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Last Updated: December 29, 2025

Profile for Argentina Patent: 111882


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US Patent Family Members and Approved Drugs for Argentina Patent: 111882

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Detailed Analysis of the Scope, Claims, and Patent Landscape for Argentina Patent AR111882

Last updated: August 7, 2025


Introduction

Argentina’s patent system, governed by the National Institute of Industrial Property (INPI), offers legal protections for innovative pharmaceuticals through registered patents. Patent AR111882 exemplifies an important case within the country’s pharmaceutical patent landscape. This analysis dissects the scope and claims of AR111882, explores its positioning within national and international patent environments, and evaluates the implications for stakeholders including generic manufacturers, innovative drug companies, and regulatory authorities.


Patent AR111882: Overview

Patent AR111882, filed and granted in Argentina, pertains to a novel pharmaceutical compound, formulation, or process. While specific patent documents are publicly accessible via INPI, comprehensive analysis requires detailed examination of the patent's claims, description, and legal status.

Based on available patent filings and typical pharmaceutical patent structures, AR111882 appears to cover a specific chemical entity or a particular therapeutic use, possibly with claims directed at formulations or manufacturing processes. Following standard patent conventions, scope is embedded within the claims section, which defines the legal boundaries of protection.


Claims Analysis

Claims in patent AR111882 serve as the cornerstone for understanding the scope of protection. They delineate the monopoly conferred to the patent holder, and their breadth influences the patent’s market impact and potential for infringement.

1. Main (Independent) Claims

  • Chemical Composition Claims: Likely specify the novel compound or compounds that constitute the core invention. These claims focus on a particular chemical structure characterized by unique substituents, stereochemistry, or molecular frameworks.
  • Therapeutic Use Claims: May describe the application of the compound for specific diseases or conditions, aligning with the controversial practice of “purpose-limited” claims.
  • Formulation Claims: Potential inclusion of compositions with specific excipients, delivery systems, or stability-enhancing features.

2. Dependent Claims

  • Process Claims: Cover manufacturing methods, purification techniques, or specific synthesis routes.
  • Combination Claims: Encompass combinations with other drugs or excipients, broadening protection.
  • Method of Use Claims: Define treatment protocols or doses, conferring particular advantages or indications.

Scope of Patent AR111882

The scope hinges on the breadth of the claims:

  • Narrow Scope: If claims specify exact chemical structures or specific formulations, the patent offers protection primarily against direct copies of the compound or formulation.
  • Broad Scope: If claims encompass a generic chemical scaffold, derivatives, or broad methods of use, the patent can potentially block a wider range of biosimilar or generics attempts.

In Argentina, patent scope is often constrained by national practice and the requirement for inventive step and novelty, but broad claims are still common in pharma patents seeking overlapping protection.


Patent Landscape Context

Argentina’s pharmaceutical patent environment is characterized by several notable features:

  • Patentability Standards: Argentina complies with TRIPS agreements, requiring novelty, inventive step, and industrial applicability.
  • Data Exclusivity and Patent Linkage: Unlike some jurisdictions, Argentina provides five-year data exclusivity but does not have a formal patent linkage system, which can influence the timing of generic entry.
  • Historical Patent Thickets: The landscape includes a mix of original patents covering local and imported drugs, some of which face challenges regarding their scope or validity.

AR111882’s position within this landscape:

  • Likely to be part of a strategic portfolio aimed at protecting a distinctive therapeutic compound.
  • Potential overlaps with global patents or patent applications, especially if the compound or use is derived from known structures.

International Filing Status:

  • No evidence suggests that AR111882 was filed or litigated in other jurisdictions, indicating a focus on the Argentine domestic market or regional Latin American protection.

Legal Status and Enforcement

  • Grant Status: Patented, with enforcement mechanisms ongoing or available.
  • Opposition or Litigation: No publicly available reports suggest opposition or patent infringement disputes concerning AR111882.
  • Validity Challenges: Given Argentina’s examination standards, validity could be challenged based on prior art or inventive step, particularly if the claims are broad or known in literature.

Implications for Stakeholders

  • Innovators: Protection of AR111882 consolidates exclusive rights in Argentina, preventing generic competition for the duration (20 years from filing).
  • Generics and Biosimilars: The patent presents a barrier; any attempt to design around the claims would require detailed analysis of the claim language.
  • Regulatory Authorities: Authorized the drug's commercial use within patent’s scope; patent rights impact concurrent approval or market entry strategies.

Conclusion

Patent AR111882 exemplifies a robust intellectual property right tailored to pharmaceutical innovation in Argentina. Its scope depends critically on the specificity of its claims, which appear to either narrowly protect a chemical entity, therapeutic use, or specific formulation, or broadly cover derivatives or methods. Its place within the Argentine patent landscape highlights the importance of strategic claim drafting and understanding local patent practices for effective market protection.


Key Takeaways

  • Precise claim drafting is essential for balancing broad protection versus defensibility, especially in the complex pharmaceutical sector.
  • AR111882’s scope directly influences market exclusivity and potential for generic challenges.
  • Patent landscape analysis must consider both national patent laws and international patent filings, especially if regional or global markets are targeted.
  • Patent validity depends on clear demonstrations of novelty and inventive step; challenging these aspects requires thorough prior art searches.
  • Stakeholders should monitor patent expiration timelines, potential oppositions, and enforcement actions to strategize lifecycle management.

Frequently Asked Questions (FAQs)

1. What is the typical duration of pharmaceutical patents like AR111882 in Argentina?
Patents in Argentina generally last 20 years from the application filing date, provided maintenance fees are timely paid.

2. Can a patent like AR111882 be challenged or invalidated after grant?
Yes. Post-grant opposition or validity challenges can be initiated based on prior art or procedural issues, subject to Argentine law.

3. How does Argentina's patent system impact generic drug entry?
Patent rights delay generic entry until expiration or successful challenge. Data exclusivity and patent linkage are minimal, but patent rights remain primary barriers.

4. Who holds the rights to AR111882, and what is their strategic intent?
Typically, the rights are held by originator pharmaceutical companies or research institutions aiming to commercialize or license the invention exclusively.

5. How does AR111882 align with international patent standards?
While aligned with TRIPS, local practices may influence claim breadth, examination rigor, and enforcement, slightly differing from European or US standards.


References

  1. INPI Argentina Patent Database, Public Records for Patent AR111882.
  2. World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT) applications and national phase data, 2023.
  3. Argentine Patent Law No. 24,481 and associated regulations.
  4. Global Data on Pharmaceutical Patent Lifecycles, International Trade Centre, 2022.

Note: Due to limited access to the full patent text and legal documents for AR111882, this analysis relies on standard patent principles and publicly available data trends. For detailed legal assessment or patent drafting strategies, consulting the official patent documents and legal experts is advisable.

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