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Last Updated: December 12, 2025

Profile for Austria Patent: E503480


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US Patent Family Members and Approved Drugs for Austria Patent: E503480

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
⤷  Get Started Free Apr 22, 2029 Genentech Inc ESBRIET pirfenidone
⤷  Get Started Free Apr 22, 2029 Genentech Inc ESBRIET pirfenidone
⤷  Get Started Free Apr 22, 2029 Genentech Inc ESBRIET pirfenidone
>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 ATE503480

Last updated: July 28, 2025


Introduction

The patent ATE503480 has garnered attention within Austria's pharmaceutical patent landscape for its potential therapeutic applications. As part of comprehensive intellectual property (IP) management, understanding the scope, claims, and broader patent environment offers critical insights for stakeholders including competitors, investors, and regulatory authorities. This analysis dissects the patent's claims, its technological scope, and contextualizes it within the evolving Austrian and European patent landscapes.


Patent Overview and Context

ATE503480 is a patent filed with the Austrian Patent Office, likely aligned with an application lodged through the European Patent Office (EPO) or an international route, considering Austria's integrated IP framework within the European system. The patent appears to focus on a novel compound, formulation, or therapeutic method relevant to a specific disease, such as oncology, neurology, or infectious diseases. However, precise technical disclosures are necessary for a detailed analysis.

The patent's priority date, filing date, and legal status influence its enforceability and lifecycle protection. As of the latest available data, ATE503480 is either granted or granted with amendments, positioning it within the active patent portfolio useful for competitive analysis.


Scope and Claims Analysis

Claims Structure and Hierarchy

The patent comprises multiple claims—independent and dependent—that delineate the breadth and depth of protection:

  • Independent Claims: Typically describe the core innovation, often a novel compound, therapeutic methodology, or unique formulation.
  • Dependent Claims: Narrow or specify aspects such as pharmaceutically acceptable salts, specific dosages, delivery forms, or use cases.

Without access to the exact claims text, this analysis infers several typical protective features based on standard patent drafting practices in the pharmaceutical sector.

Key Aspects of the Claims

  1. Compound or Composition Claims:
    Likely claim novel chemical entities or pharmaceutical compositions with specific structural motifs or properties demonstrating improved efficacy, stability, or bioavailability.

  2. Use and Method Claims:
    These claims cover the therapeutic application of the compound, including methods of administering the drug for specific indications, such as tumor suppression, immune modulation, or neurological benefit.

  3. Formulation Claims:
    Specific excipient combinations, sustained-release forms, or targeted delivery systems added to enhance pharmacokinetics or patient compliance.

  4. Manufacturing Process Claims:
    Processes for synthesizing the compound efficiently, with high purity or yield, may also be embodied in dependent claims.

Claim Scope and Validity Considerations

The scope of protection hinges on the claim language's breadth:

  • Broad Claims: Aim to cover a wide array of chemical analogs or uses but are vulnerable to invalidation if overly broad or unsupported by the disclosure.
  • Narrow Claims: Offer more specific protection around particular embodiments, reducing invalidation risk but limiting exclusivity.

Critical analysis requires comparing these claims with prior art—existing patents, scientific publications, and known compounds—to assess novelty, inventiveness (non-obviousness), and inventive step.


Patent Landscape in Austria and Europe

European Patent Strategy

Austria is part of the European Patent Convention (EPC), meaning ATE503480 may benefit from unitary or national validation upon grant by the EPO. The European landscape for drug patents is dynamic, driven by:

  • Genomics and biosimilar proliferation: As AstraZeneca or Bayer patents expire, opportunities emerge for follow-on innovations.
  • Data exclusivity vs. patent protection: EU legislation grants data exclusivity for biologics and new chemical entities, with patents serving as a primary IP tool.

Competitive Patent Environment

In Austria, the patent landscape shows a high density of pharmaceutical patents covering oncologic compounds, neurological drugs, and vaccine formulations. Notably:

  • Overlap with existing patents: The scope of ATE503480 must be scrutinized for potential infringement or freedom-to-operate issues.
  • Litigation precedents: Austria maintains a developed pharmaceutical patent litigation framework, emphasizing enforceability and validity challenges.

Relevant Patent Families

It is essential to assess:

  • Patent families related to the same inventive concept across Europe,
  • Parallel filings in major jurisdictions (e.g., US, China, Japan),
  • European Patent Office (EPO) search reports and opposition proceedings relevant to ATE503480.

Legal and Commercial Implications

Given Austria's robust IP protections, a patent like ATE503480 can serve as a valuable asset, particularly if it covers a proprietary drug candidate with strong differentiation. However, competitors may file third-party observations or challenge the patent's validity, especially if claims are broad.

For licensees, the patent provides a platform for negotiations, especially if the claimed invention covers unencumbered therapeutic indications with unmet medical needs. Conversely, generic manufacturers may seek to design-around or challenge claims to introduce biosimilar or alternative formulations.


Regulatory and Market Considerations

The patent's enforceability influences market exclusivity, especially considering Austria's integrated EMA review process and local health policies promoting affordable medicines. Patent protection enhances incentives for investment in clinical trials, registration, and commercialization.


Conclusion

Summary of the Patent ATE503480's Scope and Claims:

  • The patent aims to protect a novel chemical entity, formulation, or therapeutic method.
  • Its claims balance broad protection over its inventive concept with narrower dependent claims for specific embodiments.
  • The scope's strength depends on how well claims differentiate from prior art and withstand validity challenges.

Patent Landscape Opportunities and Risks:

  • Austria and Europe exhibit a vibrant pharmaceutical patent environment with significant overlap and innovation.
  • Strategic landscape analysis indicates potential for licensing deals, but also necessitates vigilance for challenges and invalidation risks.

Key Takeaways

  • Ensure detailed claim analysis against prior art to validate the scope’s strength.
  • Monitor European patent proceedings and oppositions affecting ATE503480.
  • Consider filing for supplementary protecting data or design-around strategies to mitigate risk.
  • Engage in early licensing discussions to maximize patent value and market penetration.
  • Maintain awareness of evolving EU patent legislation affecting biologics and small molecules.

FAQs

1. What is the primary purpose of the claims in patent ATE503480?
They define the scope of legal protection, covering specific compounds, methods, or formulations that the patent owner can prevent others from making, using, selling, or importing within Austria and Europe.

2. How does Austria's patent law influence the protection of pharmaceutical inventions like ATE503480?
Austria, as part of the EPC, offers a robust legal framework that validates European patents nationally, providing enforceable rights subject to examination of novelty, inventive step, and industrial applicability.

3. Can patent ATE503480 be challenged or invalidated?
Yes. Competitors can file third-party observations or oppositions post-grant, citing prior art that may invalidate claims if they lack novelty or inventive step.

4. How does the patent landscape in Austria impact drug market entry strategies?
A strong patent portfolio can be pivotal for exclusivity and competitive advantage; however, overlapping patents necessitate careful freedom-to-operate assessments to avoid infringement.

5. What role does patent landscape analysis play in pharmaceutical R&D investment decisions?
It helps identify white spaces, avoid infringing existing patents, and informs licensing or partnership opportunities, ultimately optimizing R&D resource allocation.


References

  1. European Patent Office, European Patent Register.
  2. Austrian Patent Office, Patent Database.
  3. EU Intellectual Property Office, Patent Legislation and Guidelines.
  4. World Intellectual Property Organization, Patent Landscape Reports.
  5. Patent legal analysis publications, relevant to European pharmaceutical patents.

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