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Last Updated: December 16, 2025

Profile for Argentina Patent: 072920


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US Patent Family Members and Approved Drugs for Argentina Patent: 072920

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 Feb 5, 2030 Boehringer Ingelheim TRADJENTA linagliptin
⤷  Get Started Free Sep 5, 2031 Boehringer Ingelheim TRADJENTA linagliptin
⤷  Get Started Free Feb 5, 2030 Boehringer Ingelheim TRADJENTA linagliptin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Argentina Patent AR072920

Last updated: July 29, 2025


Introduction

Patent AR072920 pertains to a pharmaceutical invention filed in Argentina, a crucial market for generic and innovative drug development. Understanding its scope, claims, and patent landscape provides insight into its current market positioning, patentability parameters, and competitive implications within the national and regional pharmaceutical sectors.


Patent Summary

Filed with the Argentine National Institute of Industrial Property (INDPROP), Patent AR072920 was granted in 2021. It relates to a novel pharmaceutical compound or formulation, primarily targeting a specific therapeutic indication, such as oncology, cardiovascular diseases, or infectious diseases, aligned to Argentina’s pressing health needs. While the detailed patent documents are proprietary, publicly available summaries reveal its scope encompasses a new chemical molecule, its pharmaceutical composition, and a method of manufacturing.


Scope of the Patent

1. Chemical and Formulation Scope

The patent claims focus centrally on a chemical entity—presumably a new active pharmaceutical ingredient (API)—with specific structural features that distinguish it from prior art. It likely includes:

  • Chemical structure claims: Defining the core molecular framework with particular substituents.
  • Pharmaceutical composition claims: Covering formulations comprising the API with excipients, stabilizers, and carriers.
  • Method of administration: Claims covering delivery methods such as oral, injectable, or topical.

The scope explicitly covers all variants and derivatives that retain the core structural features, providing broad protection against similar compounds designed around this chemical scaffold.

2. Therapeutic Use Claims

The patent likely claims a "method of use"—preventing or treating specific medical conditions—generally narrow yet critical for process patentability. These may include:

  • Indicators of efficacy in a specific disease.
  • Dosage ranges and schedules.

This ensures the patent covers both the compound itself and its therapeutic application, reinforcing its exclusivity.

3. Manufacturing Process Claims

The claims extend to methods of manufacturing of the compound or formulation, crucial for establishing a comprehensive patent estate. These claims define specific process steps, reagents, and conditions necessary to produce the compound efficiently and purify it.


Claims Analysis

Analyzing patent claims is critical for assessing the scope, robustness, and potential for patent challenges.

Key observations:

  • Independent Claims: They likely define the core chemical structure and composition. Broad claims may encompass various derivatives, ensuring wide coverage.
  • Dependent Claims: They narrow the scope by specifying particular substituents, dosage forms, or methods, enabling strategic defense against infringement or invalidation.
  • Claim Novelties & Inventive Step: The claims differentiate from prior art by unique substitution patterns, novel manufacturing methods, or specific therapeutic applications—elements that strengthen patent validity.

Legal strength considerations:

  • The inclusion of multiple claims covering different aspects (chemical, utility, process) provides layered protection.
  • Potential challenges from third parties could target the novelty or inventive step if similar compounds exist; however, the breadth of chemical claims appears designed to withstand such scrutiny.

Patent Landscape in Argentina and Regional Context

1. Patentability and Examination Standards

Argentina applies the Patents of Inventions Law aligned with the TRIPS agreement. Key criteria for patentability include novelty, inventive step, and industrial applicability. Patent AR072920 adheres to these with a focus on chemical and pharmaceutical innovations.

2. Patent Landscape Overview

Within the Argentine pharmaceutical patent landscape, there has been a strategic shift toward:

  • Incremental innovations in drug formulations.
  • Protection of chemical entities with therapeutic potential.
  • Increased filings related to biotechnological processes.

AR072920 fits within this emerging landscape, representing a patent that aims to carve out market exclusivity for a novel chemical entity, likely registered amidst a backdrop of existing patents covering similar therapeutic areas.

3. Patent Families and Regional Patent Strategies

Given the importance of regional patent protection, applicants often file patent families in South American countries, especially Brazil, Uruguay, and Chile, leveraging regional patent cooperation pathways. If AR072920 is part of such a family, it could extend its patent protection across multiple jurisdictions, providing a regional barrier to generic entrants.


Potential Challenges and Opportunities

Challenges:

  • Patent Obviousness: Competitors may challenge the patent if similar compounds exist in the prior art.
  • Patent Life and Maintenance: Ensuring timely payment of annuities to sustain protection.
  • Market Dynamics: Entry of generics or biosimilars post-patent expiry could impact commercial potential.

Opportunities:

  • Market Exclusivity: Patent AR072920 grants a period of market control, allowing recoupment of R&D investments.
  • Licensing and Partnerships: The patent estate can facilitate licensing agreements, especially in regional markets.
  • Strategic Positioning: Protecting a novel API positions the patent holder for future pipeline expansions.

Legal and Commercial Implications

The scope of safeguards provided by AR072920 influences drug development strategies, pricing, and competition within Argentina’s regulated pharmaceutical market. The patent’s breadth—combining composition, use, and process claims—can deter infringing generics and serve as leverage in patent litigation if challenged.

Furthermore, alignment with regional patent strategies enhances the commercial reach, integrating AR072920 into broader pharmaceutical protection and innovation frameworks.


Conclusion

Patent AR072920 embodies a comprehensive approach to patenting a novel pharmaceutical compound: broad chemical structure claims supported by therapeutic and manufacturing process claims. Its strategic positioning within Argentina’s evolving patent landscape exemplifies the country's shift towards enhanced IP protection for innovative medicines.

The patent's strength will depend on maintaining its validity against prior art challenges and effectively enforcing rights during its term. Its successful integration into the regional patent landscape further amplifies its commercial and strategic value.


Key Takeaways

  • Broad Chemical Coverage: AR072920’s claims span the core molecule, derivatives, and formulations, providing substantial protection against infringing compounds.
  • Utility and Process Claims: Inclusion of therapeutic and manufacturing claims widens scope and fortifies legal defensibility.
  • Regional Strategy: Extending protection via regional patent families amplifies commercial advantages across South America.
  • Infringement Risks: Competitors may target structural or use-based claims—vigilance in enforcement is critical.
  • Market implications: The patent supports exclusivity, enabling premium pricing and strategic licensing, but vigilance against challenges remains essential.

FAQs

1. What is the primary innovation protected by patent AR072920?
It covers a new chemical entity with specific structural features, as well as formulations and methods of manufacturing for therapeutic applications relevant to Argentina's healthcare needs.

2. How does the scope of this patent compare to other pharmaceutical patents in Argentina?
It aligns with typical chemical and formulation patents, but its broad claims and inclusion of multiple claim types make it a robust safeguard against generic competition.

3. What are the main risks to the patent's validity?
Risks include prior art that predates the invention, obviousness concerning similar compounds, or procedural issues during patent prosecution.

4. How can the patent landscape influence drug commercialization in Argentina?
A strong patent provides market exclusivity, incentivizing investment, but may also invite litigation or opposition that could limit market penetration if unsuccessful.

5. Can this patent be extended or renewed?
Yes, patents are typically valid for 20 years from the filing date, subject to annual renewal payments. Strategic extensions depend on adherence to regulatory and legal requirements.


References

  1. Argentine Patent Law (Law No. 24,481)
  2. Argentina Patent Examination Guidelines – INPI
  3. Regional patent protections and PCT strategies (World Intellectual Property Organization, 2022)
  4. Pharmaceutical patent landscapes in South America (Medicines Patent Pool, 2023)

Note: This analysis is based on publicly available patent information and standard patent practices. For proprietary details, consulting official patent documents and legal professionals is recommended.

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