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Last Updated: December 17, 2025

Profile for Austria Patent: 514003


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US Patent Family Members and Approved Drugs for Austria Patent: 514003

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
8,466,159 Sep 4, 2032 Abbvie VIEKIRA XR dasabuvir sodium; ombitasvir; paritaprevir; ritonavir
8,466,159 Sep 4, 2032 Abbvie VIEKIRA PAK (COPACKAGED) dasabuvir sodium; ombitasvir, paritaprevir, ritonavir
8,680,106 Sep 4, 2032 Abbvie VIEKIRA XR dasabuvir sodium; ombitasvir; paritaprevir; ritonavir
>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 AT514003

Last updated: July 29, 2025

Introduction

Patent AT514003 represents a notable intellectual property asset within Austria's pharmaceutical landscape. As with most patents, its scope, claims, and positioning within the broader patent landscape determine its strategic value, enforceability, and potential for innovation or litigation. This analysis provides an in-depth examination of the patent's scope and claims, contextualizing its position within Austria and Europe’s patent ecosystem.

Overview of Austria Patent AT514003

Patent AT514003, granted by the Austrian Patent Office, pertains to a specific pharmaceutical invention, with the patent filing likely initiated around the early 2010s given typical timelines and patent filing patterns. Austria, as an EPC (European Patent Convention) member, aligns its patent regulations with European standards, facilitating potential extensions or validations across key jurisdictions.

The patent addresses a novel compound, formulation, or therapeutic method, with claims designed to protect the inventive step against potential infringements or challenges.

Scope and Claims of AT514003

Type of Patent

AT514003 is classified as a standard patent focusing on pharmaceutical innovations—be it a new chemical entity, a novel formulation, or therapy method. Such patents typically aim to secure exclusivity for pharmaceutical compounds, their therapeutic applications, and sometimes specific manufacturing processes.

Scope of the Patent

The scope of AT514003 encompasses:

  • Chemical Composition: It likely claims a specific active pharmaceutical ingredient (API), including novel derivatives, salts, or formulations with unique properties.
  • Therapeutic Use: It might claim methods for treating particular diseases or conditions, especially if the invention enhances efficacy or reduces side effects.
  • Manufacturing Method: The patent may secure manufacturing processes, especially if these processes confer distinctive efficiency or purity advantages.

The scope’s breadth depends on how the claims are drafted—whether narrowly targeting a specific compound or broadly encompassing a class of related compounds and uses.

Claims Analysis

Claims are the core legal definition of the invention, defining its boundaries. A typical patent like AT514003 may feature:

  • Independent Claims: These specify the primary invention, possibly encompassing the novel compound, formulation, or method.
  • Dependent Claims: These narrow the scope, adding specific features like particular salt forms, dosage forms, or treatment protocols.

Example Insights:

  • Broad Compound Claims: If the patent claims a chemical formula, it aims to cover not just a single compound but a whole class of molecules (e.g., "a compound of formula III wherein R1 and R2 are...").
  • Use Claims: Claiming the use of the compound for specific diseases (e.g., Alzheimer's disease, cancer, etc.) broadens territorial enforceability.
  • Formulation or Method Claims: Protecting specific formulations (e.g., controlled-release tablets) or methods (e.g., administration protocols).

Claim Quality depends on balance—overly broad claims risk being invalidated for lack of inventive step or insufficiency, while overly narrow claims limit market exclusivity.

Patent Life and Legal Status

AT514003’s enforceable life, assuming standard 20-year term from priority date, remains active if resourced with timely fees. Its legal robustness involves ongoing non-challenge status, maintenance fees, and opposition proceedings, if any.

Patent Landscape in Austria and Europe

European Patent Strategy

Austria operates under the European Patent Convention, allowing patentees to validate European patents within Austria, benefiting from streamlined prosecution and enforcement. AT514003’s claims may have been drafted to align with broader European patent strategies, covering key jurisdictions like Germany, France, and beyond.

Competitive Patent Environment

Within Austria, and globally, the pharmaceutical patent landscape faces persistent innovation competition. Key aspects include:

  • Patent Thickets: Multiple overlapping patents for similar compounds or formulations create complex infringement and licensing scenarios.
  • Secondary Patents: Companies often file additional patents (e.g., secondary uses, formulations) to extend exclusivity.
  • Generic Competition: Patent expiry opens markets for generics, influencing patent holders’ strategies around lifecycle management.

Recent Litigations and Patent Challenges

While specific legal disputes involving AT514003 are not publicly documented, the broader European context shows frequent challenges to pharmaceutical patents on grounds of novelty, inventive step, or clarity [1]. The patent’s strength hinges on its ability to withstand such legal scrutiny.

Patent Filing Trends in Austria

Austria exhibits emerging trends of filings in biologics, small molecules, and personalized medicine, with recent increases in patent filings for compound modifications and combination therapies. Patent AT514003 fits into this evolving landscape, aiming to carve out protection within a crowded sector.

Strategic Considerations

  • Enforceability: Patents like AT514003 need continual monitoring and enforcement to maintain market exclusivity.
  • Lifecycle Management: Filing of divisional, continuation, or foreign patents is crucial for maintaining competitive advantage.
  • Innovation Pipeline: The patent’s validity and breadth should be leveraged to support broader R&D initiatives in Austria and Europe.

Conclusion

Patent AT514003’s scope and claims appear designed to provide substantial protection over a specific pharmaceutical compound or formulation within Austria. Its positioning within the European patent landscape allows strategic extensions into broader markets, while the competitive environment demands rigorous defense against challenges. The patent’s strength and value hinge on the precise drafting of claims, strategic enforcement, and continual innovation.


Key Takeaways

  • Scope & Claims Precision: Successful patent protection hinges on well-crafted claims balancing breadth and validity, especially in the pharmaceutical domain.
  • European Patent Strategy: Austria’s alignment with EPC standards facilitates broader protection, but enforcement requires vigilant monitoring.
  • Competitive Landscape: The densely populated patent environment necessitates proactive measures to defend patent assets against invalidation and infringement.
  • Lifecycle & Maintenance: Timely payment of renewal fees and strategic filings are essential to preserve patent rights.
  • Innovation & Litigation: Continuous innovation and readiness for potential challenges underpin long-term patent value in Austria and Europe.

FAQs

1. What are the typical elements included in the claims of pharmaceutical patents like AT514003?
Claims usually define the chemical composition, specific formulations, methods of use, and manufacturing processes to secure comprehensive protection over the invention.

2. How does Austria’s patent law influence the scope and enforceability of AT514003?
Austria’s adherence to EPC standards ensures consistent criteria for novelty and inventive step. Effective enforceability depends on claim clarity, patent maintenance, and proactive enforcement policies.

3. Can AT514003 be extended or validated across Europe?
Yes. If filed as a European patent application, it can undergo validation in Austria and other EPC member states, subject to regional law requirements.

4. What strategic risks exist for pharmaceutical patents like AT514003?
Risks include patent invalidation through legal challenges, patent within a crowded landscape, and potential infringement by generics post-expiry.

5. How does patent landscape analysis influence the commercial value of AT514003?
Understanding competing patents, potential infringements, and avenues for licensing or litigation helps maximize monetization and strategic positioning.


References
[1] European Patent Office. "Guidelines for Examination," 2022.

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