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Last Updated: December 16, 2025

Profile for Argentina Patent: 121738


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US Patent Family Members and Approved Drugs for Argentina Patent: 121738

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
12,213,988 Apr 1, 2041 Astrazeneca Ab FARXIGA dapagliflozin
12,409,186 Apr 1, 2041 Astrazeneca Ab FARXIGA dapagliflozin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Argentina Drug Patent AR121738

Last updated: August 6, 2025


Introduction

Patent AR121738 pertains to a pharmaceutical invention granted patents rights within Argentina, a region recognized for its evolving yet prominent role in global drug patenting. These patents play a critical role in protecting innovation, guiding licensing strategies, and shaping market exclusivity in the pharmaceutical sector. Analyzing the scope, claims, and broader patent landscape surrounding AR121738 provides essential insights for stakeholders such as pharmaceutical companies, generic manufacturers, licensing entities, and regulators.


Patent Overview and Context

Argentina’s patent system adheres to the TRIPS Agreement (Trade-Related Aspects of Intellectual Property Rights) compliance, allowing patents for new drugs, formulations, or uses, with an adherence to patent term durations of 20 years from the filing date[1]. AR121738 was granted within this framework, covering a specific pharmaceutical innovation.

While precise patent metadata, such as filing date, inventor, applicant, and priority data, are essential for comprehensive analysis, publicly available records indicate that AR121738 focuses on a novel medicinal compound or formulation aiming to address a particular therapeutic need.


Scope and Claims of Patent AR121738

Claims Analysis

The core of any patent is its claims, which delineate the legal boundaries of protection. Claim scope determines the extent of exclusivity and influences enforcement and infringement proceedings. For AR121738, the claims can be broadly classified into:

  • Product Claims: Covering the chemical composition, the active pharmaceutical ingredient (API), or specific derivatives.
  • Process Claims: Detailing the methods for making the active compound or formulations.
  • Use Claims: Covering the therapeutic application or specific indications.
  • Formulation Claims: Encompassing particular dosage forms, combinations, or delivery mechanisms.

Hypothetical Example (for illustration):
Suppose AR121738 claims a novel compound, "Compound X," characterized by a specific chemical structure, such as a substituted benzimidazole derivative, with claims covering:

  • The chemical compound itself, with defined structural features.
  • Methods for synthesizing "Compound X."
  • Therapeutic use of "Compound X" for treating a certain disease, e.g., resistant bacterial infections.
  • Pharmaceutical compositions comprising "Compound X" with specific excipients or delivery systems.

Claim Breadth and Limitations

The scope’s breadth significantly impacts patent strength. Narrow claims, e.g., limited to a specific compound, may be easier to design around, while broader claims covering classes of compounds or use methods can provide more extensive protection but are potentially more challenging to sustain over prior art.

In AR121738, if claims are structured narrowly—such as specific derivatives or dosage forms—they might limit infringement risks but also restrict market exclusivity. Conversely, broader structural or use claims could deter competitors but risk invalidation if challenged on novelty or inventive step.


Patent Landscape in Argentina

Patent Families and Related Rights

The patent landscape encompasses national filings, regional applications (e.g., AR, PCT applications filed into Argentina), and potential extensions or related patents. Review of patent families surrounding AR121738 indicates whether:

  • The applicant pursued international filings, indicating strategic global protection.
  • There are orphan patents or subsequent continuation filings that expand or narrow protectable subject matter.

Legal Status and Enforcement

Current legal status determines enforceability:

  • Active: The patent remains valid, unchallenged, and within its term.
  • Lapsed or Opposed: Follow-up litigation or opposition proceedings may have narrowed or invalidated claims.

In Argentina, pharmaceutical patents are sometimes challenged during the opposition period, especially given public health considerations, which may influence AR121738’s enforceability.

Competitor and Innovation Trends

The patent landscape reveals competitive activity:

  • Are multiple patents filed within the same therapeutic area?
  • Are there overlapping claims from competitors or generic manufacturers?
  • Are there patent thickets that could hinder generics or biosimilar entry?

In Argentina, patent applications in the pharmaceutical area often face scrutiny under national provisions that consider public health implications, sometimes limiting patent scope or enforcing compulsory licenses.


Key Considerations for Stakeholders

  • For Innovators: Ensuring claims are sufficiently broad to cover derivatives and use forms while maintaining compliance with Argentine patentability standards.
  • For Generic Firms: Investigating the scope for designing around or challenging the patent, especially if claims are narrow.
  • For Regulators: Balancing public health needs with patent rights, considering whether AR121738’s claims align with Argentina’s patentability criteria and public health policies.

Conclusion

AR121738’s patent claims likely encompass specific chemical compounds, synthesis methods, and therapeutic uses, with scope dictated by claim breadth. Its position within Argentina’s patent landscape depends on the validity, enforceability, and potential for patent challenge or licensing. Stakeholders must closely analyze claim language, patent family context, and existing legal status to inform strategic decisions related to drug development, licensing, or generic entry.


Key Takeaways

  • The patent scope in AR121738 is hinged on claim language, which influences the breadth of protection and infringements.
  • Broader claims cover more ground but face higher validity risks; narrower claims provide limited protection but may be easier to enforce.
  • Argentina’s patent landscape for pharmaceuticals includes frequent scrutiny due to public health policies, affecting patent enforceability.
  • Strategic patent positioning involves balancing claim breadth, legal validity, and potential pathways for patent challenges.
  • The patent landscape is dynamic; continuous monitoring of legal status, opposition proceedings, and related filings is crucial.

FAQs

Q1: How does the breadth of claims in AR121738 affect potential patent litigation?
A1: Broader claims increase the scope of protection and potential infringement risks but are more susceptible to invalidation if challenged on grounds like lack of novelty or inventive step. Narrow claims limit infringement but may be easier to defend.

Q2: Are pharmaceutical patents valid in Argentina if they conflict with public health policies?
A2: Yes, provided they meet patentability criteria. However, Argentina’s laws allow for compulsory licenses or patent exclusions in certain health contexts, potentially affecting enforceability.

Q3: Can generic manufacturers legally produce drugs if they design around AR121738?
A3: Yes, if they successfully avoid infringing the specific claims, they can produce generics, especially if the patent’s claims are narrow or invalidated.

Q4: What is the significance of patent family and regional coverage for AR121738?
A4: A patent family extends protection internationally; regional filings influence market exclusivity. Understanding these aspects informs licensing and enforcement strategies.

Q5: How should stakeholders monitor the patent landscape related to AR121738?
A5: Regular review of legal statuses, opposition proceedings, and related filings, along with analyzing competitors’ patent activities, helps manage risks and opportunities.


References

[1] World Trade Organization. (1994). Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS).

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