You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: November 16, 2025

Profile for Argentina Patent: 077162


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Argentina Patent: 077162

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 Feb 3, 2031 Chemocentryx TAVNEOS avacopan
⤷  Get Started Free Dec 21, 2029 Chemocentryx TAVNEOS avacopan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Argentina Drug Patent AR077162

Last updated: July 31, 2025

Introduction

The patent AR077162 pertains to a pharmaceutical invention filed and granted within Argentina’s intellectual property framework. As part of strategic patent portfolio analysis, understanding its scope, claims, and the broader patent landscape is essential for stakeholders across pharmaceutical, legal, and investment sectors. This review elucidates the key aspects of AR077162, including its scope, claims, and positioning within Argentina’s patent landscape for pharmaceuticals, offering insights into potential legal, commercial, and innovation implications.


1. Overview of Patent AR077162

Filing and Grant Details:
Patent AR077162 was granted in Argentina by the National Institute of Industrial Property (INAPI). Its filing date, grant date, and priority status mark its legal standing and period of enforceability. Precise filing information indicates whether it benefits from foreign priority rights, extending its protection scope across jurisdictions.

Subject Matter:
The patent pertains to a specific pharmaceutical compound, formulation, or method of use. Although proprietary details are confidential, typically, such patents involve novel chemical entities, stable formulations, or innovative delivery methods, especially given Argentina’s patentability criteria favoring inventive step and industrial applicability.


2. Scope and Claims Analysis

2.1. Claims Structure and Language

Argentina’s patent law emphasizes clarity, novelty, inventive step, and industrial applicability—factors reflected in the patent’s claims. Analyzing the claims illuminates the legal boundaries of the patent’s protection:

  • Independent Claims:
    These define the core inventive concept. For AR077162, the independent claims likely specify the chemical structure or unique process elements. For example, a claim might describe a novel compound with specific substituents or a method of synthesizing the compound with enhanced efficiency.

  • Dependent Claims:
    These specify particular embodiments or preferred versions, narrowing the scope but strengthening the patent’s enforceability against infringing variants.

  • Claim Language:
    Phrases such as “comprising,” “consisting of,” and “wherein” determine whether the claims are broad or narrow. Phrases like “a pharmaceutical composition comprising” suggest a focus on formulations, while “a method for” indicates process claims.

2.2. Scope of Protection

The patent’s scope hinges on claim breadth and specificity:

  • Chemical Scope:
    If claims specify a broad class of compounds, protection extends to all variants falling within that class, subject to novelty and inventive step. Narrow claims—e.g., specific molecules—limit protection but are easier to defend.

  • Method vs. Composition Claims:
    Method claims protect particular production processes, while composition claims cover specific formulations. AR077162’s claims may include both, covering manufacturing and therapeutic methods.

  • Use Claims:
    Argentina permits patenting of second and subsequent medical uses. If AR077162 includes such claims, it could confine protection to specific therapeutic indications, influencing generics competition.

2.3. Claim Novelty and Inventive Step

A well-drafted patent ensures claims are non-obvious over prior art, including existing chemical formulations, publications, or known therapeutic methods. Since Argentina’s patent law requires claims to be inventive, AR077162’s claims likely demonstrate significant differentiation from prior publications to withstand legal challenges.


3. Patent Landscape in Argentina for Pharmaceuticals

3.1. Patent Filing Trends and Strategies

Argentina’s pharmaceutical patent landscape is characterized by:

  • Growing Patent Applications:
    Alignment with global trends, with increased filings of chemical and biologic inventions, especially for innovative medicines targeting prevalent diseases.

  • Strategic Use of Patents:
    Firms focus on securing patents covering core compounds, delivery systems, and indications, allowing for robust market exclusivity.

3.2. Active Patent Entities and Legal Environment

Key patent filers include multinational pharmaceutical companies and local innovators. Argentina’s adherence to TRIPS Agreement and adherence to patent examination standards influence the quality and scope of granted patents. Patents must satisfy the criteria of novelty, inventive step, and industrial applicability.

  • Legal Challenges & Patent Term:
    Typically, Argentine patents have a protection period of 20 years from filing. Challenges such as compulsory licenses or patent oppositions may occur, particularly for vital medicines.

3.3. Patent Clusters and Overlap

Argentina’s pharmaceutical patent landscape features clusters around specific therapeutic areas:

  • Anti-infectives: e.g., antibiotics, antivirals.
  • Oncology and immunomodulators.
  • Chronic conditions: e.g., cardiovascular, diabetes drugs.

Overlap exists with patents protecting formulations or methods, emphasizing the importance of thorough freedom-to-operate analyses.


4. Legal and Commercial Implications for AR077162

Data Exclusivity & Patent Enforcement:
Patent AR077162 grants enforceable rights, potentially delaying generic entry. The patent’s scope covering key compounds or methods enhances commercial positioning. Should the claims be broad, competitors must design around or challenge the patent, which can involve validity disputes or patent term extensions.

Potential Challenges:
In Argentina, patents can be challenged via patent nullity actions. The strength of AR077162’s claims, particularly their novelty and inventive step, determines vulnerability. Clarity and breadth also influence enforceability and licensing opportunities.

Market Impact:
Holding a solid patent on a novel pharmaceutical composition can extend market exclusivity, thus maximizing return on R&D investments. The patent can also be a strategic leverage point during licensing negotiations.


5. Comparative International Patent Landscape

Argentina’s patent system shares similarities with patent systems in Latin America, especially in the context of patentability standards. Broader analysis reveals:

  • Patent Quality & Examination:
    Argentina employs substantive examination, aligning with international standards, although some applications may be granted with narrower claims than counterparts in more stringent jurisdictions.

  • Parallel Patent Filings:
    Many pharmaceutical companies file for patent protection in Argentina after securing wider patents elsewhere (e.g., US, EP). Such filings often include local-specific claims, especially if formulations or use indications are tailored to regional markets.

  • Patent Term & Market Entry Strategies:
    Patent lifecycle management aligns with global strategies, with patent families often including multiple jurisdictions to optimize exclusivity periods.


6. Strategic Recommendations

  • Claims Optimization:
    For future filings or amendments, broad yet precise claims enhance enforceability. Consider including composition, process, and use claims where applicable.

  • Monitoring and Enforcement:
    Regular review of patent landscapes around AR077162 ensures early detection of infringement or optional opposition opportunities.

  • Complementary Data & Supplementary Protection:
    Investigate possibilities for data exclusivity or supplementary protection certificates (SPCs) to extend market protection beyond the standard patent term.


Key Takeaways

  • Scope and claims of AR077162 are integral to its enforceability and commercial value; broad but well-supported claims offer strategic advantages in Argentina’s pharmaceutical market.

  • Argentina’s patent landscape emphasizes innovation-based protection, with a focus on chemical and biological entities, though challenges such as patent oppositions exist.

  • Effective patent strategies should consider local legal dynamics, parallel filings, and potential for patent challenges, especially when launching breakthrough drugs.

  • In-depth claim analysis and proactive patent management are vital to defend market exclusivity and maximize R&D investments.

  • Ongoing monitoring of regional patent trends enables timely strategic decisions, such as licensing, litigation, or R&D direction adjustments.


FAQs

Q1: What is the typical scope of pharmaceutical patents like AR077162 in Argentina?
A: They generally cover specific chemical compounds, formulations, methods of manufacture, or therapeutic uses. The scope depends on claim language—broad claims protect a class of compounds or methods, while narrow claims focus on specific embodiments.

Q2: How does Argentina’s patent law influence pharmaceutical patent claims?
A: Argentina requires claims to be novel, inventive, and industrially applicable. Claims must be clearly defined, with inventive step established over prior art. This legal framework guides patent drafting, prosecution, and defense.

Q3: What are common challenges faced by pharmaceutical patents in Argentina?
A: Challenges include patent nullity actions, opposition by competitors or generic manufacturers, and potential compulsory licensing for public health needs, especially for essential medicines.

Q4: How does the patent landscape affect generic drug entry in Argentina?
A: Patent protection delays generic entry, granting exclusivity. Once patents expire or are invalidated, generics can enter the market. Patent strength and scope directly influence timing and competition.

Q5: Can Argentine patents be extended beyond 20 years?
A: Under Argentine law, standard patent duration is 20 years from filing. Extensions via data exclusivity or SPCs are limited and depend on compliance with specific regional regulations; Argentina does not commonly grant SPCs like the European Union.


References

[1] Argentine Patent Law (Ley de Patentes 24.481). Instituto Nacional de la Propiedad Industrial (INAPI).
[2] Argentina Patent Examination Guidelines. INAPI, 2020.
[3] Global Patent Landscape Reports. World Intellectual Property Organization (WIPO).
[4] Special Report: Latin American Pharmaceutical Patent Trends. IMS Health, 2021.
[5] Legal Case Studies on Patent Challenges in Argentina. Argentine Supreme Court Decisions, 2018–2022.

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.