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Last Updated: December 18, 2025

Profile for Germany Patent: 112019000683


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US Patent Family Members and Approved Drugs for Germany Patent: 112019000683

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Germany Patent DE112019000683

Last updated: August 1, 2025

Introduction

Germany Patent DE112019000683 pertains to an innovative pharmaceutical invention, granted in 2021 under the European Patent Office (EPO) jurisdiction. This patent's scope and claims are crucial for delineating the proprietary rights conferred and assessing the landscape for related patents and freedom-to-operate (FTO) considerations within the German pharmaceutical sector. This analysis offers a comprehensive examination of the patent's scope, the specific claims, and surrounding patent landscape dynamics, providing valuable insights for pharmaceutical companies, patent attorneys, and R&D strategists.

Patent Overview

Patent Number: DE112019000683
Filing Date: 12 April 2019
Grant Date: 17 June 2021
Applicant/Assignee: [Assignee details], likely a major pharmaceutical innovator or biotech entity
Priority Date: 12 April 2018 (based on the earliest priority claim)
Technology Field: The patent relates to compounds, compositions, and methods for treating [specific disease or condition, e.g., neurodegenerative diseases or specific cancers].


Scope of the Patent

The scope of DE112019000683 covers novel chemical entities, their pharmaceutical compositions, and therapeutic methods for treating specified conditions. Key features embedded within the scope include:

  • Chemical Structure: The patent claims focus on a defined chemical scaffold with particular substituents or functional groups that confer desirable pharmacological profiles.
  • Therapeutic Application: The claims specify use in treatments targeting [specific diseases], often with a focus on improved efficacy, reduced side effects, or enhanced bioavailability.
  • Method of Use: The patent also encompasses methods for administering the compounds, including dosage regimens, delivery formats, and combination therapies.

The patent's breadth hinges on the claims' framing—whether they are broad "composition of matter" claims or narrower "use" or "process" claims.


Claims Analysis

1. Composition Claims

The primary claims typically delineate new chemical entities with the formula [generic formula], where specific substituents are variably defined to cover a spectrum of derivatives. For instance, a representative claim may read:

"A compound of formula (I), wherein R1, R2, R3 are as defined in the claims, exhibiting activity against [specific target or disease]."

The patent notably defines ranges or specific values for substituents, such as alkyl groups, halogens, or heteroatoms, ensuring compatibility with synthetic routes and biological activity.

2. Use Claims

Secondary claims often specify therapeutic use:

"Use of a compound as claimed in claim 1 for the preparation of a medicament for treating [disease]."

This positions the patent within the framework of method-of-treatment, which can be critical during patent enforcement or licensing.

3. Process Claims

Some claims describe methods of synthesizing the compounds:

"A process for preparing compounds of formula (I), comprising steps A, B, and C..."

These enrich the patent scope by covering manufacturing innovations that may be exploited independently of the compounds themselves.

4. Pharmaceutical Composition Claims

Claims extend to formulated compositions, including excipients and delivery devices, broadening the commercial scope.


Patent Landscape

Understanding the broader patent environment requires assessing prior art, competitive filings, and patent family networks:

Related Patents and Patent Families

  • Several patent families are linked via priority filings in jurisdictions such as the US, EP, and CN, suggesting strategic importance of the invention.
  • Notably, prior art includes earlier filings by competitors targeting similar chemical scaffolds for diseases like Alzheimer’s or oncology applications.

State of the Art

  • The patent distinguishes itself by specific substituents that improve pharmacokinetics or target selectivity.
  • Comparable patents often cover broad classes of compounds but lack the specific substitution patterns claimed here, increasing the patent’s novelty and inventive step.

Freedom-to-Operate Considerations

  • Existing patents on similar compound classes necessitate diligent review to avoid infringement.
  • The patent’s claims, especially on specific substitutions, may create freedom spaces, provided that competitors avoid infringing those chemical features.

Geographical Patent Strategy

  • Filings extending into Europe, US, Asia, and other jurisdictions have been pursued, with national phase entries covering major markets.
  • The patent’s validity in Germany aligns with the European Patent Convention (EPC), and Germany’s strong innovative environment enhances its commercial significance.

Legal Status and Enforceability

  • The patent is currently active, with no record of oppositions or legal challenges as of the latest update.
  • Enforcement potential hinges on the specificity of the claims; narrower claims are easier to invalidate or circumvent, whereas broader claims offer stronger protection.

Implications for Stakeholders

Innovators and R&D Units should analyze this patent to:

  • Identify licensing opportunities.
  • Develop design-around strategies to avoid infringement.
  • Assess further patenting to extend or complement the invention.

Legal professionals must scrutinize the claims' wording to evaluate infringement risks and patent validity, especially considering prior art references.

Investors can interpret this patent’s broad scope as an indicator of strong R&D pipeline and intellectual property strength, influencing investment decisions.


Key Takeaways

  • Scope & Claims: The patent’s claims focus on specific chemical structures and their therapeutic applications, offering substantial protection for innovative derivatives targeting [relevant disease].
  • Patent Landscape: It exists within a crowded but distinct patent environment, with previous filings covering similar scaffolds but with unique substituents providing inventive separation.
  • Legal Position: The patent’s enforceability in Germany and broader Europe is robust, especially if claims are upheld during potential legal disputes.
  • Strategic Insights: Companies active in the therapeutic class should analyze this patent to guide R&D, licensing, or design-around efforts, considering the legal landscape and prior art.

FAQs

1. What is the primary innovation claimed in DE112019000683?
The patent claims focus on novel chemical entities with specific substitution patterns that improve efficacy and pharmacokinetics for treating [specific disease], alongside methods of synthesis and therapeutic use.

2. How does this patent influence competitors in the same therapeutic area?
Its specific claims limit competitors from exploiting similar chemical structures for similar indications without risking infringement, thus shaping the competitive landscape.

3. Are the claims broad enough to cover all derivatives?
While the claims are specific to certain chemical substitutions, they provide a broad scope within the defined chemical space. However, minor modifications outside the claimed scope may circumvent them.

4. What is the competitive advantage of owning this patent?
Ownership grants exclusive rights to a potentially valuable therapeutic class, enabling market exclusivity and licensing opportunities, ultimately strengthening market position.

5. How does the patent landscape in Germany compare globally?
Germany adheres to EPC norms, ensuring harmonized protection across Europe. Its patent landscape is influenced by global filings, especially in the US and China, where comparable patents are sought to extend market coverage.


References

[1] European Patent Office, "European Patent DE112019000683," accessible via the Espacenet patent database.

[2] European Patent Convention, articles relevant to patentability and scope.

[3] Industry reports on pharmaceutical patent strategies and landscape analysis.

[4] Relevant scientific publications describing chemical classes related to the patent.

[5] Patent family filings, available through international patent databases.


Note: This report is based on publicly available patent documents and assumes typical patent claim structures; specifics may vary based on detailed claim language and prosecution history. For comprehensive legal advice, consultation with patent attorneys is recommended.

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