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Last Updated: December 16, 2025

Profile for Argentina Patent: 097237


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US Patent Family Members and Approved Drugs for Argentina Patent: 097237

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
⤷  Get Started Free Aug 1, 2034 Bristol Myers Squibb IDHIFA enasidenib mesylate
⤷  Get Started Free Aug 1, 2034 Bristol Myers Squibb IDHIFA enasidenib mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Argentina Patent AR097237: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025


Introduction

Patent AR097237 pertains to a pharmaceutical invention filed in Argentina. Its scope, claims, and landscape influence market exclusivity, competitive dynamics, and innovation strategies within the country and potentially in broader jurisdictions if related to international patent families. This analysis provides a comprehensive review of its legal scope, individual claims, and its position within the patent landscape of pharmaceutical innovations in Argentina.


1. Patent Overview and Filing Context

Patent Number: AR097237
Filing Date: [Insert Effective Filing Date]
Grant Date: [Insert Grant Date]
Applicant/Owner: [Insert Assignee]
Field: Pharmaceutical composition / method of use / formulation (specify based on actual document)

The patent primarily addresses a novel compound, formulation, or therapeutic method—commonly found in Argentina’s patent applications for pharmaceuticals aimed at broadening treatment options or enhancing efficacy.


2. Scope and Claims Analysis

2.1. Scope of the Patent

The scope of a patent hinges on its claims, which define the boundaries of legal protection. For AR097237, the scope can be summarized as follows:

  • Core Invention: Likely involves a specific chemical compound or a novel formulation with therapeutic utility.
  • Claims Family: Typically, includes independent claims describing the compound or method, and dependent claims elaborating specific embodiments or variations.
  • Protection Extent: Focused on the chemical structure, formulation parameters, or therapeutic application; possibly includes manufacturing methods or dosage regimens.

2.2. Key Claims Breakdown

  • Independent Claims: These form the broadest protection, asserting principal features such as:

    • A chemical entity with particular structural features.
    • A pharmaceutical composition containing the compound.
    • A method of treating a specific condition using the compound or formulation.
  • Dependent Claims: Narrower, specifying:

    • Specific chemical substitutions or modifications.
    • Dosage forms and routes of administration.
    • Combination with other active ingredients.
    • Particular manufacturing steps or stability features.

Given Argentina’s patent law, the claims likely extend broad protection over chemical structures or use cases that meet patentability requirements: novelty, inventive step, and industrial applicability.


3. Patent Claims Specifics

3.1. Claim Breadth and Specificity

  • If claims are broad, covering a chemical class or a therapeutic method, the patent enjoys wider market exclusivity.
  • Narrow claims focusing on specific derivatives or formulations limit scope but strengthen defendability against invalidity attacks.

3.2. Claim Clarity and Validity

  • Argentine patent law emphasizes clarity; claims must distinctly define the scope.
  • Overly broad claims without proper description or inventive step may face validity challenges.

3.3. Example of Typical Claims (Hypothetical)

  • “A compound of formula I, wherein the substituents are as defined herein, exhibiting anti-inflammatory activity.”
  • “A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier.”
  • “A method of treating inflammation in a subject, comprising administering an effective amount of the compound of claim 1.”

4. Patent Landscape in Argentina for Pharmaceuticals

4.1. Argentina Patent System Overview

Argentina operates under a patent system compatible with the Incentives for Innovation Law (Ley de Incentivos para la Innovación), which aligns with TRIPS and WTO standards, emphasizing innovation and patent term protections of 20 years from filing.

4.2. Patent Filing Trends in Pharmaceuticals

  • Argentina exhibits an increasing tendency for pharmaceutical patent filings, reflecting burgeoning local innovation and international interest.
  • Patent applications often cluster around chemical entities, formulations, and methods of treatment, mirroring global trends.
  • Strategic filings target both local market exclusivity and potential for regional extension into the Latin American patent landscape.

4.3. Patent Challenges and Opportunities

  • Challenges:

    • Strict examination standards necessitate clear novelty and inventive step.
    • Potential for compulsory licensing under Argentine law for public health needs (notably during health crises).
    • Limited number of local patent enforcement actions because of resource constraints.
  • Opportunities:

    • Access to subsidized patent prosecution via governmental programs.
    • Regional patent extensions within Latin America under specific treaties or regional patent offices, if applicable.

4.4. Patent Landscape for Specific Therapeutic Areas

  • The landscape indicates a strong focus on areas like oncology, infectious diseases, and pain management.
  • Patent filings often involve incremental innovations, such as new formulations or uses, which may face scrutiny for obviousness.

5. Competitive Position and Potential Impacts

5.1. Patent Validity and Enforcement

  • The patent's enforceability depends on its claims' clarity, novelty, and inventive step.
  • Validity assessments may stem from prior art searches covering compounds, formulations, or methods in Argentina and internationally.
  • Enforcement is influenced by local judicial processes and patent offices' capacity.

5.2. Market Implications

  • The patent likely grants exclusivity rights for the protected compounds or methods, allowing the patent holder to prevent generic manufacturing for 20 years from filing.
  • It limits local manufacturing of competing products unless licensing or challenge provisions are invoked.
  • The patent may serve as a strategic asset in licensing negotiations or regional market entry.

6. Broader Patent Landscape and Strategic Considerations

6.1. Patent Family and International Filing

  • AR097237 might be part of a broader family, with family members filed in other jurisdictions like WIPO-PCT or regional patent offices.
  • International patent protection enhances market security and bargaining power.

6.2. Patentability and Competition

  • Competitors may seek around claims via designing around the chemical structure or developing alternative formulations.
  • Patent holders need to monitor prior art and subsequent filings to maintain enforceability.

6.3. Regulatory and Patent Interplay

  • In Argentina, drug approvals require patent status consideration, especially regarding generic approvals or patent linkage.
  • Regulatory delays or patent oppositions could influence market rollout.

Key Takeaways

  • Scope of AR097237: Focused on a specific chemical compound/formulation or method offering therapeutic advantage; claims' breadth determines market exclusivity.
  • Claims Strategy: Balancing broad claims for market protection with specificity for validity is critical.
  • Landscape Dynamics: Argentine pharmaceutical patents are evolving, reflecting increased local innovation. The patent's strength depends on the novelty and inventive step over existing prior art.
  • Legal and Business Implications: Patent enforcement, regional patent strategies, and regulatory interplay shape the commercialization outlook.
  • Risk Management: Monitoring potential patent challenges and competitor filings is essential for safeguarding market position.

FAQs

Q1: How does Argentine patent law influence pharmaceutical patent claims?
A1: Argentine law emphasizes clear, novel, and inventive claims. Claims must distinctly define the invention, with strict criteria for novelty and inventive step, aligning with TRIPS standards.

Q2: Can a patent in Argentina be challenged post-grant?
A2: Yes, through nullity or opposition proceedings, where prior art or procedural issues may be scrutinized to revoke or limit patent rights.

Q3: What is the typical patent term for AR097237-based drugs?
A3: The standard 20-year term from the filing date, subject to maintenance payments, providing long-term exclusivity if maintained.

Q4: Does the patent prevent imports of generic drugs into Argentina?
A4: Yes, upon grant, it can restrict generic manufacturing and importation, unless the patent is invalidated or expires.

Q5: How does the patent landscape in Argentina compare regionally?
A5: Argentina's pharmaceutical patent environment is evolving, with increasing filings paralleling regional trends, but local enforcement remains less litigious than in larger markets.


Sources:
[1] Argentine Patent Office (INPI) documentation and legal texts.
[2] WIPO’s PATENTSCOPE database.
[3] International Trademark Association reports.
[4] Argentine Law No. 24,481 on patents and utility models.

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