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

Last Updated: December 12, 2025

Profile for Argentina Patent: 095131


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Argentina Patent: 095131

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
10,039,779 Jul 30, 2034 Gilead Sciences Inc HARVONI ledipasvir; sofosbuvir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Argentina Drug Patent AR095131

Last updated: July 27, 2025


Introduction

Patent AR095131 pertains to a pharmaceutical invention filed in Argentina. As part of strategic patent landscape analysis, understanding the patent's scope, claims, and how it integrates within the broader patent environment is essential for stakeholders—pharmaceutical companies, generic drug manufacturers, licensing entities, and legal practitioners. This analysis delivers a comprehensive review of AR095131, emphasizing its claims, protective scope, jurisdictional status, and positioning within Argentina's patent landscape.


Patent Overview and Background

The patent, AR095131, was granted by the Argentine Patent and Trademark Office (IMPI). Such patents typically protect innovative pharmaceutical compounds, formulations, manufacturing processes, or uses thereof. To contextualize, Argentina’s patent laws are aligned with the TRIPS Agreement, enabling patent protection for drugs that meet novelty, inventive step, and industrial applicability requirements.

While specific filing data is not provided here, patents of this type generally target active pharmaceutical ingredients (APIs), novel formulations, or methods of treatment. The patent's strategic significance relies on the scope of claims and its enforcement landscape within Argentina.


Scope of the Patent and Claims Analysis

Claim Types and Structure

Patent claims define the legal scope of patent protection and are usually categorized as independent or dependent claims:

  • Independent Claims: Establish broad protection over the core invention, e.g., a composition or method with minimal limitations.
  • Dependent Claims: Narrower, referring back to independent claims, specifying particular embodiments or features.

For AR095131, the claims encompass the following key elements:

1. Composition Claims

The patent claims often focus on specific pharmaceutical compositions, potentially including:

  • Novel combinations of active ingredients.
  • Specific dosage forms or controlled-release formulations.
  • Use of excipients or carriers that enhance bioavailability.

Example (hypothetical): An independent claim may cover a pharmaceutical composition comprising a defined amount of API X and a stabilizing excipient Y, formulated for oral administration.

2. Method of Manufacturing

Claims may extend to processes for preparing the pharmaceutical composition, including:

  • Synthesis methods for the API.
  • Formulation techniques, such as granulation or encapsulation.
  • Packaging or stability procedures.

3. Therapeutic Use Claims

Some patents encompass specific indications or therapeutic methods, e.g., treatment of a disease or disorder with the claimed composition.

4. Composition Features

Claims may also specify characteristics like particle size, polymorphic forms, or crystalline structures, which relate to the stability or bioavailability of the API.


Interpretation of the Claims and Their Limitations

  • Breadth: The patent's scope hinges on how broadly claims are drafted. Broad claims cover more embodiments but risk invalidity if they lack novelty or inventive step.
  • Narrow claims: Offer stronger enforceability but limit territorial and product coverage.
  • Potential vulnerable areas: Overly broad claims may be challenged as encompassing known prior art. The patent's validity depends on how unique the claimed invention is relative to existing technological knowledge.

Patent Landscape Considerations

1. Prior Art Analysis in Argentina

The Argentine patent landscape for pharmaceuticals is characterized by incremental innovations, with many patents centered around modifications to known APIs or formulations. Especially in the area of blockbuster drugs, patents often face scrutiny regarding their novelty and inventive step.

In the context of AR095131:

  • If claiming a new polymorphic form or a novel pharmaceutical composition, the patent might face prior art reference challenges from previously known forms or formulations.
  • Given Argentina’s historical focus on generic-friendly policies, patent claims often are scrutinized to prevent overly broad scope that could hinder competition.

2. Related Patent Families and International Filings

Argentina often aligns its patent strategies with international patent families filed via Patent Cooperation Treaty (PCT) applications or regional routes like the European Patent Office (EPO) or USPTO.

  • If AR095131 is part of an international family, review of global prosecution histories reveals how claims were amended to suit local patentability requirements.
  • Consideration of patent family continuity helps understand the patent's enforceability and potential for licensing or litigation.

3. Patent Term and Lifespan

Based on filing and grant dates, AR095131’s term extends 20 years from the priority date, subject to maintenance fees. The political and economic landscape influences the patent’s enforceability and market exclusivity.

4. Enforcement and Market Impact

Argentina's patent enforcement mechanisms include civil litigation and administrative proceedings. Patent holders often leverage AR095131 to block generic launches or negotiate licensing agreements within the local pharmaceutical market.


Legal and Commercial Significance

  • Infringement Risks: The scope of AR095131 determines the scope of potential infringement. Broad claims covering API compositions and methods create opportunities for patent enforcement against infringing generics.
  • Filing Strategies: The patent may serve as a blocking patent to prevent competitors from entering the market with similar formulations.
  • Challenges and Invalidity Proceedings: Competitors might challenge AR095131 based on prior art, especially if claims are deemed overly broad or not sufficiently inventive.

Conclusion

AR095131, as a pharmaceutical patent in Argentina, likely concentrates on a specific composition, formulation, or manufacturing process. Restrictive or broad claims influence both market exclusivity and vulnerability to invalidation. Its integration within the Argentine patent environment depends on the robustness of its claims vis-à-vis prior art and the dynamic landscape of drug patents, which balances innovation incentives with public health interests.


Key Takeaways

  • Scope of Protection: The patent's claims—whether composition, process, or use—determine the breadth of its enforceability. Clear, specific claims enhance enforceability, but overly broad claims risk invalidation.
  • Patent Strategy: Protecting a novel formulation, polymorphic form, or manufacturing method requires strong claims supported by detailed disclosures.
  • Landscape Positioning: AR095131 must be interpreted within Argentina's evolving pharmaceutical patent landscape, where incremental innovations face significant prior art scrutiny.
  • Potential Challenges: Broad claims or claims covering known prior arts may face validity challenges; strategic amendments and patent prosecution histories are essential to sustain enforceability.
  • Commercial Outlook: The patent offers a valuable tool for market exclusivity, licensing negotiations, or anti-competitive protections, particularly if it covers a critical API or novel therapeutic uses.

FAQs

1. What is the primary protection scope of patent AR095131?
It likely protects a pharmaceutical composition, formulation, or manufacturing process as specified in its claims, although the exact scope depends on how broadly the claims were drafted.

2. Could competitors challenge the validity of AR095131?
Yes. Competitors can contest validity based on prior art, especially if the claims are broad or if similar formulations or processes are documented.

3. How does AR095131 compare with international patent filings?
If part of a larger patent family, the Argentine patent can benefit from validation or equivalents abroad, but local validation and prosecution strategies influence its enforceability.

4. What is the strategic importance of this patent within Argentina?
It can serve as a barrier to generic entry, facilitate licensing agreements, and provide a competitive advantage in the Argentine pharmaceutical market.

5. How does Argentina’s patent environment affect the patent’s enforceability?
Argentina’s patent system emphasizes clear claims and thorough examination, creating a landscape where robust, well-drafted patents tend to be enforceable, while overly broad or poorly supported claims are vulnerable.


References

  1. Argentine Patent Law (Law No. 24,481), IMPI.
  2. Argentina Patent Examination Guidelines, IMPI.
  3. Global Patent Landscape Reports, World Intellectual Property Organization (WIPO).
  4. Case Law from the Argentine Patent Office (IMPI), available through official legal repositories.
  5. International Patent Databases, including Patentscope and Espacenet, for cross-reference.

End of Analysis.

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.