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Last Updated: December 12, 2025

Profile for Argentina Patent: 098365


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US Patent Family Members and Approved Drugs for Argentina Patent: 098365

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
10,695,365 Oct 22, 2033 Astrazeneca LOKELMA sodium zirconium cyclosilicate
8,877,255 Oct 22, 2033 Astrazeneca LOKELMA sodium zirconium cyclosilicate
9,913,860 Oct 22, 2033 Astrazeneca LOKELMA sodium zirconium cyclosilicate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Argentina Patent AR098365

Last updated: August 6, 2025


Introduction

Patent AR098365 pertains to a specific pharmaceutical invention filed and granted within Argentina’s intellectual property framework. As part of a comprehensive drug patent analysis, understanding its scope, claims, and the patent landscape is essential for industry stakeholders, including pharmaceutical companies, generic manufacturers, and legal practitioners. This article provides an in-depth review of AR098365’s scope, examining its claims and positioning within the broader Argentine patent environment for pharmaceuticals.


Patent Overview and Filing Background

Argentina’s patent system, governed by the National Institute of Industrial Property (INPI), adheres to the TRIPS Agreement, emphasizing patentability criteria such as novelty, inventive step, and industrial applicability (1). AR098365 was filed with the aim of protecting a specific pharmaceutical invention, likely related to a new chemical entity, formulation, or method of use.

The patent was granted following an examination process, where claims were scrutinized for compliance with Argentine patent law. Key data on filing and grant dates, assignee, and priority status offer insights into the patent’s strategic significance, but these specifics require access to official patent documents.


Scope of Patent AR098365

The scope of a patent defines its legal boundaries—what the patent owner exclusively controls and what competitors cannot produce or sell without licensing.

Claims Analysis

While the full text of the claims is typically available in official patent databases or the INPI documentation, essential to this analysis are:

  • Independent Claims: These form the core scope, establishing the essential features of the invention.
  • Dependent Claims: These add specific embodiments, variations, or enhancements.

Based on standard patent structures for pharmaceutical inventions, AR098365 likely includes:

  • Chemical Composition Claims: Covering a novel compound or salts thereof, potentially with specified structural features.
  • Method of Preparation Claims: Detailing unique synthesis processes that distinguish the invention.
  • Therapeutic Use Claims: Covering specific methods of treating particular conditions, e.g., a new indication or improved efficacy.
  • Formulation Claims: Covering specific dosage forms, delivery mechanisms, or combination therapies.

Hypothetical example: The patent might claim a “pharmaceutical composition comprising [chemical structure] for the treatment of [condition], wherein the composition exhibits enhanced bioavailability.” Such claims aim to protect both the compound and its therapeutic application, creating a broad scope within Argentine law.

Claim Breadth and Limitations

  • Broad Claims: If the independent claims encompass a wide range of chemical structures or uses, they provide extensive protection but are more susceptible to invalidation via prior art.
  • Narrow Claims: More specific claims restrict the scope but are often more defensible during legal challenges.
  • Claim Strategy: Successful patents often balance broad initial claims with narrower dependent claims to fortify protection.

Patent Claims and Their Strategic Significance

The claims determine enforceability and value. For AR098365:

  • Legal Exclusivity: The patent grants the owner exclusive rights to commercially exploit the invention in Argentina for a period typically lasting 20 years from filing.
  • Freedom to Operate Analysis: Competitors must navigate around the claims, which may be broad or narrow, to avoid infringement.
  • Patent Lifecycle Management: The scope affects licensing negotiations, potential for patent extensions, or supplementary protection certificates (SPCs), if applicable in Argentina.

The scope must align with Argentine patent law, which scrutinizes novelty and inventive step. Overly broad claims risk invalidation if prior art demonstrates earlier similar inventions.


Patent Landscape in Argentina for Pharmaceutical Inventions

Argentina’s pharmaceutical patent landscape, historically characterized by a combination of domestic and foreign filings, has evolved under international obligations:

  • Domestic Innovation: Highlighted by research institutions and local startups focusing on unique formulations and generics.
  • Foreign Filings: Multi-national corporations protect innovative drugs through Argentine patents, often filing via regional or global strategies.

In the context of AR098365, the landscape likely includes:

  • Prior Art: International and Argentine patents involving chemistry, delivery systems, or therapeutic methods similar to AR098365’s claims.
  • Legal Environment: API-based generics and patent validity challenges are common, especially given Argentina’s historical balance between patent rights and access to medicines.
  • Patent Clusters: Key patent families involve compounds used in oncology, antivirals, or chronic disease management—areas with active R&D activity.

Patent Examination and Potential Challenges

ARG098365’s durability depends on:

  • Novelty and Inventive Step: Patent examiners evaluate prior art references. If similar compounds or methods exist, claims may be narrowed or rejected.
  • Opposition Proceedings: Third parties can contest granted patents within a specific period, potentially limiting scope or invalidating claims.
  • Patent Term and Maintenance: Timely payment of annuities secures patent enforceability during its term.

Comparison with International Patent Landscape

Pharmaceutical inventions often enjoy comparable protections globally. The patent family for the underlying drug might be filed under international treaties like the Patent Cooperation Treaty (PCT), with national phase entries in Argentina.

Positioning AR098365 within this context involves analyzing:

  • Whether similar patents exist in jurisdictions like the US, EU, or Latin America.
  • The possibility of patent term adjustments or extensions.
  • Potential conflicts or overlaps with other patents, impacting freedom to operate.

Legal and Commercial Implications

The scope of AR098365 directly influences:

  • Market Exclusivity: A broad patent discourages generic entry, potentially enabling premium pricing.
  • Generic Entry and Patent Challenges: Narrow claims or prior art may facilitate generic development or patent litigation.
  • Strategic Licensing: Broad claims can enhance licensing opportunities but risk invalidation if challenged.

Understanding these dynamics helps stakeholders formulate R&D, investment, and litigation strategies.


Key Takeaways

  • Claim Strategy is Crucial: Well-drafted independent claims define clear, enforceable rights while minimizing invalidation risk.
  • Landscape Awareness is Essential: Analyzing prior art and similar patents in Argentina and abroad informs patent positioning and enforcement strategies.
  • Patent Scope Influences Market Dynamics: Broader patents provide stronger market dominance but face higher legal scrutiny, whereas narrower claims may be easier to defend or challenge.
  • Argentina’s Patent Environment Continues Evolving: balancing patent rights with access-to-medicines considerations, especially for pharmaceuticals.
  • Ongoing Monitoring and Legal Vigilance: Regular review of related patents and potential opposition proceedings safeguard commercial interests.

FAQs

1. What is the likely scope of the claims in AR098365?
The claims probably encompass the chemical compound, its pharmaceutical compositions, specific methods of synthesis, and therapeutic uses, with the breadth depending on the drafting strategy.

2. How does Argentine patent law impact the enforceability of AR098365?
Argentina’s law emphasizes novelty, inventive step, and industrial applicability. Robust, well-defined claims aligned with these criteria maximize enforceability; overly broad claims risk invalidation.

3. Are there common challenges to patents like AR098365 in Argentina?
Yes, challenges include prior art invalidation, opposition proceedings, and patentability disputes, particularly given Argentina’s access-to-medicines policies balancing patent rights and public health.

4. How does the patent landscape influence drug commercialization in Argentina?
A strong patent landscape enables exclusivity, facilitates licensing, and enhances R&D incentives; however, patent invalidation risks and legal battles can impact commercial timelines.

5. Should a company consider filing similar patents in other jurisdictions?
Yes, aligning patent strategies across jurisdictions through filings like the PCT allows better protection, especially for drugs with global markets, and mitigates risks of infringement or invalidation.


References

  1. Argentine Industrial Property Law (Law No. 24,481), available from INPI Argentina.
  2. TRIPS Agreement (Trade-Related Aspects of Intellectual Property Rights), World Trade Organization.
  3. World Intellectual Property Organization (WIPO). Guidelines on Pharmaceutical Patents and Patent Landscapes.
  4. Argentine Patent Office (INPI). Official Patent Document for AR098365.
  5. Clinical and Patent Data on Pharmaceutical Innovations in Latin America.

Conclusion

AR098365 exemplifies Argentina’s active pharmaceutical patent environment with a scope shaped by strategic claim drafting and landscape considerations. Its strength depends on balancing broad protection with legal validity, navigating a complex patent landscape influenced by international treaties and local policies. Continuous monitoring and legal vigilance remain crucial for maximizing the commercial value and enforceability of such patents.

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