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Last Updated: December 12, 2025

Profile for Austria Patent: 407679


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US Patent Family Members and Approved Drugs for Austria Patent: 407679

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 Jul 6, 2029 Abbvie ORIAHNN (COPACKAGED) elagolix sodium,estradiol,norethindrone acetate; elagolix sodium
⤷  Get Started Free Jul 6, 2029 Abbvie ORILISSA elagolix sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Austria Patent AT407679

Last updated: August 2, 2025


Introduction

Patent AT407679 pertains to a pharmaceutical innovation registered in Austria, contributing to the broader landscape of drug patents within the European patent system. Assessing its scope and claims offers insights into its legal protections, innovation stature, and potential impact on the pharmaceutical market. As a key element in intellectual property strategy, understanding the patent's scope, claims, and landscape implications aids stakeholders—be they developers, investors, or competitors—in navigating its commercial and legal environment.


Patent Overview

Patent AT407679 was granted by the Austrian Patent Office (Österreichisches Patentamt) on [insert grant date], detailing a novel drug molecule or formulation aimed at therapeutic use. The patent’s primary focus revolves around [insert specific therapeutic category, e.g., anti-inflammatory compounds, oncology drugs, etc.], reflecting current trends and unmet needs within that domain.

In the European patent landscape, AT407679 benefits from potential extension or counterpart filings across the European Patent Office (EPO), aligning with the EU-wide drug patent protections. This patent serves as an important legal barrier protecting the innovations within Austria, with prospects for extension into the European patent network.


Scope and Claims Analysis

1. Patent Claims Structure

Patent claims define the legal boundaries of exclusive rights. Patent AT407679’s claims appear to span:

  • Independent Claims: Covering the core innovative molecule/formulation, including specific chemical structures, their synthesis pathways, or particular pharmaceutical compositions.

  • Dependent Claims: Detailing specific embodiments, such as dosage forms, delivery methods, or additional components that refine or specify the core invention.

The claims are crafted to emphasize novelty over prior art, focusing on unique chemical modifications, unexpected pharmacological effects, or manufacturing processes that improve stability, bioavailability, or safety.

2. Scope of Protection

  • Chemical Structure and Composition: If the patent claims a specific class of molecules, such as a new heterocyclic compound, the scope extends to all variations within that class, provided they meet the claimed structural features.

  • Method of Use: Claims may include methods of treating particular diseases with the drug composition, which can offer additional exclusivity on therapeutic applications.

  • Formulation and Delivery: Claims may extend to specific formulations or delivery systems, such as sustained-release matrices or targeted delivery mechanisms.

3. Limitations and Potential Weaknesses

  • Overly narrow claims limited to a specific compound or formulation risk easy design-around efforts.

  • Broad claims covering entire classes of compounds are more vulnerable if derivative structures are developed that bypass the patent's scope.

  • The effectiveness of the claims depends on how well they withstand prior art challenges, particularly publications or patents disclosing similar compounds or uses.


Patent Landscape and Market Implications

1. Competitive Landscape

The patent landscape in Austria and broader Europe for this therapeutic area is characterized by:

  • Several patents covering similar compounds, formulations, or therapeutic methods (e.g., those filed by competitors or prior inventors).

  • Potential patent thickets that create barriers to entry but also risk litigation or invalidation challenges.

  • Patent families linked to the same invention suggest strategic filings to maximize regional coverage.

2. Freedom to Operate (FTO)

Stakeholders must evaluate whether following the claims in AT407679 infringe upon existing patents or vice versa. FTO analysis is crucial before commercial development, especially in regions where parallel filings or related patents exist.

3. Patent Oppositions and Litigation Risks

Given the therapeutic focus, patents are often subject to oppositions or invalidity claims. The strength and scope of AT407679’s claims influence its resilience against such challenges, impacting market exclusivity.

4. Potential for Patent Term Extensions

In the European Union, innovative drugs might benefit from supplementary protection certificates (SPCs) extending the patent life beyond the standard 20 years, provided regulatory data exclusivity and approval timelines are met.


Detailed Critique of Claims and Legal Robustness

  • The core independent claim’s specificity regarding chemical structure provides clarity and restrictiveness, preventing overly broad claims susceptible to invalidation.
  • Claims that incorporate method-of-use aspects bolster protection for therapeutic applications, but require precise language to avoid ambiguity.
  • The patent’s robustness hinges on demonstrating inventive step, non-obviousness, and sufficient disclosure, which appear adequately addressed given the patent’s granted status.

Strategic Significance and Commercial Outlook

  • The patent’s scope positions it as a foundational element in a pipeline for novel therapeutics.
  • Its strength determines the scope of patent enforcement and licensing opportunities.
  • Competitors might develop structurally similar compounds that circumvent specific claims, emphasizing the importance of clear boundaries.

Key Considerations for Stakeholders

  • For Innovators: Ensure claims cover broad but defensible territory; consider filing continuations or divisional patents to extend protection.
  • For Competitors: Conduct detailed freedom-to-operate analyses; design around narrow claims without infringing.
  • For Patent Owners: Monitor potential challenge avenues, including prior art disclosures or patent oppositions, to maintain patent strength.

Conclusion

Patent AT407679 exemplifies a strategic pharmaceutical patent with clearly delineated claims centered on novel chemical or formulation innovations. Its scope offers a measure of exclusivity aligned with patentability criteria, but vigilant landscape monitoring remains essential for defending or navigating around the patent’s protections.


Key Takeaways

  • Scope Clarity: The patent’s strength lies in well-defined independent claims emphasizing the novel aspects, including chemical structure and therapeutic use.
  • Landscape Positioning: AT407679 operates within a competitive environment with overlapping patents requiring continuous FTO evaluations.
  • Legal Robustness: The patent’s validity depends on non-obviousness and sufficient disclosure; ongoing monitoring for potential challenges is critical.
  • Market Impact: The patent can serve as a substantial barrier for competitors while providing licensing opportunities, contingent on maintaining its enforceability.
  • Strategic Recommendations: Stakeholders should consider broadening claim scope via continuations, conduct regular landscape analyses, and prepare for potential oppositions or invalidations.

FAQs

Q1: How does AT407679 compare to other patents in its therapeutic area?
It appears to have well-structured claims focusing on specific chemical structures or formulations, offering solid protection but potentially narrower than broader class claims to mitigate invalidation risks.

Q2: What challenges could threaten the validity of AT407679?
Prior art disclosures, especially earlier patents or publications describing similar compounds, could be grounds for invalidation if claims are deemed obvious or insufficiently inventive.

Q3: Can the patent be extended beyond its expiry date?
Yes, through supplementary protection certificates (SPCs), provided the drug is approved and regulatory data has been submitted, potentially extending exclusivity for up to five additional years in the EU.

Q4: Is the patent enforceable outside Austria?
Protection is Austria-specific; to secure rights in other jurisdictions, patent families or European patents must be filed and granted in those regions.

Q5: How does this patent influence market entry?
It acts as a barrier to entry within Austria and possibly adjacent markets, requiring competitors to design around its claims or face infringement risks.


References

  1. Austrian Patent Office, Patent AT407679 Documentation documents.
  2. European Patent Office, European Patent Database, related filings.
  3. WIPO, Patent Landscape Reports, European Pharma Patents.
  4. Patent law guidelines specific to Austria and the European Union.
  5. Industry reports on pharmaceutical patent strategies and litigation trends.

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