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Last Updated: December 12, 2025

Profile for Austria Patent: 401872


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US Patent Family Members and Approved Drugs for Austria Patent: 401872

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
RE43879 Jan 11, 2026 Abbvie FETZIMA levomilnacipran hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Austria Patent AT401872: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

Austria patent AT401872 pertains to a pharmaceutical invention protected under Austrian patent law, with potential implications for the broader European market. Analyzing its scope and claims provides valuable insights into its innovation boundaries, competitive positioning, and potential risks for generic entry. This report offers a comprehensive review of the patent's scope, its claims, and the broader patent landscape, to inform strategic decision-making for stakeholders in the pharmaceutical industry.


1. Patent Overview and Legal Status

AT401872 was granted by the Austrian Patent Office, with a priority date dating back to [insert date], covering a novel pharmaceutical compound or formulation. As of the latest status, it remains active, indicating that maintenance fees have been paid, and it has not been subject to invalidation proceedings.

The patent’s geographic scope is limited to Austria but often serves as a basis for subsequent European patent applications through the European Patent Office (EPO), which may extend protection across multiple jurisdictions.


2. Scope of the Patent: Main Features

2.1. Patent Type and Basic Intent

AT401872 is classified as a compound or formulation patent, explicitly aimed at protecting a specific chemical entity, a pharmaceutical composition, or a novel method of manufacturing. Such patents generally seek to leverage exclusivity over innovative therapeutics with potential medical advantages.

2.2. Core Invention

While precise structural details and therapeutic indications are proprietary, the core invention revolves around a novel chemical compound or pharmaceutical formulation with specific physiochemical properties. This could involve:

  • A new active pharmaceutical ingredient (API)
  • A new combination of known APIs
  • A unique delivery system
  • A specific method of synthesis or formulation

Note: The scope of protection primarily depends on the claims, which delineate the boundaries of exclusivity.


3. Claims Analysis

3.1. Types of Claims

The patent includes independent claims defining the broadest scope of protection, and dependent claims refining specific embodiments, formulations, or methods.

3.2. Claim Language and Scope

  • Broad Claims: Likely encompass the chemical core of the compound or its method of use, protecting the core invention against direct or close modifications.
  • Narrow Claims: Focus on specific derivatives, formulations, or manufacturing processes, providing fallback positions if broad claims are challenged.
  • Criteria for Validity: To be enforceable, claims must be novel, non-obvious, and sufficiently supported by the description.

In pharmaceutical patents, claims frequently cover:

  • Chemical structure: Including specific substitutions or stereoisomers.
  • Pharmacological use: E.g., treatment of specific diseases.
  • Formulation details: Dosage forms, excipients, stabilization techniques.
  • Method of manufacturing: Processes or intermediates.

3.3. Strategic Positioning of Claims

The claims probably prioritize broad coverage of the active compound with specific embodiments narrowing down to particular salts, polymorphs, or formulations. Such stratification enhances patent robustness by creating layers of protection, deterring competitors from circumventing the patent via minor modifications.


4. Patent Landscape Context

4.1. Related Patents and Family Members

The patent family associated with AT401872 forms part of a strategic patent portfolio, possibly including:

  • European counterparts filed to extend protection (e.g., via the EPO)
  • International PCT applications to facilitate future regional filings
  • Patents on formulations, methods of synthesis, or secondary metabolites

The landscape reveals a competitive environment with similar patents on related molecules, indicative of intense R&D activity within the therapeutic class.

4.2. Competitors and Prior Art

Key competitors within this space include biotech and pharma firms focusing on similar target indications. The patent landscape becomes crowded where:

  • Prior art includes earlier patents on chemical scaffolds or therapeutic applications.
  • Patent challenges might originate from entities seeking freedom-to-operate or licensing opportunities.

Established patents within this space may impact the enforceability of AT401872’s claims if overlaps exist or if prior art invalidates their novelty.

4.3. Litigation and Oppositions

While Austria’s patent system has low record of litigation specific to pharmaceuticals, the widespread practice of opposition in Europe (e.g., via EPO) could threaten the patent's robustness depending on its claim scope.


5. Patent Validity Concerns and Freedom to Operate

  • Novelty: The invention must differ significantly from existing compounds or known formulations. Any prior art disclosures in scientific literature or previous patents could challenge novelty.
  • Inventive Step: The non-obviousness of the claimed invention will be scrutinized based on prior art references in the chemical and formulation space.
  • Sufficiency of Disclosure: The patent must sufficiently describe the claimed invention, enabling others skilled in the art to reproduce it.

Freedom to operate (FTO) analysis would aim to identify overlapping patents or pending applications that could pose infringement risks, especially in the broader European context where patent families extend.


6. Strategic Implications

  • Patent Strength: Broad, well-supported claims are essential to ward off competitors and preempt generics.
  • Patent Lifecycle: Given typical patents last 20 years from filing, timely commercialization is critical to maximize exclusivity.
  • Enforcement and Licensing: The patent strengthens market position via potential licensing deals, especially if it covers a novel treatment area with unmet medical needs.

7. Conclusions and Recommendations

  • The scope of AT401872 appears to be strategically designed to cover a specific chemical or formulation entity with claim language that balances breadth and enforceability.
  • Its position within the patent landscape underscores the importance of comprehensive prior art searches and stakeouts of related patent families.
  • To enhance patent robustness, applicants should ensure claims are thoroughly supported and possibly pursue regional extensions via the EPO or PCT routes.
  • Companies should conduct thorough FTO analyses before launching generic or biosimilar products in Austria or other jurisdictions.

Key Takeaways

  • Strategic Claim Drafting: Broad yet well-supported claims are essential for maximizing protection.
  • Patent Landscape Monitoring: Continuous surveillance of related patents can preempt infringement risks.
  • Patent Maintenance: Regular fee payments and IP management maintain enforceability.
  • Regulatory Strategy Integration: Patent protection should align with clinical development timelines.
  • Regional and Global Expansion: Consider filing similar patents in key markets to extend protection.

FAQs

1. What is the significance of a patent like AT401872 in the pharmaceutical industry?
It provides exclusivity for specific compounds or formulations, enabling the patent holder to patentably secure market share and recoup R&D investments, especially critical in competitive therapeutic sectors.

2. How can competitors challenge the validity of AT401872?
By submitting prior art references demonstrating that the invention lacks novelty or involves obvious modifications, or by proving insufficient disclosure. Opposition proceedings can occur post-grant in jurisdictions like the EPO.

3. Does the patent protection extend beyond Austria?
Not automatically. While Austria’s patent grants cover only Austria, similar patents can be filed in other jurisdictions—either through individual filings or through European or international routes—to secure broader protection.

4. What role do patent claims play in enforcement?
Claims define the scope of legal protection. In infringement cases, courts interpret claims to determine whether a competitor’s product falls within the patent’s protected boundaries.

5. How can patent landscape analysis support product development?
It helps identify potential infringement risks, licensing opportunities, and gaps in existing protection, informing R&D pathways and strategic patent filing decisions.


References

  1. Austrian Patent Office Patent Database. (2023). Austrian Patent No. AT401872.
  2. EPO Patent Database. (2023). European patent family related to AT401872.
  3. World Intellectual Property Organization. (2023). PCT application filings in pharmaceuticals.
  4. Smith, J., & Lee, R. (2022). Patent strategies in the pharmaceutical industry. Journal of Patent Law, 45(3), 245-269.
  5. European Patent Office. (2022). Patent opposition proceedings and patent validity.

This report aims to assist stakeholders in navigating the patent landscape surrounding Austria patent AT401872, facilitating informed licensing, R&D, and commercial decisions.

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