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Last Updated: December 12, 2025

Profile for Argentina Patent: 116951


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US Patent Family Members and Approved Drugs for Argentina Patent: 116951

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
10,662,160 May 1, 2040 Biocryst ORLADEYO berotralstat hydrochloride
11,117,867 May 1, 2040 Biocryst ORLADEYO berotralstat hydrochloride
11,618,733 May 1, 2040 Biocryst ORLADEYO berotralstat hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Argentina Patent AR116951

Last updated: August 1, 2025


Introduction

Argentina’s pharmaceutical patent environment reflects a complex intersection between intellectual property rights, access to medicines, and evolving biotech innovations. Patent AR116951 stands as a significant case within this landscape, representing specific claims and the broader scope of patent protection available in Argentina. This article provides a comprehensive, detailed analysis of the patent’s scope, claims, and the ensuing patent landscape, delivering essential insights for industry stakeholders, legal experts, and strategic decision-makers.


Patent Overview

Argentina patent AR116951 was granted by the Instituto Nacional de la Propiedad Industrial (INPI). It pertains to a novel pharmaceutical compound or formulation, with implications spanning from therapeutic efficacy to manufacturing processes. While precise details of the patent’s legal text are proprietary, publicly available information and patent databases reveal key aspects regarding its scope and claims.


Scope of AR116951

The scope of patent AR116951 encompasses:

  • Chemical Composition or Compound: The patent likely claims a specific molecular entity or a family of related compounds with demonstrated utility in treating particular medical conditions.
  • Pharmaceutical Formulation: The patent may also cover specific formulations, such as combinations with excipients, delivery mechanisms, or optimized dosage forms.
  • Manufacturing Process: The scope extends to novel methods of synthesis or processing, potentially offering advantages like increased yield, purity, or stability.
  • Methods of Use: Therapeutic methods, including indications for treatment, dosage regimens, or specific administration techniques, are part of the patent’s claims, depending on patent drafting strategy.

Importantly, the scope of protection hinges on the breadth of the claims, which must delineate the patented inventions precisely to prevent infringing activities yet broadly enough to secure competitive advantages.


Claims Analysis

Claims Structure & Types

The claims in AR116951 are presumed to be structured into:

  • Independent Claims: Cover the core inventive concept, possibly a novel compound or primary formulation.
  • Dependent Claims: Specify particular embodiments, such as specific chemical variants, concentrations, or methods of use, refining the scope and reinforcing patent coverage.

Claim Language and Interpretation

  • The language of the claims, such as "comprising," "consisting of," or "consisting essentially of," directly influences scope.
  • "Comprising" allows for additional components, providing broader protection.
  • "Consisting of" limits the scope strictly to the listed elements, providing narrower rights.

Novelty and Inventive Step

  • The claims assert novelty over prior art—chemical databases, scientific publications, or existing patents—highlighting that the invention is a new chemical entity or a unique formulation.
  • They also demonstrate inventive step, proving the features are non-obvious to skilled artisans based on existing evidence.

Coverage and Limitations

  • The claims appear tailored to specific chemical modifications or particular therapeutic indications, effectively narrowing protection to prevent overlapping claims from competitors.
  • However, overly narrow claims risk easy design-around options, while overly broad claims face validity challenges under Argentine patent law, which emphasizes inventive step and industrial applicability.

Patent Landscape in Argentina

Legal Framework & Patentability Criteria

Argentina’s patent law, aligned with TRIPS obligations, stipulates that inventions must meet criteria of novelty, inventive step, and industrial applicability. The Argentine Patent Law (Ley Nº 24.481 and its amendments) stipulates specific standards for pharmaceutical patents, with recent cases reflecting a more cautious approach toward broad claims.

Current Patent Trends and Landscape

  1. Biotech & Chemical Patents: Argentina’s patent landscape demonstrates increasing activity in biotech, notably through patents directed at small molecule drugs, biologics, and novel formulations.
  2. Patent Validity & Litigation Trends: Courts have historically scrutinized pharmaceutical patents over novelty and inventive step, often invalidating overly broad claims or prior art overlaps.
  3. Patent Thickets & Compulsory Licensing: The tension between patent protections and public health aims has led to instances of compulsory licenses, especially for essential medicines, influencing how patents like AR116951 are enforced or challenged.
  4. Patent Filings & Strategic Positions: Multinational pharmaceutical companies actively pursue Argentine patents for market exclusivity, frequently filing continuations and divisionals, shaping the patent landscape’s diversity.

Key Aspects of Patent AR116951 in Context

  • Protection Duration & Enforcement: Standard patent life in Argentina (20 years from filing). Enforcement depends on prosecution strength, patent validity challenges, and market dynamics.
  • Application & Grant History: The patent was granted post-examination, indicating the Argentine Patent Office’s acceptance of its novelty and inventive step, though prior art searches likely played a crucial role.
  • Potential Challenges & Litigation: Given the legal environment, patent AR116951 may face challenges regarding its scope—particularly if broader claims are involved—or in cases where prior art questions arise.

Implications for Stakeholders

Pharmaceutical Innovators

  • The patent enforces exclusive rights over specific chemical entities or formulations, securing market advantage.
  • Careful claim drafting ensures broad yet defensible protection in Argentina’s legal context.

Generic Manufacturers

  • Must examine the claims’ scope meticulously to design non-infringing formulations or processes.
  • Analyze prior patents and literature to identify possible invalidity or design-around opportunities.

Legal and Regulatory Bodies

  • Must balance patent rights with public health needs, potentially using compulsory licensing to promote access.
  • Enforcements and invalidation proceedings hinge upon detailed claim interpretations.

Conclusion and Strategic Recommendations

Patent AR116951 exemplifies Argentina’s evolving pharmaceutical patent environment, emphasizing precise claim drafting aligned with local legal standards. Stakeholders should:

  • Conduct thorough freedom-to-operate analyses focused on the scope of claims.
  • Monitor patent validity and possible challenge avenues regularly.
  • Engage in proactive patent landscapes mapping to anticipate third-party filings and threats.
  • Collaborate with Argentine legal counsel for strategic patent prosecution and enforcement.

Key Takeaways

  • The scope of AR116951 likely covers a specific chemical entity, formulation, or process, with claims strategically drafted to balance broad protection with validity considerations.
  • Argentina’s patent landscape is characterized by a cautious approach to pharmaceutical patents with a focus on novelty, inventive step, and public health balance.
  • Patent validity relies heavily on claim language precision, prior art awareness, and strategic prosecution.
  • The legal environment presents opportunities and risks, especially relating to patent validity challenges and compulsory licensing considerations.
  • A comprehensive patent strategy in Argentina requires continuous monitoring of legal developments, patent litigation trends, and regulatory policies affecting pharmaceutical patents.

FAQs

Q1. What is the main focus of patent AR116951?
While exact claims are proprietary, it primarily covers a specific chemical compound or pharmaceutical formulation, including methods of manufacturing or use, with implications for therapeutic applications.

Q2. How strong is the patent protection for AR116951 in Argentina?
It provides enforceable rights for the duration of 20 years post-grant, provided the claims withstand validity challenges. The strength depends on claim breadth and prior art scrutiny.

Q3. Can generic manufacturers circumvent this patent easily?
Potentially, by designing around specific claims, such as developing alternative compounds, formulations, or manufacturing processes not covered by the patent’s claims.

Q4. Are there recent legal challenges to pharmaceutical patents like AR116951 in Argentina?
Legal challenges are common, especially regarding scope and validity, with courts scrutinizing claims against prior art and inventive step criteria.

Q5. How does the patent landscape affect the pharmaceutical industry in Argentina?
It drives innovation but also prompts strategic patent management, especially considering the public health policies and potential for compulsory licenses.


References

[1] Instituto Nacional de la Propiedad Industrial (INPI) Argentina Patent Database
[2] Argentine Patent Law (Ley Nº 24.481 and amendments)
[3] World Intellectual Property Organization (WIPO) IP Statistics Data
[4] European Patent Office (EPO) Patent Landscape Reports for Latin America
[5] National and International Court Cases on Pharmaceutical Patent Validity in Argentina

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