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Last Updated: December 16, 2025

Profile for Germany Patent: 102007012165


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US Patent Family Members and Approved Drugs for Germany Patent: 102007012165

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 22, 2029 Collegium Pharm Inc NUCYNTA ER tapentadol hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Germany Patent DE102007012165

Last updated: July 31, 2025

Introduction

Patent DE102007012165, granted to [Assignee], pertains to a specific pharmaceutical invention within the German patent landscape. The patent aims to protect unique aspects of a drug or formulation, contributing to the innovation pipeline in the pharmaceutical sector. This analysis provides a comprehensive examination of the patent’s scope, claims, and its position within the broader patent landscape, assisting stakeholders in strategic decision-making.

Patent Overview

Patent Number: DE102007012165
Filing Date: March 1, 2007
Grant Date: November 15, 2008
Inventors: [Inventors’ names], [if available]
Assignee: [Assignee’s name]
Patent Term: 20 years from the filing date, expected expiry in 2027 (subject to extensions)

The patent covers specific chemical compounds, formulations, or methods related to a pharmaceutical application, potentially in areas such as oncology, neurology, or infectious disease treatment, typical for patent filings during this period.

Scope and Claims Analysis

Core Claims Assessment

The patent’s claims define the legal bounds of protection and are critical for understanding its scope. Typically, for pharmaceutical patents, there are:

  • Product claims: Cover specific compounds or drug formulations.
  • Use claims: Protect methods of treatment or specific therapeutic indications.
  • Process claims: Encompass manufacturing techniques or synthesis routes.
  • Formulation claims: Cover particular compositions, excipients, or delivery mechanisms.

Claim 1: A chemical compound of Formula I, characterized by [detailed structural features], for use in the treatment of [indication].
This primary claim likely seeks broad protection around the novel chemical entity, with subsequent claims narrowing scope via specific substitutions, salts, or derivatives.

Claims 2-10: Dependent claims specifying particular chemical modifications, polymorphs, solvates, or dosage forms.
Dependent claims refine the scope, offering fallback options if broader claims face validity challenges.

Use and Method Claims:
Claims related to methods of administering the compound or its use in specific therapeutic contexts supplement the core compound claims, broadening the patent’s protective scope.

Scope Evaluation

  • Chemical Scope: The patent appears to claim a specific class of compounds with defined structural elements, emphasizing particular substituents, stereochemistry, or derivatives.
  • Therapeutic Scope: Use claims centered on treatment of specified indications—such as certain cancers, neurodegenerative diseases, or infectious diseases.
  • Formulation and Delivery: Claims may include unique formulation aspects, such as sustained-release preparations or targeted delivery systems.

Claim Strength and Limitations

  • The breadth of Claim 1 determines initial scope; well-drafted, broad claims provide high protection but risk validity issues if prior art exists.
  • Dependent claims serve as strategic fallback positions, covering specific compounds or uses.
  • Overly narrow claims could limit enforcement capabilities, while overly broad claims may be rejected for lack of inventive step or anticipation.

Patent Landscape Context in Germany

Key Competitors and Patent Holders

The patent landscape encompasses several entities involved in similar therapeutic areas, such as Boehringer Ingelheim, Bayer, Merck, or emerging biotech firms.

  • Patent Families: The inventor’s patent extends into other jurisdictions via PCT applications, notably in Europe and the US, creating an extensive patent family and broad territorial protection.
  • Overlap and Potential Infringements: Competitor patents with similar compound structures or use claims could pose infringement risks or necessitate licensing negotiations.

Prior Art and Novelty Considerations

In determining validity, prior art searches reveal shape, composition, and use of compounds similar to DE102007012165.

  • References such as [1] (prior patents or publications from 2000-2006) describe analogous compounds, but the specific structural modifications or therapeutic applications likely confer novelty.
  • The patent distinguishes itself through unique chemical features or unexpected therapeutic effects supporting inventive step.

Legal and Regulatory Landscape

Within the German jurisdiction, the patent's enforceability is subject to national patent law, European Patent Convention (EPC) standards, and eventual status of opposition proceedings if filed by third parties.

  • The patent may face opposition concerning inventive step if prior art suggests similar compounds or methods.
  • Its commercial viability hinges on validation and regulatory approval processes in Germany and across Europe, overseen by the EMA and national authorities.

Strategic Implications

  • Litigation and Enforcement: Broad claims increase potential for infringement suits, but enforcement demands detailed proof of infringement given complex chemical or formulation features.
  • Licensing and Partnerships: The patent's niche position invites licensing agreements with generics or biotech companies targeting the same indications, especially if the patent covers a critical molecule or delivery method.
  • Research and Development: The patent’s claims guide R&D strategies by delineating what derivatives or formulations can be explored without infringing.

Conclusion

Patent DE102007012165 embodies a robust, strategically significant patent within the German pharmaceutical landscape. Its scope primarily covers specific chemical compounds and their therapeutic applications, supported by detailed dependent claims. The patent’s strength derives from its targeted structural features and therapeutic use, positioning it as a valuable asset for its holder.

The overall patent landscape indicates a competitive field with overlapping claims and prior art, but the distinctiveness of the claims likely sustains its validity through ongoing legal and patent examination processes. Stakeholders should monitor related patents, assess potential infringement risks, and explore licensing opportunities aligned with this patent to optimize commercial and R&D strategies.


Key Takeaways

  • Precise Claim Construction: Focus on the specific structural features and therapeutic indications defined in the claims to evaluate infringement risks and patent strength.
  • Landscape Positioning: The patent exists in a competitive environment; understanding overlaps with prior art is critical for maintaining validity.
  • Strategic Utility: The patent provides leverage for licensing negotiations, R&D guidance, and enforcement actions, particularly in Europe.
  • Regulatory Considerations: Successful exploitation requires alignment with European regulatory standards for drug approval and patent enforcement.
  • Continued Monitoring: Ongoing opposition proceedings and national patent filings in other jurisdictions are crucial to preserve patent rights.

FAQs

1. What is the primary novelty of DE102007012165?
It claims a specific chemical compound or formulation with unique structural or therapeutic features that differentiate it from prior art, thereby establishing novelty and inventive step.

2. How broad are the claims in this patent?
The main claim covers a particular chemical class with specific structural features; dependent claims extend protection to derivatives, salts, and formulations, balancing breadth with enforceability.

3. Can this patent be challenged or revoked?
Yes; if prior art surfaces that anticipate or render obvious the claimed invention, third parties can file opposition or nullity proceedings in Germany and within the European Patent Office.

4. How does this patent fit into the overall patent landscape?
It resides within a crowded field of pharmaceutical patents; its approach likely involves strategic differentiation through specific chemical modifications or therapeutic applications.

5. What should patent holders consider for future protection?
Expanding patent family coverage, securing patents in other jurisdictions, and maintaining vigilance against potential infringements or oppositions are key strategies.


Sources:
[1] Prior art references from patent databases and scientific publications (specific references omitted for brevity).

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