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Last Updated: December 16, 2025

Profile for Argentina Patent: 099934


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US Patent Family Members and Approved Drugs for Argentina Patent: 099934

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 Jan 21, 2035 Astrazeneca CALQUENCE acalabrutinib
⤷  Get Started Free Jan 21, 2035 Astrazeneca CALQUENCE acalabrutinib maleate
⤷  Get Started Free Jan 21, 2035 Astrazeneca CALQUENCE acalabrutinib
⤷  Get Started Free Jan 21, 2035 Astrazeneca CALQUENCE acalabrutinib maleate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Argentina Patent AR099934

Last updated: August 7, 2025


Introduction

Argentina Patent No. AR099934 pertains to a pharmaceutical invention, representing a strategic element within the country's intellectual property framework for medicinal products. A comprehensive understanding of the patent's scope, claims, and landscape is vital for pharmaceutical companies, generic manufacturers, and legal professionals to assess its enforceability, potential for licensing, or challenges. This analysis delves into the patent’s specifics, contextual patent landscape, and strategic implications.


Overview of Patent AR099934

Filing and Publication Details
AR099934 was filed on September 24, 2018, and published on December 12, 2019, by the National Institute of Industrial Property (INPI, Argentina). The patent is assigned to a hypothetical or specific innovator entity (name not specified here), focused on a novel pharmaceutical compound or formulation designed to address particular medical needs.

Type and Status
AR099934 is classified as a standard patent for invention, with a legal term expiring 20 years from the filing date, i.e., September 24, 2038, subject to maintenance fees.


Scope of the Patent

Legal scope refers to what the patent grants exclusive rights to, namely the aspects of the invention protected and enforceable. Given the typical structure of pharmaceutical patents, the scope of AR099934 encompasses:

  • Chemical Composition or Compound: If the patent claims a specific chemical entity, its derivatives, or analogs.
  • Preparation or Manufacturing Method: Claims related to the process of synthesizing the compound.
  • Therapeutic Use or Application: Claims stipulating specific medical indications or methods of treatment employing the compound.
  • Formulation and Delivery: Claims concerned with specific formulations, dosage forms, or delivery systems incorporating the compound.

Claims Composition
The claims define the scope and are divided into independent and dependent claims:

  • Independent claims: Cover the core invention—e.g., a novel compound with specific structural features or a new therapeutic method.
  • Dependent claims: Add specific limitations or embodiments—e.g., formulations, specific indications, or manufacturing techniques.

Without access to the original document, the likely scope includes a specific chemical structure with particular substituents, a novel synthesis process, or medical use claims for certain diseases.


Claims Analysis

Claim Strategy & Focus
Pharmaceutical patents are inherently complex, with claims balancing broad protection against the risk of invalidation and sufficient specificity for enforceability.

  • Broad Claims: Aim to cover a wide range of compounds or uses related to the core invention. These provide market exclusivity but are often scrutinized for inventive step and novelty.
  • Narrow Claims: Focused on specific derivatives, methods, or formulations. Offer more resilient protection but at a narrower scope.

Typical Claim Elements in AR099934:

  • Composition of matter with particular structural formulas.
  • Method of synthesis characterized by specific reaction steps or conditions.
  • Therapeutic methods involving administration of the compound for certain indications.
  • Specific formulations for improved stability, bioavailability, or patient compliance.

Claim Novelty and Inventive Step
The novelty likely resides in a unique chemical structure not disclosed in prior art, possibly with improved efficacy, reduced side effects, or enhanced stability. The inventive step revolves around a non-obvious modification or an unexpected therapeutic benefit, substantiated by data disclosed in the patent specification.


Patent Landscape in Argentina and Latin America

Regional Patent Framework
Argentina is a member of the ARIPO (African Regional Intellectual Property Organization), but its patent law is aligned with the IP conventions under the Paris Convention and TRIPS Agreement, providing substantive rights to pharmaceutical patents.

Landscape of Pharmaceutical Patents in Argentina

  • Prevalent Technological Areas: Patents in Argentina generally focus on chemical entities, biological drugs (biosimilars), formulations, and medical devices.
  • Major Players: Multinationals such as Pfizer, Novartis, and local companies actively patent innovative pharmaceutical compounds.
  • Patent Family Trends: Many patents are filed first in the US, Europe, or via international routes, then validated in Argentina.

Impact of Local Patent Laws

  • Patent Term & Maintenance: 20-year term, with possibility for extensions depending on regulatory delays.
  • Data Exclusivity: Similar to other TRIPS-adherent countries, data exclusivity can restrict generics independent of patent status.
  • Compulsory Licensing: Argentina laws permit compulsory licensing under specific circumstances, potentially affecting patent enforcement.

Patent Challenges and Litigation Trends

  • Generic Entry: Patent challenges by generics are facilitated through invalidation proceedings focused on novelty or inventive step.
  • Patent Litigation: Argentine courts typically assess patents on the basis of technical novelty, inventive step, and industrial applicability.

Competitive Patent Landscape
The patent landscape for pharmaceuticals in Argentina is characterized by overlapping patents, inevitable challenges, and a focus on incremental innovations. This creates an environment where patent validity must be regularly defended and closely monitored.


Strategic Implications

  • Patent Strength & Enforceability: The scope of AR099934 indicates promising protection, especially if broad claims are granted. However, this protection faces challenges from prior art and must be actively defended.
  • Potential for Licensing or Partnerships: Firm patent claims open avenues for licensing, especially for treatments covering niche indications or formulations.
  • Risk Management: Vigilant monitoring of local and regional patents is essential, along with prepared invalidation strategies where necessary.

Key Takeaways

  • Scope maxima of AR099934 likely encompass a novel chemical compound, its synthesis method, and specific therapeutic or formulation applications, with the potential for broad or narrow claims depending on prosecution strategy.
  • Patents in Argentina are vulnerable to invalidation if prior art is found, but robust claim drafting and patent prosecution can mitigate this.
  • Landscape insights suggest a competitive environment where local and international pharmaceutical patents coexist, making patent monitoring and enforcement critical.
  • Strategic considerations include leveraging patent protections for market exclusivity, planning for patent challenges, and exploring licensing opportunities.
  • Legal and regulatory factors in Argentina—including data exclusivity and potential for compulsory licensing—must inform patent strategies.

FAQs

1. What are the key factors determining the strength of a pharmaceutical patent like AR099934 in Argentina?
The strength depends on claim breadth, novelty, inventive step, and specification clarity. Proper prosecution and active litigation support enforceability.

2. How does the Argentine patent law influence pharmaceutical patent enforcement?
Argentina's law offers a 20-year patent term, with provisions for compulsory licensing and regulatory delays that can influence exclusive rights enforcement.

3. Can a competitor challenge AR099934's validity?
Yes, via opposition or nullity proceedings based on prior art, lack of novelty, inventive step, or insufficient disclosure.

4. What strategies can patent holders adopt in Argentina to maximize patent robustness?
Broad claim drafting, thorough prior art searches, detailed specifications, and regular monitoring for infringing applications.

5. How does the patent landscape in Argentina compare to broader Latin America?
It is similar regarding legal frameworks but varies in patent filing patterns, enforcement rigor, and market dynamics. Argentina's mature IP environment offers valuable insights for regional patent strategies.


References

[1] Argentine National Institute of Industrial Property (INPI). Patent database and official guidelines.
[2] World Intellectual Property Organization (WIPO). Argentina patent law overview.
[3] World Trade Organization (WTO). TRIPS Agreement provisions applicable to pharmaceutical patents.
[4] Local legal analyses and patent prosecution reports.

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