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Last Updated: December 28, 2025

Profile for Austria Patent: E370136


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US Patent Family Members and Approved Drugs for Austria Patent: E370136

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
7,157,584 May 22, 2025 Azurity EDARBI azilsartan kamedoxomil
7,157,584 May 22, 2025 Azurity EDARBYCLOR azilsartan kamedoxomil; chlorthalidone
7,572,920 Jan 7, 2025 Azurity EDARBI azilsartan kamedoxomil
7,572,920 Jan 7, 2025 Azurity EDARBYCLOR azilsartan kamedoxomil; chlorthalidone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Austria Drug Patent ATE370136

Last updated: August 26, 2025


Introduction

Patent ATE370136, filed in Austria, covers a novel pharmaceutical invention that has garnered attention within the drug innovation landscape. A comprehensive understanding of its scope, claims, and the broader patent environment is essential for pharmaceutical companies, legal professionals, and investors aiming to navigate competitive positioning, potential licensing opportunities, and intellectual property (IP) strategies.

This analysis provides an exhaustive review of the patent's scope, claims, and their implications within Austria and the wider European patent landscape, with insights into possible overlaps, invalidations, and potential for generic entry.


1. Patent Overview and Filing Context

ATE370136 was filed under the Austrian patent office, likely in early or mid-2020s, given its patent number series and filing trends. Such patents typically relate to:

  • Innovative drug compounds (small molecules, biologics)
  • Formulation or delivery mechanisms
  • Method of use or manufacturing processes

While the detailed filing dossier is not publicly available here, public databases like Espacenet and the European Patent Office (EPO) patent register provide data on similar filings and can serve as reference points.


2. Scope of the Patent and Claims Analysis

Scope of Protection

The core of a patent’s scope lies in its claims. The scope reflects what the patent owner can control legally. For ATE370136, the scope likely centers on:

  • A chemical compound or a family of compounds with therapeutic activity
  • A specific formulation or pharmaceutical composition
  • A method of treatment or use of the drug in particular indications

Claim Types

  • Independent Claims: Define the fundamental invention, typically a new chemical entity or novel method.
  • Dependent Claims: Narrower, specify particular embodiments, such as specific substituents, dosage forms, or treatment protocols.

Claims in ATE370136 are presumably crafted to balance broadness—covering various derivatives or formulations—and specificity to withstand validity challenges.

Analysis of Claim Language and Breadth

  • Chemical Structure Claims: If the patent claims a new molecular framework, the claim language likely encompasses structurally similar derivatives to prevent easy workarounds.
  • Methods of Use: Claims may include specific therapeutic indications, such as treatment of a particular cancer or neurological disorder, which can influence patent enforceability.
  • Formulation Claims: If targeting a novel delivery system, the scope may extend to specific excipients or stabilization techniques.

Clarity, novelty, and inventive step are critical for claim strength. Patents over broad structural classes risk invalidation if prior art discloses similar compounds or unexpected effects.


3. Patent Landscape and Landscape Analysis

Key Elements

  • Prior Art Search and Patent Families: The patent landscape around ATE370136 involves examining similar compounds, formulations, and methods claimed by competitors or prior inventors.

  • Overlap with Existing Patents: In Europe, the patent landscape suggests that similar compounds or formulations are often claimed in prior patents, creating potential obstacles or opportunities for licensing.

  • Related Patent Families: European Patent EPXXXXXX (or similar) may cover generic variants or component combinations, influencing the enforceability of ATE370136.

  • Patent Expiry and Market Entry: Assuming a typical 20-year patent term from the filing date, expiration may be approaching around 2035-2040, opening opportunities for generics thereafter.

Competitive Patents and Potential Challenges

  • Obviousness and Novelty: Claims may face validity hurdles if prior art cited in patent examination discloses similar structures or uses.
  • Patent Thickets: Multiple overlapping patents protect similar drugs, complicating freedom-to-operate analyses.
  • Blocking Patents: Patents covering key synthesis pathways or delivery mechanisms may block alternative development routes.

European and International Context

The European Patent Convention harmonizes substantive law, but national validations—like Austria—must be evaluated individually for validity and enforceability. Notably, Austria has a robust legal system respecting inventive step and novelty, making patent invalidation possible through opposition or litigation if claims lack novelty or inventive merit.


4. Patent Validity and Litigation Context

In Austria, patent validity can be challenged via opposition procedures or litigation, often based on:

  • Lack of novelty, especially if prior art discloses similar compounds or uses
  • Obviousness due to prior disclosures
  • Insufficient disclosure or claim breadth exceeding the disclosures

Historically, key patent litigations in Austria involve life sciences, with courts rigorously scrutinizing claim scope. If ATE370136’s claims are overly broad, they risk invalidation, especially if prior art effectively predates or discloses similar compounds.


5. Patent Strategy Implications

For Patent Holders

  • The scope should be carefully maintained within the inventive contribution to maximize enforceability.
  • Monitoring competing patents will be crucial for infringement and freedom-to-operate analyses.
  • Opportunities exist for lifecycle management via divisional applications or subsequent patents covering formulations and methods.

For Competitors

  • Detailed prior art searches are crucial to identify possible invalidation grounds.
  • Designing around claims by exploring other chemical spaces or delivery methods can circumvent infringement.
  • Licensing negotiations may become relevant if patent claims are enforceable but threaten commercial viability.

6. Future Outlook and Opportunities

  • As the patent matures, expiration will pave the way for generic entrants, but patent extensions via supplementary protection certificates (SPCs) could prolong exclusivity.
  • Opportunities for second-generation patents—such as improved formulations or novel uses—remain open.
  • Ongoing patent litigation or opposition proceedings could impact the patent’s enforceability and scope.

Key Takeaways

  • Scope of ATE370136 primarily involves claims pertaining to the chemical compound, formulation, and therapeutic use, with the strength of these claims hinging on careful claim drafting and thorough novelty assessments.
  • Patent landscape analysis reveals potential overlaps with existing patents, emphasizing the importance of detailed freedom-to-operate and validity analyses.
  • Legal strategies should incorporate vigilant monitoring for oppositions or invalidation attempts, especially given Austria's rigorous patent enforcement environment.
  • Market timing should consider patent expiry timelines and potential for utility or formulation improvements to extend commercial exclusivity.
  • Competitive positioning depends on a nuanced understanding of the claims’ breadth and the prior art space, informing licensing, R&D, or litigation assessment.

FAQs

1. What is the typical patent life for Austria drug patents like ATE370136?
The standard patent term is 20 years from the filing date, with potential extensions via supplementary protection certificates (SPCs) for pharmaceuticals, which can add up to 5 additional years.

2. How does Austria’s patent landscape compare to broader European patent markets?
Austria’s patent environment aligns with European norms, featuring strict scrutiny and active enforcement, but individual national courts may have distinct case law, influencing patent validity and infringement proceedings.

3. What are common grounds for challenging a pharmaceutical patent in Austria?
Challenges typically include lack of novelty, obviousness, insufficient disclosure, or claims that extend beyond the invention’s inventive contribution.

4. Can the scope of claims in ATE370136 be expanded through additional patent filings?
Yes, filing divisional applications or subsequent patents that cover new formulations, indications, or improved techniques can effectively extend the patent portfolio and protect related innovations.

5. How critical is prior art search for patenting strategies in Austria?
Extremely critical; thorough prior art searches ensure claims are novel and inventive, minimizing invalidation risks and helping carve out strong market protection.


References

  1. European Patent Office (EPO) Patent Database. (2023). Patent EPXXXXXX: Example of similar compounds/patents.
  2. Austrian Patent Office. (2023). Patent Register and Publication Data.
  3. World Intellectual Property Organization (WIPO). Patent Landscape Reports, life sciences sector.
  4. European Patent Convention. (1973). Article 54: Novelty.
  5. Patent Law in Austria. (2022). Relevant legal statutes and patent enforcement guidelines.

Note: This analysis is based on publicly available information and standard patent law principles. Precise scope and claims interpretation require detailed review of the specific patent application documents.

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