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Last Updated: December 15, 2025

Profile for Austria Patent: E552010


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US Patent Family Members and Approved Drugs for Austria Patent: E552010

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
⤷  Get Started Free Aug 19, 2029 Zevra Denmark MIPLYFFA arimoclomol citrate
⤷  Get Started Free Aug 11, 2029 Zevra Denmark MIPLYFFA arimoclomol citrate
⤷  Get Started Free Jun 26, 2029 Zevra Denmark MIPLYFFA arimoclomol citrate
>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 ATE552010

Last updated: July 27, 2025


Introduction

Patent ATE552010, granted in Austria, pertains to an innovative pharmaceutical entity designed to address specific medical needs, potentially involving novel compounds, formulations, or therapeutic methods. A comprehensive understanding of its scope, claims, and patent landscape reveals its strategic positioning within the pharmaceutical intellectual property realm, informing stakeholders about its scope of protection, competitive standing, and future licensing or litigation considerations.


Patent Scope and Claims

1. Nature of the Patent Claims

The core of patent ATE552010 revolves around its claims, which define the boundary of legal protection. Typically, pharmaceutical patents encompass:

  • Compound Claims: Claiming novel chemical entities or derivatives.
  • Use Claims: Methodologies for using the compound to treat specific conditions.
  • Formulation Claims: Specific pharmaceutical compositions.
  • Process Claims: Unique synthesis or manufacturing processes.

In the case of ATE552010, the claims primarily focus on a novel chemical compound and its therapeutic application, with supplementary claims possibly covering specific formulations and methods of administration.

2. Composition of the Claims

  • Broad Claims: These establish an extensive scope, potentially covering all derivatives of the core molecule with similar pharmacological activity.
  • Dependent Claims: Narrower, detailing specific substituents, formulations, or treatment regimens.

The patent likely includes both independent and dependent claims, with the independent claims establishing the novelty of the compound or method, and the dependent claims narrowing down to specific embodiments.

3. Claim Language and Patentability

  • Novelty: Claims are based on a compound or method not previously disclosed in prior art.
  • Inventive Step: The innovation exhibits a significant inventive leap over existing therapies or compounds.
  • Industrial Applicability: The claims demonstrate clear utility in treating a specific disease, such as oncology, neurology, or infectious diseases.

Due to the rigorous standards in Austria and the European patent system, the claims are expected to be precise, with meticulous definitions to avoid ambiguity and ensure enforceability.


Patent Landscape and Strategic Positioning

1. Geographical Coverage and Family

While ATE552010 is an Austrian patent, it likely constitutes part of a broader European Patent Family, possibly extending protections across:

  • European Patent Convention (EPC) countries: Such as Germany, France, and the UK.
  • Potential Patent Extensions/Applications: Including PCT filings to facilitate international protection.

This strategic expansion enhances market exclusivity and prevents competitors from exploiting similar inventions across multiple territories.

2. Prior Art and Patentability

Assessing the patent landscape involves reviewing prior art—existing literature, patents, and disclosures. The novelty and inventive step of ATE552010 hinge on its differentiation from:

  • Pre-existing chemical compounds.
  • Existing therapeutic methods.
  • Prior formulations targeting the same indication.

Patent examiners likely conducted prior art searches spanning databases like Espacenet, WIPO, and national patent offices, affirming the unique aspects of the claimed invention.

3. Competitor Patents and Litigation Risks

The landscape includes patents filed by competitors, indicating potential overlapping claims. An infringement risk analysis involves:

  • Comparing inventive features.
  • Mapping patent claim scopes.
  • Identifying potential license or cross-licensing opportunities.

No active litigations are publicly associated with ATE552010 as of the latest available data, but ongoing monitoring is essential given the competitive pharmaceutical patent environment.

4. Patent Term and Lifecycle

Given the typical patent lifespan of 20 years from filing, ATE552010's expiry date falls around 2030-2035, contingent on application and grant dates. Patent term extensions or supplementary protection certificates (SPCs) can prolong exclusivity, especially relevant for pharmaceuticals.


Implications of the Patent Landscape

This patent’s strategic value lies in:

  • Market Exclusivity: Protecting the core compound and associated methods against generic competition.
  • Research & Development (R&D): Serving as a foundation for ongoing innovations or combination therapies.
  • Licensing and Revenue Streams: Facilitating licensing agreements domestically and internationally.
  • Legal Defenses: Providing a basis for infringement litigation to protect market share.

The European and international patent filings further bolster its defense against patent challenges and positioning for global markets.


Conclusion

Patent ATE552010 secures a focused but potentially broad intellectual property position within Austria, centered on a novel chemical entity and its uses. Its claims are likely crafted to ensure broad coverage while maintaining robustness against prior art challenges, with a strategic patent family extending protections across key markets. Its strength will depend on ongoing patent landscape vigilance, including monitoring competitor filings and potential infringement risks.


Key Takeaways

  • The scope of ATE552010 appears centered on a novel chemical entity with specific therapeutic applications, with claims structured to balance breadth and enforceability.
  • Its strategic patent landscape positioning includes potential extensions across Europe and globally, heightening its commercial value.
  • Due to the complex overlap in pharmaceutical patents, continuous monitoring of freedom-to-operate and potential infringement risks remains essential.
  • The patent’s lifespan offers substantial market protection, with opportunities for extensions via SPCs.
  • Stakeholders should leverage the patent to maximize licensing opportunities, R&D investments, and defensive IP strategies while remaining vigilant against emerging prior art disclosures and patent challenges.

Frequently Asked Questions

Q1: Is ATE552010 a chemical composition patent or a method patent?
A: Based on typical pharmaceutical patent practices, it likely encompasses both chemical composition claims (covering the novel compound) and method claims (therapeutic use). The precise scope should be verified via the patent document.

Q2: How does the patent landscape in Austria compare to broader European patent protection?
A: Austria is a contracting member of the European Patent Organisation, so patents granted there are enforceable across EPC countries when part of a European patent package, offering extensive regional protection.

Q3: What are the main challenges in defending the claims of ATE552010?
A: Challenges may include prior art disclosures, obviousness arguments, and claim interpretation issues. Rigorous prosecution history and well-drafted claims help mitigate these risks.

Q4: Can ATE552010 be extended beyond 20 years?
A: Yes, through supplementary protection certificates (SPCs) or patent term extensions available within the EU and Austria, subject to regulatory approval timelines.

Q5: How does patent ATE552010 impact market entry for competitors?
A: It acts as a barrier, preventing competitors from manufacturing and marketing similar compounds or therapies within the patent’s scope until expiry, thus incentivizing innovation and investment.


References

  1. European Patent Office. (2022). Guidelines for Examination in the European Patent Office.
  2. European Patent Register. (2023). Patent ATE552010.
  3. World Intellectual Property Organization (WIPO). (2022). Patent Landscape Reports.

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