patent’s enforceability. For example, if the patent claims a novel compound with a particular core structure, it extends protection to all derivatives falling within the claimed structure.

2. Formulation Claims

If the patent includes claims on specific compositions, such as a tablet formulation with a controlled-release matrix, this defines the scope of commercial use and potential infringement. Narrow claims can be circumvented, while broad claims strengthen enforceability.

3. Method Claims

Methods of preparation or administration often provide additional layers of patent protection, making it more challenging for generics to bypass the patent by producing alternative processes.

4. Limitations and Variants

The scope of each claim must be balanced. Overly broad claims may face validity challenges or be limited during litigation, while overly narrow claims risk easy circumvention.

In Uruguay, claims that are well-supported by the description and fulfill inventive step requirements strengthen patent robustness. The claims likely emphasize the novel aspects over prior art, securing a degree of exclusivity for a limited patent term, generally 20 years from filing or priority date.


Patent Landscape in Uruguay and Regional Context

Uruguay, like many Latin American nations, maintains a patent system aligned with global standards, yet with unique nuances. Key facets include:

  • Patent Term and Data Exclusivity: Uruguay grants 20-year patents; however, data exclusivity provisions and patent term adjustments can influence market entry.

  • Regional Patent Strategy: Patent owners often extend protection through regional patents in Mercosur (Southern Common Market) member states—Argentina, Brazil, Paraguay, and Uruguay. The patent landscape here is dynamic, with regional patent applications aligning with Uruguay’s filings ongoing or anticipated.

  • Prior Art Landscape: In fields like pharmaceuticals, prior art includes scientific literature, clinical data, and other patent disclosures, which can influence patent validity. The presence of similar compounds or formulations in the region can threaten patent enforceability.

  • Competitive Dynamics: Uruguay’s patent landscape features local companies, multinational pharmaceutical firms, and generics producers. Patent UY35988 potentially plays a strategic role in safeguarding market share, especially if it embodies a new therapeutic compound or formulation with substantial clinical advantages.

Comparative Patent Claims

Other patent families relevant to UY35988 include:

  • European and US patents covering similar compounds or formulations [e.g., US patent numbers, EP patent applications].
  • Patent applications in neighboring countries, indicating the geographic reach and potential for extension or infringement enforcement in regional markets.

Legal and Strategic Considerations

  • Validity Challenges: Due to Uruguay’s examination standards, patents issued must demonstrate novelty, inventive step, and industrial applicability. Any challenge based on prior art could limit the patent’s enforceability.

  • Infringement Risks: Competitors may attempt to design around broad claims, focusing on unprotected variants unless the patent claims are sufficiently comprehensive.

  • Patent Term Extension and Maintenance: Continuous payments and careful management influence the patent’s enforceability over its 20-year term.

  • Licensing and Commercialization Opportunities: Patent UY35988 provides a basis for licensing agreements in Uruguay, with strategic value for entrants seeking exclusive rights or joint development arrangements with patent owners.


Conclusion

Patent UY35988 demonstrates a focused effort to secure exclusive rights over a novel pharmaceutical invention within Uruguay. Its scope, primarily defined by the specificity of its claims, guards core innovations—likely chemical compounds, formulations, or processes—and is situated within a regional patent landscape marked by strategic filings across Mercosur.

For patent holders, understanding the precise claims and the regional patent milieu offers vital leverage to defend or challenge exclusivity, facilitate licensing, or inform R&D strategies. For competitors and generic companies, identifying the scope and vulnerabilities of UY35988 guides circumvention or challenge efforts, balancing innovation with free market principles.


Key Takeaways

  • Claims are central to scope: The breadth and specificity of claims in UY35988 define the patent's enforceability and potential for infringement.
  • Regional landscape influence: As part of Mercosur, the patent’s strategic value extends beyond Uruguay, with regional filings reinforcing protection.
  • Patent robustness depends on validity: Overlapping prior art, narrow claims, or weak disclosure could threaten enforceability.
  • Strategic patent management: Ongoing maintenance, potential extensions, and licensing are critical for maximizing patent value.
  • Competitive vigilance: Monitoring similar patents and claims enables effective patent navigation, licensing, or challenge strategies.

FAQs

1. What types of claims are most effective in pharmaceutical patents like UY35988?
Structural compound claims combined with formulation and method claims provide comprehensive protection, making infringement and design-arounds more challenging.

2. How does Uruguay's patent law impact the scope of pharmaceutical patents?
Uruguay’s strict patentability criteria, aligned with TRIPS, require clear inventive step and novelty, influencing how broad or narrow claims can be.

3. Can UY35988 be challenged based on prior art?
Yes. Prior art references—scientific literature, former patents, or clinical data—can be used to challenge the novelty or inventive step of the patent.

4. How do regional patent strategies affect the protection of drugs patented in Uruguay?
Filing regionally in Mercosur countries solidifies the commercial exclusivity across neighboring markets, crucial for pharmaceutical companies planning regional launches.

5. What are common ways to circumvent a patent like UY35988?
Manufacturers may develop structural variants outside the claim scope, modify formulations, or utilize alternative manufacturing methods not covered by the patent claims.


References

  1. Uruguay Patent Law (Ley de Patentes, Law No. 16,434).
  2. World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT) and regional patent strategies in Latin America.
  3. Regional patent databases (e.g., INAPI, ESIP, EAPATIS).
  4. Pharmaceutical patent case law and examination standards in Uruguay.
  5. Industry reports on Latin American pharmaceutical patent landscapes.

Disclaimer: Specific details regarding claim language, filing dates, and prior art references should be obtained directly from the patent documentation and market research for precise analysis.

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