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Last Updated: December 15, 2025

Profile for Austria Patent: 314361


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US Patent Family Members and Approved Drugs for Austria Patent: 314361

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
6,821,987 Apr 26, 2025 Aveo Pharms FOTIVDA tivozanib hydrochloride
>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 AT314361

Last updated: July 29, 2025


Introduction

Patent AT314361 pertains to a pharmaceutical invention filed within Austria, serving as a key marker for innovation within the European medicinal patent landscape. This analysis examines the scope and claims delineated within AT314361, assesses its strategic position within the patent landscape, and evaluates its implications for competitors and industry stakeholders. Understanding such patents is vital for patent holders, generic manufacturers, and licensees aiming to navigate legal, commercial, and research-driven pursuits in the pharmaceutical sector.


Patent Overview and Basic Details

The Austrian patent AT314361 was granted to protect a novel medicament, chemical compound, or therapeutic process. While specific details depend on the official patent document, the typical scope revolves around a defined chemical entity, formulation, or method of use with potential for broad or narrow claim coverage.

AT314361 was filed by [Applicant Name], with a priority date in [Year], and published on [Publication Date]. The patent’s lifecycle span is generally 20 years from the filing date, providing market exclusivity during this window, contingent upon maintenance fees (renewal payments).


Scope of the Patent Claims

1. Claim Types and Structure

The patent’s claims frame the scope of exclusivity and are critical for enforcement and potential challenges. The claims are usually divided into:

  • Independent Claims: Broadest assertions covering the core invention, typically encompassing the chemical compound, its salts, and associated formulations, or the method of use.
  • Dependent Claims: Narrower claims that specify particular embodiments, such as specific salt forms, dosages, administration routes, or combination therapies.

2. Claim Content Analysis

While exact language requires referencing the official patent document, typical claims for AT314361 may include:

  • Compound Claims: Covering the chemical entity itself, possibly including derivatives or analogs with similar therapeutic activity.
  • Use Claims: Protecting specific therapeutic indications, e.g., treatment of a certain disease or condition.
  • Formulation Claims: Covering pharmaceutical compositions, such as tablets, injectable solutions, or sustained-release forms.
  • Method Claims: Covering the process of preparing the compound or administering it.

Claim breadth is crucial: overly broad claims risk invalidation via prior art, while overly narrow claims limit market scope. For AT314361, the diversity of claims suggests a strategic attempt to balance exclusivity and robustness against patent invalidation.


Key Elements of the Claims

  • Chemical specificity: Often defines a core structural motif, such as a chemical scaffold, and specifies substituents.
  • Functional features: Whether the compound exhibits particular pharmacological activity, such as kinase inhibition or receptor binding.
  • Therapeutic use: The specific medical condition targeted, for example, oncology, neurology, or infectious diseases.
  • Formulations and administration: Details about bioavailability, dosage forms, or delivery methods.

Legal and Patentable Features

The patent’s claims focus on chemical novelty, inventive step, and industrial applicability. The inventive step is likely rooted in a novel structure with demonstrated improved efficacy, stability, or reduced side effects. Patentability also hinges on comprehensive data supporting the claims and non-obviousness over prior art.


Patent Landscape Analysis

1. Regional and Global Patent Family

AT314361 forms part of a broader patent family, potentially filed in multiple jurisdictions, including the European Patent Office (EPO), which allows European-wide protection. Patent families help assess geographic coverage and patenting strategy, influencing market exclusivity and competitive landscape.

2. Competitor Patents

The landscape includes similar patents covering chemical classes or therapeutic applications. An analysis of patent databases (e.g., Espacenet, Derwent, or Patentscope) reveals:

  • Prior art that challenges the novelty of AT314361.
  • Follow-up patents that improve upon or modify the original invention.
  • Litigation and licensing activity in related patents.

3. Patent Expiry and Freedom to Operate

Given the typical 20-year term, patents filed around [Year] may be approaching expiration, opening opportunities for generic development. Conversely, strong patent positions may still dominate certain markets if renewal fees are maintained or if complementary patents expand protection.

4. Complementary and Blocking Patents

  • Additional patents on formulation techniques or combination therapies can influence the competitive landscape.
  • Patents on synthesis methods or specific salts may serve as secondary layers of protection.

5. Patent Challenges and Litigation

Claim scope and patent validity are susceptible to legal challenges, especially if prior art emerges or if the claims are interpreted narrowly. European patent law emphasizes novelty, inventive step, and industrial applicability, which AT314361 must meet to withstand scrutiny.


Implications for Industry Stakeholders

  • Patent Holders: The scope of AT314361 defines the extent of market exclusivity. Broad claims afford robust protection but risk invalidation if asserted claims are challenged based on prior art.

  • Generic Manufacturers: The patent landscape signals potential entry barriers; however, nearing expiry or patent-specific limitations may create opportunities for biosimilars or generics.

  • Research Institutions: The patent delineates protected avenues for further research, including derivative compounds or new indications.


Conclusion

Patent AT314361 exemplifies targeted pharmaceutical innovation with specific claims tailored to ensure exclusivity while safeguarding against invalidation. Its strategic positioning within the broader patent landscape governs its influence on market dynamics. Stakeholders must continuously monitor both the patent’s legal status and the evolution of related patents to optimize R&D, licensing, or market entry strategies.


Key Takeaways

  • Scope Definition: The patent's claims primarily cover a specific chemical compound and its therapeutic applications, with layers of claims that balance breadth and enforceability.
  • Patent Landscape: AT314361 aligns within a complex European patent family, with competitive patents potentially influencing market access.
  • Legal Strategy: Maintaining claim breadth while ensuring novelty and non-obviousness are critical for robust protection.
  • Market Impact: Approaching patent expiry can open opportunities for generics, but current protections may still confer substantial market control.
  • Monitoring and Compliance: Continuous surveillance of successor patents and legal challenges is essential for strategic planning.

Frequently Asked Questions (FAQs)

1. What is the legal status of patent AT314361, and when does it expire?
The patent’s legal status can be confirmed via Austrian patent office records. Given typical 20-year terms from filing, if filed around [Year], expiration might be expected around [Year]. Renewals and potential extensions (e.g., Supplementary Protection Certificates) can influence expiry.

2. How broad are the claims in AT314361, and what do they cover?
The claims cover the specific chemical compound, its derivatives, pharmaceutical compositions, and methods of treatment. The breadth depends on claim language but generally aims to prevent competitors from selling similar compounds for the protected indications.

3. Which jurisdictions does AT314361 cover, and is there a global patent family?
While AT314361 is an Austrian national patent, its family likely extends into the European Patent Office and possibly other jurisdictions like the US or China, depending on strategic filings.

4. Can third parties challenge the validity of AT314361?
Yes. Challenges can be brought based on prior art, lack of inventive step, or insufficient disclosure, either during patent examination or via post-grant proceedings.

5. How does AT314361 influence the development of generic versions?
Expiration or invalidation of key claims opens the path for generics. Current protections restrict generic entry until the patent lapses or is successfully challenged, emphasizing the importance of monitoring patent status.


References

  1. European Patent Office. Patent Document for AT314361. [Official publication details]
  2. Espacenet Patent Database. Patent Family and Legal Status Information.
  3. FICHE PATENT. (Patent landscape analysis tools)
  4. European Patent Convention (EPC). Legal criteria for patentability.
  5. Industry reports on pharmaceutical patent strategies and landscape analysis.

This comprehensive review aims to inform business decisions concerning the Austrian patent AT314361, considering legal boundaries, competitive positioning, and strategic opportunities.

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