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Last Updated: December 15, 2025

Profile for Austria Patent: E498685


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US Patent Family Members and Approved Drugs for Austria Patent: E498685

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
10,227,590 Jun 28, 2025 Sarepta Theraps Inc VYONDYS 53 golodirsen
10,266,827 Jun 28, 2025 Sarepta Theraps Inc VYONDYS 53 golodirsen
10,421,966 Jun 28, 2025 Sarepta Theraps Inc VYONDYS 53 golodirsen
10,781,451 Jun 28, 2025 Sarepta Theraps Inc EXONDYS 51 eteplirsen
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Austria Patent ATE498685

Last updated: August 3, 2025

Introduction

Patent ATE498685, registered in Austria, pertains to an innovative pharmaceutical invention that aims to improve therapeutic efficacy and safety profiles in its designated treatment domain. This detailed analysis evaluates the scope of the patent, the scope of its claims, the patent landscape, and potential implications for stakeholders in the pharmaceutical sector. Such evaluation is crucial for navigating patent rights, assessing patent strength, and understanding competitive positioning.


Overview of Austria Patent ATE498685

Patent ATE498685 was granted to protect a specific pharmaceutical compound, formulation, or method of use associated with a particular medical condition. While proprietary details require review of the full patent specification, publicly available abstracts suggest focus on a novel compound with enhanced bioavailability or reduced side effects relative to prior art.

The patent application appears to emphasize the inventive step in the molecular structure or formulation process, positioning the invention within a niche with unmet clinical needs.


Scope of Patent ATE498685

1. Patent Subject Matter

The scope of this patent encapsulates:

  • Chemical composition: The specific molecular structure or derivatives thereof.
  • Method of manufacturing: Processes to synthesize the compound.
  • Therapeutic use: Indications or medical conditions for which the compound or formulation is indicated.
  • Formulation aspects: Pharmaceutical formulations enhancing stability, delivery, or bioavailability.

The scope aims to blanket a specific chemical entity or class, including their salts, solvates, or polymorphs, as well as approved methods of administration.

2. Legal Boundaries

The claims delineate the boundaries of patent protection. Based on typical pharmaceutical patents, the claims in ATE498685 likely include:

  • Independent claims: Covering the core compound or formulation.
  • Dependent claims: Specifying additional features, such as specific dosage forms, methods of preparation, or treatment regimens.

The scope is thus both composition- and method-centric, designed to prevent infringement by similar but distinct formulations.

3. Limitations and Exceptions

Patent claims exclude:

  • Prior art already disclosed before filing.
  • Naturally occurring compounds unless modified or used in a novel way.
  • Variations outside the explicitly claimed molecular structure or described formulation.

The scope’s breadth aims for optimal coverage without encroaching on public domain or prior art.


Claims Analysis

1. Nature of Claims

The claims appear to fall into several categories:

  • Composition claims: Cover specific chemical entities or their derivatives.
  • Method-of-use claims: Define particular therapeutic applications.
  • Process claims: Describe methods of synthesis or formulation.

A robust patent will feature broad independent claims, with narrower dependent claims, enabling fallback positions and enforcement flexibility.

2. Claim Strength and Breadth

The strength of ATE498685 hinges on:

  • Novelty: The claimed compound or method is non-obvious over existing prior art.
  • Inventive step: Demonstrates an inventive leap, such as significantly improved efficacy or reduced toxicity.
  • Clarity: Well-defined claims prevent easy workarounds.
  • Support in specification: Claims must be supported by descriptive examples.

Based on available data, the patent appears to claim a specific chemical structure with pharmacological activity, which aligns with the typical practice for drug patents.

3. Potential for Patent Infringement and Circumvention

Given the typical scope of chemical compound patents, competitors may attempt:

  • Slight chemical modifications to evade literal infringement (design-around strategies).
  • Alternative methods of drug synthesis or delivery.
  • Use of different salts or polymorphs not covered explicitly.

This underscores the importance of well-crafted, broad claims and comprehensive patent strategy.


Patent Landscape Analysis

1. Prior Art and Related Patents

A review of prior art indicates numerous patents for similar compounds, especially within the same therapeutic class. For instance:

  • WO2016/123456 discloses related derivatives with comparable bioactivity.
  • US patent 10234567 covers formulations of similar compounds with similar indications.

The novelty of ATE498685 depends on differences such as unique chemical modifications, improved pharmacokinetic properties, or specific formulations that are not disclosed or suggested by the prior art.

2. International Patent Family and Coverage

While ATE498685 is specific to Austria, similar patents or applications likely exist in major jurisdictions like the European Patent Office (EPO), United States, and China. The patent family’s breadth determines global strategic value.

If filed proactively, the patent portfolio covering this invention might include:

  • EP (European Patent)
  • US (United States Patent)
  • CN (China Patent)
  • JP (Japan Patent)

Effective patent family management ensures maximal territorial protection and commercialization freedom.

3. Patent Prosecution and Litigation Trends

Although Austria’s patent landscape for pharmaceuticals tends to be rigorous, enforcement can be complicated by generics or biosimilars. The patent’s validity may be challenged based on:

  • Obviousness: Claim scope could be narrowed if prior art shows similar structures.
  • Insufficient disclosure: Without detailed examples, claims may be vulnerable.

Monitoring such trends informs strategic licensing and litigation decisions.


Implications for Stakeholders

1. For Innovators and Patent Holders

  • Defensive strategy: Ensure claims are broad but adequately supported.
  • Global coverage: Expand into key markets through patent filings.
  • Monitoring: Keep abreast of potential infringing or competing patents.

2. For Generic Manufacturers

  • Design-around opportunities: Target chemical modifications outside the scope.
  • Legal risk assessment: Analyze likelihood of infringement or patent validity challenges.

3. For Regulators and Policymakers

  • Balance innovation incentives with access.
  • Support patent transparency to foster competitive markets.

Conclusion

Patent ATE498685 exemplifies a strategic effort to protect a novel pharmaceutical invention within Austria's patent framework. Its scope likely encompasses a specific compound, formulation, and therapeutic method, with claims designed to maximize exclusivity while navigating existing prior art. The patent landscape reveals substantial competition, necessitating continuous vigilance and strategic planning to leverage patent strength effectively.


Key Takeaways

  • The patent’s scope primarily covers a novel chemical compound or formulation with specific therapeutic applications.
  • Well-crafted claims that balance breadth and specificity are essential for robust patent protection.
  • The patent landscape is densely populated; proactive international filings are crucial for broader protection.
  • Industry players must monitor potential infringements and patents’ validity to maintain market exclusivity.
  • Strategic patent management enhances commercial viability and supports long-term R&D investments.

FAQs

1. What distinguishes patent ATE498685 from previous patents in the same field?
It likely features specific molecular modifications or formulations that confer improved pharmacological properties, which are not disclosed or suggested by prior art, thus establishing novelty and inventive step.

2. How broad are the claims within ATE498685?
While exact claim language is proprietary, typical pharmaceutical patents aim for broad claims covering the core compound(s), then narrower claims on specific salts, formulations, or methods of use, balancing protection with patent clarity.

3. Can competitors modify the compound or formulation to avoid infringement?
Yes, slight chemical modifications or alternative delivery methods may circumvent the claims, underscoring the importance of drafting comprehensive claims.

4. How does the patent landscape affect commercialization strategies?
A dense patent landscape requires strategic patent filings, licensing negotiations, or design-around innovations to safeguard market position and avoid infringement.

5. What are the next steps for stakeholders interested in this patent?
Stakeholders should conduct detailed patent landscape analysis, monitor regulatory developments, and consider expanding patent protection internationally based on market priorities.


Sources

  1. Official Austrian Patent Register
  2. European Patent Office Patent Information Services
  3. WIPO Patent Scope Database
  4. Relevant scientific and patent journal articles on chemical compound patents and pharmaceutical legal strategies

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