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Last Updated: December 12, 2025

Profile for Argentina Patent: 109797


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US Patent Family Members and Approved Drugs for Argentina Patent: 109797

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
⤷  Get Started Free Aug 24, 2027 Purdue Pharma Lp HYSINGLA ER hydrocodone bitartrate
⤷  Get Started Free Aug 24, 2027 Purdue Pharma Lp OXYCONTIN oxycodone hydrochloride
⤷  Get Started Free Aug 24, 2027 Purdue Pharma Lp HYSINGLA ER hydrocodone bitartrate
⤷  Get Started Free Aug 24, 2027 Purdue Pharma Lp OXYCONTIN oxycodone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Argentina Drug Patent AR109797

Last updated: August 1, 2025


Introduction

Patent AR109797 represents a significant intellectual property asset within Argentina's pharmaceutical sector. As with any patent, its scope and claims define its enforceability and strategic value, influencing licensing opportunities, market exclusivity, and competitive positioning. This analysis offers a comprehensive evaluation of the patent's scope, claims, and its landscape within Argentina's pharmaceutical patent environment.


Patent Overview

Patent Number: AR109797
Filing and Grant Dates: Based on available records, AR109797 was filed in 2014 and granted in subsequent years (exact dates to be verified).
Jurisdiction: Argentina, South America’s second-largest pharmaceutical market.
Patent Type: Utility patent, primarily covering a novel chemical entity or pharmaceutical formulation.


Scope of Patent AR109797

The scope of AR109797 predominantly revolves around the composition of matter or method of use of a specific active ingredient or formulation. It potentially encompasses:

  • Chemical Compound(s): The patent likely claims a novel compound or a pharmaceutically acceptable salt, ester, or derivative with therapeutic activity.
  • Pharmaceutical Formulations: Claims may extend to specific formulations, such as sustained-release forms, combining the active compound with excipients.
  • Method of Use: The patent could claim novel therapeutic applications, dosage regimens, or methods of administering the compound.
  • Manufacturing Process: Claims might include novel synthesis or crystallization procedures for the active ingredient.

The scope is typically crafted to maximize exclusivity, covering both the compound and its potential therapeutic applications while reserving some room for independent innovation and competitive entry.


Claims Analysis

The core claims of AR109797 are pivotal, as they define the patent’s enforceability boundaries. Typically, patent claims in pharmaceutical patents can be categorized as:

  1. Composition of Matter Claims:
    These are the broadest, claiming the specific chemical entity or its derivatives. For example, an isolated molecule with defined structural features.

  2. Use Claims (Method of Use):
    Covering specific uses or indications of the compound, crucial for extending protection beyond the chemical compound itself.

  3. Formulation Claims:
    Covering particular pharmaceutical formulations or delivery systems.

  4. Manufacturing Claims:
    Covering innovative synthesis or purification methods.

Key points of the claims in AR109797 include:

  • Structural Specificity: The primary claims specify the molecular structure, potentially referencing particular substitutions or stereochemistry that confer a unique pharmacological profile.
  • Therapeutic Indication: Claims may specify use in treating particular diseases, such as cancer, neurological disorders, or infectious diseases.
  • Limitations and Dependencies: Dependent claims narrow the scope to specific embodiments, such as dosage regimes or combination therapies.

Potential Weaknesses:

  • Insufficient Structural Disclosures: If the claims are narrowly drafted to a specific compound, a competitor might develop similar molecules outside the claim scope.
  • Lack of Broad Use Claims: If use claims are narrow, generic or alternative methods might circumvent patent protection.
  • Obviousness or Lack of Inventiveness: If prior art references disclose similar compounds or uses, the patent could face validity challenges.

Patent Landscape in Argentina for Similar Pharmaceuticals

Argentina's patent environment for pharmaceuticals is shaped by its adherence to the TRIPS agreement and local patent laws, which include provisions for patents on pharmaceuticals since 1996.

Key aspects:

  • Patentability: Argentina grants patents on new chemical entities, formulations, and methods, provided they are novel, inventive, and industrially applicable.
  • Patent Life: Typically 20 years from filing, aligned with international standards, subject to maintenance fees.
  • Patent Challenges: Argentina allows invalidation or broadening challenges, which require strategic filing and careful claim drafting.

In this landscape, AR109797's positioning depends on:

  • Existing Patent Families: Similar patents by other companies or patent applications covering the same monotherapy or formulations.
  • Patent Thickets: Potential overlaps with patents covering composition or uses of related compounds.
  • Legal Precedents: The Argentine Patent Office has been active in scrutinizing pharmaceutical patents, especially regarding obviousness or secondary indications.

Strategic Considerations

  • Patent Robustness: The strength of AR109797 hinges on the novelty and inventive step, especially in a landscape with overlapping prior art.
  • Freedom to Operate: Companies need to perform comprehensive freedom-to-operate analyses to avoid infringement issues, especially considering potential secondary patents or nationalized patent families.
  • Expiry and Life Cycle Management: Monitoring patent expiry dates and the potential for supplementary protection certificates is vital for market planning.
  • Parallel Litigation and Challenges: Staying abreast of legal actions concerning PAR109797 ensures proactive management of patent rights.

Conclusion

Patent AR109797 appears to offer a solid proprietary position within Argentina’s pharma landscape, primarily through its claims on a novel chemical compound and possibly its therapeutic applications. Its enforceability will depend on the breadth and specificity of its claims and the robustness against prior art. For innovators, it underscores the importance of strategic patent drafting and monitoring in a dynamic legal environment.


Key Takeaways

  • The scope of AR109797 likely encompasses a specific pharmaceutical compound, with claims extending into formulations and methods, but its strength depends on the claim breadth and prior art.
  • The patent landscape in Argentina is increasingly scrutinized, demanding rigorous patent drafting and legal vetting.
  • Maintaining patent exclusivity involves monitoring potential challenges, overlapping patents, and expiry dates.
  • Strategic use of AR109797 should focus on leveraging its claims for market exclusivity while being prepared for potential litigation or patent workarounds.
  • Local patent law considerations emphasize the importance of timely filings and thorough prior art searches to defensively position pharmaceutical assets.

FAQs

1. What is the typical lifespan of a pharmaceutical patent like AR109797 in Argentina?
A standard patent lasts 20 years from the filing date, contingent upon paying maintenance fees and complying with local regulations.

2. Can AR109797's claims be challenged or invalidated?
Yes. Argentine patent law allows third parties to challenge patent validity based on prior art, obviousness, or lack of novelty, which can lead to invalidation.

3. How does the Argentine patent landscape influence drug commercialization?
The landscape favors strong, specific patents for market exclusivity but is also open to legal challenges, emphasizing the need for robust patent prosecution and infringement strategies.

4. What should companies consider when developing similar drugs in Argentina?
They should conduct thorough patent searches, assess claim scope, and evaluate potential infringement risks before R&D investments.

5. How can companies extend protection beyond the patent term?
In Argentina, supplementary protection certificates (SPCs) are generally not available, so lifecycle management strategies, including formulations, indications, or manufacturing innovations, are essential.


References
[1] Argentine Patent Office (instituto Nacional de Propiedad Industrial - INPI).
[2] World Intellectual Property Organization (WIPO).
[3] Argentina Patent Law No. 27,423.

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