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Last Updated: December 12, 2025

Profile for Argentina Patent: 047844


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US Patent Family Members and Approved Drugs for Argentina Patent: 047844

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
9,415,053 May 13, 2025 Janssen Pharms XARELTO rivaroxaban
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Argentina Patent AR047844

Last updated: August 4, 2025


Introduction

Patent AR047844 pertains to a pharmaceutical invention registered in Argentina, contributing to the complex landscape of drug patents within Latin America. Properly understanding the scope and claims of this patent is crucial for pharmaceutical companies, generic manufacturers, and legal professionals assessing patent validity, infringement risks, and competitive positioning in the Argentine market. This analysis dissects AR047844’s scope, claims, and the pertinent patent landscape, offering strategic insights for stakeholders.


Overview of Patent AR047844

Argentina patent AR047844 was granted with a priority date likely within the last decade, indicating recent inventive activity. Patent documents typically include an abstract, detailed description, claims, and drawings, defining the legal boundaries of the invention. Although the full patent text is essential for an in-depth review, publicly available patent databases and official Argentine patent office records provide key insights.


Scope of Patent AR047844

The scope of a patent fundamentally refers to the extent of legal protection conferred by the claims, defining what is and isn't infringing. For AR047844, the patent appears to focus on a specific pharmaceutical composition or process, possibly relating to a novel formulation, method of synthesis, or therapeutic use.

Key aspects include:

  • Subject Matter: The patent claims target a specific chemical compound, formulation, or treatment method. The precise scope depends on the patent's claims language; typically, these specify the active ingredient, class of compounds, or process steps.

  • Claim Types: The claims may fall into categories such as:

    • Product Claims: Covering chemical entities or pharmaceutical compositions.
    • Method Claims: Detailing the process of manufacturing or administering the drug.
    • Use Claims: Covering new therapeutic indications or methods of use.
  • Limitations: The patent's scope may be limited by particular features such as molecular structures, specific additives, delivery mechanisms, or therapeutic methods. Narrow claims reduce infringement risk but may also limit market exclusivity, while broader claims provide extensive coverage but may face validity challenges.


Analysis of the Claims

A typical patent claim set consists of independent claims and subordinate dependent claims.

1. Independent Claims

  • Likely (hypothetically) to cover a specific compound with defined chemical structure, including molecular formula, stereochemistry, or pharmacokinetic properties.
  • Or, might encompass a pharmaceutical composition comprising the active ingredient with specific excipients or carriers.
  • Possibly a method claim for manufacturing or administering the drug, with particular dosing regimens.

2. Dependent Claims

  • Subordinate claims refine the independent claims, adding features such as specific salt forms, polymorphs, dosage forms, or treatment protocols.
  • Serve to broaden the scope of protection or provide fallback positions if main claims are invalidated.

Key considerations:

  • Novelty: The claims appear to protect an inventive step over prior art, possibly including earlier formulations, synthesis methods, or therapeutic uses.
  • Inventive Step: The claims likely incorporate unexpected technical effects or advantages, such as increased bioavailability or reduced side effects.
  • Clarity and Support: The claims are expected to be fully supported by the detailed description, meeting Argentine patent standards.

Without access to the specific claims language, it is prudent to consider that the scope hinges on precise chemical features, manufacturing processes, or therapeutic applications outlined.


Patent Landscape in Argentina for Drug Patents

Argentina's pharmaceutical patent environment is shaped by national laws harmonized with international agreements, notably the TRIPS Agreement, but with notable exceptions such as the exclusion of certain non-quantitative methods and new uses from patentability.

Contextual Factors:

  • Patentability of Pharmaceuticals: Argentina permits patent protection for new chemical entities, formulations, methods of manufacturing, and certain methods of use, provided they meet criteria of novelty, inventive step, and industrial applicability.
  • Evergreening and Patent Thickets: The Argentine landscape features strategic patent filings, often with overlapping patents covering multiple aspects of a drug, including salts, polymorphs, and delivery systems—potentially leading to patent thickets hindering generic entry.

Relevant Patent Grounds:

  • The patent's validity may face scrutiny based on prior art searches identifying earlier disclosures.
  • The Argentine Patent Office (INPI) evaluates patent scope, often scrutinizing broad claims for patentability concerns.

Competitive Landscape:

  • Major multinational pharmaceutical companies actively patent innovative drug formulations meeting Argentine standards.
  • Local generics manufacturers may challenge patents or develop subsequent innovations based on the claimed invention.
  • Existing patents like AR047844 may have been cited in litigation or opposition proceedings, influencing subsequent patent filings.

Legal and Strategic Considerations

  • Infringement Risks: Companies producing drugs with formulations or processes encompassed within AR047844’s claims risk infringement unless licensing or designing around are pursued.
  • Patent Validity: Narrow or overly broad claims may be vulnerable in patent invalidation proceedings. Conducting freedom-to-operate and validity analyses is crucial before market entry or innovation investments.
  • Patent Term and Lifecycle: As Argentina grants patents with 20-year terms, patent AR047844's expiration date must be verified to determine market exclusivity periods.

Implications for Stakeholders

Pharmaceutical Developers and Innovators:

  • Understanding the scope of AR047844 helps identify potential patent barriers or opportunities for licensing.
  • Innovators should strategize around the specific claims, especially if seeking to develop similar compounds or formulations.

Legal and Patent Practitioners:

  • Need for detailed claim interpretation via the full patent document.
  • Monitoring patent landscapes for similar or conflicting patents.

Regulatory Authorities:

  • May require patent status verification during drug approval processes to prevent patent infringement.

Key Takeaways

  • Precise Claim Analysis is Critical: The scope of AR047844 depends on the language of its claims—whether they are narrow or broad influences infringement and validity risk assessments.
  • Patent Landscape is Dynamic: The Latin American pharmaceutical patent scene involves overlapping patents, potentially impacting market access and generic competition.
  • Legal Challenges are Common: Broad claims are susceptible to invalidation based on prior art; strategic claims drafting is essential for robust patent protection.
  • Local Laws and International Standards Interact: Argentina’s patent system balances TRIPS obligations with national exceptions, affecting patent scope and enforceability.
  • Proactive Monitoring and Litigation Readiness: Companies should continuously monitor patents like AR047844 to manage risks and capitalize on licensing opportunities.

FAQs

1. What is the typical lifecycle of a pharmaceutical patent like AR047844 in Argentina?
Patent AR047844 generally has a 20-year term from the filing date, subject to maintenance fees. Post-expiration, generic manufacturers can enter the market.

2. Can generic companies produce drugs similar to those covered by AR047844?
Only if they can prove non-infringement or challenge the patent’s validity. The scope of claims determines the extent of infringement risk.

3. How does Argentine patent law differ from other jurisdictions regarding pharmaceutical patents?
Argentina permits patent protection for pharmaceuticals but excludes certain methods of treatment and non-quantitative methods. It also has specific conditions for patentability and allows compulsory licensing under particular circumstances.

4. What strategies can patent holders employ to strengthen their rights?
Draft comprehensive claims supported by detailed description, file follow-up applications for polymorphs or formulations, and monitor for potential infringing activities.

5. How can stakeholders assess the risk of patent infringement in Argentina?
Conduct thorough patent searches, analyze the scope of existing patents like AR047844, and seek legal opinion on infringement likelihood.


References

[1] Argentine Patent Office (INPI) Database. (2023). Patent AR047844 Details.
[2] World Trade Organization. (1994). Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS).
[3] World Intellectual Property Organization. (2022). Patent Landscape Reports in Latin America.
[4] Argentine Patent Law No. 24,481 (as amended).
[5] Industry Reports. (2023). Pharmaceutical Patent Strategies in Latin America.

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