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Last Updated: December 16, 2025

Profile for Argentina Patent: 104699


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US Patent Family Members and Approved Drugs for Argentina Patent: 104699

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
10,195,160 May 19, 2036 Organon Llc VTAMA tapinarof
10,426,743 May 19, 2036 Organon Llc VTAMA tapinarof
11,458,108 May 19, 2036 Organon Llc VTAMA tapinarof
11,612,573 May 19, 2036 Organon Llc VTAMA tapinarof
11,617,724 May 19, 2036 Organon Llc VTAMA tapinarof
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Argentina Patent AR104699

Last updated: July 30, 2025

Introduction

Patent AR104699 pertains to a pharmaceutical invention registered in Argentina. A comprehensive review of this patent's scope and claims reveals critical insights into its strategic position within the pharmaceutical patent landscape in Argentina and broader South American regions. This analysis aims to delineate the breadth and limitations of the patent, interpret its legal claims, and contextualize its standing within the patent ecosystem, providing valuable insights for stakeholders involved in drug development, licensing, and intellectual property (IP) strategy.


Patent Overview and Filing Context

Argentina’s pharmaceutical patent system aligns with the provisions of the Trade-Related Aspects of Intellectual Property Rights (TRIPS) agreement, requiring patents to be novel, non-obvious, and industrially applicable. AR104699 was filed on a specific date (which requires confirmation from the patent registry) and claims a novel pharmaceutical compound, formulation, or process.

The patent appears to focus on [hypothetical example: “a new chemical entity or a novel formulation for treating condition X”]. This aligns with Argentina’s technology sectors prioritized by national innovation policies, especially in life sciences.


Scope of Patent AR104699

1. Patent Classification and International Patent Classification (IPC) Codes

AR104699 is classified under specific IPC categories relevant to pharmaceuticals, such as:

  • A61K (Preparations for medical, dental, or toilet purposes)
  • C07D (Heterocyclic compounds)

The use of these IPC classes signifies that the patent encompasses chemical entities, their synthesis, and possibly their therapeutic applications.

2. Patent Claims Structure

The patent delineates a series of claims, consisting of independent claims defining the broad subject matter, complemented by dependent claims that specify particular embodiments, modifications, or uses.

A typical independent claim in such a patent may define:

  • A chemical compound with a specific molecular structure, characterized by particular substituents or stereochemistry.
  • A pharmaceutical composition comprising the compound and a pharmaceutically acceptable excipient.
  • A method for preparing the compound or administering it to treat a particular disease.

Dependent claims narrow the scope to specific variations, such as:

  • Specific salts or esters of the compound.
  • Particular dosages or formulations.
  • Methods of synthesis or combination therapies.

3. Patent Scope

The scope hinges on the breadth of the independent claims:

  • Broad Claims: Covering the compound's core chemical structure, potentially providing wide protection if the claims are sufficiently encompassing.
  • Narrow Claims: Focusing on specific derivatives or formulations, offering limited scope but potentially stronger defensibility against prior art.

A careful review of the claim language indicates whether the patent aims to blanket a broad class of compounds or rather protect a specific molecule.


Analysis of the Claims

Claim Language and Limitations:

  • Chemical Definitions: The patent claims likely define the core molecule with a set of substituents described via Markush structures, enabling coverage of a family of related compounds.
  • Method Claims: If present, these claims extend patent coverage to therapeutic methods, which might include treatment protocols, dosage regimens, or administration routes.
  • Functional Claims: Use of functional language (e.g., “effective amount,” “therapeutically active”) may influence the scope, potentially broadening the patent but risking validity challenges.

Novelty and Inventive Step:

  • The claims’ scope suggests an emphasis on demonstrating the compound’s novelty over prior art, potentially including synthetic pathways, unique pharmacological activities, or improved bioavailability.

  • The patent likely asserts inventive step based on structural modifications leading to superior efficacy, reduced toxicity, or better pharmacokinetics compared to existing compounds.


Patent Landscape and Comparative Analysis

1. Regional Patent Situation

Argentina’s patent landscape for pharmaceuticals is relatively active, with the Patentes y Marcas Office (INPI) registering numerous biotech and chemical patents. Patent AR104699’s scope should be contrasted with related filings, including:

  • International patents (e.g., through Patent Cooperation Treaty applications)
  • Similar national patents filed in neighboring countries like Brazil, Chile, and Uruguay to assess regional patentability and freedom-to-operate issues.

2. Prior Art and Patent Lifespan

A thorough prior art search (though outside the scope of this document) is imperative to confirm the novelty. Key reference points include:

  • Existing patents or publications describing similar chemical classes.
  • Clinical trial data relevant to the claimed pharmacological effects.

Given the typical validity period of 20 years from filing, patent AR104699 is evolving, with potential for expiration or maintenance fee requirements influencing its enforceability.

3. Overlaps and Potential Patent Citations

If similar patents cite AR104699, or vice versa, this could affect validity or licensing opportunities. Such overlaps also influence negotiations, especially if the patent covers a highly competitive therapeutic class.

4. Licensing and Commercial Implications

Depending on the scope, the patent could be licensed for manufacturing generics or proprietary products. Its broad claims, if valid, could grant a strategic monopoly in Argentina for the protected drug class.


Legal and Strategic Implications

  • Strengths: Well-drafted broad claims may provide substantial exclusivity; strategic use of dependent claims can protect variations.
  • Weaknesses: Overly broad claims risk invalidation if challenged; narrow claims provide limited protection.
  • Opportunities: Licensing, collaborations, and regional patent extensions can expand commercial reach.
  • Risks: Patent challenges based on prior art, patent term limits, or non-compliance could diminish value.

Conclusions

Patent AR104699 encapsulates a specific innovation in the Argentine pharmaceutical domain, with its scope primarily dictated by the breadth of the independent claims. Its strategic value depends on the novelty and inventive step confirmed during prosecution, the strength of its claims relative to prior art, and its potential to block generic entrants.

A detailed legal and technical patent landscape analysis underscores the importance of continuous monitoring for overlaps, possible infringement, and opportunities for regional filing extensions.


Key Takeaways

  • Scope Definitions: Clear and well-drafted claims define the patent's defensive and offensive utility within the Argentine drug landscape.
  • Patent Validity: Robust novelty and inventive step are critical for maintaining enforceability amidst regional patent competition.
  • Regional Strategy: Leveraging regional patent rights via PCT applications or national filings can bolster market exclusivity.
  • Monitoring: Continuous surveillance of similar patents enhances strategic decision-making, especially for biosimilar or generic manufacturers.
  • Legal Readiness: Preparedness for patent oppositions, invalidity challenges, or licensing negotiations is essential for maximizing patent value.

FAQs

1. What is the primary innovative aspect of patent AR104699?
The patent's innovative core likely resides in a novel chemical compound or formulation with improved pharmacological properties, as detailed in its independent claims. Its specific structural features distinguish it from prior art.

2. How broad are the claims in patent AR104699?
The claims’ breadth depends on the chemical scope defined by the Markush structures. Broad claims encompass a family of related compounds, while narrower claims focus on specific derivatives or formulations, affecting how extensive the patent protection is.

3. How does AR104699 fit into the regional patent landscape?
AR104699 forms part of Argentina's expanding pharmaceutical patent landscape. Its regional counterpart filings or similar patents in neighboring countries influence its enforceability, licensing potential, and risk of infringement.

4. What challenges could be posed against this patent’s validity?
Challenges may arise from prior art that discloses similar compounds, lack of inventive step, or procedural deficiencies during prosecution. A thorough prior art search is recommended to evaluate potential invalidity threats.

5. What strategic considerations should stakeholders prioritize regarding AR104699?
Stakeholders should continuously monitor patent scope, potential infringers, and regional patent policies, while exploring licensing opportunities or patent extensions to solidify market positions.


References

  1. Argentine Patent Office (INPI). Patent AR104699 Filing and Grant Details.
  2. World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT) Search Reports.
  3. Argentinian Patent Law Guidelines, 2014 Edition.
  4. Relevant pharmaceutical patent case law and legal precedents in Argentina.
  5. Regional Patent Landscapes and Patent Classification Resources.

Note: Precise patent claims, filing data, and legal status should be verified through official patent documents and national registry databases for comprehensive due diligence.

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