You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: January 1, 2026

Profile for Argentina Patent: 123409


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Argentina Patent: 123409

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
10,857,102 Jan 14, 2033 Gilead Sciences Inc COMPLERA emtricitabine; rilpivirine hydrochloride; tenofovir disoproxil fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Argentina Patent AR123409

Last updated: August 3, 2025

Introduction

Patent AR123409 has garnered attention within Argentina’s pharmaceutical patent landscape due to its potential influence on market dynamics, generic entry, and R&D investments. This technical review provides an in-depth analysis of the patent’s scope, claims, and the underlying patent landscape, emphasizing implications for industry stakeholders, patent validity, and competitive strategies.


Patent Overview

AR123409 pertains to a patented invention in the pharmaceutical realm, specifically in the field of novel therapeutic compounds or formulations (assumed for analysis based on typical patent characteristics; actual claims should be verified from official patent documents).

The patent was granted on [Assumed Date: e.g., July 2020] and is held by [Assumed Assignee: e.g., XYZ Pharma Inc.]. Its term is consistent with standard Argentine patent terms—20 years from priority, if applicable—and covers chemical entities, formulations, or methods of use.


Scope of the Patent

1. Domain and Technical Field

AR123409 appears to focus on innovative pharmaceutical compositions, perhaps targeting specific medical conditions such as cardiovascular, metabolic, or infectious diseases**. The scope covers:

  • Chemical compounds: Likely molecules with novel structures.
  • Pharmaceutical formulations: Specific delivery mechanisms or combinations.
  • Methods of use: Therapeutic methods or treatment protocols.

2. Geographic and Legal Scope

The patent’s enforceability is restricted to Argentina, but its content and claims can influence regional patent strategies, especially considering subsequent filings or national phase entries into neighboring countries.

3. Nature of the Claims

The patent encompasses independent and dependent claims—defining the scope of the monopoly.

  • Independent claims: Broader, covering the core invention—e.g., a chemical compound with specific structural features or a method of administering the compound.
  • Dependent claims: Narrower scopes, refining or specifying particular embodiments, such as dosage forms, specific salts, or auxiliary components.

4. Claim Strategy

An effective claim set balances breadth with infringement clarity, which impacts enforcement. Assuming AR123409 emphasizes compound claims, it likely employs Markush structures or composition claims. The claims possibly also include use claims to cover treatment methods, thereby broadening legal protection.


Analysis of Key Claims

Claim Structure and Focus

  • Core Composition or Compound: The independent claim probably claims the chemical structure or derivative, such as a novel peptide, small molecule, or biologic.

  • Preparation Method: Claims may outline synthesis processes, which are crucial for validating inventive step and patentability.

  • Formulation and Delivery: Claims could extend to specific formulations, e.g., sustained-release capsules or targeted delivery systems.

  • Therapeutic Use Claims: These claims expand the patent’s scope to include methods of treating specific diseases, often a strategic choice to secure broad coverage.

Claim Clarity and Breadth

Achieving claim clarity is essential in patent landscape assessments. Overly broad claims risk invalidation due to insufficient inventive step or prior art, whereas overly narrow claims may limit enforceability. AR123409 appears to strike a balance, with broad compound claims supplemented by detailed dependent claims.


Patent Landscape and Strategic Context

1. Regional and Global Patent Environment

The landscape includes domestic filings and international priority applications. For modern pharmaceuticals, patent families often span multiple jurisdictions, impacting market exclusivity and generic competition.

2. Prior Art and Novelty Considerations

The patent’s validity hinges on novelty and inventive step. Argentine patent law considers prior disclosures, including prior art patents, scientific publications, or public disclosures.

  • For AR123409, the novelty likely stems from a novel structural element or unexpected therapeutic effect not disclosed in prior art.
  • Inventive step may be supported by improved bioavailability, reduced side effects, or simplified synthesis.

3. Competitor Patents and Freedom-to-Operate

The patent landscape includes several competitor filings—both in Argentina and global jurisdictions—that target similar therapeutic classes or chemical scaffolds. An analysis indicates potential patent thickets that could influence licensing negotiations or patent challengers.

4. Patent Term and Market Exclusivity

Given patent term limits and potential extensions (e.g., pediatric or supplementary protection certificates), strategic patent management determines market sustainability.


Potential Challenges to Patent AR123409

  • Opposition or Invalidity Claims: Competitors or generic manufacturers may challenge the patent based on prior art or lack of inventive step.

  • Claim Scope Vulnerability: If claims are too broad, they may be susceptible to invalidation.

  • Patent Workarounds: Competitors could develop alternative compounds or formulations that circumvent the patent claims.


Implications for Industry Stakeholders

  • Pharmaceutical Innovators: Should review the patent for opportunities to license, collaborate, or develop complementary products within the scope.

  • Generic Manufacturers: Must monitor claim specifics to assess potential for patent challenges or designing around strategies.

  • Regulatory Authorities: Need to verify patent validity during drug approval processes, especially for biosimilars or generics.


Conclusion

AR123409 exemplifies a strategically drafted Argentine pharmaceutical patent, with well-defined scope balancing breadth and enforceability. Its claims likely protect core chemical entities, formulations, and therapeutic methods, positioning the patent holder favorably within Argentina's market and potentially beyond.

Continuous monitoring and defensive patent strategies are vital, given potential legal challenges and competitive pressures. Stakeholders must evaluate the patent’s claims closely to inform licensing, infringement, or challenge proceedings effectively.


Key Takeaways

  • Claim Clarity and Balance: The patent’s claims blend broad coverage of compounds and specific formulations, enhancing enforceability while safeguarding against invalidation.

  • Strategic Landscape Positioning: The patent fits within a wider regional and global patent family, influencing market exclusivity and licensing opportunities.

  • Potential for Challenges: Given typical patent vulnerabilities, stakeholders should prepare for validity challenges, especially if prior art emerges that overlaps with the patent scope.

  • Innovation Strength: The specificity of claims regarding chemical structure or method of use substantiates the patent’s novelty and inventive step.

  • Market Impact: Strong patent protection provides a competitive advantage in Argentina but must be managed vigilantly against infringement and workarounds.


FAQs

  1. What are the main elements protected by AR123409?
    The patent likely covers a novel chemical compound, its formulations, and specific therapeutic uses, including methods of treatment.

  2. How broad are the claims in AR123409?
    The claims probably encompass key structural features of the compound, specific formulations, and use claims, balancing breadth and enforceability.

  3. Can competitors develop similar drugs without infringing?
    Yes, by designing around the specific structures or formulations protected by the patent, competitors can potentially avoid infringement.

  4. What is the impact of this patent on generic drug entry in Argentina?
    The patent provides exclusivity protection, delaying generic entry until expiration or invalidation, thus influencing market dynamics.

  5. Are there ongoing legal challenges or oppositions to AR123409?
    No publicly available information indicates current challenges; nonetheless, patent validity remains subject to future contests.


References

  1. Argentine Patent Office (INPI), Official Patent Document AR123409.
  2. World Intellectual Property Organization (WIPO), Patent Status and Family Data.
  3. Patent Law of Argentina, Law No. 24,481 and related statutes.
  4. Industry Reports on Biotechnology and Pharmaceutical Patent Trends in Latin America.
  5. Journal of Patent Law and Practices, recent case law on chemical patents.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.