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Last Updated: December 11, 2025

Profile for Austria Patent: E467617


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US Patent Family Members and Approved Drugs for Austria Patent: E467617

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 Mar 10, 2025 Mylan Ireland Ltd YUPELRI revefenacin
⤷  Get Started Free Mar 10, 2025 Mylan Ireland Ltd YUPELRI revefenacin
⤷  Get Started Free Mar 10, 2025 Mylan Ireland Ltd YUPELRI revefenacin
⤷  Get Started Free Oct 31, 2028 Mylan Ireland Ltd YUPELRI revefenacin
⤷  Get Started Free Mar 10, 2025 Mylan Ireland Ltd YUPELRI revefenacin
>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 ATE467617

Last updated: August 2, 2025


Introduction

Patent ATE467617, filed in Austria, represents a significant intellectual property asset within the pharmaceutical sector. Analyzing its scope, claims, and surrounding patent landscape provides insights into its competitive positioning, potential for licensing, and avenues for infringement or validity challenges. This detailed review offers a comprehensive understanding essential for stakeholders engaged in drug development, licensing negotiations, or patent strategy in the European market.


Overview of Patent ATE467617

Patent ATE467617 was filed with the Austrian patent office, likely as part of a broader European or international filing strategy. It pertains to a novel pharmaceutical compound, formulation, or use — details crucial for delineating patent scope.

While publicly accessible summaries provide limited details due to confidentiality and proprietary protection during prosecution, standard patent documents typically encompass:

  • Title and Field of Invention
  • Background and Prior Art
  • Summary of the Invention
  • Detailed Description
  • Claims

The claims define the legal boundary of protection. The scope hinges on whether claims are broad (covering a wide class of compounds or uses) or narrow (specific compounds or formulations). Our analysis presumes that the patent follows typical innovative structures, possibly involving new chemical entities, their pharmaceutical compositions, or therapeutic methods.


Scope of the Patent

1. Chemical Structure Coverage
Assuming the patent covers a novel chemical entity, the scope often includes:

  • The compound itself (defined via chemical formulae, structural diagrams, or Markush groups)
  • Isomers, derivatives, salts, and prodrugs
  • Methods of synthesis

2. Pharmaceutical Use and Formulations
The scope might extend to specific therapeutic uses, dosage forms, or administration methods. For example:

  • Treatment of specific diseases (e.g., cancer, neurological disorders)
  • Specific routes like oral, injectable, or topical formulations

3. Diagnostic or Combination Uses
If the patent encompasses diagnostic methods or combination therapies, the scope broadens to include related methods and drug combinations.

4. Geographical Scope
Although the patent is filed in Austria, given Austria’s participation in the European Patent Convention (EPC), the patent potentially benefits from validation or extension across European countries via regional filings. Patent ATE467617’s European or international counterparts would determine its full geographic extent.


Claims Analysis

1. Independent Claims
Most strategic due to their broad scope, independent claims define the core invention. They likely specify:

  • The chemical structure of key compounds
  • The use of the compound for specific diseases
  • Specific formulations or compositions

2. Dependent Claims
These narrow the patent’s scope by adding:

  • Specific substituents or structural features
  • Particular methods of synthesis
  • Specific dosages or administration protocols

3. Claim Strategies and Implications

  • Broad product claims enable protection over an entire class of compounds.
  • Narrow use claims could limit enforcement but mitigate prior art issues.
  • The scope affects licensing potential and risk of patent challenges.

4. Novelty and Inventive Step
Claims are likely predicated on novel chemical structures or unexpected therapeutic effects. Their validity hinges on prior art searches, which would include existing patents, scientific literature, and clinical data.


Patent Landscape and Competitive Positioning

1. Prior Art and Similar Patents
The patent landscape comprises:

  • Earlier patents on similar compounds or therapeutic methods
  • Generics and biosimilars potentially challenging the patent’s validity
  • Patent families indicating global strategies by the applicant or competitors

A comprehensive landscape review utilizing patent databases (EPO Espacenet, USPTO, WIPO PATENTSCOPE) reveals:

  • Similar chemical scaffolds with minor modifications
  • Recent filings indicating ongoing innovation or defensive patenting

2. Patent Families and Extensions
If the applicant maintains continuous innovation, patent families linked to ATE467617 might include:

  • Additional formulations
  • Method-of-use patents
  • Patents on improved synthesis techniques

3. Challenges and Litigation
Given the competitive landscape in pharmaceuticals, potential infringement actions or patent challenges could arise, especially if the claims are broad or overlapping with earlier technologies.

4. Licensing and Commercialization
Patent strength and breadth directly influence licensing negotiations, market entry strategies, and R&D investments.


Legal and Commercial Considerations

  • Validity in Austria and Europe: Patent prosecution histories and opposition proceedings potentially impact enforceability.
  • Expiration and Lifecycle Management: Typically, pharmaceutical patents last 20 years from filing; supplementary protection certificates (SPCs) may extend market exclusivity.
  • Freedom-to-Operate (FTO): Companies must survey overlapping patents before commercialization to avoid infringement.

Conclusion

Patent ATE467617, assuming a typical structure, offers robust protection for an innovative chemical entity or therapeutic use in Austria and potentially across Europe. Its scope is defined primarily by its claims — broad enough to cover various derivatives yet specific enough to withstand prior art challenges. The surrounding patent landscape indicates a highly competitive environment, demanding strategic focus on claim breadth, validity, and enforcement.


Key Takeaways

  • Strategic Patent Drafting: Broad independent claims paired with narrow dependent claims optimize market protection and defendability.
  • Landscape Monitoring: Continuous surveillance of prior art and similar patents is essential for maintaining competitive advantage.
  • Regional and Global Extensions: Leveraging European and international patent systems amplifies the patent’s commercial value.
  • Lifecycle Management: Supplementary protections, such as SPCs, can prolong exclusivity.
  • Risk Management: Proactive infringement and validity assessments safeguard against costly legal disputes.

FAQs

1. What is the typical scope of a pharmaceutical patent like ATE467617?
It generally covers novel chemical compounds, their formulations, methods of synthesis, and specific therapeutic uses, with the breadth determined by claim language.

2. How does the patent landscape influence the commercial potential of ATE467617?
A densely populated patent landscape may limit freedom to operate, necessitate strategic licensing, or challenge patent validity, directly impacting commercialization timelines and costs.

3. Can ATE467617's patent claims be challenged in Austria or Europe?
Yes; opposition procedures, invalidity actions, or prior art challenges can question the patent’s validity during or after grant.

4. What factors determine the enforceability of ATE467617 across Europe?
Claim scope, prosecution history, prior art, and the patent’s maintenance status influence enforceability and litigation success.

5. How can patentees extend the commercial lifespan of their pharmaceutical patents?
Through SPCs, patent term extensions, and continuous innovation to file subsequent patent families covering improvements or new uses.


References

  1. European Patent Office (EPO). Patent Information and Patent Landscapes. https://www.epo.org
  2. WIPO Patent Landscape Reports. Worldwide Patent Landscape Reports. https://www.wipo.int
  3. European Patent Convention (EPC) and patent procedures. https://www.epo.org/law-practice/legal-texts/epc.html
  4. Official Austrian Patent Office Database. https://www.patentamt.at
  5. Patent documentation related to ATE467617 (hypothetical reference based on the initial query).

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