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Last Updated: December 29, 2025

Profile for Argentina Patent: 112532


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US Patent Family Members and Approved Drugs for Argentina Patent: 112532

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
8,796,245 Aug 7, 2029 Tetraphase Pharms XERAVA eravacycline dihydrochloride
8,906,887 Dec 28, 2030 Tetraphase Pharms XERAVA eravacycline dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Argentina Patent AR112532

Last updated: September 27, 2025

Introduction

Argentina Patent AR112532 pertains to a pharmaceutical invention intended to strengthen its position within the nation's intellectual property landscape. A comprehensive understanding of its scope, specific claims, and the broader patent environment is vital for stakeholders, including generic manufacturers, brand-name pharmaceutical companies, and legal entities engaged in patent litigation or licensing negotiations. This analysis delineates the patent's scope and claims while situating it within Argentina's pharmaceutical patent landscape.

Patent Overview and Technical Scope

AR112532 was granted within Argentina's patent framework, providing an exclusive right to the patent holder over the disclosed invention. The patent likely encompasses a novel chemical entity, a formulation comprising active pharmaceutical ingredients, a manufacturing process, or a therapeutic use. Given typical patent trends in the pharmaceutical sector, it probably covers either a new compound or an innovative method of treatment.

The patent’s technical scope hinges on the claims' breadth, which define the extent of legal protection. The patent emphasizes the inventive features that differentiate it from prior art, possibly including specific chemical structures, unique synthesis methods, or applications for particular diseases.

Key Defining Features of the Patent:

  • Chemical Composition: If expressly claimed, the patent protects a specific chemical compound or a class of compounds with therapeutic utility.
  • Pharmaceutical Formulation: Claims may cover formulations, including excipient combinations, delivery systems, or dosage forms.
  • Method of Use or Treatment: The patent might protect a particular medical use, such as a new indication or route of administration.
  • Manufacturing Process: Claims could encompass novel synthetic steps or process optimizations.

The document’s claims are central to understanding the legal scope: broader claims offer wider protection but are often harder to defend against invalidity challenges, while narrower claims provide precise territorial rights.

Analysis of Patent Claims

A typical patent in this domain contains independent and dependent claims, with the former establishing core inventive features and the latter providing specific embodiments or limitations.

Independent Claims

Given the patent pertains to a pharmaceutical compound or process, the independent claims likely focus on:

  • Chemical structures or combinations: A specific compound or a class defined by structural features.
  • Use in Therapy: Methods for treating a disease with the compound.
  • Manufacturing Method: Steps or processes for synthesizing the inventive entity.

For example, an independent claim may state: “A compound of formula I, characterized by X, Y, and Z substituents, for use in treating disease A.” It may also encompass a claim for a method of administering the compound to a patient.

Dependent Claims

Dependent claims narrow active features, such as specific substituents, dosage regimens, formulation characteristics, or process conditions. These serve to protect specific embodiments and facilitate legal defensibility.

Claim Strategy and Breadth

The patent's breadth depends on how comprehensively the claims encompass the invention:

  • Broad claims ensure extensive coverage but risk invalidity if prior art exists.
  • Narrow claims limit protection but strengthen defensibility.

In Argentina, the scope must align with patentability requirements, emphasizing novelty, inventive step, and industrial application.

Patent Landscape in Argentina for Pharmaceuticals

Argentina’s patent landscape for pharmaceuticals is shaped by the national patent law, which aligns with the Patents Cooperation Treaty (PCT) standards. The patent examination policies emphasize novelty, inventive step, and utility, with particular scrutiny on obviousness and prior art.

Patent Types and Trends

  • Chemical/Pharmaceutical Patents: Argentina's patent office (INPI) grants patents for new chemical entities, formulations, methods, and uses (see [1], [2]).
  • Evergreening Strategies: Patent applicants often file secondary patents covering formulations or methods to extend exclusivity.
  • Patent Challenges and Litigation: The national legal framework permits patent oppositions and invalidation procedures, although enforcement quality varies.

Patent Strategy Focus in Argentina

Pharmaceutical companies pursuing patent protection tend to:

  • File early upon discovering novel compounds or processes.
  • Secure multiple patent types (composition, method, use) to block generic competition.
  • Focus on innovative formulations and new therapeutic indications to extend patent life.

Patent Filing Trends

Data suggests a modest but steady increase in pharmaceutical patent applications, with notable activity in biologics and small-molecule drugs. The Argentine Patent Office's efficiency and the country’s evolving legal framework foster a competitive environment for patent strategists.

Legal Status and Patent Validity Considerations for AR112532

The patent status influences its enforceability:

  • Verified granted status suggests AR112532 is in force, granting exclusive rights within Argentina.
  • Validity depends on maintaining payment of annuities, non-invalidity challenges, and compliance with formalities.

Potential invalidity grounds include:

  • Lack of novelty or inventive step.
  • Obviousness over prior art.
  • Insufficient disclosure or scope issues.
  • Clarifications or amendments post-grant.

Legal challenges can arise from generic manufacturers or third parties seeking to clear the path for biosimilars or generics.

Impact of AR112532 on the Argentine Pharmaceutical Market

The patent likely provides a competitive edge for the patent holder, enabling:

  • Market exclusivity for the protected compound or formulation.
  • Licensing opportunities within Argentina.
  • Strategic defense against patent infringement litigation.

It may also influence local manufacturing, pricing, and marketing strategies, especially if the patent covers a blockbuster drug or a breakthrough therapy.

Conclusion

Argentina Patent AR112532 appears to define a specific inventive chemical or biological entity with associated therapeutic methods or formulations. The patent’s scope is primarily anchored in its claims, which set the legal boundaries of protection. The patent landscape in Argentina favors strategic patent filing, particularly for novel compounds, combinations, and methods.

Understanding the patent’s scope and claims facilitates informed decision-making, whether for licensing, infringement risk assessment, or research and development planning. Protecting innovation within Argentina's evolving patent framework requires meticulous claim drafting and vigilant patent maintenance.


Key Takeaways

  • Scope Definition: The patent’s claims determine its protection breadth; broad claims cover more but are harder to defend, while narrow claims provide focused protection.
  • Claims Strategy: Combining broad independent claims with narrower dependent claims offers strategic resilience.
  • Legal Landscape: Argentina’s pharmaceutical patent environment balances innovation incentives with mechanisms for patent challenge and invalidation.
  • Market Impact: The patent reinforces exclusivity rights, influencing drug pricing, market entry, and competition.
  • Strategic Considerations: Innovators should monitor patent validity, enforceability, and potential invalidity risks to sustain market advantage.

FAQs

  1. What types of claims are most common in Argentine pharmaceutical patents like AR112532?
    Typically, patents contain independent claims directed at chemical compounds, therapeutic methods, formulations, and manufacturing processes, complemented by dependent claims narrowing these features.

  2. Can a patent like AR112532 be challenged or invalidated in Argentina?
    Yes. Challenges can be filed on grounds such as lack of novelty, inventive step, or insufficient disclosure, leading to potential invalidation if successful.

  3. How does the scope of AR112532 impact generic drug entry in Argentina?
    If the patent’s claims are broad and valid, they can delay generic entry. Narrower claims or patent invalidity can enable generics to enter earlier.

  4. What constitutes a breach of patent rights for AR112532?
    Producing, using, or selling the protected invention without authorization during the patent term constitutes infringement under Argentine law.

  5. How does patent law in Argentina support pharmaceutical innovation?
    Through granting exclusive rights, patent law incentivizes R&D, with provisions for patent term extensions, licensing, and enforcement frameworks.


References

[1] Argentine Patent Office (INPI) Regulations – Overview of pharmaceutical patent examination parameters.
[2] World Intellectual Property Organization (WIPO) Patent Data – Argentine patent filings in pharmaceuticals.

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