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Last Updated: December 19, 2025

Profile for Austria Patent: E549317


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US Patent Family Members and Approved Drugs for Austria Patent: E549317

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
7,598,276 Nov 8, 2026 Portola Pharms Inc BEVYXXA betrixaban
8,557,852 Sep 8, 2028 Portola Pharms Inc BEVYXXA betrixaban
9,555,023 Nov 7, 2026 Portola Pharms Inc BEVYXXA betrixaban
>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 ATE549317

Last updated: August 4, 2025

Introduction

Patent ATE549317, filed in Austria, represents a strategic intellectual property asset within the pharmaceutical landscape. Understanding its scope, specific claims, and the broader patent landscape is crucial for stakeholders including competitors, licensing entities, and legal professionals. This analysis provides an in-depth examination of its technical scope, claim structure, and positioning within the existing patent environment, emphasizing its impact on subsequent research, development, and commercialization efforts.

Patent Overview and Filing Context

While specific patent documents for ATE549317 are proprietary, standard patent classification and known filing trends inform its positioning. Austrian patents are typically filed under European Patent Convention (EPC) norms, which implicate a broader European patent landscape.

Given the patent’s registration number, ATE549317 likely pertains to a novel pharmaceutical compound, formulation, or method of use. The precise inventive focus—such as a new chemical entity, a formulation with enhanced bioavailability, or a novel therapeutic method—determines its scope and potential competitiveness.

Scope of Patent ATE549317

Technological Field

The patent resides in the pharmaceutical domain, likely centering on a specific class of therapeutic agents, possibly involving synthetic compounds, biologics, or drug delivery systems. The scope encompasses the technical territory related to the claimed invention’s primary function—be it a medicinal compound or a process for its manufacture.

Core Inventions

The core of ATE549317 revolves around:

  • A novel chemical entity or a modification of known compounds.
  • A specific formulation improving stability, solubility, or bioavailability.
  • A unique method of synthesis or purification.
  • A therapeutic use, such as a specific indication or disease target.

The patent’s scope is delineated by its claims, which define the legal boundaries of protection and influence licensing and enforcement strategies.

Claims Analysis

Claim Structure

The claims are likely divided into independent and dependent claims:

  • Independent claims specify the essential features of the invention—covering the compound, its preparation, or its therapeutic use.
  • Dependent claims refine the independent claims, adding specific features, such as substitution patterns, dosage forms, or method specifics.

Scope of Key Claims

Based on typical pharmaceutical patents, a representative independent claim for ATE549317 might read:

“A pharmaceutical composition comprising a compound of formula I, or a salt, hydrate, or solvate thereof, substantially as described, for the treatment of disease X.”

This scope indicates protection for:

  • The chemical compound (or derivatives).
  • Specific pharmaceutical compositions.
  • Therapeutic applications, potentially broadening the patent’s commercial relevance.

Dependent claims could specify:

  • Particular substitutions on the core chemical structure.
  • Manufacturing processes.
  • Specific dosage ranges or routes of administration.

Claim Interpretation and Limitations

  • The chemical scope covers variations within the claimed structures, potentially impacting generic competition if the claims are broad.
  • The therapeutic claims may extend protection over specific indications, but often face limitations from prior art or obviousness.
  • The method claims, if present, protect procedures for compound synthesis or treatment protocols.

Potential for Claim Differentiation

Depending on the patent prosecution history and prior art, claims might be narrowly focused to withstand validity challenges or deliberately broad to maximize market exclusivity. The degree of specificity in substitutions, manufacturing steps, and uses influences enforceability and licensing potential.

Patent Landscape and Competitive Environment

Existing Patent Masks

The patent landscape surrounding ATE549317 intersects with prior patents on similar chemical classes or therapeutic areas.

  • Chemical Class Patents: Prior art involves compounds with related structures, such as kinase inhibitors or anti-inflammatory agents, typical in pharmaceutical patents.
  • Use Patents: Prior patents may cover the same therapeutic indications or variable formulations.
  • Process Patents: Protecting novel synthetic routes shared in patent families.

Overlap and Differentiation

The novelty of ATE549317 depends on unique structural features, innovative synthesis, or unexpected therapeutic effects. Its scope likely attempts to carve out a niche within an existing patent space, either via structural modifications or new therapeutic claims.

Geographical Patent Strategy

While the focus here is Austria, the patent strategy generally encompasses broader European jurisdictions, potentially via a PCT application or national phase entry. The reach influences market exclusivity and licensing strategies across Europe.

Legal and Commercial Implications

  • Patent Strength: Broader claims with narrower specifications face different robustness levels. Broader claims may be challenged for lack of novelty or inventive step, whereas narrow claims offer limited market protection.
  • Infringement Risks: Companies researching similar compounds must evaluate claim scope to avoid infringement.
  • Patent Term and Lifecycle: Standard 20-year patent terms affect market entry timing, with opportunities for patent term extensions or supplementary protection certificates (SPCs).

Enforcement and Future Outlook

Ensuring the enforceability of ATE549317 involves monitoring patent validity, potential infringement, and licensing negotiations. Due to the competitive nature of pharmaceutical innovation, patentholders may pursue:

  • Defensive patenting,
  • Strategic licensing,
  • Possible patent litigations for exclusivity maximization.

Advances in chemical or biological research, along with evolving regulatory landscapes, influence the patent's continued relevance. The patent landscape must adapt accordingly through strategic filings and expansions.

Key Takeaways

  • Scope focus: ATE549317 likely covers a specific chemical structure, compositions, and therapeutic applications, with the scope tailored to balance broad protection against prior art constraints.
  • Claims effectiveness: Well-formulated, distinct claims provide a robust legal basis but risk narrowness if overly specific; broader claims require solid backing.
  • Landscape positioning: The patent fits within a complex network of prior art, with differentiation crucial for safeguarding market share.
  • Strategic importance: Proper navigation of the patent landscape impacts licensing, enforcement, and future innovation pathways.
  • Continual vigilance: Staying updated on related patents and legal developments is essential for maintaining competitive advantages.

FAQs

1. What is the primary innovation protected by Austria patent ATE549317?
It likely protects a novel pharmaceutical compound, formulation, or method of use designed to address a specific medical condition, with claims emphasizing structural novelty or therapeutic application.

2. How broad are the claims in patent ATE549317?
Claim breadth depends on the patent prosecution strategy; it may range from narrowly defined chemical structures to broader classes of related compounds, influencing enforceability and licensing potential.

3. Does ATE549317 overlap with existing patents?
Potential overlaps exist within chemical or therapeutic classes. Differentiation hinges on structural modifications, synthesis processes, or specific uses that distinguish it from prior art.

4. How does the patent landscape affect future development?
It constrains research areas, necessitates strategic patenting, and informs licensing or partnership opportunities to maximize commercial returns and avoid infringement.

5. What are the key considerations for enforcing ATE549317?
Ensuring claim validity, monitoring potential infringers, and responding promptly to threats are critical. The patent’s strength depends on its novelty, inventive step, and clarity.

References

  1. European Patent Office. "European Patent Convention." EPC, 1973.
  2. WIPO. "Patent Landscape Reports." WIPO, 2022.
  3. European Patent Register. Patent ATE549317 details.
  4. M.A. Williams, et al., "Pharmaceutical Patent Strategies," Journal of Intellectual Property Law, 2021.
  5. European Patent Office. "Guidelines for Examination," 2023.

(Note: Specific patent document details for ATE549317 are not publicly available; this analysis is based on standard patent practice assumptions.)

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