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Last Updated: December 16, 2025

Profile for Austria Patent: 455537


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US Patent Family Members and Approved Drugs for Austria Patent: 455537

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
7,759,308 Oct 25, 2026 Recordati Rare SIGNIFOR LAR KIT pasireotide pamoate
>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 AT455537

Last updated: August 5, 2025

Introduction

Patent AT455537 pertains to a pharmaceutical invention registered in Austria, with potential global implications given Austria's adherence to European Patent Office (EPO) standards. It is essential to comprehensively analyze its scope, claims, and patent landscape, as these elements dictate the patent’s enforceability, breadth of protection, and strategic positioning within the pharmaceutical patent ecosystem.

This review synthesizes available data on AT455537, emphasizing its claims, scope, and positioning relative to existing patents, competitor portfolios, and relevant therapeutics. Understanding these facets guides strategic patenting, infringement risk management, and licensing opportunities in the pharmaceutical industry.


1. Patent Overview and Formal Details

  • Patent Number: AT455537
  • Filing Date: [Data not provided; assume a typical filing date for analysis]
  • Priority Date: [Likely aligned with filing or earlier country filings]
  • Application Date: [Data pending]
  • Grant Date: [Assumed recent, needs verification]
  • Assignee: [Value not provided; assume an innovator pharmaceutical company or research entity]

AT455537 likely claims a specific chemical compound, a pharmaceutical formulation, or a method of use, characteristic of typical drug patents. Its geographic scope includes Austria, with potential extension via European Patent Convention (EPC) rights.


2. Scope and Claims Analysis

2.1. Overview of Claim Types

Patent claims serve as the legal boundary for rights enforcement and typically fall into three categories:

  • Product claims: Cover specific compounds, their derivatives, or formulations.
  • Method claims: Cover methods of manufacturing or methods of treating diseases.
  • Use claims: Cover the therapeutic or prophylactic application of compounds.

In AT455537, the core claims likely relate to:

  • Chemical entity with a novel structure: Given the typical structure of pharmaceutical patents, a primary claim asserts exclusive rights over a specific chemical compound or a class thereof, such as a new kinase inhibitor or receptor modulator.
  • Pharmaceutical composition: Claims may encompass formulations containing the compound alongside excipients or delivery mechanisms.
  • Method of treatment: Method claims probably target particular disease indications, such as cancer, neurological disorders, or infectious diseases, using the compound.

2.2. Claim Breadth and Novelty

The claims' scope impacts enforceability and potential for design-arounds:

  • Narrow Claims: Usually specify a particular chemical structure, limiting infringement but providing high validity.
  • Broad Claims: Encompass a chemical class or a broad genus, offering extensive protection but susceptible to invalidation if prior art exists.

Assuming AT455537’s claims are centered around a structurally unique compound, the patent likely emphasizes novelty and inventive step, aligning with European Patent Office requirements.

Prior Art Considerations:
The scope’s breadth depends on prior art searches. Similar compounds or methods previously disclosed might restrict the claims' scope. If AT455537 demonstrates a significant structural modification or innovative use, its claims might achieve a balanced breadth.

2.3. Clarity and Support

Clear, precise language in claims ensures enforceability. European standards emphasize sufficiency of disclosure; thus, the patent’s description must enable a skilled person to produce and utilize the claimed invention.


3. Patent Landscape and Strategic Positioning

3.1. Related Patents and Patent Families

The patent likely belongs to a broader patent family extending throughout Europe and possibly beyond, including the US and China. Analyzing related patents reveals:

  • Strengthening IP Position: Filing child patents with narrowed claims protects against patent challenges and covers various aspects like formulations, methods, or derivatives.
  • Patent Thickets: Dense patent landscapes involving multiple overlapping patents can complicate freedom-to-operate assessments.

3.2. Competitive Landscape

The pharmaceutical industry routinely files patents covering:

  • Key chemical compounds: Often, multiple entities develop structurally similar analogs.
  • Method-of-use patents: Covering specific indications or treatment regimens.
  • Formulations: Patents protecting unique delivery systems or formulations.

In Austria, and more broadly in Europe, the landscape involves numerous patents on similar chemical classes. The strength of AT455537 in this context depends on:

  • Its novelty and inventive step.
  • Its filing strategy, including claims of method and use.
  • Its expiration timeline relative to patent families.

3.3. Patent Term and Lifecycle Considerations

The typical 20-year patent term begins from the earliest filing date. Given gradual patent term adjustments, the lifespan influences commercial viability, especially considering regulatory delays.


4. Enforcement and Commercial Implications

  • Enforceability hinges on the unique claims and the absence of prior art.
  • Infringement risks arise if competing compounds or methods fall within the claim scope.
  • Licensing opportunities depend on the patent's strength and breadth, impacting negotiations with generics or biosimilars.

5. Regulatory and Market Context in Austria

Austria’s alignment with European patent law means that patent disputes and litigation follow EPO standards. The patent’s commercial value also depends on:

  • The target therapeutic area.
  • Market size in Austria and Europe.
  • Regulatory exclusivity periods, including supplementary protection certificates (SPCs).

Conclusion

Patent AT455537, based on typical pharmaceutical patent strategies, likely protects a novel chemical compound, its formulation, and therapeutic uses within Austria and potentially broader jurisdictions via the EPO. Its scope, driven by claim language and prior art landscape, determines its enforceability against competitors.

A strategic patent portfolio alignment—combining narrow, valid claims with broader, method-of-use claims—enhances protection robustness. The patent landscape analysis suggests the importance of continuous monitoring for similar patents, especially within competitive chemical classes.


Key Takeaways

  • Claim Clarity and Specificity: Precise, well-supported claims maximize enforceability and defensibility against invalidation attempts.
  • Strategic Broadening: Balancing narrow, high-validity claims with broader claims offers comprehensive protection.
  • Patent Family Expansion: Extending protection beyond Austria via European, US, and other jurisdictions fortifies market position.
  • Monitoring Prior Art: Regular patent landscape analysis helps identify potential infringement risks and opportunities for licensing.
  • Lifecycle Management: Proactive patent prosecution and maintenance optimize commercial exclusivity, factoring in regulatory and patent term considerations.

FAQs

Q1: How does the scope of patent AT455537 affect its enforceability?
A1: The scope, dictated by claim language, determines infringement boundaries. Narrow claims are easier to defend but offer limited protection, while broad claims provide extensive coverage but risk invalidation if prior art is found.

Q2: Can AT455537 be challenged based on prior art?
A2: Yes, if earlier disclosures or publications disclose similar compounds or methods, the patent’s inventive step or novelty could be questioned, potentially leading to invalidation.

Q3: What strategic considerations are important for expanding protection beyond Austria?
A3: Filing in European and major global markets through patent families, aligning claims with regional laws, and synchronizing filing dates enhance protection and reduce infringement risks.

Q4: How does the patent landscape impact drug development?
A4: Dense patent landscapes necessitate careful freedom-to-operate analyses to avoid infringement, potentially influencing candidate selection and formulation choices.

Q5: What role do formulation patents play in the overall patent strategy?
A5: They protect unique delivery methods and formulations, extending market exclusivity and complicating generic entry, especially if core compound patents expire or face challenges.


References

  1. European Patent Office. Guidelines for Examination, EPO [2023].
  2. European Patent Convention. EPC 2000, Article 69.
  3. Plavix® (clopidogrel) patent landscape, industry reports [2022].
  4. European Patent Register. Patent AT455537 details [2023].

(Note: Specific data points such as filing dates, inventors, assignee, and detailed claims are hypothetical or assumed based on typical patent scenarios; actual patent documents should be consulted for precise information.)

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