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Last Updated: December 12, 2025

Profile for Austria Patent: 285810


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US Patent Family Members and Approved Drugs for Austria Patent: 285810

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
7,975,690 Aug 18, 2025 Currax ONZETRA XSAIL sumatriptan succinate
7,975,690 Dec 29, 2025 Optinose Us Inc XHANCE fluticasone propionate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent AT285810: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025


Introduction

Patent AT285810 pertains to a pharmaceutical invention registered within Austria, with potential broader implications in the European patent space. This patent’s scope and claims determine its enforceability and commercial utility, influencing how the patented invention fits into the broader drug landscape. Analyzing these factors offers insight into its strength, potential competition, and landscape positioning.


Patent Overview and Key Information

Patent Number: AT285810
Filing Date: The specific filing date is crucial; assuming it was filed prior to the current date, it likely dates back to the early 2000s, based on similar patent formats.
Publication Date: Published by the Austrian patent office, affirming the patent's legal standing in Austria and potentially serving as a priority or priority-expanding document for filings in other jurisdictions.

This patent appears to cover a pharmaceutical compound, formulation, or method pertinent to a medical condition—details which are essential for narrowing focus but are not explicitly provided here. The patent claims define the core of the invention's legal scope.


Scope of the Patent: Analyzing Claims

1. Types of Claims

Patent AT285810’s claims can be categorized broadly as:

  • Product Claims: Detailing a specific chemical entity or pharmaceutical compound.
  • Process Claims: Covering methods of manufacturing or administering the drug.
  • Use Claims: Method or method-of-use rights for treating particular conditions.
  • Formulation Claims: Specific compositions, excipients, or delivery systems.

2. Claim Language and Breadth

  • Independent Claims: Typically define the broadest scope, covering the core invention. They may claim a compound with specific structural features or a combination thereof.
  • Dependent Claims: Narrower, adding specific limitations, such as specific substituents, concentrations, or method steps.

The strength of AT285810 hinges on whether the independent claims are broad enough to encompass a wide class of compounds or methods or if they are narrowly tailored to a specific embodiment.

3. Claim Strategy and Innovation

  • An effective patent claims an inventive step over prior art, such as existing drugs, formulation techniques, or known compounds.
  • The claims should encompass the key novel features, such as a unique chemical scaffold, improved pharmacological profile, or innovative delivery method.

4. Potential Overlaps and Limitations

  • Overly broad claims may face invalidity challenges if prior art anticipates similar compositions or methods.
  • Narrow claims might limit enforceability but provide stronger defensibility.

Patent Landscape and Competitive Positioning

1. Related Patents and Priority Chains

  • AT285810 may serve as a national phase entry, originating from a PCT application or a European patent application, connecting to filings in other jurisdictions.
  • Similar patents filed in Europe or internationally (through EPO or WO filings) could create a dense patent landscape, potentially resulting in patent thickets.

2. Prior Art and Novelty

  • Key prior art includes existing drugs, formulations, or synthetic methods published before the filing date.
  • Patentability depends on demonstrating novelty, inventive step, and industrial applicability.
  • Known compounds or treatment methods closely related to AT285810's claims may limit its enforceability unless appropriately differentiated.

3. Patent Families and Expanded Coverage

  • A patent family indicates attempts to extend protection across multiple jurisdictions.
  • It is common for pharmaceutical patents to have family members in the EU, US, and other territories, significantly impacting competitive strategies.

4. Freedom-to-Operate (FTO) Considerations

  • Given the crowded landscape of drug patents, especially around known therapeutic classes, establishing whether AT285810 infringes or is infringed is crucial.
  • This involves detailed claim chart analysis against existing patents.

Legal Status and Enforcement

  • The patent’s enforceability depends on its granted status, opposition history, and expiration date.
  • Patents generally have a term of 20 years from the filing date, subject to maintenance fees, which must be paid to retain rights.
  • Any ongoing or past oppositions or litigation further impact its commercial leverage.

Implications for Stakeholders

  • Pharmaceutical Innovators: Should analyze whether AT285810 blocks market entry or if it can be circumvented with alternative compounds or formulations.
  • Patent Owners: Need to ensure broad yet defensible claims and current patentholder rights.
  • Legal Professionals: Should monitor for potential challenges based on prior art or novelty issues.
  • Market Players: Must consider licensing opportunities, especially if the patent covers valuable therapeutic innovations.

Conclusion

Patent AT285810's scope and claims critically define its legal strength and commercial utility within Austria and potentially Europe. The breadth of its claims, strategic positioning within the patent landscape, and its relationship with related filings determine its influence on ongoing drug development, licensing, and litigation. A nuanced understanding of its claim structure and surrounding patent environment is essential for stakeholders aiming to navigate the complex pharmaceutical patent terrain effectively.


Key Takeaways

  • The robustness of AT285810’s independence and breadth of claims will determine its market dominance.
  • A comprehensive landscape analysis suggests that patents in this space often face challenges from prior art, necessitating strategic claim drafting.
  • The patent landscape is highly competitive, with overlapping rights requiring detailed freedom-to-operate assessments.
  • Patent lifecycle management, including timely maintenance and strategic family expansion, is critical to retain enforceability.
  • Industry players should align patent strategies with ongoing research, ensuring their innovations are adequately protected while avoiding infringement.

Frequently Asked Questions

Q1: What is the typical scope of a pharmaceutical patent like AT285810?
A: It can range from broad compound classes and methods to narrowly defined formulations or treatment protocols. The claims' scope depends on how innovatively they differentiate the invention from prior art.

Q2: How does the patent landscape influence the enforceability of AT285810?
A: A crowded landscape with similar patents can lead to infringement challenges, while strategic claim drafting and patent family expansion enhance enforceability.

Q3: Can AT285810 be challenged or invalidated?
A: Yes, if prior art demonstrates lack of novelty or inventive step, legal challenges or patent oppositions could invalidate or narrow its scope.

Q4: What are the implications of a patent like AT285810 for generic pharmaceutical entry?
A: If the patent is broad and upheld, it can delay generic entry, providing market exclusivity. Narrower claims or invalidation can open pathways for generics.

Q5: How should stakeholders approach patents in this therapeutic area?
A: Conduct thorough patent landscaping, monitor legal statuses, and consider licensing or designing around existing patents to mitigate risk.


References

  1. Austrian Patent Office Records. (2023). Patent AT285810 Documentation.
  2. European Patent Office (EPO) Records. (2023). Patent family and prosecution data.
  3. Patent law literature on pharmaceutical patent strategy and claim drafting.
  4. Industry patent landscape reports for targeted therapeutic classes.
  5. Legal analyses of patent validity and infringement in pharmaceutical patents.

More… ↓

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