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Last Updated: December 28, 2025

Profile for Austria Patent: E392889


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US Patent Family Members and Approved Drugs for Austria Patent: E392889

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
8,263,120 May 3, 2025 Cosmo Technologies AEMCOLO rifamycin sodium
8,486,446 May 3, 2025 Cosmo Technologies AEMCOLO rifamycin sodium
8,529,945 May 3, 2025 Cosmo Technologies AEMCOLO rifamycin sodium
8,741,948 May 3, 2025 Cosmo Technologies AEMCOLO rifamycin sodium
>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 ATE392889

Last updated: July 28, 2025


Introduction

Patent ATE392889, registered in Austria, embodies critical intellectual property rights related to a pharmaceutical entity. This patent’s scope—particularly its claims—dictates the extent of proprietary protection granted, influencing market exclusivity, licensing potential, and competitive landscape. This analysis delineates the patent’s scope, critically examines its claims, and contextualizes its landscape within Austria's broader pharmaceutical patent environment.


Overview of Patent ATE392889

Patent ATE392889 was filed to secure exclusive rights over a novel drug compound or formulation. While specific details of the patent's prosecution documents are proprietary, typical pharmaceutical patents encompass claims covering:

  • The active compound or its analogs.
  • The pharmaceutical composition or formulation.
  • Method of preparation or synthesis.
  • Therapeutic use and method-of-use claims.

Given the standard practices and common patent strategies in pharmaceuticals, the scope of ATE392889 likely integrates composition claims and possibly method-of-use claims.


Scope of the Patent

1. Composition and Structure Claims:
These claims define the chemical structure of the active ingredient(s). They specify the molecular formula, stereochemistry, and purity standards. Such claims aim to protect a specific chemical entity or a class of analogs, thereby blocking competitors from producing or selling the same or closely related compounds.

2. Formulation Claims:
Protection extends to specific formulations, such as sustained-release, injectable, or oral dosage forms. These are crucial in establishing a broad protective net around the drug’s commercial embodiments.

3. Method of Manufacturing and Synthesis:
Claims may cover patented synthesis protocols, which secure exclusivity over specific production methods. This prevents competitors from manufacturing the compound via alternative processes that might bypass composition claims.

4. Therapeutic and Method-of-Use Claims:
Claims may encompass novel therapeutic indications or methods of treatment. These are particularly strategic in blocking generic competitors from marketing the same compound for the claimed indications without licensing.


Claims Analysis

1. Independent Claims:
Typically, the patent’s most robust claims are broad, covering the chemical entity and fundamental methods. For instance, an independent claim might claim the active compound with a specific molecular structure or its pharmaceutically acceptable salts.

2. Dependent Claims:
These narrow the scope further by specifying particular salts, polymorphs, crystal forms, or specific dosage ranges. Dependent claims add layers of protection and are often used to defend the core invention against design-around strategies.

3. Claim Interplay:
Effective patents balance broad independent claims with narrower dependent claims to maximize territorial and temporal scope without risking invalidation due to overbreadth. In Austria, patent examination adheres to EPO standards, emphasizing novelty, inventive step, and industrial applicability, influencing claim phrasing and scope decisions.

Legal Considerations:
In Austria, patent claims must be clear and concise, explicitly supported by the description. Ambiguous or overly broad claims risk rejection or invalidation, especially if they attempt to cover prior known compounds or obvious modifications.


Patent Landscape in Austria and EU Context

1. Austria’s Patent Law Framework:
Austria complies with the European Patent Convention (EPC). Once granted, patents have a 20-year term, subject to annual fees and renewal requirements. The Austrian Patent Office (Österreichisches Patentamt) evaluates applications based on EPC criteria.

2. European Patent Strategy:
Many pharmaceutical companies file for European patents covering Austria via the European Patent Office (EPO). These patents are uniformly valid across member states, including Austria, simplifying medicinal patent protection strategy.

3. Overlapping Patent Rights:
In Austria, the patent landscape often involves overlapping rights—national patents, European patents, and supplementary protection certificates (SPCs). For a drug like the one protected by ATE392889, concurrent patent rights may exist for formulations, methods, or methods of use, complicating the competitive landscape.

4. Patent Challenges and Litigation Trends:
Austria’s judiciary and patent offices have upheld strict standards for patentability, especially concerning obviousness and inventive step. Invalidations often target overly broad claims or insufficient disclosure. Litigation frequency remains moderate but impactful, influencing patent value and licensing strategies.


Competitive and Innovation Implications

1. Patent Life Cycle:
The patent’s expiration—likely in around 20 years from filing—dictates market exclusivity length. Secondary patents (e.g., for formulations or methods) can extend protection or create patent thickets to delay generic entry.

2. Freedom-to-Operate Analysis:
Manufacturers assessing commercialization in Austria must analyze claims to avoid infringement. Similarly, patentees must vigilantly monitor prior art to defend or enforce the patent.

3. Patent Strategies:
Innovators often combine broad structure claims with method-of-use patents to safeguard multifaceted aspects of the drug. Licensing negotiations frequently hinge on the scope and enforceability of such claims.


Conclusion

Patents like ATE392889 exemplify targeted protection strategies within Austria’s pharmaceutical patent landscape. The patent’s scope, centered on structure and formulation claims, significantly influences its enforceability and market exclusivity. Meticulous drafting aligned with EPC standards ensures robust protection, while awareness of the landscape helps optimize licensing and litigation strategies.


Key Takeaways

  • Patent ATE392889 likely covers the chemical compound, its formulations, and specific methods, providing layered protection.
  • Effective claims balance breadth and specificity, safeguarding against design-arounds and invalidation.
  • Austria’s adherence to EPC standards and its position within the EU context makes the patent landscape highly structured, with potential overlaps requiring careful strategic planning.
  • Patent validity, enforceability, and potential challenges depend heavily on precise claim language and thorough disclosure.
  • Companies should conduct comprehensive freedom-to-operate analyses and consider secondary patents to prolong market exclusivity.

FAQs

1. What types of claims are typically included in pharmaceutical patents like ATE392889?
Patent claims typically encompass chemical structure/class, formulations, manufacturing processes, and therapeutic methods. Each type offers layered protection, covering both the active compound and its applications.

2. How does Austria's patent law influence the scope of pharmaceutical patents?
Austria applies EPC standards, emphasizing novelty, inventive step, and industrial applicability. Broad claims are carefully scrutinized, requiring clear support in the description to avoid invalidation.

3. Can a European patent provide protection in Austria?
Yes. A granted European patent, validated in Austria, provides unitary protection across multiple EU member states, including Austria, streamlining patent management.

4. How can companies extend patent protection beyond the initial 20 years?
Secondary patents for formulations, polymorphs, or new uses can extend effective protection. Additionally, applying for supplementary protection certificates (SPCs) can extend exclusivity for certain drugs.

5. What strategies can be used to challenge a patent like ATE392889?
Opposition proceedings, patent invalidation trials, or non-infringement defenses can be employed. Validity challenges often focus on prior art, inventive step, or disclosure adequacy.


Sources
[1] European Patent Convention (EPC) standards for patentability.
[2] Austrian Patent Act (Patentgesetz).
[3] European Patent Office (EPO) guidelines on patent claims and validity.
[4] Industry reports on pharmaceutical patent enforcement and litigation in Austria.

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