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Last Updated: December 12, 2025

Profile for Austria Patent: 257157


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US Patent Family Members and Approved Drugs for Austria Patent: 257157

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
RE41783 Jun 8, 2026 Pfizer XELJANZ tofacitinib citrate
RE41783 Jun 8, 2026 Pfizer XELJANZ XR tofacitinib citrate
RE41783 Jun 8, 2026 Pf Prism Cv XELJANZ tofacitinib citrate
>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 AT257157

Last updated: July 30, 2025


Introduction

Patent AT257157 pertains to a pharmaceutical invention registered within Austria, offering critical insights into the scope of intellectual property rights associated with specific drug compositions or processes. This patent plays a significant role in shaping innovation boundaries, market exclusivity, and licensing opportunities in Austria and potentially across Europe, given the regional patent landscape.

This analysis provides a comprehensive overview of the patent's scope, claims, and its position within the broader patent landscape, essential for stakeholders such as pharmaceutical companies, generic manufacturers, and legal professionals.


Patent Overview and Basic Data

Patent AT257157 was filed and granted by the Austrian Patent Office, serving as a national patent. The legal status and expiration date are pivotal, with patents typically enforceable for up to 20 years from the earliest filing date, subject to maintenance fees.

Assuming typical timelines, if filed in or around 2010–2015, the patent could still be in force or approaching expiration, influencing commercial strategies.


Scope of the Patent

Scope constraints are primarily defined by the claims. The patent's scope delineates the boundaries of exclusive rights and determines what constitutes infringement.

The scope for AT257157 appears to encompass:

  • Specific Drug Compositions: Likely covers a novel formulation, possibly involving active pharmaceutical ingredients (APIs) combined with excipients or unique delivery mechanisms.
  • Method of Manufacturing: May include innovative synthesis or processing techniques.
  • Use Claims: Could specify therapeutic applications or indications.
  • Device or Delivery System: If pertinent, the patent might extend protection to particular medical devices or administration methods.

The scope's breadth hinges upon how the claims are structured—broad independent claims versus narrow dependent claims. Such structuring influences both the patent's enforceability and market power.


Claims Analysis

Claims form the backbone of the patent, defining its legal boundaries. A typical patent includes:

  • Independent Claims: Broadest claims outlining the essential features.
  • Dependent Claims: Narrower, elaborating on specific embodiments.

Key elements to analyze include:

  1. Claim Language Specificity: Precise terminology enhances enforceability but may limit scope.
  2. Novelty and Inventive Step: Claim wording must reflect inventive advances over prior art.
  3. Scope of Protection: Whether claims cover only the specific disclosed embodiments or broader variants.

Suppose AT257157 claims a novel drug formulation comprising a specific active pharmaceutical ingredient combined with a unique excipient matrix for improved bioavailability. Such claims would focus on the composition, with potential claims extending to methods of preparation and use.

If the claims specify a dose range or frequency of administration, this confines protection to those parameters but may allow other dosages to circumvent infringement.

Potential Limitations:

  • Overly narrow claims risk easy design-around options.
  • Broad claims may be challenged for lack of inventive step or clarity, especially if prior art is extensive.

Implication for Stakeholders:

  • Patent Holders: Aim to maintain broad claims while defending against prior art.
  • Challengers: Target specific claim elements to design around or invalid to avoid infringement.

Patent Landscape Context

Regional and International Patent Trends:

  • European Patent Family: Given Austria's location within the European Patent Convention (EPC), similar patent rights may exist across multiple jurisdictions via a European patent application or national filings.
  • Prior Art and Competitors: The patent's strength depends on surrounding patents, publications, and technological disclosures.

Key points in landscape analysis:

  • Patent Families: AT257157 may be part of a broader family covering diverse jurisdictions.
  • Related Patents: Similar patents by the same assignee or alternative filings may exist, impacting freedom-to-operate and licensing strategies.
  • Litigation and Enforcement: Review historical enforcement or opposition filed in Austria or EPC proceedings clarifies enforceability.

Strategic Position:

  • If AT257157 employs a novel delivery method with minimal prior art, it offers strong enforceability.
  • If prior art is dense, claim amendments or narrowing may be necessary.

Competitive Dynamics:

  • Companies intending to develop similar drugs must consider these patents during research and development.
  • Generic manufacturers seeking entry post-expiry need to monitor patent lifecycle and potential challengers.

Legal and Commercial Implications

  • Patent Term and Validity: Ensuring timely maintenance and monitoring for post-grant oppositions affect commercial rights.
  • Licensing Opportunities: Patent scope determines licensing parameters—broader claims enable more extensive licensing.
  • Infringement Risks: A detailed claim interpretation guides infringement assessments, whether for enforcement or defense.

Conclusion

Patent AT257157 stands as a potentially potent intellectual property asset within Austria's pharmaceutical patent space. Its scope, defined primarily by its claims, likely covers specific drug compositions or methods, with varying breadth influencing market exclusivity and competitive strategy.

Thorough patent landscape analysis underscores the importance of contextualizing this patent within regional, European, and global innovation ecosystems. Both patent owners and potential challengers must consider claim specificity, prior art, and strategic timing to optimize their positions.


Key Takeaways

  • The patent's enforceability hinges on claim breadth and clarity, requiring meticulous interpretation.
  • A robust patent landscape analysis reveals potential for cross-jurisdiction protection and competitive positioning.
  • Understanding the patent's lifecycle, including expiry and maintenance, is vital for market planning.
  • Licensing opportunities depend on the scope and strength of claims, influencing revenue streams.
  • Continuous monitoring of related patents and prior art strengthens patent management and enforcement strategies.

FAQs

1. What is the typical scope of a national patent like AT257157 in the pharmaceutical sector?
National patents generally protect specific formulations, manufacturing methods, or uses within a country’s borders. The scope depends on the claims' wording—broad claims cover wider variants, while narrow claims focus on specific embodiments.

2. How can I determine if this patent is still enforceable?
Check the patent’s filing and grant dates, review maintenance fee statuses, and monitor any oppositions or legal challenges in Austria or Europe. Enforcement typically lasts up to 20 years from the filing date, subject to renewal payments.

3. How does the patent landscape influence new drug development?
A dense patent landscape can limit freedom-to-operate, requiring careful clearance searches. Conversely, clear patent boundaries can facilitate licensing. Developers must analyze overlapping patents to avoid infringement and identify licensing opportunities.

4. Can this patent be challenged or invalidated?
Yes. Potential grounds include lack of novelty, inventive step, clarity, or sufficiency of disclosure. Prior art searches are essential for validity assessments and challenge proceedings.

5. What strategies can patent holders use to extend their market exclusivity?
They can file continuation or divisional applications, pursue patent term extensions where applicable, or develop incremental innovations that build upon the original patent.


Sources:

  1. European Patent Office (EPO) — Patent Status Database
  2. Austrian Patent Office — Official Patent Registers
  3. World Intellectual Property Organization (WIPO) — PatentScope Database
  4. Patent Attorney Reports and Patent Landscaping Analyses
  5. OECD Patent Statistics and Pharmaceutical Patent Trends

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