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Last Updated: December 12, 2025

Profile for Uruguay Patent: 30021


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US Patent Family Members and Approved Drugs for Uruguay Patent: 30021

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
8,933,097 Aug 2, 2030 Chattem Sanofi CHILDREN'S ALLEGRA ALLERGY fexofenadine hydrochloride
8,933,097 Aug 2, 2030 Chattem Sanofi CHILDREN'S ALLEGRA HIVES fexofenadine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Uruguay Drug Patent UY30021

Last updated: July 29, 2025

Introduction

Patent UY30021, filed and granted in Uruguay, represents a significant intellectual property asset within the pharmaceutical sector. Understanding its scope, claims, and position in the patent landscape is crucial for industry stakeholders, including generic manufacturers, research entities, and legal professionals. This analysis dissects the patent’s claims, delineates its coverage, and contextualizes its landscape within global and regional patent environments.

Patent Overview

Uruguayan patent UY30021 was filed to protect a specific pharmaceutical invention. Its patent application number indicates regulatory approval and commercial exclusivity in the Uruguayan market. The patent’s filing date, grant date, and expiry date are crucial benchmarks for assessing its competitive and legal timeout, although specifics require access to official patent databases.

Although publicly available data on UY30021 is limited, typical pharmaceutical patents filed in Uruguay encompass compounds, formulations, manufacturing processes, or therapeutic methods. For the purpose of this analysis, the assumed focus is on a novel pharmaceutical compound with potential therapeutic indications, as is common in patent filings within the sector.

Scope of the Patent

The scope of UY30021 primarily depends on the breadth of its claims. In pharmaceutical patents, claims can range from broad structural formulas covering multiple derivatives or analogues to narrower claims specifying specific chemical entities, doses, or methods of use. The scope defines the legal protection and commercial exclusivity, shaping subsequent R&D, potential licensing, or patent challenges.

Key Aspects Influencing the Scope:

  • Independent Claims: Typically define the core invention, often encompassing a chemical compound or composition with specific structural features, or a method of achieving a therapeutic effect.
  • Dependent Claims: Narrow the scope, adding specific substituents, concentration ranges, or particular methods.
  • Use Claims: Cover specific therapeutic applications, enabling protection beyond the compound itself.
  • Manufacturing Claims: Address process-specific aspects, which can extend patent coverage into production methods.

For UY30021, assuming a typical pharmaceutical patent, the scope likely includes:

  • The chemical entity with unique structural features.
  • A pharmaceutical composition comprising the compound.
  • A method of treating certain diseases using the compound or composition.
  • Processes for synthesizing the compound.

Implications of Scope

A broad patent claim covering a chemical class may enable protection over multiple derivatives, discouraging generic entry. Conversely, narrow claims protect specific compounds but risk ease of design-around strategies.

In Uruguay, the patent examination process emphasizes novelty, inventive step, and industrial applicability, leading to well-defined claim scopes aligned with these criteria.

Claims Analysis

An in-depth review entails analyzing each independent claim, understanding their inventive features, and potential vulnerabilities.

Typical Claims in UY30021:

  • Structural Claims: Covering the core chemical structure with specific substituents. For example, a chemical formula representing a novel compound with pharmacologically relevant modifications.
  • Method of Use Claims: Describing treatment of specific conditions, such as certain cancers, neurological disorders, or metabolic diseases.
  • Combination Claims: Protecting the compound when used in combination with other therapeutic agents.
  • Process Claims: Detailing novel synthesis routes that improve yield, purity, or process efficiency.

Claim Scope and Patentability

The claims' breadth impacts enforceability and risk of infringement or invalidation. Broad claims must demonstrate sufficient inventive step and clear description, aligning with Uruguay's patent standards. Narrower claims, though easier to defend, may limit commercial scope.

Claim Challenges and Limitations

  • Prior art may limit the scope if similar compounds or methods exist, reducing claim breadth.
  • Patentability in Uruguay also depends on the novelty of the claims relative to existing regional or international patents, such as those in the INPI (Argentina) or INPI Brazil, or international databases.

Patent Landscape Context

Regional and Global Patent Filings

Pharmaceutical companies often file for patent protection across multiple jurisdictions, creating a robust landscape to analyze. Uruguay’s patent law aligns with standards under the TRIPS Agreement, integrating with regional systems like the Andean Community (CAN) or the Patent Cooperation Treaty (PCT), facilitating broader protection.

Adjacent Patent Families

  • Patent Families: For UY30021, examining related patents filed regionally or internationally can reveal the scope of the invention’s protection.
  • Prior Art References: Globally, key patents and publications in the same chemical class limit the claim scope unless the invention demonstrates a significant inventive step.

Competitive Landscape and Freedom-to-Operate

The presence of similar patents, especially in larger markets like Brazil or Argentina, impacts the freedom to operate in Uruguay. Companies must analyze whether UY30021 or related patents pose potential infringement risks or if further licensing is required.

Legal and Market Implications

  • The patent’s validity and enforceability depend on its claim novelty, inventive step, and compliance with Uruguayan patent law.
  • The patent can serve as a barrier to generic entry, influencing market dynamics and pricing.
  • Lifecycle management strategies in Uruguay should consider patent expiration and potential patent term extensions, if applicable.

Conclusion

Patent UY30021 plays a critical role in protecting a pharmaceutical innovation within Uruguay’s legal framework. Its scope is determined by carefully crafted claims that balance broad protection with patentability requirements. The patent landscape surrounding UY30021—both regionally and globally—shapes its strength, enforceability, and competitive significance.

For stakeholders, key considerations involve strategic patent claim drafting, ongoing landscape monitoring, and navigating regional patent systems to sustain market exclusivity and support R&D investments.


Key Takeaways

  • The scope of UY30021 depends on the breadth of its independent claims, influencing its enforceability and ability to prevent generic competition.
  • Precise claim drafting and strategic positioning in the regional patent landscape optimize commercial protection.
  • The patent landscape, including prior art and similar filings, guides assessment of validity and freedom-to-operate.
  • Regional patent systems and international treaties influence the patent’s strength and cross-border enforcement possibilities.
  • Continuous monitoring of patent expiry dates, potential challenges, and new filings is critical for maintaining market exclusivity.

FAQs

  1. What is the typical scope of pharmaceutical patents like UY30021 in Uruguay?
    They can range from broad structural claims covering drug classes to narrow claims on specific compounds, formulations, or methods of use, depending on strategic patent drafting.

  2. How does Uruguay’s patent law influence the scope of pharmaceutical patents?
    Uruguay’s law emphasizes novelty, inventive step, and industrial application, ensuring claims are sufficiently specific and non-obvious, which influences how broad or narrow claims can be.

  3. Can similar patents filed across Latin America affect UY30021’s exclusivity?
    Yes, regional patent overlaps or prior art can limit claim scope or threaten validity, emphasizing the need for comprehensive landscape analysis.

  4. What lifecycle management options are available for patents like UY30021?
    Strategies include patent term extensions, filing additional pediatric or supplementary protection certificates, and pursuing new claims for derivatives or methods.

  5. How can patent disputes in Uruguay impact pharmaceutical companies?
    Disputes can lead to patent invalidation, injunctions, or licensing requirements, affecting market stability and revenue projections.


Sources

  1. Uruguayan Patent Office (DNPI) database.
  2. World Intellectual Property Organization (WIPO) – PATENTSCOPE.
  3. Patent laws and regulations of Uruguay.
  4. Regional patent systems (CAN, INPI Brazil, INPI Argentina).
  5. Industry-standard patent strategies for pharmaceuticals.

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