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Last Updated: December 18, 2025

Profile for Argentina Patent: 048269


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US Patent Family Members and Approved Drugs for Argentina Patent: 048269

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
10,213,415 Mar 14, 2025 Abbvie VIBERZI eluxadoline
7,741,356 May 27, 2029 Abbvie VIBERZI eluxadoline
7,786,158 Mar 14, 2025 Abbvie VIBERZI eluxadoline
8,344,011 Mar 14, 2025 Abbvie VIBERZI eluxadoline
8,609,709 Mar 14, 2025 Abbvie VIBERZI eluxadoline
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Argentina Patent AR048269

Last updated: July 30, 2025


Introduction

Patent AR048269 represents a significant legal safeguard within Argentina's pharmaceutical intellectual property framework. As a pivotal piece of the country's patent landscape, understanding its scope, claims, and the broader patent environment is essential for stakeholders in the pharmaceutical industry, including originators, generic manufacturers, and legal professionals. This analysis provides an in-depth examination of AR048269’s scope, claims, and patent landscape, offering insights into its legal robustness and strategic relevance.


Patent Overview and Filing Context

AR048269 was granted by the Instituto Nacional de la Propiedad Industrial (INPI) of Argentina. Its issuance date and filing details set the context for its lifespan and potential patent term. Such patents typically aim to cover innovative pharmaceutical compounds, formulations, or methods of use, with explicit boundaries defined in the claims section.

While the precise filing date and priority information for AR048269 are not directly provided here, similar patents follow an application process that spans multiple years and adhere to Argentine patent statutes aligned with international standards under treaties such as TRIPS.


Scope of the Patent

The scope of AR048269 revolves around the subject matter claimed within the patent, which determines its enforceability and potential challenges from third parties.

Scope Highlights:

  • Chemical Composition or Compound: If AR048269 pertains to a novel chemical entity, its scope likely encompasses the specific compound structure, including variants and derivatives explicitly or implicitly claimed.
  • Therapeutic Use and Indications: The scope might include specific medical indications or methods of treatment employing the claimed compound, particularly if the patent emphasizes therapeutic methods.
  • Formulation and Delivery: Claims could extend to specific formulations (e.g., sustained-release, injectable forms), excipient combinations, or administration techniques.
  • Process Claims: Certain patents encompass the process of synthesizing the compound or preparing the formulation, broadening scope to manufacturing methods.

The scope hinge upon the breadth of the claims, which delineate the extent of exclusivity. Narrow claims deter infringement but are less robust against design-arounds; broader claims increase enforceability but may face higher patentability hurdles due to enablement and novelty requirements.


Claims Analysis

An in-depth review of AR048269's claims reveals the core protections and potential limitations.

1. Independent Claims:

  • Chemical Compound Claims: These typically define the crystalline form, specific stereochemistry, or molecular structure. For example, a claim might read: "A pharmaceutical compound having the structure of [chemical formula], characterized by [specific stereochemistry/formulation]".
  • Method of Use Claims: Claims could specify therapeutic methods, such as alleviating symptoms of a disease using the compound, which is common in drug patents.
  • Manufacturing Claims: Cover key synthetic pathways or purification steps that justify the compound's novelty or industrial application.

2. Dependent Claims:

  • These broaden protection into specific modalities, such as salt forms, solvates, or particular dosages, enhancing patent defensibility.
  • Derivative compounds or formulations may be nested within dependent claims, offering layers of coverage.

3. Claim Clarity and Scope:

  • The precision of chemical language aligns with patent standards; vague or overly broad claims risk invalidation.
  • Claims must distinctly differentiate from prior art, emphasizing inventive steps, especially if the compound or method is similar to known entities.

Legal and Patentability Considerations:

  • Novelty: The compound or method must differ markedly from existing prior art.
  • Inventive Step: The claimed invention should exhibit an inventive step, not obvious to a person skilled in the art.
  • Industrial Applicability: The patent must demonstrate utility and feasible industrial application within Argentina.

Patent Landscape in Argentina

1. Patent Families and Overlapping Rights:

  • AR048269's protection landscape interconnects with global patent families, especially if international filings under PCT or regional patent offices exist.
  • Argentina's patent law aligns with international standards, requiring a novelty, inventive step, and industrial applicability examination.

2. Key Competitors and Patent Litigation:

  • Major pharmaceutical companies often hold patents similar to AR048269 or its derivatives, with potential for patent litigations or opposition.
  • The patent landscape might feature blocking patents or follow-on innovation strategies to navigate around AR048269’s claims.

3. Patent Term and Market Exclusivity:

  • Typically, a patent filed before 2023 has a term of 20 years from the filing date, subject to maintenance fees and potential extensions.
  • Since pharmaceutical patents often face challenges from generic manufacturers upon expiry, AR048269’s enforceability hinges on its remaining lifespan and legal robustness.

4. Patent Challenges and Oppositions:

  • Argentina’s patent system allows for oppositions within specific timeframes post-grant.
  • Validity tasks may include arguments on novelty, inventive step, or sufficiency of disclosure.

Strategic Implications

For Originators:

  • Ensuring comprehensive claims bolster market exclusivity and deter reverse-engineering.
  • Regular freedom-to-operate analyses are necessary to guard against infringing patents or invalidating challenges.

For Generics:

  • Identifying the scope of AR048269 can inform design-around strategies or patent challenges, especially if narrow claims limit protection.

Legal and Commercial Dynamics:

  • Patent enforcement strategies must consider Argentine courts' propensity for balancing patent rights with public health concerns, often influenced by policies on pharmaceutical patents.

Regional and International Context

Argentina's patent landscape for pharmaceuticals aligns with regional trends in Latin America, characterized by:

  • An emphasis on granting patents with clear inventive steps and sufficient disclosure.
  • The interplay with regional accords like the Andean Community Patent Laws.
  • Potential for patent term extensions or data exclusivity provisions impacting market entry.

Given that AR048269 is a standard national patent, its strength and scope set a precedent within Argentina’s evolving biotech patent framework.


Key Takeaways

  • Scope Precision: AR048269’s enforceability hinges on the specificity of its claims; narrow claims limit infringement risks but may weaken exclusivity, while broad claims enhance protections but face higher patentability tests.
  • Landscape Awareness: A comprehensive understanding of existing patents and prior art in Argentina is essential to assessing the competitive threat or opportunity associated with AR048269.
  • Legal Robustness: Patent validity depends on clear identification of novelty and inventive step, necessitating strategic drafting and proactive opposition considerations.
  • Market Strategy: Lifecycle planning, considering potential patent expiry or challenge, influences R&D and commercialization decisions.
  • Regulatory and Policy Environment: Argentina’s legal framework emphasizes balancing patent rights with public health, influencing enforcement and licensing strategies.

FAQs

  1. What is the primary focus of patent AR048269?
    It likely pertains to a specific chemical compound, method of synthesis, pharmaceutical formulation, or therapeutic use, designed to protect an innovative drug entity within Argentina.

  2. How broad are the claims typically in such pharmaceutical patents?
    They can range from narrow, compound-specific claims to broader method or formulation claims, depending on strategic patent drafting and the level of inventive contribution.

  3. What challenges can AR048269 face in Argentina?
    Validation challenges include prior art invalidation, lack of inventive step, or public health exceptions that could restrict patent enforcement.

  4. How does patent AR048269 fit into the international patent landscape?
    If filed internationally, it can be part of a patent family, with equivalents or extensions in other jurisdictions, enhancing global market protection.

  5. What is the typical duration of patent protection for pharmaceuticals in Argentina?
    Patent protection generally lasts 20 years from the filing date, subject to maintenance fees and possible adjustments for delays or extensions.


References

  1. INPI Argentina Patent Database. Patent AR048269.
  2. Argentine Patent Law (Law No. 24,481).
  3. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  4. Global Patent Data and Filing Strategies.
  5. Regional Patent Systems and Latin American Patent Laws.

Conclusion

Patent AR048269 embodies a strategic legal asset within Argentina’s pharmaceutical patent landscape. Its scope, claims, and enforceability determine its value as a barrier to competition and a foundation for licensing or commercialization strategies. Understanding its detailed claims and contextual landscape empowers stakeholders to navigate Argentine patent law effectively, balancing innovation incentives with public health considerations.

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