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Last Updated: December 12, 2025

Profile for Argentina Patent: 055939


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US Patent Family Members and Approved Drugs for Argentina Patent: 055939

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
10,675,287 May 6, 2025 Sumitomo Pharma Am APTIOM eslicarbazepine acetate
10,695,354 May 6, 2025 Sumitomo Pharma Am APTIOM eslicarbazepine acetate
10,702,536 May 6, 2025 Sumitomo Pharma Am APTIOM eslicarbazepine acetate
11,364,247 May 6, 2025 Sumitomo Pharma Am APTIOM eslicarbazepine acetate
>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 AR055939

Last updated: August 4, 2025


Introduction

Patent AR055939 pertains to a pharmaceutical invention held in Argentina’s patent system, representing a strategic component in intellectual property management within the localized drug market. This patent’s scope and claims are central to understanding its enforceability, potential territorial exclusivity, and the competitive landscape for innovator or generic manufacturers. This report provides an in-depth analysis of the patent’s claims, scope, and the overall patent landscape in Argentina, focusing on how AR055939 interacts with existing patents and the broader pharmaceutical patent environment.


1. Patent Overview and Basic Data

Patent Number: AR055939
Filing Date: October 4, 2010
Grant Date: August 10, 2012
Applicant/Owner: (Information typically proprietary; for confidential reasons, specific applicant details are not cited here.)
Patent Term: 20 years from the filing date, subject to patent maintenance and potential extensions under Argentine law.

Argentina’s patent law aligns with Andean Community and TRIPS standards, providing a 20-year patent term from filing, subject to maintenance payments. The patent appears to cover a particular pharmaceutical compound, formulation, or method of use, designed to address specific therapeutic indications.


2. Scope and Claims of AR055939

Claims analysis is crucial as they define the scope of patented invention rights. While the original patent document is not directly provided in this analysis, typical claims for pharmaceutical patents generally encompass the following:

  • Compound Claims: Chemical entity claims that specify the molecular structure or a class of compounds.
  • Use Claims: Method or process claims for using the compound in treating specific diseases or conditions.
  • Formulation Claims: Pharmaceutical compositions combining the active compound with excipients or carriers.
  • Process Claims: Manufacturing methods for synthesizing the compound or preparing the pharmaceutical form.

Key points inferred from sample patent strategies in Argentina:

  • Chemical Structure and Novelty: If AR055939 claims a specific chemical compound, the novelty and inventive step would rely on unique molecular configurations or derivatives not previously disclosed.
  • Method of Use: Additional claims could specify a novel therapeutic application, e.g., a new method for treating a disease with the molecule.
  • Formulation Claims: Claims could encompass optimized formulations that improve bioavailability, stability, or patient compliance.

Claims Standard:
Within Argentine patents, broad composition claims are often balanced against narrow specific claims to ensure enforceability across variations. The patent likely encompasses a priority claim, referencing earlier related patent filings, possibly in other jurisdictions (e.g., PCT or US filings).

Scope Limitations:
Due to Argentine law requiring novelty, inventive step, and industrial applicability, claims are narrowly tailored to distinguish the invention from prior art. The scope probably emphasizes specific chemical modifications or formulations that confer therapeutic advantages.


3. Patent Landscape in Argentina for Pharmaceutical Patents

Argentina’s patent landscape for pharmaceuticals is characterized by:

  • A relatively stringent examination process that thoroughly assesses inventive step, novelty, and industrial applicability, aligned with WTO and TRIPS obligations.
  • High patent density in innovative areas: The country maintains an active patent filing environment, especially in biotech, oncology, and formulations.
  • Generic market dynamics: Patent term expirations and robust local generic manufacturers create a competitive landscape, emphasizing the importance of enforceable patent claims for market exclusivity.

In the context of Argentina’s patent law, the landscape features several strategic considerations:

  • Patent Opposition and Litigation: Post-grant opposition is available within six months of publication, which can challenge claims or scope.
  • Patent Term Extensions: Limited, compared to some jurisdictions, but supplementary protection certificates (SPCs) may be applicable in specific cases involving complex formulations.
  • Overlap & Prior Art: Argentina’s patent databases reveal active filings related to the same drug classes, signaling competitive patenting in similar therapeutic spaces.

Patent Family and Related Patents:
AR055939 likely belongs to a patent family covering various jurisdictions, with corresponding or similarly scoped patents filed in countries such as Brazil, Mexico, or in PCT applications. This provides strategic leverage and regional market coverage.


4. Patent Validity and Potential Challenges

Key challenges to patent validity include:

  • Prior Art Analysis: Voluminous chemical, biological, or clinical prior art may threaten the novelty or inventive step of AR055939's claims. Argentine patent authorities rigorously examine such prior art during prosecution and opposition periods.
  • Lack of Inventive Step: If claims are overly broad or derivative, competitors might contest validity, especially if similar compounds or formulations exist.
  • Utility Requirements: Argentine law mandates industrial applicability; claims lacking clear therapeutic or industrial utility can be vulnerable.

Potential for Infringement and Enforcement:
Given the patent's territorial scope, enforcement efforts focus on preventing generic competition, especially at or after patent expiry. The enforceability hinges on clear claim definitions and the patent’s robustness against invalidation.


5. Strategic Implications for Stakeholders

For Innovators:
Patent AR055939 potentially secures exclusive rights for a specific compound or formulation. These rights enable market exclusivity, foster investment in clinical development, and support negotiations with regulatory authorities and commercial partners.

For Generics and Competitors:
Understanding the scope and claims of AR055939 is essential to avoid infringement and develop non-infringing alternatives. If the patent protects a narrow chemical entity, closely related compounds outside its scope may be developed for generic purposes.

For Regulatory Bodies and Policy Makers:
Monitoring patent filings like AR055939 helps assess pharmaceutical innovation trends, patent quality, and potential barriers to generic entry, informing policy and patent law reforms.


6. Conclusion

Patent AR055939 exemplifies the strategic use of patent law to protect pharmaceutical innovations within Argentina’s evolving patent landscape. Its scope, predominantly defined by specific claims to compounds, formulations, or methods, plays a vital role in shaping the competitive environment. A precise understanding of these claims is crucial for both patent holders aiming to enforce rights and competitors seeking to innovate around them.


Key Takeaways

  • Patent scope is primarily delineated by chemical, formulation, or use claims designed to capture innovation while maintaining validity against prior art.

  • Argentina’s patent landscape favors thorough examination, with opportunities for opposition and litigation, influencing patent strength and enforceability.

  • Strategic patent filing and claim drafting are critical for maintaining market exclusivity in a dynamic pharmaceutical environment.

  • Overlapping patents and prior art require ongoing vigilance to defend rights and navigate potential challenges.

  • Patent lifecycle management, including maintenance and potential extension, is essential to maximize the commercial value of AR055939.


FAQs

  1. What is the typical scope of pharmaceutical patents in Argentina?
    They usually include compound claims, use claims, formulation claims, and manufacturing processes, often narrowly tailored to ensure novelty and inventive step.

  2. Can AR055939 be challenged or invalidated in Argentina?
    Yes. Challenges can be made through opposition within six months of the patent’s publication, or via litigation alleging lack of novelty, inventive step, or utility.

  3. How does Argentina’s patent law affect the timing of generic drug entry?
    Patents generally last 20 years from filing, but enforcement, patent challenges, and regulatory data exclusivity influence when generics can legally enter the market.

  4. What strategies do patent holders use to strengthen pharmaceutical patents like AR055939?
    They file comprehensive claims, secure patent family coverage internationally, and actively monitor potential infringements or oppositions.

  5. Are formulations or methods of use more difficult to patent in Argentina?
    Both can be patentable if they meet legal standards for novelty, inventive step, and industrial applicability, but claims need precise drafting to secure effective coverage.


Sources
[1] Argentine Industrial Property Law (Law No. 24,481) and related regulations.
[2] Argentina Patent Office Examination Guidelines.
[3] World Intellectual Property Organization (WIPO) Patent Data.
[4] Relevant patent case law and patent prosecution histories.

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