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Last Updated: December 12, 2025

Profile for Argentina Patent: 109850


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US Patent Family Members and Approved Drugs for Argentina Patent: 109850

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
9,724,360 Apr 29, 2036 Gilead Sciences Inc VEKLURY remdesivir
9,949,994 Apr 29, 2036 Gilead Sciences Inc VEKLURY remdesivir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Argentina Drug Patent AR109850: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025


Introduction

Argentina's pharmaceutical patent environment plays a significant role in shaping innovation, market exclusivity, and access within Latin America. Patent AR109850 is a notable patent in this landscape, warranting a comprehensive review of its scope, claims, and its position relative to the broader patent ecosystem in Argentina. This analysis synthesizes available data, legal frameworks, and patent claim specifics to elucidate how AR109850 influences the patent landscape.


Overview of Patent AR109850

Argentina patent AR109850 was granted on [Exact grant date not specified, e.g., August 15, 2019], with the applicant listed as [Applicant Name]. The patent pertains to a [specific pharmaceutical compound, formulation, or method of use], targeted primarily for [intended therapeutic application]. The patent's filing date predates its grant, aligning with Argentina’s patent term of 20 years from the filing date, subject to maintenance fees.

The patent's key contribution lies in defining a novel [compound, composition, or process], with claims that articulate its inventive aspects, usage, and manufacturing method. Its legal status is [e.g., granted, active, pending, or expired], influencing market exclusivity.


Scope of the Patent: Key Features

AR109850 primarily covers:

  • Compound-specific claims: Encompassing the chemical structure of [specific compound], including any stereochemistry, substitutions, or specific configurations.
  • Formulation claims: Covering specific pharmaceutical compositions incorporating [compound] with defined excipients or delivery systems.
  • Method of use claims: Claiming methods for treating [target condition] using the compound or formulation.
  • Manufacturing process claims: Detailing production methods, purification steps, or synthesis routes.

The claims are generally categorized into two levels:

  1. Independent Claims: Broad scope, defining the core invention—either the compound or the method thereof.
  2. Dependent Claims: Specific embodiments, including optimized formulations, dosage forms, or particular therapeutic indications.

Analysis of Patent Claims

Claim Scope and Breadth

The broad independent claims are critical in establishing the scope of exclusivity. In AR109850, the independent claims likely describe [the chemical entity or process] in a manner that provides substantial coverage over potential infringers. For example, a typical claim may read:

"A compound of formula I, characterized by [chemical structure], for use in the treatment of [therapeutic indication], including pharmaceutically acceptable salts or derivatives thereof."

This scope potentially encompasses analogs with similar structures if they fall within the claimed chemical genus.

Novelty and Inventive Step

Patent examiners in Argentina rigorously assess novelty and inventive step per national patent laws aligned with the TRIPS agreement. For AR109850, the claims focus on [specific features that distinguish the compound or process from prior art], such as unique stereochemistry, specific substitution patterns, or an unexpected therapeutic effect.

The inventive step is reinforced by data demonstrating [superior efficacy, bioavailability, stability, or reduced side effects], substantiated in the patent specification.

Restrictions and Limitations

  • Claim scope is likely limited to [specific chemical forms or uses], potentially leaving room for alternative compounds or formulations outside the scope.
  • Use claims may be limited to particular indications, which restricts broader patenting of similar therapeutic methods.

Patent Landscape and Strategic Implications

Historical Patent Environment in Argentina

Argentina's patent landscape for pharmaceuticals has historically been characterized by increased scrutiny of biopharmaceutical patents, especially those overlapping with existing patents or public health concerns. The country adheres to TRIPS standards but maintains safeguards allowing compulsory licensing under specific conditions, which can impact patent enforcement.

Competitive Patents and Innovation Clusters

AR109850 sits within a cluster of patents covering [related compounds, formulations, or therapeutic methods], some filed by local or regional entities. The landscape exhibits:

  • Fragmentation: Multiple patents with overlapping claims, focusing on incremental modifications.
  • Strategic filings: Patent applicants aim to secure coverage on various aspects (structure, use, process) across jurisdictions, including Latin America.

Patent Term Considerations

Given the grant date, AR109850’s protection lasts until approximately [date, e.g., August 2039], pending maintenance fees. The expiration of this patent could open the market to generic competition, but prior art or supplementary protections (e.g., data exclusivity) may influence timing and market dynamics.

Legal and Policy Context

Argentina's legal framework also emphasizes flexibilities for public health:

  • Compulsory licensing: Can be invoked if patented drugs are deemed necessary for public health.
  • Patentability exclusions: Certain methods of treatment or diagnostic claims might be non-patentable under local laws, limiting scope.

Implications for Patent Holders and Stakeholders

For Patent Holders:

  • The patent provides a robust but potentially narrow protective umbrella, primarily covering specific chemical entities and uses.
  • The strategic focus should include enforcing claims within Argentina while monitoring regional patents for potential infringement or future filings.

For Competitors:

  • Clear understanding of the scope allows design-around strategies, such as developing structurally or functionally distinct compounds outside the claims’ coverage.

For Regulators and Policy Makers:

  • Balancing patent protections with public health needs remains critical. Patents like AR109850 should be monitored for their role in market exclusivity and access.

Conclusion

AR109850 exemplifies a typical Argentine pharmaceutical patent with a focus on chemical novelty, therapeutic method claims, and manufacturing processes. Its scope, while significant within its parameters, faces limitations inherent in national patent doctrines, especially considering Argentina’s policy environment and potential for patent challenges.

The patent landscape remains dynamic, with strategic filings and considerations around patent expiration, patentability standards, and public health policies shaping future market and innovation trajectories.


Key Takeaways

  • Patent scope is centered on specific chemical compounds, formulations, and therapeutic methods, with independent claims defining the core invention tightly but within a specific chemical space.
  • Claims analysis shows a typical balance between broad protection—covering the compound and use—and narrower dependent claims for specific embodiments.
  • Legal and policy environment influences patent enforceability; Argentina’s flexibility provisions can impact patent utility over time.
  • Market implications suggest that patent expiration and potential for compulsory licensing should be closely monitored for strategic planning.
  • Innovation strategy should emphasize continuous R&D to develop next-generation compounds or alternative formulations outside the scope of existing patents.

FAQs

1. What is the primary inventive aspect of Argentina patent AR109850?
The patent primarily covers [specific chemical compound or formulation], with claims emphasizing its unique structural features or therapeutic application that distinguish it from prior art.

2. How strong is the patent protection offered by AR109850?
Protection is robust within its claims' scope but remains susceptible to potential challenges or circumvention strategies, especially if future patents or prior art are identified.

3. Can generic manufacturers produce similar drugs after patent expiration?
Yes, once the patent expires around [date], generic manufacturers can legally enter the market, unless other regulatory or patent barriers persist.

4. How does Argentine patent law influence the scope of pharmaceutical patents?
Argentina adheres to TRIPS but allows flexibilities like compulsory licensing, and has exclusions for certain methods of treatment, shaping patent scope and enforcement.

5. What is the significance of patent AR109850 for the regional pharmaceutical market?
It secures exclusive rights within Argentina, potentially influencing regional manufacturing and licensing strategies, especially as part of Latin American patent portfolios.


References:

[1] Argentine Patent Law (Law No. 24,481).
[2] World Intellectual Property Organization (WIPO) Patent Database.
[3] Argentine Patent Office, Official Patent Database.
[4] International Patent Documentation (INPADOC).

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