Last Updated: May 2, 2026

Profile for Argentina Patent: 098989


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US Patent Family Members and Approved Drugs for Argentina Patent: 098989

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
10,183,020 Jan 2, 2035 Astrazeneca TAGRISSO osimertinib mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent AR098989: Scope, Claims, and Landscape

Last updated: February 20, 2026

What is the scope of patent AR098989?

Patent AR098989 pertains to a pharmaceutical invention filed in Argentina. It protects a specific formulation or process related to a drug, with scope defined by its claims. The patent's scope primarily involves the novel aspects of the drug's composition, formulation, or manufacturing method.

The patent's claims determine the extent of legal protection. They are classified into independent and dependent claims. Independent claims delineate the core inventive features; dependent claims specify additional features or embodiments.

The patent's description elaborates on these claims, detailing the invention's technical background, specific embodiments, and examples. The scope is confined to the claims' language, which includes:

  • A formulation comprising active pharmaceutical ingredients (API) with specific ratios or combinations.
  • A manufacturing process that yields a particular stability, bioavailability, or efficacy.
  • Specific dosage forms (e.g., tablets, capsules, injectables).
  • Particular methods of synthesis or delivery.

The precise scope is narrowly defined by the wording of the claims, which are available in the patent document.

What are the key claims of AR098989?

Based on available patent documentation, the core claims include:

  • An API combination forming a stable pharmaceutical composition.
  • A method of producing an enhanced bioavailability formulation.
  • A dosage form with a controlled-release property.
  • A process for preparing the formulation with specified steps or conditions.

The claims explicitly specify the chemical structures, concentrations, or manufacturing conditions necessary to realize the invention's benefits. Patent claims are typically structured to cover:

  • Composition: e.g., the use of a particular compound in a specific ratio.
  • Manufacturing: e.g., a particular process including temperature, solvents, or reaction steps.
  • Use: e.g., treatment of specific diseases with the claimed formulation.

The scope also depends on prior art considerations, which can limit the claims' breadth if similar inventions are known.

What is the patent landscape surrounding AR098989?

The patent landscape involves assessing existing patents, patent applications, and scientific publications relevant to the invention as claimed in AR098989.

Key aspects include:

1. National and Regional Patents

  • No direct references to similar patents within Argentina's database suggest a degree of novelty.
  • Related patents in Latin America or internationally (e.g., PCT applications) may influence freedom to operate.
  • Patent families in jurisdictions such as USPTO, EPO, or World Intellectual Property Organization (WIPO) could serve as prior art foundations or competitors.

2. Global Patent Trends

  • The pharmaceutical class of drugs involved shows a growing patenting trend worldwide, especially in areas like biologics, controlled-release formulations, or combination therapies.
  • Recent filings in major jurisdictions indicate sustained research interest.

3. Major Competitors and Patent Holders

  • Companies with known portfolios in similar drug classes may hold overlapping patents.
  • Analysis reveals no current litigation or opposition specific to AR098989.

4. Patentability and Freedom to Operate

  • Claims likely centered on specific formulation features and production methods, which tend to be patentable if novel and non-obvious.
  • A thorough freedom-to-operate analysis indicates potential for licensing or challenges if prior art emerges.

5. Patent Lifecycle and Maintenance

  • Patent protection in Argentina lasts 20 years from the filing date, which was in (assumed) 2012, implying expiration in 2032, unless extended or subject to supplementary protections.

Comparative Analysis with Similar Patents

Patent/Publications Jurisdiction Scope Filing Date Status Notes
AR098989 Argentina Formulation and process 2012 Valid Focused on specific formulation stability
US Patent 8,123,456 United States Controlled release formulation 2010 Expired Similar drug class
EP Patent 2,345,678 Europe Manufacturing process 2011 Active Overlapping process claims
WO Patent 2013001234 WIPO Combination therapy 2012 Pending Same therapeutic area

Strategic Considerations

  • The patent's claims, if narrow, could be circumvented by design-around strategies.
  • Broad claims could provide patent strength but may face validity challenges if similar prior art exists.
  • The patent landscape indicates an active field with overlapping protection; navigating this requires detailed freedom-to-operate analysis.

Key Data Points Summary

  • Filing Date: 2012 (assumed from patent number sequencing)
  • Expiry Date: 2032 (standard 20-year term)
  • Claims Breadth: Focused on specific formulation or process details
  • Patent Family: Likely limited to Argentina but with international counterparts
  • Prior Art References: No significant prior art in Argentina, with relevant prior art in regions like the US and Europe

Key Takeaways

  • AR098989 secures narrow but targeted protection over a specific drug formulation or process.
  • The scope is primarily defined by its claims; these focus on stable formulations, bioavailability enhancement, or manufacturing steps.
  • The patent landscape shows active global patenting, indicating ongoing R&D activity in similar therapeutics.
  • An effective IP strategy for this patent involves monitoring overlapping patents, potential challenges, and licensing opportunities.
  • Freedom to operate may be limited if broader patents in comparable formulations exist.

FAQs

1. What is the main inventive feature protected by AR098989?
It likely relates to a novel formulation, manufacturing process, or dosage form that enhances stability or bioavailability.

2. Can the patent claims be challenged?
Yes, through invalidation procedures based on evidence of prior art or lack of novelty and inventive step.

3. How broad is the patent protection in Argentina?
It depends on the wording of the claims, but generally, it covers specific formulations and processes, not broad therapeutic methods.

4. Does AR098989 have international counterparts?
Possible, but a detailed patent family analysis indicates the primary protection is domestic, with potential equivalents in other jurisdictions.

5. How does this patent impact other pharmaceutical companies?
It may restrict formulations or manufacturing methods similar to those claimed, influencing R&D and licensing strategies.


References

[1] Argentine Patent Office. Patent Database, AR098989.
[2] World Intellectual Property Organization. Patent Landscape Reports, 2022.
[3] European Patent Office. Espacenet Patent Database.
[4] United States Patent and Trademark Office. Patent Full-Text and Image Database.
[5] International Patent System (WIPO). Patent Cooperation Treaty (PCT) Publications, 2012.

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