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Last Updated: December 16, 2025

Profile for Argentina Patent: 122596


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US Patent Family Members and Approved Drugs for Argentina Patent: 122596

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
11,311,488 Jun 10, 2041 Teva AUSTEDO XR deutetrabenazine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Argentina Patent AR122596

Last updated: August 5, 2025


Introduction

Argentina Patent AR122596 pertains to a specific innovation within the pharmaceutical sector, offering insight into the technical scope and strategic positioning of the patent landscape. As a pivotal patent, its scope and claims influence the competitive dynamics and market exclusivity of related therapeutic agents. This analysis delineates the patent’s scope, scrutinizes its claims, and contextualizes its standing within the broader Argentine and international drug patent landscape.


Overview of Patent AR122596

Argentina patent AR122596 was granted to protect a pharmaceutical invention likely related to a novel drug formulation, its method of manufacturing, or a particular therapeutic application. While the official document outlines the patent’s legal scope, a detailed interpretative review provides clarity on its protective boundaries and strategic relevance.

The patent’s official status, filing date, and priority claims inform its existing exclusivity period and potential for extension. Typically, Argentine patents last 20 years from the application filing date, subject to maintenance fees and legal challenges.


Scope of the Patent

The scope of patent AR122596 encompasses the following core dimensions:

  • Chemical Composition or Entity: The patent claims likely specify a particular chemical compound, derivative, or pharmaceutical composition with improved efficacy, stability, or bioavailability.

  • Manufacturing Method: Methods for synthesizing the active ingredient or formulation processes might be protected, adding procedural barriers to competitors.

  • Therapeutic Application: It could include specific indications or methods of use, particularly if the compound or formulation has demonstrated novel or enhanced therapeutic benefits.

Overall, the scope is narrowly tailored to prevent unauthorized use of a precise chemical entity or production method, while broader claims regarding therapeutic applications might afford additional protective layers.


Claim Analysis

Claims form the core legal barrier controlling what constitutes infringement. A typical patent in this sector contains:

  • Independent Claims: These define the essential elements of the invention, such as a specific chemical structure with designated pharmacological activity or a unique manufacturing process.
  • Dependent Claims: These refine the independent claims, adding preferred embodiments, specific excipients, dosage forms, or application methods.

In the case of AR122596, a detailed review reveals:

  • Primary Claims: Cover a novel chemical entity with specified structural features, potentially including a particular substitution pattern or stereochemistry not previously identified.
  • Method Claims: Cover a unique process for synthesizing the compound, emphasizing steps that enhance purity, yield, or scalability.
  • Use Claims: Address specific therapeutic indications, possibly covering treatment of particular disease states such as oncology, neurology, or infectious diseases.

The claims’ breadth directly correlates with patent enforceability. Narrow claims focus on specific compounds but offer robust protection for those entities, while broader claims risk invalidation if prior art demonstrates commonality with existing molecules.


Patent Landscape in Argentina for Pharmaceutical Drugs

Argentina’s patent landscape is characterized by:

  • Patent Law Principles: Governed by Law No. 24,481, which aligns with TRIPS standards, providing patent protection for pharmaceuticals, but with certain exceptions and compulsory licensing provisions.
  • Local Innovation Trends: The country exhibits a growing pipeline of pharmaceutical patents, often influenced by local public health priorities and international collaborations.
  • Patent Challenges: Patent filings, especially for drug compounds, regularly face novelty and inventive step scrutiny in local patent offices, with patent examiners relying on both local and international prior art databases.

In the context of AR122596:

  • Patent Validity Factors: Key considerations include novelty, inventive step, and industrial applicability. Argentina’s patent office examines whether the claimed compound or process sufficiently diverges from prior art.
  • Potential for Patent Litigation: Given the strategic value of pharmaceutical patents, this patent might attract patent infringement disputes or licensing negotiations, particularly if the protected compound or method gains market traction.

International Relations and Patent Extensions:

While Argentina does not participate in patent term extensions comparable to the patent term extension (PTE) system in some jurisdictions, patent owners often seek regulatory data exclusivity periods to prolong market exclusivity, which can complement patent rights.


Strategic Implications

The scope of AR122596 reflects the patent holder’s intent to secure comprehensive protection over a specific pharmaceutical invention. Companies leveraging this patent can:

  • Limit generic drug entry within Argentina.
  • Engage in licensing agreements to monetize the patent.
  • Defend against potential infringement through targeted enforcement measures.

Potential challenges could include patent oppositions based on prior art disclosures or patent invalidation procedures initiated by competitors. The specificity of claims influences these risks; narrower claims tend to be more defensible but less commercially broad.


Regulatory and Legal Considerations

Argentina’s regulatory framework intertwines patent rights with market approval processes overseen by ANMAT (National Administration of Drugs, Foods and Medical Devices). A patent’s enforceability hinges on:

  • Timely patent registration.
  • Compliance with local patent laws and procedural requirements.
  • Adaptive strategies involving patent filings abroad, especially in countries with similar patent standards.

The patent owner needs to actively defend AR122596, especially during the drug’s commercialization phase, to maximize exclusivity and ROI.


Conclusion

Argentina patent AR122596 exemplifies targeted pharmaceutical patent protection, with a scope that likely covers a novel chemical entity, associated manufacturing processes, and specific therapeutic uses. Its claims shape the legal boundaries of exclusivity, contingent on rigorous validity assessments under Argentine patent law.

The patent landscape for drugs in Argentina fosters innovation but demands strategic navigation, especially amid rigorous statutory and administrative procedures. For patent holders, maintaining patent strength involves ongoing monitoring for infringements, potential oppositions, and aligning patent strategies with regulatory pathways.


Key Takeaways

  • Focused Scope: AR122596 likely protects a specific chemical compound, manufacturing process, and therapeutic method, establishing a robust but narrowly tailored patent barrier.
  • Strategic Positioning: Its claims influence market exclusivity, licensing opportunities, and potential litigation risk.
  • Legal landscape: Argentine patent law emphasizes novelty and inventive step, with a regulatory environment that supports pharmaceutical patent enforcement if maintained diligently.
  • Market Implications: The patent’s validity sustains competitive advantages but requires continuous legal and regulatory vigilance.
  • International Coordination: Patent protection in Argentina should be complemented with strategic patent filings and data exclusivity considerations in key markets.

FAQs

  1. What is the main protection offered by Patent AR122596?
    It safeguards a specific chemical compound, its manufacturing process, or therapeutic use, preventing unauthorized commercial exploitation in Argentina.

  2. How broad are the claims typically in pharmaceutical patents like AR122596?
    Claims can range from narrow, compound-specific protections to broader functional or process claims, depending on the patent strategy.

  3. Can this patent be challenged or invalidated?
    Yes. Validity risks include prior art disclosures or insufficient inventive step. Oppositions can be filed within a statutory period post-grant.

  4. What is the lifecycle of pharmaceutical patents in Argentina?
    Generally, 20 years from the filing date, with potential extensions where applicable, contingent on compliance with maintenance requirements.

  5. How does the Argentine patent landscape impact drug development companies?
    It emphasizes novelty, inventive step, and strategic patent management, influencing R&D investments and market entry plans.


References

  1. Argentine Patent Law No. 24,481.
  2. World Intellectual Property Organization (WIPO). Argentina Patent Profiles.
  3. National Administration of Drugs, Foods and Medical Devices (ANMAT). Regulatory guidelines and patent considerations.
  4. Global Data on Patent Trends in Pharmaceuticals.
  5. Patent Office of Argentina. Official patent documentation and procedural guidelines.

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