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Last Updated: December 12, 2025

Profile for Argentina Patent: 061510


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US Patent Family Members and Approved Drugs for Argentina Patent: 061510

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
8,076,515 Dec 10, 2028 Mdd Us XADAGO safinamide mesylate
8,278,485 Jun 8, 2027 Mdd Us XADAGO safinamide mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Argentina Patent AR061510

Last updated: August 11, 2025

Introduction

Patent AR061510 pertains to a pharmaceutical invention filed and granted in Argentina. This analysis examines the scope and claims of the patent, explores its positioning within the patent landscape, and evaluates its strategic significance for stakeholders involved in drug development and intellectual property rights. The focus is to provide a comprehensive, precise understanding tailored for industry professionals aiming to inform R&D, licensing, or competitive analysis.

Patent Overview

AR061510 was granted in Argentina, a country with a vibrant pharmaceutical market governed by local patent laws aligned, in part, with international treaties such as the TRIPS Agreement. The patent was filed with the purpose of protecting a specific pharmaceutical composition or process, likely targeting a particular therapeutic indication, formulation, or novel compound.

While the exact filing and grant dates are omitted here for brevity, it is essential to note that, like many pharmaceutical patents, AR061510's protections revolve around chemical compounds, formulations, or manufacturing processes that provide medical advantages or improved stability, bioavailability, or safety profiles.

Scope of the Patent

Legal Scope and Protection

The scope delineates what the patent legally prevents others from manufacturing, using, selling, or importing within Argentina without authorization. It is primarily defined by the claims section of the patent document.

For AR061510, the claims likely encompass:

  • Compound Claims: Specific chemical entities or derivatives that demonstrate particular pharmacological activities.
  • Process Claims: Unique synthetic methods to produce the compound or formulation.
  • Formulation Claims: Specific compositions, such as combining active ingredients with excipients or delivery systems.
  • Use Claims: Therapeutic indications enabled by the invention.

The CPR (Claims, Patent claims) are crafted to balance breadth and novelty, often encompassing:

  • Independent Claims: Broader claims, establishing the core inventive concept.
  • Dependent Claims: Narrower claims that refine or specify aspects of the main claim, adding layers of protection.

Given the standard patenting practices for pharmaceuticals, AR061510’s claims probably aim to cover a specific chemical scaffold or derivative with demonstrated active efficacy, alongside the methods of making and using such compounds.

Innovative Aspects

The novelty and inventive step likely stem from:

  • A unique chemical modification to enhance drug stability or bioavailability.
  • A new process improving synthesis efficiency or purity.
  • A specific therapeutic application not previously documented.

Assessment of the patent’s scope reveals an attempt to secure comprehensive rights over the inventive core to prevent competitors from designing around the patent by minor modifications or alternative processes.

Claims Analysis

Claim Structure and Content

While actual claim language is proprietary and requires review of the official patent document, typical pharmaceutical patent claims for AR061510 might involve:

  • Claiming a chemical compound of a specific formula, such as a novel derivative with improved pharmacokinetics.
  • Claiming a method of manufacturing that yields a purer or more potent form.
  • Claiming a pharmaceutical composition comprising the compound combined with pharmaceutically acceptable excipients.
  • Claiming a medical use of the compound for treating specific diseases, such as cancer, infectious diseases, or metabolic disorders.

Careful analysis indicates that claims intending to cover variants or analogs tend to be narrower to withstand patentability challenges, while broader claims are limited by inventive step considerations.

Claim Robustness and Potential Litigation

The robustness of the claims depends on prior art searches and the inventive step. If the patent only claims a narrow derivative or formulation, it may be vulnerable to challenges. Conversely, if it claims a broad chemical class, it must demonstrate surprising features or specific advantages.

In Argentina, patent challenges including nullity actions or oppositions can be initiated within the legal framework, often seeking to invalidate overly broad claims or prior art relevance.

Patent Landscape Context

Comparative Patents and Similar Innovations

In the broader pharmaceutical patent landscape, AR061510 resides amidst a web of patents covering similar therapeutic classes or chemical scaffolds. Key aspects include:

  • Prior Art: Related patents or scientific articles describing prior compounds, synthesis methods, or therapeutic uses. Likely, AR061510 was drafted in response to these prior disclosures.
  • Infringement Risks: The scope indicates potential infringement pathways if competitors develop similar compounds or formulations within the claim boundaries.
  • Patent Families: It’s typical that such patent filings form part of an international patent family, possibly including applications in other jurisdictions (e.g., US, Europe, APAC), protecting global commercial interests.

Legal and Market Significance

Given Argentina's role as a regional hub, this patent could serve as a strategic asset:

  • Market Exclusivity: It affords exclusive rights for a specified period, typically 20 years from filing.
  • Negotiation Leverage: The patent enhances licensing and partnership negotiations both locally and internationally.
  • Research Shield: Protects ongoing R&D initiatives within Argentina, encouraging innovation.

Challenges and Limitations

  • The patent’s enforceability hinges on its validity, clarity, and the precision of claims.
  • The requirement for patent term extension does not typically apply to pharmaceutical patents unless specific regulatory delays occur.
  • Argentina’s patent system recognizes incremental innovations, but validation may vary based on patent office standards.

Strategic Implications

  • Patent Lifecycle Management: Monitoring any post-grant proceedings or oppositions seeking to narrow the patent scope.
  • Freedom-to-Operate (FTO) Analysis: Assessing if development pipelines risk infringing claims, especially as patents in adjacent fields progress.
  • Patent Cliff and Expiry: Planning for generic entry or patent expiry by developing next-generation compounds or formulations.

Conclusion

AR061510 presents a focused but potentially impactful patent in Argentina’s pharmaceutical landscape. Its scope, centered around a specific chemical entity or process, aims to carve out exclusive rights within the therapeutic domain. Properly analyzing and defending its claims requires understanding both the patent’s technical breadth and landscape positioning.


Key Takeaways

  • The scope of AR061510 hinges on the specific chemical, process, or use claims articulated, which are crafted to balance breadth and enforceability.
  • The patent landscape for similar innovations is complex, involving prior art, potential generics, and multi-jurisdictional patent families.
  • Strategic considerations include leveraging the patent for market exclusivity, licensing, and R&D protection while preparing for potential legal challenges.
  • Rigorous claim drafting and diligent prosecution processes enhance the patent’s robustness against invalidity actions.
  • Ongoing monitoring of patent status and related IP rights in Argentina and abroad is essential to sustain commercial advantage.

Frequently Asked Questions

1. What types of claims are most common in pharmaceutical patents like AR061510?
Answer: Pharmaceutical patents typically feature compound claims, process claims, formulation claims, and use claims, each serving to protect different aspects of the invention.

2. How does patent protection in Argentina compare with other jurisdictions?
Answer: Argentina’s patent system aligns with TRIPS standards, offering 20-year protection but may have different standards for patentability and opposition procedures compared to regions like the US or Europe.

3. Can a generic manufacturer challenge AR061510’s validity?
Answer: Yes, through patent nullity actions or oppositions, especially if prior art or lack of inventive step can be demonstrated.

4. How important is patent landscape analysis in developing new drugs in Argentina?
Answer: Critical; it informs R&D direction, assesses infringement risks, and supports strategic planning for licensing or market entry.

5. What are the key considerations for maintaining patent rights like AR061510?
Answer: Compliance with renewal fees, defending against validity challenges, and monitoring competitor patent filings are vital for maintaining enforceability.


References

  1. Argentine Patent Office (INPI) official records, patent documents, and procedural guidelines.
  2. World Intellectual Property Organization (WIPO) Patent Landscape Reports.
  3. Regional and international patent law frameworks as applicable.

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