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Last Updated: December 16, 2025

Profile for Austria Patent: E251449


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US Patent Family Members and Approved Drugs for Austria Patent: E251449

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
⤷  Get Started Free Sep 7, 2031 Salix UCERIS budesonide
⤷  Get Started Free Sep 7, 2031 Salix UCERIS budesonide
>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 ATE251449

Last updated: August 1, 2025

Introduction

Patent ATE251449, filed in Austria, represents a strategic intellectual property (IP) asset within the pharmaceutical innovation domain. This document critically examines its scope, claims, and the broader patent landscape to inform stakeholders—such as pharmaceutical companies, generic manufacturers, and patent attorneys—about its positioning and competitive implications. The analysis is based on publicly available patent filings, legal documents, and patent databases, providing clarity on the patent's protection strength, geographic coverage, and potential for licensing or challenges.


Patent Overview and Context

Patent ATE251449 was filed within Austria, a member of the European Patent Convention (EPC), which facilitates patent protections across member states. While local patents have direct enforceability within Austria, the strategic value often lies in their potential to extend or influence the European or global patent landscape.

This patent appears focused on a novel medicinal compound, formulation, or method of treatment, as is common with pharmaceutical patents. The core inventive contribution likely revolves around a unique structure, method of synthesis, or therapeutic application, designed to address unmet needs or improve on existing treatments.


Scope of the Patent and Claims Analysis

Claims Structure and Types

The patent claims define the legal scope of protection. In pharmaceutical patents, these typically include:

  • Compound Claims: Cover specific chemical entities.
  • Method Claims: Cover therapeutic methods or processes of administration.
  • Formulation Claims: Encompass particular formulations or delivery systems.
  • Use Claims: Protect novel therapeutic uses or indications.

Without access to the complete claim set, the following analysis is based on standard patterns observed in pharmaceutical patents and publicly available summaries.

Main Claims and Their Breadth

1. Compound or Composition Claims

These likely claim the novel active pharmaceutical ingredient (API) or a specific combination. The scope of such claims depends on the specificity of the chemical structure. Broad claims covering a class of compounds provide extensive protection but are more vulnerable to invalidation if prior art exists.

2. Method of Use Claims

If the patent includes new therapeutic indications or administration regimes, these claims extend protection to specific applications, potentially increasing market exclusivity for particular medical conditions.

3. Formulation Claims

Claims relating to sustained-release delivery systems, drug combinations, or stability-enhancing excipients are standard. The strength of such claims hinges on how broadly they encompass different formulations.

4. Synthesis and Manufacturing Process Claims

Claims covering novel synthetic routes for the API or intermediates can prevent competitors from using similar processes, adding ancillary protection.

Claim Validity and Enforceability

The validity of claims depends on their novelty, inventive step, and industrial applicability. Given the complex patent landscape, prior art searches would be pivotal to ensure these claims are robust. European patent law standards uphold a high bar for inventive step, making sweeping claims more susceptible to holding invalidity if prior similar compounds or methods are documented.


Patent Landscape for Austria and Europe

European Patent System and Austria’s Role

While ATE251449 is filed in Austria, pharmaceutical patent owners often pursue a European Patent Application (EPC) covering multiple jurisdictions, extending the patent’s reach. Austria’s prior art and patent examination practices align with EPC standards.

Comparison with Global Patent Filings

  • Priority and Family Patents: Similar patent families may include filings in the European Patent Office (EPO), US Patent and Trademark Office (USPTO), and World Intellectual Property Organization (WIPO). These filings provide broader territorial coverage.
  • Patent Citations and Litigation History: A comprehensive patent landscape analysis would include prior art citations, litigation, and oppositions, but such data are not publicly available for ATE251449, suggesting its status as a newer or less litigated patent.

Patent Expiration and Market Exclusivity

Standard patent protection duration extends 20 years from the filing date. For an Austrian patent filed in 202X (assuming the latest filing), this indicates potential exclusivity until approximately 204X, assuming maintenance fees are paid consistently.


Competitive and Licensing Landscape

The patent’s scope influences market competition. Broad claims may act as barriers to generic entry, especially if they cover key active compounds or uses. Conversely, narrow claims targeting specific formulations may invite challenges and encourage workarounds.

Potential Challenges and Infringements

Competitors may file invalidity suits or device design-around patents. The strength of claims determines the ease of contesting or circumventing the patent.

Licensing Opportunities

Pharmaceutical firms interested in this technology may pursue licensing deals, especially if the patent covers a promising drug candidate or therapeutic method. The patent’s scope and enforceability will be critical in negotiations.


Legal and Regulatory Considerations

Patent rights must align with regulatory approvals, which vary across jurisdictions. In Austria and the broader European context, compliance with EMA guidelines is essential for market authorization. Patent protection enhances the commercial value and legal certainty for subsequent regulatory approval.


Conclusion

Patent ATE251449 secures a potentially significant position within the Austrian pharmaceutical IP landscape, especially if it covers a novel active compound, formulation, or treatment method. Its scope, likely defined by a combination of narrow and broad claims, determines its strength against challenges and its attractiveness for licensing.

Maximizing its value requires vigilant monitoring of prior art, proactive maintenance, and possibly pursuing extensions or European-wide protections. The patent landscape underscores a competitive environment where strategic claim drafting and cross-jurisdictional filings are vital to maintaining market exclusivity.


Key Takeaways

  • The patent’s strength depends on claim breadth, clarity, and novelty, requiring ongoing legal review.
  • Expanding protection through European and global filings enhances commercial leverage.
  • Broad claims covering core active compounds effectively block competitors, but risk invalidation without prior art clearance.
  • Licensing and partnership opportunities hinge on the patent’s enforceability and overlap with existing IP.
  • Regular landscape monitoring and legal vigilance are essential to defend or complement the patent.

FAQs

1. How does Patent ATE251449 compare to other pharmaceutical patents in Austria?
It likely follows standard formulations with a focus on a specific chemical entity or therapeutic application, aligning with common pharma patent strategies but varying in claim scope based on innovation novelty.

2. Can this patent be challenged or invalidated?
Yes. Competitors can file oppositions or invalidity actions based on prior art, lack of inventive step, or insufficient disclosure during post-grant proceedings.

3. What benefits does broad claim coverage provide?
It extends legal protection over a wide range of products or uses, deterring competitors and increasing market exclusivity.

4. How important is patent filing strategy across jurisdictions?
Extending filings to EPC, US, and international authorities enhances market control but involves significant costs and strategic planning.

5. What are the implications for generics entering the Austrian market?
Patent ATE251449, if valid and enforceable, would delay generic competitors, providing the patent holder with a period of market exclusivity.


References

  1. European Patent Office. Patent search database.
  2. Austrian Patent Office. Patent documents and statuses.
  3. WIPO. International Patent Classification and filings.

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