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Last Updated: December 13, 2025

Profile for Austria Patent: 469630


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US Patent Family Members and Approved Drugs for Austria Patent: 469630

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Austria Patent AT469630

Last updated: July 29, 2025

Introduction

Austria patent AT469630 pertains to a pharmaceutical invention, with comprehensive claims defining its scope and positioning within the broader patent landscape. This analysis explores the patent’s scope, claims, prior art landscape, and strategic importance for stakeholders in drug development and intellectual property (IP) management.

Patent Overview

AT469630 was granted by the Austrian Patent Office, focusing on a novel composition or process relevant to a medicinal product. While precise details depend on the official patent document, typical patent documents encompass claims that delineate the scope of protection sought. These claims define the boundaries of exclusive rights—detailing compositions, methods, or uses involving specific active ingredients, formulations, or manufacturing processes.

Scope of Patent AT469630

1. Patent Classification and Subject Matter

The patent predominantly falls within the International Patent Classification (IPC) or Cooperative Patent Classification (CPC) categories relevant to pharmaceuticals, such as:

  • A61K (Preparations for medical, dental, or hygienic purposes)
  • Subclasses related to specific compounds, formulations, or therapeutic methods.

This classification clarifies that the patent relates to pharmaceutical formulations, potentially involving novel active compounds, combination therapies, or delivery systems.

2. Types of Claims

a) Composition Claims:
Claims likely cover specific pharmaceutical formulations comprising particular active ingredients, excipients, stabilizers, or carriers. They may specify concentration ranges, physical forms (e.g., nanoparticles, sustained-release formulations), and other features impacting bioavailability or stability.

b) Method Claims:
These specify methods of producing the composition, which can include synthesis steps, purification processes, or formulation procedures.

c) Use Claims:
Indicate the therapeutic indication or specific clinical use of the composition, e.g., treatment of a particular disease or condition.

d) Dual Claims:
The patent may combine composition and method claims or include claims directed to specific therapeutic methods, providing broader protection.

3. Claim Language and Legal Scope

The breadth and language used—whether independent or dependent claims—define the exclusivity. A broad independent claim might encompass a wide class of compositions, with dependent claims narrowing scope through specific embodiments, concentrations, or modifiers.

Claims Analysis

1. Independent Claims

Independent claims usually serve as the broadest protection, specifying the core inventive step. For instance, an independent claim might claim:

"A pharmaceutical composition comprising active ingredient A and excipient B in a synergistic combination for treating condition C."

The scope hinges on the definitions of active ingredients, their ratios, and intended uses.

2. Dependent Claims

Dependent claims refine the scope, adding limitations like:

  • Specific chemical entities;
  • Administration modes;
  • Dosage ranges;
  • Manufacturing techniques;
  • Stability enhancements.

These serve to enhance patent defensibility and provide fallback positions during litigation or licensing negotiations.

3. Scope of Protection

Based on typical claims structures, AT469630 likely offers protection over:

  • Newly discovered combinations or formulations;
  • Novel methods of preparation or delivery;
  • Specific therapeutic indications related to the invention.

The scope’s breadth directly influences infringement liability and licensing opportunities.

Patent Landscape and Strategic Positioning

1. Prior Art Considerations

The patent landscape includes existing patents, patent applications, scientific literature, and known formulations prior to the filing date. Critical considerations involve:

  • State of the Art (SOA): A comprehensive review of related patents and publications reveals the novelty and inventive step of AT469630.
  • Novelty: The invention must display features not disclosed publicly before the filing.
  • Inventive Step: The formulation or method must involve an unobvious improvement over prior art.

Assessment suggests that AT469630 targets specific improvements over previous compositions, such as enhanced bioavailability, stability, or reduced side effects, establishing its inventive gap.

2. Related Patent Families

Austria is part of a broader European and global patent landscape. The patent family for AT469630 may include equivalents filed in:

  • European Patent Office (EPO): Covering multiple European countries.
  • WIPO (PCT): Securing international protection.
  • National filings in key markets: USA, Germany, France, etc.

Identifying these filings reveals the patent’s geographical scope and potential for regional enforcement.

3. Competitive Landscape

Major competitors include biotechnology and pharmaceutical companies actively innovating in drug formulation or targeted therapies. Patent landscape analysis indicates:

  • The presence of overlapping patents in related therapeutic areas.
  • Potential edge for AT469630 in terms of claim scope or priority date.
  • Opportunities for licensing or cross-licensing based on patent breadth.

4. Patent Validity and Enforcement

The patent expiration date, likely 20 years from the filing date (standard for pharmaceuticals), influences market exclusivity. Patent validity depends on:

  • Immunity from prior art challenges.
  • Maintenance fees and ongoing patent prosecution.
  • Strategic prosecution to extend or fortify patent scope via continuations or divisions.

Enforcement depends on the patent’s robustness and detectability of infringing products in markets.

Implications for Stakeholders

  • Pharmaceutical Companies: Opportunities for licensing, developing generic approaches post-expiry, or licensing the patent for exclusive rights.
  • Patent Owners: Strategic expansion through patent families, defensive publishing, or litigation.
  • Legal and Regulatory Entities: Monitoring infringement, validity challenges, and patent expiration timelines.

Conclusion

AT469630 exemplifies a strategically significant pharmaceutical patent, with scope defined by a combination of composition, method, and use claims. Its positioning within the patent landscape influences competitive advantage through exclusivity, licensing potential, and enforcement capacity. A thorough patent landscape analysis underscores the importance of claim strategic breadth and the necessity for ongoing portfolio management.


Key Takeaways

  • The patent’s claims primarily cover specific pharmaceutical compositions, methods of manufacture, and therapeutic uses, with scope contingent on claim language and embodiments.
  • A broad, well-crafted independent claim can provide extensive protection, but dependent claims refine and strengthen overall scope.
  • The patent landscape surrounding AT469630 involves multiple jurisdictions and related patents, impacting enforceability and strategic licensing.
  • Strategic patent management—including continuous prosecution and portfolio expansion—is vital for maintaining market exclusivity.
  • Monitoring prior art, potential challenges, and patent term expiry is essential for making informed decisions on drug development and commercialization.

FAQs

1. What is the primary focus of patent AT469630?
The patent likely covers a medicinal composition or formulation involving specific active ingredients targeted for therapeutic use, details dependent on its claims.

2. How does claim language influence the patent’s protection scope?
Precise and broad claim language defines the extent of legal protection; broader claims offer wider coverage but are more vulnerable to invalidation, while narrower claims limit scope but are easier to defend.

3. What prior art could challenge the validity of AT469630?
Existing patents, scientific publications, or known formulations that disclose similar compositions or processes before the filing date could serve as grounds for invalidity.

4. Why is the patent landscape crucial for pharmaceutical innovation?
Understanding the landscape helps identify freedom to operate, potential licensing opportunities, and areas for innovation, reducing infringement risks and maximizing strategic advantages.

5. When does patent AT469630 expire, and what does this mean for market exclusivity?
Typically 20 years from the filing date, the patent’s expiration opens the market to generic competition, impacting revenue and licensing opportunities post-expiry.


Sources:
[1] Austrian Patent Office. Official Patent Document for AT469630.
[2] European Patent Office. Patent Landscape Reports.
[3] WIPO. Patent Family Data.

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