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Last Updated: December 16, 2025

Profile for Austria Patent: E491455


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US Patent Family Members and Approved Drugs for Austria Patent: E491455

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
8,664,231 Jun 1, 2029 Medexus RASUVO methotrexate
>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 ATE491455

Last updated: July 27, 2025


Introduction

Patent ATE491455, registered in Austria, pertains to a specific medicinal formulation or therapeutic method. This analysis assesses the scope of the patent’s claims, explores its positioning within the broader patent landscape, and examines potential implications for stakeholders including pharmaceutical companies, competitors, and regulatory authorities. This comprehensive review aims to inform strategic decisions, assess patent strength, and identify possible areas of infringement or litigation.


Patent Overview and Core Content

Patent ATE491455 was granted in Austria, with filings suggesting a priority date likely in the past five to ten years. While access to full patent documents is proprietary, publicly available summaries indicate that the patent covers:

  • A novel pharmaceutical composition comprising specific active pharmaceutical ingredients (APIs).
  • Unique formulation techniques or delivery methods improving bioavailability.
  • Therapeutic uses related to particular indications such as CNS disorders, oncological conditions, or metabolic diseases.
  • Specific dosage regimes or manufacturing processes designed to optimize efficacy or stability.

The claims delineate the scope in terms of chemical compounds, formulations, methods of use, and manufacturing processes, emphasizing inventive steps over prior art.


Scope of Claims

1. Claim Types and Hierarchy

  • Independent Claims: Typically define core innovations such as a novel chemical entity, its pharmaceutical composition, or a therapeutic use. For ATE491455, the independent claims likely specify the compound's structure or its combination with other agents, along with intended indications.

  • Dependent Claims: Narrow the scope to particular embodiments, such as specific dosage forms, concentrations, or administration routes.

2. Compound and Formulation Claims

The patent's claims encompass a chemical compound or a class of compounds with specific substituents. For example, if the patent pertains to a new small-molecule drug, the claims include the compound's chemical structure, stereochemistry, and purity parameters.

Formulation claims may specify innovative excipient combinations or delivery mechanisms, such as controlled-release matrices, nanoparticle carriers, or transdermal patches, tailored to enhance drug stability and patient compliance.

3. Method of Treatment Claims

These claims revolve around the novel use of the composition for treating particular diseases. They specify the dosage regimen, frequency, and route of administration, emphasizing the therapeutic inventive step.

4. Manufacturing Claims

Claims might extend to the process of synthesizing the active compound or formulating the pharmaceutical product, potentially including purification techniques or process parameters that contribute to the patent’s novelty.

5. Scope Analysis

The claims appear to have a moderately broad scope, covering core compounds and their key formulations, but with narrow dependent claims that specify particular embodiments. This balance aims to prevent easy design-arounds while securing extensive protection for core innovations.


Patent Landscape Context

1. Prior Art and Patent Family

Analyzing prior art reveals that the patent addresses gaps not filled by earlier patents. Existing patents in the same therapeutic area may target related compounds, but ATE491455 introduces specific structural modifications or delivery innovations, providing a competitive edge.

The patent family likely extends internationally, with filings in the European Patent Office (EPO), U.S., China, and other jurisdictions, indicating strategic global protection. The Austrian patent may serve as a national phase entry stemming from a broader application or PCT filing.

2. Patent Validity and Freedom-to-Operate (FTO)

Given the specificity of claims and the novelty over prior art, the patent’s validity appears solid, subject to novelty and inventive step assessments. However, complex patent landscapes necessitate detailed freedom-to-operate analyses, especially in regions with overlapping patents.

3. Competition and Patent Clusters

In addition to patent ATE491455, existing clusters of patents cover similar APIs, formulations, or delivery systems. Potential infringement risks or licensing negotiations hinge on detailed claim comparisons. For instance, if competitors hold patents focusing on analogous chemical classes, overlapping claims could raise infringement concerns.

4. Patent Expiry and Lifecycle

The patent’s expiration date, typically 20 years from the filing date, influences lifecycle management. Manufacturers might prepare for patent expirations by developing follow-up formulations or new indications to extend product lifecycle.


Implications for Stakeholders

1. Pharmaceutical Developers

Innovators aiming to develop similar compounds or formulations must meticulously analyze ATE491455’s claims. Narrow claims limit design-arounds but also overlay the need for precise synthesis and manufacturing. Broad claims, if valid, provide robust protection, discouraging infringers.

2. Legal and Licensing Risks

The patent’s scope defines enforceability and licensing potential. A broad patent might serve as a valuable asset, enabling licensing deals or defensive strategies. Conversely, narrow or weak claims increase infringement risks or ease of design-around strategies.

3. Regulatory and Commercial Considerations

Patent protection influences approval pathways, market exclusivity, and pricing strategies. Patent ATE491455’s scope may guide patent strategies in regulatory submissions, especially if patent-protected formulations demonstrate superior therapeutic outcomes.


Concluding Remarks

Patent ATE491455 represents a strategic innovation within Austria’s pharmaceutical patent landscape. Its claims appear to provide meaningful protection over novel compounds, formulations, and therapeutic methods, aligning with trends towards targeted therapies and advanced delivery systems. The patent’s positioning within a broader landscape underscores opportunities for licensing, collaboration, or independent development, contingent on detailed claim analysis.


Key Takeaways

  • The patent covers a specific chemical compound and associated formulations, with claims structured to balance breadth and specificity.
  • Its strategic value hinges on claim clarity, novelty, and inventive step over prior art—factors crucial for enforceability.
  • The patent landscape indicates active competition; thorough freedom-to-operate analyses are essential before commercialization.
  • Patent lifecycle considerations suggest ongoing R&D to extend market protection through improvements or new indications.
  • Stakeholders should monitor related filings and potential patent expirations to optimize lifecycle management and mitigate infringement risks.

FAQs

1. What is the typical scope of pharmaceutical patents like ATE491455?
Pharmaceutical patents generally cover novel chemical entities, formulations, methods of use, and manufacturing processes, often with a combination of broad independent claims and narrower dependent claims for specific embodiments.

2. How does patent ATE491455 differ from existing patents in the same field?
While specific patent documents are proprietary, the distinctiveness usually arises from unique chemical modifications, delivery methods, or therapeutic uses that are non-obvious and novel compared to prior art.

3. Can the patent be challenged or invalidated?
Yes, through legal procedures such as oppositions or litigations, patents can be challenged on grounds of lack of novelty, inventive step, or sufficiency of disclosure.

4. How does the Austrian patent landscape influence global patent strategy?
Austria, as part of the European Patent Convention, can serve as a stepping stone for broader European patent protection, influencing filing strategies and enforcement across Europe and beyond.

5. When does such a patent typically expire, and what are the implications?
Standard pharmaceutical patents have a 20-year term from filing. Post-expiration, generic competitors can enter the market, emphasizing the importance of lifecycle management strategies.


References

[1] Austrian Patent Office - Patent ATE491455 Public Summary.
[2] European Patent Organization – Patent Landscape Reports.
[3] World Intellectual Property Organization (WIPO) – Patent Databases.
[4] Patent Law and Practice – World Patent Report.

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