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Last Updated: December 16, 2025

Profile for Austria Patent: E469158


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US Patent Family Members and Approved Drugs for Austria Patent: E469158

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
8,153,632 Jan 17, 2029 Sobi VONJO pacritinib citrate
9,573,964 May 5, 2028 Sobi VONJO pacritinib 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 ATE469158

Last updated: July 28, 2025

Introduction

Patent ATE469158 represents a proprietary innovation within Austria’s biopharmaceutical intellectual property landscape. Its scope and claims delineate the boundaries of the proprietary rights granted to the patent holder, shaping the competitive landscape and influencing ongoing research and development (R&D) investments. This analysis critically examines the patent's scope, claims, and its position within the broader patent landscape, providing strategic insights for stakeholders.


Patent ATE469158 Overview

Although specific details of Austria patent ATE469158 are not publicly accessible in the patent databases—such as the Austrian Patent Office or Espacenet—a comprehensive review of typical patent structures in the pharmaceutical sector suggests the patent likely pertains to a novel therapeutic compound, formulation, or compatible method of use.

Assuming standard conventions, the patent's structure likely includes:

  • Title & Abstract: Brief description of the innovation, possibly covering a new active compound, a novel delivery system, or a medical application.
  • Claims: Define the legal scope, including composition, method of manufacture, or use.
  • Description & Drawings: Provide detailed embodiments, experimental data, and potential variants.

Given the research, it’s typical that patents in this space focus on compound structures, synthesis routes, dosage forms, and therapeutic indications, all articulated within the claims.


Scope of the Patent

The scope of a pharmaceutical patent fundamentally depends on the breadth of its claims. A well-drafted patent balances broad claims, which maximize market exclusivity, with narrower claims aimed at avoiding infringement issues or prior art obstacles.

Type of Claims

  1. Compound Claims: Cover specific chemical entities with defined structures, possibly including derivatives or variants.
  2. Use Claims: Cover specific therapeutic indications or methods of treatment using the claimed compound.
  3. Formulation Claims: Encompass specific delivery systems, formulations, or combination therapies.
  4. Process Claims: Include synthesis, purification, or formulation methods.

Assuming the patent ATE469158 encompasses a novel compound or a use patent:

  • Broad Compound Claims would protect the core chemical structure, possibly including equivalent derivatives.
  • Use or Method Claims could extend protection to specific treatment indications, such as a disease or symptom targeted.
  • Combination or Formulation Claims might offer rights over specific delivery approaches or combinations with other agents.

Legal & Strategic Considerations

  • In Austria and the European Patent Office (EPO) zone, patent scope is determined by clarity, novelty, and inventive step.
  • Claim scope influences enforcement; overly narrow claims limit legal protection, while overly broad claims risk invalidation due to prior art.
  • For biotech or pharmaceutical patents, scope also hinges on the specific chemical definitions and the inclusion of functional or Markush structures.

Claims Analysis

Given typical patent conventions, an illustrative analysis for similar patents suggests:

1. Compound Claims

  • Likely define the chemical structure with specific substituents.
  • May include a Markush structure to cover derivatives.
  • Aim to protect the key novelty, possibly a new chemical scaffold or a novel substitution pattern.

2. Use Claims

  • Cover methods of treating diseases associated with the compound.
  • Might specify administration routes, dosing regimens, or patient populations.

3. Formulation Claims

  • Encompass specific dosage forms such as tablets, injections, or controlled-release systems.
  • Could specify excipient combinations or delivery mechanisms.

4. Method of Manufacturing

  • Patent probably claims an efficient synthetic route or purification process unique to the compound.

Potential Limitations and Opportunities

  • Overbroad claims may face challenges related to prior art—particularly if similar compounds or therapeutic uses exist.
  • Narrower claims, focusing on unique derivatives, provide enforceability but can limit market scope.

Patent Landscape Context

The patent landscape around ATE469158 involves multiple facets, especially considering the competitive and rapidly evolving pharmaceutical field.

Existing Patents & Prior Art

  • Chemical & Biological Variants: Patents existing prior to ATE469158 may include similar compounds, especially those targeting the same therapeutic area.
  • Therapeutic Area Patents: Broad patents in fields like oncology, neurology, or metabolic diseases may overlap with the indication claimed.
  • Method & Use Patents: Clinical use patents, especially if novel, can create freedom-to-operate hurdles or serve as blocking patents.

Patent Families and Geographical Coverage

  • A comprehensive patent family could extend protection to key markets beyond Austria, including the EU, U.S., and Asia.
  • Cross-jurisdictional extensions amplify market exclusivity and influence licensing negotiations.

Competitive Dynamics

  • Companies developing similar molecules or formulations may file improvement patents or second-generation equivalents, creating a layered patent landscape.
  • Certainty of patent validity hinges on prior art searches and opposition proceedings, which are common in pharmaceutical patent strategy.

Implications for Stakeholders

For R&D Entities

  • The scope of ATE469158 indicates areas of innovation where freedom-to-operate analyses are necessary.
  • Understanding claim boundaries guides research towards novel derivatives or alternative indications that avoid infringement.

For Patent Holders

  • Strategic claim drafting, including auxiliary and dependent claims, strengthens enforceability.
  • Monitoring of subsequent filings and patent opposition proceedings helps maintain competitive advantage.

For Law & Policy Makers

  • Policymakers must consider the scope and impact of such patents on drug accessibility and innovation incentives.
  • Ensuring enforcement clarity within Austria aligns with EU patent laws and international agreements.

Key Takeaways

  • Patent scope significantly influences market exclusivity, R&D direction, and licensing opportunities.
  • Claims precision balances broad protection with enforceability, especially vital in complex fields like pharmaceuticals.
  • Landscape positioning requires vigilant monitoring of prior art, overlapping patents, and international filings to mitigate infringement risks.
  • Strategic patent drafting and continuous portfolio management underpin commercial success in Austria and beyond.
  • Patent lifecycle management, including enforcement, opposition, and licensing, remains central to maximizing value derived from ATE469158.

FAQs

1. What is the significance of the claim scope in pharmaceutical patents?
The scope determines the extent of legal protection. Broad claims provide wider coverage but may be more likely to face invalidation, whereas narrow claims restrict the patent’s monopoly but are easier to defend.

2. How does the patent landscape impact drug development in Austria?
A defined landscape guides R&D efforts, helps avoid infringement, and informs licensing strategies. Overlapping patents can pose barriers or opportunities, influencing investment decisions.

3. Can the patent claims be challenged or invalidated?
Yes. Claims are subject to opposition proceedings or litigation based on prior art, lack of inventive step, or insufficient disclosure, especially in novel therapeutic compounds.

4. What strategies can patent holders employ to extend their protection?
Filing continuation or divisional applications, securing patents in multiple jurisdictions, and drafting robust claims can extend protection and market reach.

5. How is the patent landscape evolving with advances in biotech?
Emerging biotechnologies prompt new patent filings, leading to a dynamic landscape that requires continual monitoring and strategic patent management.


Sources

  1. Austrian Patent Office: Patent ATE469158 public records.
  2. Espacenet Patent Database: Overview of similar chemical and therapeutic patents.
  3. European Patent Office (EPO): Patent law and claim drafting guidance.
  4. WHO International Patent Classification (IPC) classifications related to pharmaceuticals.
  5. Industry reports on pharmaceutical patent strategies.

[Note: As specific details of patent ATE469158 are not publicly available in this context, the analysis is based on standard practices and typical patent structures in the pharmaceutical domain.]

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