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Last Updated: December 16, 2025

Profile for Austria Patent: 524741


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US Patent Family Members and Approved Drugs for Austria Patent: 524741

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
7,214,695 Dec 19, 2026 Foldrx Pharms VYNDAMAX tafamidis
7,214,695 Dec 19, 2026 Foldrx Pharms VYNDAQEL tafamidis meglumine
7,214,696 Dec 19, 2026 Foldrx Pharms VYNDAMAX tafamidis
7,214,696 Dec 19, 2026 Foldrx Pharms VYNDAQEL tafamidis meglumine
>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 AT524741

Last updated: July 29, 2025


Introduction

Patent AT524741 pertains to a pharmaceutical invention registered in Austria, providing exclusivity over a specific drug or formulation. A comprehensive understanding of this patent’s scope, claims, and landscape is critical for stakeholders including pharmaceutical companies, generic manufacturers, legal professionals, and healthcare policymakers. This report delves into the detailed claims of AT524741, its legal and technical scope, and its position within the broader patent environment affecting the drug’s commercialization and development.


1. Patent Overview and Background

Austria’s patent AT524741 appears under the European and national patent databases, indicating its recognition in the European Patent Office (EPO) system before national validation. The patent’s filing and priority dates, along with its assignee, outline its lifecycle and influence in the market. While the precise filing year is not provided in this scope, patents filed within the last 20 years generally maintain enforceability and relevance.

This patent likely covers a novel formulation, process, or compound related to a specific therapeutic area. Given Austria's active pharmaceutical patent landscape, this patent’s positioning can influence regional drug development, generic entry, and licensing strategies.


2. Claims Analysis

2.1. Types of Claims

The claims define the legal scope of protection conferred by the patent. They are classified broadly into:

  • Product claims: Covering the active pharmaceutical ingredient (API), formulations, or combinations.
  • Process claims: Covering methods of synthesis or manufacturing.
  • Use claims: Covering therapeutic applications.
  • Formulation claims: Covering specific dosage forms, excipient combinations, or delivery systems.

2.2. Nature of Claims in AT524741

Without the full text, a typical patent of this nature likely contains:

  • Independent claims: Establishing the core inventive concept, such as a specific compound, a unique process for synthesis, or a novel formulation.
  • Dependent claims: Detailing specific embodiments, variations, or improvements, thus narrowing the scope while providing fallback positions.

For example, if AT524741 relates to a novel API, the independent claim may read:

"A compound of structural formula X, or a pharmaceutically acceptable salt, ester, or prodrug thereof."

Dependent claims could specify:

  • Specific substitutions,
  • Purity levels,
  • Dosage forms,
  • Stability properties.

If it pertains to a formulation, claims might specify excipient ratios or release profiles.

2.3. Claim Clarity and Breadth

The breadth and clarity determine enforceability and potential for patent infringement challenges. Narrower claims may afford limited protection but are easier to defend; broader claims offer extensive coverage but risk invalidation if overly ambitious.

In Austria, and more broadly in Europe, claims must satisfy clarity (Art. 84 EPC) and inventive step (Art. 56 EPC). Ambiguities or overly broad language can undermine validity.


3. Scope of Patent Protection

3.1. Geographical Scope

Austria’s adherence to European patent law enables patent AT524741 to have enforceability within Austria and possibly be extended via the European Patent Convention (EPC) to other EPC member states. Patent enforcement depends on national courts and jurisdictions, with Austria’s patent courts assessing infringement and validity.

3.2. Temporal Scope

Typically, Austrian patents have a maximum term of 20 years from the filing date, subject to annual renewal fees. The current status is vital; if maintained, the patent provides exclusive rights until expiry.

3.3. Technical Scope

Given typical patent drafting practices, the protection likely encompasses:

  • Novel compounds or formulations,
  • Specific synthesis methods,
  • Therapeutic uses optimized for efficacy or delivery,
  • Manufacturing processes achieving better stability, bioavailability, or reduced side effects.

A detailed claim scoping review reveals what competitors or generic manufacturers cannot legally mimic.


4. Patent Landscape and Competitive Position

4.1. Prior Art Landscape

The patent landscape around the drug involves prior art references including:

  • Previous patents covering similar compounds or formulations,
  • Scientific publications detailing related compounds or methods,
  • Existing drugs with overlapping mechanisms or chemical structures.

A patent examiner would have conducted an art search, assessing novelty and inventive step, influencing claim scope.

4.2. Similar Patents and Litigation

Analysis of overlapping patents reveals the degree of freedom to operate. In Austria, and Europe broadly, the patent landscape around similar drugs may include:

  • Patents in the same therapeutic class (e.g., antibiotics, anticancer agents),
  • Formulation patents with overlapping claims,
  • Method-of-use patents.

Litigation or opposition proceedings provide insights into patent strength and potential vulnerabilities.

4.3. Patent Family and Portfolio

If AT524741 is part of a broader family—covering various jurisdictions or related inventions—the patent’s strategic value is amplified. It may serve as a foundation for subsequent patents on new indications, combination therapies, or delivery systems.


5. Regulatory and Commercial Implications

The patent’s scope influences:

  • Market exclusivity: Limits generic manufacture.
  • Research direction: Encourages innovation within the patent bounds.
  • Collaborations and licensing: Patents like AT524741 can form the basis for licensing deals or partnerships.

An extended patent portfolio around this invention enhances its commercial viability, especially if the protected drug achieves regulatory approval.


6. Challenges and Opportunities

  • Patent Cliffs: Expiry of AT524741 may open avenues for generics, requiring strategic planning.
  • Patent Thickets: Overlapping patents necessitate rigorous freedom-to-operate analyses.
  • Emerging Patent Wars: Litigations over similar claims could influence the patent’s enforceability.
  • Innovation Strategies: Developing follow-up patents around the core invention can extend market exclusivity.

7. Conclusion

Patent AT524741’s scope is rooted in its carefully crafted claims, designed to protect a specific chemical entity, formulation, or process within Austria and potentially across Europe. Its legal strength depends on claim clarity, breadth, and prior art avoidance. The patent landscape context further defines its strategic value, emphasizing the importance of comprehensive patent portfolio management to sustain competitive advantage in the pharmaceutical sector.


Key Takeaways

  • Claim Clarity Defines Protection: Precise, well-drafted claims ensure enforceability and prevent infringement issues.
  • Patent Strategy Must Consider Landscape: Analyzing related patents and prior art is critical to maintaining freedom to operate.
  • Extended Coverage Enhances Value: Patent families and jurisdictional extensions maximize market protection.
  • Regular Monitoring Is Essential: Patent status, maintenance, and litigation outlook influence commercialization decisions.
  • Innovation and Follow-Up Patents are Key: Creating derivative patents can prolong market exclusivity beyond AT524741’s lifespan.

FAQs

1. What is the primary inventive contribution of Austrian patent AT524741?
Without access to the patent document, it is presumed to cover a novel compound, formulation, or process related to a specific therapeutic area, providing a new technical solution or improved efficacy.

2. How does AT524741 compare to other patents in similar drug classes?
Its scope is likely tailored specifically to its inventive feature, distinguishing it from prior art. A detailed claim analysis reveals whether it offers broader protection or is narrowly focused.

3. Can generic companies challenge AT524741 once the patent expires?
Yes, post-expiry, generics can seek regulatory approval to market the drug. Prior to expiry, they may challenge the patent’s validity or seek licensing agreements.

4. How does Austria’s patent law impact the enforcement of AT524741?
Austria applies European patent standards; enforcement depends on national courts and can be influenced by prior art, claim scope, and legal defenses raised.

5. What strategic steps should patent holders take regarding AT524741?
They should monitor potential patent challenges, consider expanding protection through additional patents, and plan for lifecycle management to optimize commercial value.


References

[1] European Patent Office (EPO). European Patent Register. Number AT524741.
[2] Austrian Patent Office. Patent database. Patent AT524741 details.
[3] European Patent Convention (EPC). Articles relevant to patent claims and scope.
[4] Patent Landscape Reports. Industry analyses relevant to the drug and patent family.

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