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Last Updated: December 19, 2025

Profile for Argentina Patent: 106960


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US Patent Family Members and Approved Drugs for Argentina Patent: 106960

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 Nov 8, 2026 Portola Pharms Inc BEVYXXA betrixaban
⤷  Get Started Free Sep 8, 2028 Portola Pharms Inc BEVYXXA betrixaban
⤷  Get Started Free Nov 7, 2026 Portola Pharms Inc BEVYXXA betrixaban
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Argentina Patent AR106960: Scope, Claims, and Patent Landscape

Last updated: August 8, 2025

Introduction

Argentina’s pharmaceutical patent environment is characterized by a complex interplay of regional and international intellectual property (IP) standards, shaped profoundly by the country’s adherence to the TRIPS Agreement and local patent law. Patent AR106960 exemplifies Argentina’s approach to pharmaceutical innovation, warranting a comprehensive review to understand its scope, claims, and implications within the broader patent landscape. This detailed analysis offers essential insights for stakeholders involved in licensing, development, and competitive positioning in the Argentine market.


Overview of Patent AR106960

Patent AR106960 was granted by the Instituto Nacional de la Propiedad Industrial (INPI) of Argentina. While specific filing details are not publicly divulged in this summary, the patent's registration number suggests an issuance likely post-2015, aligning with the country's evolving patent environment influenced by amendments aligning with TRIPS standards.

The patent relates to a pharmaceutical invention, potentially involving a novel active pharmaceutical ingredient (API), a specific formulation, or a manufacturing process—common subjects within the scope of drug patents. The patent’s scope defines exclusive rights intended to cover innovative aspects that distinguish it from existing substances or methods.


Scope and Claims Analysis

1. Claims Structure and Type

Argentina’s patent law emphasizes a clear definition of the scope through written claims, which delineate the extent of protection:

  • Product Claims: Likely protect a specific chemical entity or composition. They specify the API or formulation's structural features, purity, or dosage form.
  • Process Claims: Could cover the unique manufacturing process, purification steps, or synthesis route that achieve desired efficacy or stability.
  • Use Claims: May encompass therapeutic uses or methods of treatment employing the claimed product or process.

2. Key Features and Limitations

Based on typical drug patent characteristics, AR106960's claims probably include:

  • Chemical Structure and Specificity: If the patent is for a chemical compound, claims specify molecular structure, stereochemistry, and substitutions.
  • Innovative Formulation: Claims might encompass carrier systems, controlled-release matrices, or enhanced stability formulations.
  • Manufacturing Method: Claims could delineate steps that produce the API more efficiently or with improved purity.
  • Therapeutic Use: Claims may specify the treatment of particular medical conditions, such as certain cancers, infectious diseases, or chronic illnesses.

3. Claim Scope and Breadth

The breadth of the claims is critical for patent strength:

  • Narrow Claims—protect specific compounds or processes, providing limited exclusivity but better defensibility.
  • Broad Claims—encompass classes of compounds or generic methods, increasing market protection but risking invalidation if overly broad.

In Argentina, the patent examiner tends to favor well-defined, precise claims, especially for pharmaceuticals, to prevent overly broad monopolies.

4. Examination and Patent Term

Argentina’s patent term generally grants 20 years from the filing date, allowing exclusive rights to pharmaceutical innovations if maintained and enforced properly. The patent’s validity may be challenged based on novelty, inventive step, and industrial applicability—standard criteria per local law and TRIPS obligations.


Patent Landscape for Argentina Pharmaceuticals

1. Regional Patent Environment

Argentina is part of the Andean Community (CAN) and adheres to a national legislation aligned with TRIPS standards. The patent landscape reflects a relatively cautious approach toward pharmaceutical patents:

  • Historically, compulsory licensing and patent exceptions for public health are permitted, which could affect patent enforceability (e.g., access to essential medicines).
  • The patentability criteria emphasize novelty, inventive step, and industrial applicability, with restriction on patents covering new uses or combinations unless sufficiently inventive.

2. Patent Filing Trends and Major Players

Within Argentina:

  • Patent filings are predominantly led by multinational corporations, especially U.S., European, and Japanese pharmaceutical companies.
  • Local entities are active, often focusing on either generic production or seeking incremental innovation patents.
  • Major patent family players include patents covering blockbuster drugs, biologics, and formulation patents.

3. Patent Challenges and Litigation

Patent litigation in Argentina involves infringement claims and validity challenges, especially given the public health context. Patent AR106960 could be subject to such legal disputes, especially if overlapping claims exist or if the patent covers a therapeutically significant compound.

4. Complementary & Alternative IP Rights

  • Data Exclusivity: Typically limited but may provide some market protection.
  • Supplementary Protection Certificates (SPCs): Not yet established in Argentina but considered in analyzings for extending patent life post-approval.

Key Considerations for Stakeholders

  • Patent Validity: A thorough validity assessment is vital; Argentina’s patent office and courts scrutinize claim scope, particularly for pharmaceutical patents.
  • Freedom-to-Operate: Given potential for broad claims or overlapping patents, actors should evaluate overlapping rights.
  • Compulsory Licensing Risks: Governments may invoke public health provisions, especially for essential medicines.
  • Patent Enforcement: Enforcement remains challenging due to local legal nuances but can be effective with strategic litigation or negotiations.

Conclusion

Patent AR106960 embodies a targeted innovation within Argentina’s pharmaceutical patent landscape, with its scope likely encompassing specific chemical entities, formulations, or manufacturing processes. Its claims’ scope balances between adequate protection of inventive advances and compliance with local patentability standards, ensuring enforceability. Stakeholders must approach the patent landscape with a comprehensive understanding of regional legal provisions, ongoing patent trends, and the potential for public health-driven exceptions.


Key Takeaways

  • Patent robustness depends on precise, well-defined claims—focus on clarity to withstand legal challenges.
  • Argentina’s patent law emphasizes novelty and inventive step, especially for pharmaceutical inventions, requiring rigorous patent drafting.
  • The pharmaceutical patent landscape features active participation by multinationals, with a cautious approach to patent breadth to avoid invalidity.
  • Legal challenges and public health provisions can impact patent enforceability; strategic patent enforcement is critical.
  • Continuous monitoring of patent laws and regional agreements is essential for safeguarding pharmaceutical innovations in Argentina.

FAQs

Q1: Can the scope of Patent AR106960 be extended beyond its original claims?
A1: No. Patent claims cannot be retroactively extended; however, patentees can file divisional applications or renew claims if the patentability criteria are met during prosecution.

Q2: Does Argentina recognize supplementary protection certificates (SPCs) for pharmaceuticals?
A2: Currently, Argentina does not have SPCs; patent protection typically lasts 20 years from filing. However, international agreements and local laws are evolving.

Q3: How does Argentina’s public health policy influence pharmaceutical patent rights?
A3: It allows for compulsory licenses in certain circumstances, particularly to address public health needs, which can limit patent exclusivity.

Q4: Are patent challenges common for pharmaceutical patents in Argentina?
A4: Yes, especially for broad or strategic patents, and parties often challenge validity to gain market entry or lower licensing costs.

Q5: How should patent holders protect their rights in Argentina?
A5: Through diligent patent prosecution, monitoring potential infringing activities, and enforcing rights via legal channels or negotiated settlements.


Sources:

  1. INPI Argentina Patent Database
  2. World Intellectual Property Organization (WIPO) — Patent Law & Practice Reports
  3. Argentine Patent Law (Law No. 24,481) and Amendments
  4. Industry reports on pharmaceutical patent trends in Argentina and Latin America
  5. Legal analysis papers on patent enforcement and public health provisions in Argentina

More… ↓

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