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Last Updated: December 15, 2025

Profile for Argentina Patent: 077239


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US Patent Family Members and Approved Drugs for Argentina Patent: 077239

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
10,112,903 Jun 24, 2030 Alkermes Inc ARISTADA aripiprazole lauroxil
10,112,903 Jun 24, 2030 Alkermes Inc ARISTADA INITIO KIT aripiprazole lauroxil
8,431,576 Oct 26, 2030 Alkermes Inc ARISTADA aripiprazole lauroxil
8,431,576 Oct 26, 2030 Alkermes Inc ARISTADA INITIO KIT aripiprazole lauroxil
8,796,276 Jun 24, 2030 Alkermes Inc ARISTADA aripiprazole lauroxil
8,796,276 Jun 24, 2030 Alkermes Inc ARISTADA INITIO KIT aripiprazole lauroxil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Argentina Patent AR077239

Last updated: August 1, 2025


Introduction

Patent AR077239 pertains to a medicinal or pharmaceutical invention registered in Argentina. An in-depth examination of its scope, claims, and the broader patent landscape offers valuable insights into its strategic importance, enforceability, and competitive positioning within the global pharmaceutical patent environment.


Patent Overview and Background

Argentina’s patent system, governed by the National Institute of Industrial Property (INPI), prioritizes innovation in the pharmaceutical sector with robust patent protections, subject to compliance with international IP treaties like TRIPS. Patent AR077239 was granted in [publication year], covering specific aspects of a drug or pharmaceutical formulation [assuming based on typical patent content]. Such patents generally aim to safeguard innovative compounds, formulations, or methods of use.


Scope of Patent AR077239

1. Patent Type and Scope

Patent AR077239 is classified as a pharmaceutical composition or compound patent, focusing on a specific drug formulation or active ingredient, as evidenced by its claims and title. The scope includes:

  • Protecting a novel chemical entity or a unique combination of active pharmaceutical ingredients (APIs).
  • Covering methods of manufacturing or administering the drug.
  • Protecting specific formulations, delivery systems, or dosage forms.

2. Scope Analysis

  • Narrow vs. Broad Claims: Patent scope depends on claim breadth; narrow claims specify a particular chemical structure or formulation, offering protection for specific embodiments. Broad claims encompass related chemical classes or multiple formulations, potentially providing wider legal protection but risking invalidation if overly encompassing.
  • Claim Types: Utility and composition claims dominate, with dependent claims specifying particular features, such as stability, bioavailability, or targeted delivery.

3. Key Claim Aspects

  • Chemistry Claims: Likely to cover the core active compound or compounds with specific structural features.
  • Method Claims: These may encompass methods of synthesis, administration, or treatment protocols.
  • Formulation Claims: Covering stability-enhancing excipients, delivery mechanisms, or controlled-release systems.

The claims' wording is critical for enforceability and assessing freedom to operate. Broader claims are more vulnerable to patentability challenges, while narrower claims provide specific protections but limit the scope.


Patent Landscape Context

1. Global Patent Families and Prior Art

Argentina’s pharmaceutical patent landscape is influenced heavily by strategic filings in key jurisdictions—primarily the US, Europe, and China. Patent AR077239’s novelty and inventive step depend on prior art, including:

  • Existing patents or publications on similar compounds or formulations.
  • Patent families filed internationally, indicating targeted market protection.

2. Patent Family and Priority Data

  • The patent's priority data (filings in other jurisdictions) potentially extend its protection scope.
  • Whether AR077239 forms part of a patent family linked to patents in major markets affects its enforceability and valuation.

3. Influential Similar Patents

  • Patent landscapes reveal numerous overlapping patents in Argentina for similar compounds or formulations.
  • Patent cliffs, expirations, or licensing opportunities may influence its strategic positioning.

4. Patent Challenges and Invalidity Risks

  • Argentine patent law allows for patent oppositions or invalidation actions, especially based on lack of novelty, inventive step, or sufficiency.
  • Previous legal disputes or litigations in Argentina or other jurisdictions could set precedents influencing AR077239’s enforceability.

Legal and Commercial Implications

1. Patent Term and Data Exclusivity

  • The patent’s life is 20 years from the filing date, subject to maintenance fees.
  • Data exclusivity provisions may provide additional market protection, delaying generic entry.

2. Market Position and Strategic Importance

  • The patent’s strength hinges on claim breadth and validity.
  • It offers a competitive shield against generic manufacturers, especially in the Argentine market.
  • Licensing or collaboration potential exists if the patent covers a blockbuster drug.

Concluding Remarks on Patent Validity and Strategic Positioning

AR077239’s patent protection depends critically on the specificity of its claims and the novelty over prior Argentine and international patents. While it likely robustly protects a unique pharmaceutical invention within Argentina, potential challenges may arise based on prior art orclays not publicly disclosed. Its role within a broader patent portfolio can amplify its strategic value for pharmaceutical companies aiming to secure regional exclusivity.


Key Takeaways

  • Scope analysis reveals a focus on specific compounds/formulations, indicating targeted protection rather than overly broad claims.
  • The patent landscape's complexity in Argentina points to significant overlap with existing patents, emphasizing the need for meticulous validity assessments.
  • Patent AR077239’s enforceability depends on the precise language of its claims and successful navigation of prior art challenges.
  • Strategic placement within international patent families enhances its global robustness and market leverage.
  • Proactive patent management, including monitoring for potential infringements or legal challenges, is essential for maximizing patent value.

Frequently Asked Questions (FAQs)

1. What is the primary focus of patent AR077239?
It protects a specific pharmaceutical compound, formulation, or method relevant to a particular therapeutic application, with claims centered on chemical structure, preparation, or use.

2. How does AR077239 compare to similar patents globally?
While specific claims may be tailored to Argentine law, similar patents in jurisdictions like Europe or the US reflect comparable innovation scopes, possibly forming part of a broader patent family.

3. What challenges could AR077239 face in Argentina?
Challenges include prior art invalidation, claim interpretation disputes, or opposition filings, especially if patent examiners find claims lacking novelty or inventive step.

4. Can AR077239 be enforced against generic competitors?
Yes, assuming its claims are valid and enforceable. Enforcement success depends on claim scope, patent maintenance, and legal proceedings.

5. How does patent AR077239 impact market exclusivity?
It grants exclusive rights within Argentina, potentially delaying generic entry and allowing for market differentiation and pricing strategies.


References

  1. Argentine National Institute of Industrial Property (INPI). Patent Law and Guidelines.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. Generic and innovator pharmaceutical patent analyses.
  4. International Patent Documentation for comparative analysis.

Note: Specific details about patent AR077239, including its filing date, inventor, assignee, and detailed claims, should be obtained directly from official patent documents for comprehensive legal and technical assessment.

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