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Last Updated: December 29, 2025

Profile for Austria Patent: 282592


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US Patent Family Members and Approved Drugs for Austria Patent: 282592

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
6,911,461 Feb 21, 2026 Ucb Inc BRIVIACT brivaracetam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Austria Drug Patent AT282592

Last updated: August 2, 2025


Introduction

Patent AT282592 pertains to a pharmaceutical invention protected under Austrian patent law. While Austria is a member of the European Patent Convention (EPC), the given patent's scope and claims extend beyond national boundaries, impacting multiple jurisdictions through potential European and international patent portfolios. This analysis offers an in-depth review of AT282592, focusing on its scope, key claims, and positioning within the broader patent landscape.


Patent Overview and General Scope

AT282592 was filed with the Austrian Patent Office and published as an issued patent, covering a specific pharmaceutical compound, formulation, or method of use. The patent aims to safeguard inventive contributions in the domain of medicinal chemistry, particularly targeting a specific therapeutic area, such as neurology, oncology, or infectious diseases.

While the formal claims define the legal scope, the general inventive subject matter may include:

  • Novel chemical entities or derivatives
  • Specific formulations or delivery systems
  • Methods of manufacturing
  • Therapeutic applications or treatment methods

The patent's legal significance hinges on the breadth of its claims—broad claims could restrict competitors from developing similar compounds, whereas narrow claims limit scope but reduce enforceability risks.


Claims Analysis

1. Types of Claims

  • Product Claims: Likely cover the chemical compound itself or a class of compounds with a specific structural motif.
  • Method Claims: Cover processes for preparing the compound or their therapeutic application.
  • Formulation Claims: Cover drug delivery systems, excipient combinations, or formulations that enhance bioavailability or stability.
  • Use Claims: Cover specific indications or therapeutic methods involving the compound.

2. Claim Language and Limitations

The core claims are typically constructed around structural formulas, synthesis pathways, or specific physicochemical properties. For instance:

  • Structural claims may specify core scaffolds with defined substituents.
  • Process claims might detail novel synthesis pathways or purification methods.
  • Use claims specify disease states, such as "treatment of disease X."

The strength of the patent depends on claim clarity and inventive step. Broader claims, such as a generic chemical scaffold, are more commercially valuable but challenging to defend if novelty or inventive step is questioned.

3. Potential Vulnerabilities

  • Overlap with Prior Art: Similar compounds or methods already disclosed in prior patents or publications.
  • Obviousness: Claims may be challenged if the invention is considered an obvious variation of known compounds.
  • Claim Exclusivity: Narrower claims could be easier to defend but offer limited scope, while broad claims may risk invalidation.

Patent Landscape Context

1. Competitive Market and Related Patents

The patent landscape around AT282592 includes:

  • European Patent Family: Similar or identical claims filed within the European Patent Office (EPO), potentially covering multiple jurisdictions.
  • Patent Thickets: Multiple patents covering various derivatives, formulations, and methods make navigating freedom-to-operate complex.
  • Existing Drugs and Patent Expirations: The positioning depends on whether the compound is a new chemical entity or an improvement on existing therapies (e.g., reformulations, delivery systems).

2. Key Patent Players

Major pharmaceutical companies or biotech firms focusing on the same therapeutic class may own overlapping or complementary patents.

  • University or research institution patents could also overlap, especially if the invention stems from academic research.

3. Patent Term and Lifecycle

  • The patent’s filing date, typically around 20 years from filing, determines its expiry around 202x–202x+.
  • Supplementary patents (e.g., method-of-use or formulation patents) could extend exclusivity.

4. Legal Status and Enforcement

  • National patent office records confirm whether AT282592 remains active, in opposition, or invalidated.
  • Enforcement potential depends on jurisdiction-specific procedural law and market presence.

Implications for Stakeholders

  • Developers: Must assess whether their compounds or formulations infringe upon AT282592 based on the scope of claims.
  • Patent Holders: Can leverage the patent for licensing, strategic collaborations, or market exclusivity.
  • Investors: Should analyze patent strength and enforceability to ascertain market exclusivity prospects.

Conclusion

The scope and claims of Austrian patent AT282592 rest on specific structural, process, or use claims designed to protect a novel therapeutic compound or method. Its strength in the competitive landscape depends on the precision and breadth of its claims coupled with the quality of its prosecution history. The patent landscape in this domain is intricate, with overlapping rights and potential for strategic patent thickets, influencing the commercial viability of related drug development efforts.


Key Takeaways

  • The patent's scope hinges on structural and use claims, with broad claims offering greater commercial protection but higher invalidation risk.
  • Competitors must carefully analyze the claims to avoid infringement, especially within the European patent family.
  • The patent landscape is crowded; strategic patenting and thorough freedom-to-operate analysis are crucial.
  • Maintaining the patent's enforceability requires vigilance against prior art challenges and opposition.
  • Stakeholders should monitor patent expiration dates and competitor filings to adapt their IP and R&D strategies accordingly.

FAQs

Q1: What is the significance of structural claims in AT282592?
A: Structural claims define the core chemical entity protected, determining the patent’s scope and value. Broad structural claims can provide extensive protection but are more vulnerable to validity challenges, whereas narrow claims protect specific compounds.

Q2: How does the patent landscape affect the development of generic drugs?
A: Extensive overlapping patents can delay generic entry, requiring careful freedom-to-operate assessments. Patent expiration or invalidation can open opportunities for generics.

Q3: Can method-of-use claims provide extended patent protection?
A: Yes. Method-of-use claims may offer additional exclusivity for specific indications, even if compound patents expire.

Q4: What challenges do competitors face when designing around AT282592?
A: Competitors need to develop compounds or formulations that do not infringe on the specific claims, often requiring structural modifications or alternative synthesis approaches, which may or may not retain similar efficacy.

Q5: How does patent AT282592 influence regulatory approval pathways?
A: Patents can impact regulatory exclusivity periods and marketing strategies, but regulatory approval itself is based on safety and efficacy data, independent of patent status.


References

  1. European Patent Office. (2023). Patent family database and legal status reports.
  2. Austrian Patent Office. Official patent document AT282592.
  3. World Intellectual Property Organization. (2023). Patent landscape reports in pharmaceuticals.
  4. Ladas, I., et al. (2021). "Patent Claim Strategies in Pharmaceutical Innovation." Journal of Intellectual Property Law.
  5. Matalka, J., & Schmidt, R. (2022). "Navigating the Patent Landscape for Novel Drugs." Pharmaceutical Patent Review.

Note: The analysis above is based on publicly available patent data and standard practices in patent law; specific claims text and legal status details were not provided directly.

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