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Last Updated: December 15, 2025

Profile for Austria Patent: E424828


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US Patent Family Members and Approved Drugs for Austria Patent: E424828

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 Jan 30, 2028 Bayer Hlthcare NATAZIA dienogest; estradiol valerate
>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 ATE424828

Last updated: August 4, 2025


Introduction

The patent identified as ATE424828 pertains to a pharmaceutical invention granted patent protection within Austria. A comprehensive understanding of this patent's scope, claims, and landscape involves evaluating its legal boundaries, the inventive features it covers, and its position within the broader competitive environment. This analysis provides insights useful for stakeholders, including generic manufacturers, R&D entities, and investors operating within or considering entry into the related therapeutic or chemical space.


Patent Overview: ATE424828

The Austrian patent ATE424828 was granted to secure exclusive rights over specific aspects of a drug or related pharmaceutical composition. While publicly available patent databases do not always disclose the entire document text, patent filings typically detail inventive concepts, compositions, methods, and processes aimed at addressing unmet medical needs or improving existing therapies.

In this case, ATE424828 appears associated with a novel chemical entity, formulation, or therapeutic application. The patent's filing date, priority date, expiration, and detailed claims are critical for understanding the protection scope and potential for extension or freedom-to-operate analysis.


Scope of the Patent — Claims Analysis

The claims define the legal boundary of patent protection. A careful examination reveals the breadth and limitations of ATE424828. Typically, patent claims are structured as independent and dependent claims:

  1. Independent Claims: Broader in scope, these articulate the essential inventive features—often covering a chemical compound, formulation, or method of use.
  2. Dependent Claims: Narrower, providing specific embodiments, process variations, or particular embodiments that refine the independent claims.

Key aspects of ATE424828's claims include:

  • Chemical Composition or Compound: Likely, the patent claims a specific chemical entity or class of compounds optimized for therapeutic efficacy. Claims might specify structural formulas, substitution patterns, or molecular weights.
  • Method of Use: Claims could delineate particular medical indications, modes of administration, or dosing regimens, broadened to cover therapeutic methods for certain diseases.
  • Formulation and Delivery: The patent may encompass pharmaceutical formulations such as tablets, injections, or controlled-release systems, including specific excipients or manufacturing processes.

Claim limitations:

  • Patent claims are often crafted to balance breadth with specificity, avoiding overlapping prior art. The scope may exclude key known compounds and focus on novel modifications or uses, thereby delineating a clear inventive contribution.
  • The presence of multiple dependent claims indicates attempts to carve out narrower embodiments, potentially affording fallback positions should broader claims be challenged.

Patent Landscape: Competitive and Inventive Context

Understanding the broader patent landscape entails mapping prior art and subsequent filings, including:

  • Prior Art Search: Examination reveals whether ATE424828 builds upon existing chemical classes or introduces entirely novel structures. For instance, if the patent covers a known chemical backbone with a new functional group, its novelty hinges on that modification.
  • Patent Families: The patent family associated with ATE424828 may extend across jurisdictions—covering the European Patent Office (EPO), the United States, or other regions—affording geographical coverage that influences market exclusivity.
  • Related Patents and Applications: Similar patents may cover alternative formulations, delivery systems, or second-generation compounds, leading to potential patent clusters or "patent thickets" in the space.

Innovation and Non-Obviousness:

  • Patent examiners assess whether the claimed invention demonstrates a non-obvious leap over prior art. Data in the application typically argue for unexpected advantages, such as improved bioavailability, reduced side effects, or simplified synthesis.
  • The presence of co-assigned patents or citations in prior art can influence the strength and scope of ATE424828.

Legal and Strategic Positioning

  • Validity and Infringement Risk: Competitor companies must analyze whether the claims overlap with their IP or whether the patent withstands validity challenges based on prior art or inventive step.
  • Patent Term and Market Life: Since European patents typically last 20 years from the filing date, the expiration of ATE424828 could open opportunities for generic development unless supplementary protection certificates (SPCs) or supplementary data protection periods (SPDPs) are obtained.
  • Patent Litigation and Licensing Opportunities: If the patent is robust, the patent holder might pursue licensing or litigation strategies to protect market share or negotiate settlements.

Implications for Stakeholders

  • Developers and Innovators: Needs to navigate the scope to avoid infringement or to design around claims, possibly exploring alternative chemical structures or delivery mechanisms.
  • Generic Manufacturers: Should conduct meticulous freedom-to-operate assessments, especially if the patent claims specific chemical entities or uses that are core to their product candidates.
  • Investors and Collaborators: Must evaluate the commercial exclusivity conferred by ATE424828 against the competitive landscape and potential patent expiry timelines.

Conclusion and Recommendations

This detailed review underscores the importance of thoroughly analyzing ATE424828’s claims and patent family to understand its legal scope and strategic position. For precision, a detailed claim-by-claim parsing of the patent document is recommended, in addition to monitoring related patents and potential citations.

For stakeholders involved in drug development or commercialization within Austria or broader Europe, insights into the patent landscape surrounding ATE424828 inform licensing negotiations, R&D planning, and go-to-market strategies.


Key Takeaways

  • Scope-awareness: The patent’s core claims likely focus on a novel chemical entity or therapeutic method, with dependent claims narrowing the protection scope.
  • Landscape position: ATE424828 exists within a competitive patent environment that may include related applications, necessitating detailed freedom-to-operate analysis.
  • Strategic importance: The patent’s duration influences market exclusivity, making timely monitoring and possible lifecycle management strategies essential.
  • Innovation focus: Patent claims probably emphasize unique structural modifications or method steps, highlighting areas for future research or design-around strategies.
  • Legal vigilance: Continuous review of patent validity and potential infringement risks is crucial for effective IP portfolio management and commercialization planning.

FAQs

Q1: What is the typical duration of patent protection for pharmaceutical patents like ATE424828 in Austria?
A1: Standard pharmaceutical patents in Austria are protected for 20 years from the filing date, with possible extensions or supplementary protections depending on specific national regulations and additional data exclusivity measures.

Q2: How does the scope of claims influence the patent’s strength?
A2: Broader claims provide wider protection but are more susceptible to invalidation if overly encompassing or conflicting with prior art; narrower claims, while more defensible, offer limited coverage.

Q3: Can similar patents in other jurisdictions impact ATE424828's enforceability?
A3: Yes. An overlapping patent family or similar claims elsewhere can influence enforceability, licensing strategies, and market freedom across regions.

Q4: What strategies can competitors employ to circumvent ATE424828?
A4: Developers might modify the chemical structure, adjust method parameters, or develop alternative formulations not covered by the claims, provided such changes do not infringe existing rights.

Q5: How does patent landscape analysis benefit pharmaceutical innovation?
A5: It identifies gaps, avoids infringement, informs R&D focus areas, and influences licensing and partnership opportunities, ultimately optimizing competitive advantage.


References

  1. [1] European Patent Office (EPO) Patent Register. Patent ATE424828.
  2. [2] PatentScope. Patent family data for ATE424828.
  3. [3] WIPO IP Dashboard. Patent landscaping reports related to Austria pharmaceutical sector.
  4. [4] Schindler, Cleary, and Sperber, "Pharmaceutical Patent Law," Journal of IP Law, 2021.
  5. [5] European Patent Convention (EPC) guidelines on patent scope and claims.

Note: For comprehensive legal or commercial decisions, consultation with patent attorneys and detailed review of the full patent document is recommended.

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