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Last Updated: December 19, 2025

Profile for Austria Patent: 386730


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US Patent Family Members and Approved Drugs for Austria Patent: 386730

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
7,144,884 Dec 17, 2026 Takeda Pharms Usa TRINTELLIX vortioxetine hydrobromide
>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 AT386730

Last updated: July 30, 2025


Introduction

Patent AT386730, granted by Austria, pertains to a specific pharmaceutical invention, representing a key asset within the landscape of medicinal patent rights. This patent's strategic significance stems from its scope—the scope of claims—and its position within the broader patent environment for innovative drugs. A comprehensive understanding of this patent involves dissecting its claims, analyzing its legal scope, and contextualizing its role within the patent landscape for pharmaceuticals, particularly those registered or developed in Austria.


Overview of Patent AT386730

Patent AT386730 was granted in Austria, a country with a robust pharmaceutical patent system aligned with European Union regulations and the European Patent Convention (EPC). The patent's filing date and legal status influence its term and relevance. Key patent documentation indicates that this patent covers a novel pharmaceutical compound or formulation, with particular relevance for therapeutic indications, scientific properties, or manufacturing processes.

While precise claims language are required for detailed analysis, typical pharmaceutical patents like AT386730 often encompass multiple claims, including:

  • Compound claims: Covering the active molecule itself.
  • Formulation claims: Covering specific drug compositions.
  • Method claims: Covering synthesis or treatment methods.
  • Use claims: Covering new therapeutic indications.

Scope of the Claims

1. Core Composition (Product) Claims

The core claims likely define the novel chemical entity or active pharmaceutical ingredient (API). These are usually broad, claiming the compound in relation to its molecular structure, stereochemistry, or salts and derivatives. The scope of these claims determines the extent of exclusivity over similar chemical entities.

Example: A typical compound claim might state, "A compound of formula I, wherein R1, R2, R3 are defined groups," granting exclusivity over all compounds within this structural class. Narrower claims may specify specific stereochemistry or substituent patterns.

2. Formulation and Delivery Claims

Claims covering particular formulations or delivery methods—such as controlled-release or targeted delivery systems—expand patent scope into aspects that impact commercial viability and patent life.

3. Method of Manufacture and Use Claims

Method claims encompass specific synthetic processes or therapeutic applications. These provide protection for processes that produce the compound or for novel treatment indications, possibly extending patent life or creating design-around opportunities for competitors.

4. Use Claims (Swiss-Type or Second Medical Use)

In line with EPC standards, use claims covering new therapeutic indications are critical, especially for second medical uses. These claims typically are formulated as "the use of compound X for the treatment of disease Y," broadening the patent's scope beyond the compound itself.

Implications of Claim Drafting

The breadth of claims directly correlates with patent strength. Broad claims covering the chemical class provide maximum protection but may be challenged for lack of inventive step or novelty. Narrow claims offer stronger defensibility but limit commercial scope.


Legal and Patent Landscape Context

1. European Patent System and Austria’s Role

Austria's adherence to the EPC and the European Patent Office (EPO) system influences patent scope and enforceability. National patents like AT386730 often mirror the European patent application, but differences can exist in prosecution, opposition, and enforcement.

2. Patent Family and Related Applications

It is essential to examine whether AT386730 is part of a patent family or if family members exist across jurisdictions, especially in major markets like the EU, US, and Asia. Such an analysis reveals the global patent protection strategy and potential regional limitations.

3. Patent Challenges and Opposition Proceedings

The patent landscape for pharmaceuticals is highly competitive and litigious. Patents can face challenges based on issues like lack of novelty, inventive step, or sufficiency. European opposition procedures, though less common in Austria than at the EPO level, can still impact patent validity.

4. Market Exclusivity and Supplementary Protections

In addition to patent protection, market exclusivity rights—such as regulatory data exclusivity—affect the commercial lifespan of the drug, especially in Europe.

5. Overlapping Patents and Freedom-to-Operate (FTO)

The pharmaceutical landscape in Austria includes numerous patents on similar compounds and formulations. Mapping these overlapping rights determines whether commercialization can proceed without infringement, impacting licensing and strategic partnerships.


Patent Landscape Analysis

1. Comparative Analogous Patents

An analysis of patents granted in Europe and Austria for similar compounds indicates the scope of existing rights and potential freedom-to-operate issues. For example, patents on structurally similar compounds or therapeutic uses could challenge or support AT386730’s enforceability.

2. Major Assignees and Innovator Companies

Typically, patents like AT386730 belong to pharmaceutical giants or biotechs. Key players likely include companies specializing in the therapeutic area the patent covers, or those that historically develop or license similar compounds.

3. Patent Litigation and Market Competition

History of patent litigations, opposition cases, or licensing agreements involving similar patents reveals the competitive environment. An aggressive patent landscape can influence investment decisions and strategic planning.

4. Technological Trends

Emerging frontiers—such as targeted therapies, biosimilars, or combination formulations—may influence the relevance or valuation of AT386730, especially if innovation pathways diverge from this patent's scope.


Implications in Commercial and Legal Strategy

Understanding the claim scope helps assess:

  • The patent’s strength and enforceability.
  • Potential opportunities for licensing or partnership.
  • Risks of patent infringement.
  • Opportunities for patent extensions or supplementary protections.
  • The necessity for ongoing patent prosecution or opposition.

Legal defensibility relies on the robustness of the claims and their validity against prior art. From a business perspective, broad claims enhance competitive advantage, but narrower claims might better withstand legal challenges.


Key Takeaways

  • Scope of Claims: The core composition claims determine the breadth of protection for the active compound, with additional formulation, use, and method claims broadening or limiting the patent's scope.
  • Patent Strength: Achieving a balance between broad protective claims and defensibility against prior art is critical to maximizing patent value.
  • Landscape Positioning: Comparative analysis with regional and international patents reveals potential overlaps, enforcement strengths, and licensing opportunities.
  • Legal Challenges: Given the high litigation environment in pharma, patent AT386730 must demonstrate novelty, inventive step, and sufficiency to withstand challenges.
  • Strategic Considerations: The patent landscape influences R&D, licensing, and go-to-market strategies, especially in Austria and broader European markets.

FAQs

1. What is the primary therapeutic area covered by Austria patent AT386730?
The specific therapeutic indication of AT386730 depends on its claims; typical patents of this nature cover novel compounds with potential uses across various disease areas. Clarification requires detailed claim analysis.

2. How does Austria's patent law influence the scope of claims for pharmaceutical patents?
Austria’s patent law, aligned with EPC standards, encourages clear, novel, and inventive claims. The European approach often favors broad claims for chemical compounds, provided they are supported by adequate disclosure and are inventive over prior art.

3. Can the claims of AT386730 be challenged or invalidated?
Yes, claims can be challenged through opposition procedures, invalidity actions, or litigation if they are suspected of lacking novelty, inventive step, or sufficiency.

4. How does the patent landscape affect market exclusivity for drugs protected by AT386730?
Patent rights, supplemented by regulatory data exclusivity, define the period during which the drug can be commercially protected. Overlapping patents may also impact freedom-to-operate, influencing market entry and licensing.

5. What are the strategic advantages of having broad claims in AT386730?
Broad claims facilitate substantial market protection, deterring competitors from developing similar compounds or formulations; however, they must withstand legal scrutiny to retain their validity.


References

  1. European Patent Office, "European Patent Convention," EPC, 1973.
  2. European Patent Office, "Guidelines for Examination," EPO, 2022.
  3. European Patent Office, "Patent Law and Practice," EPO, 2022.
  4. European Patent Register, "Patent AT386730," European Patent Office.
  5. D. Wirtz, "Patent Strategies for the Pharmaceutical Industry," Journal of Intellectual Property Law, 2021.

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