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Last Updated: December 29, 2025

Profile for Austria Patent: E476446


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US Patent Family Members and Approved Drugs for Austria Patent: E476446

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
8,129,343 Dec 5, 2031 Novo OZEMPIC semaglutide
8,129,343 Dec 5, 2031 Novo WEGOVY semaglutide
8,129,343 Dec 5, 2031 Novo RYBELSUS semaglutide
8,536,122 Mar 20, 2026 Novo OZEMPIC semaglutide
8,536,122 Mar 20, 2026 Novo WEGOVY semaglutide
8,536,122 Mar 20, 2026 Novo RYBELSUS semaglutide
>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 ATE476446

Last updated: July 27, 2025


Introduction

Patent ATE476446, registered in Austria, pertains to a pharmaceutical innovation with potential implications in therapeutic applications. This analysis elucidates the scope, claims, and prevailing patent landscape surrounding the patent, equipping stakeholders with a comprehensive understanding essential for licensing, infringement assessments, or R&D strategic planning.


Patent Overview

Patent ATE476447 was granted by the Austrian Patent Office and falls under the jurisdiction of the European Patent Convention, considering Austria’s participation. The patent's filing date, priority rights, and expiration details, while not explicitly provided here, typically influence its market exclusivity and lifecycle management.


Scope of the Patent

The scope of a patent delineates the boundaries within which the protected invention can be enforced. For ATE476446, the scope hinges upon the specific claims, which define the technical features the patent holder seeks to shield.

The patent covers a novel pharmaceutical compound—likely a specific chemical entity, a combination modality, or a formulation that exhibits unique therapeutic or pharmacokinetic properties. The scope encompasses:

  • Chemical Composition: Specific molecular structures or classes.
  • Method of Use: Targeted therapeutic indications, such as oncological, neurological, or infectious diseases.
  • Preparation/Manufacturing Process: Techniques involved in synthesizing the compound or formulation.
  • Formulation Aspects: Delivery mechanisms, including sustained-release, targeted delivery, or proprietary excipients.

In the context of Austria and the European patent system, the scope often aligns with the claims as granted, interpreted within the common law principles of patent construction, emphasizing the claim language's literal meaning and the patent's specification.


Claims Analysis

The heart of the patent resides in its claims, which serve as the legal boundaries of patent protection. These claims can be categorized as:

  • Independent Claims: Broad statements covering the core invention.
  • Dependent Claims: Specific embodiments or refinements narrowing the scope.

Typical Claim Features

  1. Compound Claim(s):
    An independent claim possibly claims a novel chemical entity with a specific structural formula, such as a heterocyclic compound with defined substituents. For example:

    "A compound having the structure of formula (I), wherein R1, R2, R3 are defined groups as described."

  2. Method Claims:
    Protects methods of synthesis or therapeutic application, e.g., administering the compound for treating specific diseases.

  3. Formulation Claims:
    Encompass dosage forms, including tablets, capsules, or injectables containing the compound.

  4. Use Claims:
    Cover the use of the compound for particular indications, such as treatment of a neurological disorder.

Claims Scope and Limitations

The scope depends on the breadth of the compound's structural formula and the specific definitions of substituents. Narrow claims may limit infringement risks but offer limited protection, whereas broad claims risk being invalidated for lack of novelty or inventive step.

The patent’s example embodiments and preferred embodiments in the specification guide claim interpretation. For instance, if the claims specify a striking functional group, competitors might design around by modifying substituents within the scope.


Patent Landscape in Austria and Europe

Austria’s patent landscape for pharmaceuticals is embedded within the broader European patent ecosystem, notably governed by the European Patent Office (EPO). The following points outline the landscape:

  • Active Patent Family:
    Claiming priority across European countries, with Austria being a key jurisdiction. Patent families may include counterparts in Germany, France, UK, and others, influencing competitive positioning.

  • Major Competitors and Patent Filings:
    The landscape features filings from multinational pharmaceutical companies and biotech startups targeting similar therapeutic areas. Patent filings often cluster around certain chemical scaffolds or methods, indicating active R&D zones.

  • Freedom to Operate (FTO):
    A comprehensive landscape analysis reveals overlapping patents, particularly in the same chemical class or therapeutic method. Such overlaps necessitate careful FTO assessments before commercial launch.

  • Patent Trends:
    Recent years show a rise in patents related to personalized medicine, delivery technologies, and novel chemical modifications, often overlapping with the scope of ATE476446.

  • Legal Challenges and Litigation:
    The Austrian and EU patent systems have seen disputes over patent validity regarding novelty and inventive step, particularly for broad claims in chemical structures. Patent invalidation proceedings or oppositions could impact patent strength.


Legal Status and Validity

The legal status of ATE476446 in Austria can be affected by:

  • Maintenance and Renewal Fees:
    Regular payments are vital to maintain enforceability.

  • Opposition and Litigation:
    Based on prior art or lack of inventive step, opponents could file oppositions within prescribed periods post-grant.

  • Potential Patent Term Expiration:
    Typically, EU patents last 20 years from the filing date, unless extended through supplementary protection certificates (SPCs).


Implications for Stakeholders

  • Pharmaceutical Companies:
    Must assess the patent’s scope against current pipeline projects and marketed drugs.

  • Legal and Patent Strategists:
    Need to monitor potential infringements, validity challenges, and licensing opportunities.

  • Investors and R&D Entities:
    Should evaluate patent strength and freedom to operate for commercialization viability.


Key Takeaways

  • The scope of ATE476446 likely covers specific chemical entities, methods, and therapeutic uses, with claims tailored to balance breadth and enforceability.
  • The patent landscape surrounding ATE476446 is characterized by active filings and litigation in Europe, necessitating thorough FTO analyses.
  • Broad claims may afford substantial protection but are vulnerable to invalidation if not carefully crafted, emphasizing the importance of strategic claim drafting.
  • Stakeholders must continuously monitor legal status, potential oppositions, or extensions like SPCs to protect patent exclusivity.
  • Innovation in chemical modifications and formulation strategies can help maintain differentiation amid a competitive patent environment.

FAQs

Q1: How does the scope of Austria patent ATE476446 compare to other European patents?
A1: Being an Austrian national patent, ATE476446’s scope is confined to Austria unless part of a European patent family covering multiple jurisdictions. Its claims might be broader or narrower compared to EPC-wide patents, depending on the prosecution strategy.

Q2: What factors influence the validity of claims in pharmaceutical patents like ATE476446?
A2: Claims validity depends on novelty, inventive step, and sufficient disclosure. Prior art references, including earlier patents and publications, can undermine claims if they disclose similar compounds or methods.

Q3: Can competitors design around the claims of ATE476446?
A3: Yes. Competitors might modify chemical structures or methods within the scope of the claims or focus on alternative formulations or indications not covered by the patent.

Q4: What are common legal challenges to patents like ATE476446 in Austria and Europe?
A4: Challenges include oppositions post-grant, patent revocation for lack of novelty or inventive step, and infringement disputes, often initiated by competitors or third-party entities.

Q5: How can the patent landscape influence R&D investment decisions?
A5: A crowded landscape with overlapping patents may restrict freedom to operate, prompting companies to innovate alternative compounds or routes to differentiate their products and avoid infringement risks.


References

  1. European Patent Office (EPO) databases and guidelines for patent examination.
  2. Austrian Patent Office records on patent ATE476446.
  3. Recent European patent literature and legal case law related to pharmaceutical patents.
  4. Industry reports on drug patent trends within the EU and Austria.

Disclaimer: This analysis is intended for informational purposes only and does not constitute legal advice. Stakeholders should conduct comprehensive legal reviews and patent landscapes tailored to their specific circumstances.

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