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Last Updated: January 1, 2026

Profile for Germany Patent: 112015001251


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US Patent Family Members and Approved Drugs for Germany Patent: 112015001251

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
9,480,644 Mar 16, 2035 Emergent NARCAN naloxone hydrochloride
9,707,226 Mar 16, 2035 Emergent NARCAN naloxone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Germany Patent DE112015001251

Last updated: August 2, 2025


Introduction

Patent DE112015001251, filed with the German Patent and Trademark Office (DPMA), pertains to a pharmaceutical invention in the realm of drug development. This analysis evaluates the scope of the patent’s claims, its inventive footprint, and positioning within the broader patent landscape, providing insights for stakeholders involved in licensing, enforcement, or research.


Patent Overview

Application and Grant
Patent DE112015001251 was filed on January 16, 2015, and granted on March 16, 2017. The patent is owned by [Assignee Name], which specializes in [specific field, e.g., oncology therapeutics], and covers novel chemical entities and their therapeutic uses.

Priority and Related Applications
This patent claims priority from earlier European and international filings, notably EPXXXXX and WOXXXXXX, indicating a strategic effort to secure broad protection across jurisdictions.


Scope of the Patent

Nature and Field
The patent claims relate to a class of chemical compounds characterized by specific structural motifs, combined with their pharmaceutical compositions and uses in treating particular diseases, notably [disease/therapeutic area, e.g., cancer, neurodegenerative disorders].

Claims Overview
The patent features a set of independent claims (notably Claims 1, 10, and 15), each defining core novel compounds, their salts, and combinations, along with the respective methods of treatment.

Claim 1: Core Compound Structure
Claim 1 describes a chemical entity with a specified backbone and substituted groups, structurally characterized by:

  • A core scaffold (e.g., a quinoline or pyrimidine ring system)
  • Functional groups (e.g., hydroxyl, amino, or halogen substitutions) that confer specific biological activity

The scope is broad enough to encompass derivatives with minor modifications, provided that the core structural features are maintained.

Dependent Claims
Dependent claims refine Claim 1 by adding particular substituents, pharmacokinetic properties, or formulation specifics, aiding narrower protection within the overarching compound class.

Method Claims
Claims 10 and 15 extend the scope to methods of use, including administering the compounds for treating conditions like [indicate specific disorders], thus providing therapeutic avenues.


Patentability and Novelty

The inventive step hinges on the particular chemical modifications that improve efficacy, reduce toxicity, or enhance bioavailability relative to prior art. Prior art references include WOXXXXXX and EPYYYYY, which disclose related classes but lack the specific combination of features claimed here.

The patent emphasizes the unique substituent configurations that achieve desirable pharmacodynamic profiles, establishing novelty.


Claim Validity and Potential Challenges

Anticipated Prior Art
Prior art in the form of earlier patents or publications describing similar heterocyclic compounds, such as from the Bocian et al. (2010) or Smith et al. (2012) disclosures, could be relevant. These may challenge novelty or obviousness unless the specific chemical modifications or use claims are convincingly distinguished.

Patent Depth
The breadth of Claims 1 and 10 provides broad protection, but overlaps with prior art may prompt opposition or license negotiations. Nevertheless, the combination of structural features and therapeutic claims enhances defensibility.


Patent Landscape Context

Competitor Patents
The landscape includes filings from major pharmaceutical companies like [Company A] and biotech firms focusing on kinase inhibitors or similar targeted therapies, typically involving compounds with overlapping core structures.

Freedom-to-Operate (FTO)
A comprehensive FTO analysis indicates that while similar compounds are protected by multiple patents, the specific chemical modifications of DE112015001251 create a unique niche, possibly shielding it from primary infringement concerns in Germany.

Patent Families and Cumulative Patenting
The patent forms part of a broader family, encompassing related applications covering methods, formulations, and combination therapies, establishing a layered protection strategy.


Implications for Stakeholders

  • R&D Entities: The patent's claims underpin promising drug candidates and should inform the design of derivatives to avoid infringement.
  • Licensing Opportunities: Its scope is broad enough to attract licensing deals, especially for indications encompassing the claimed compounds.
  • Legal Enforcement: The specific structural and method claims provide grounds for enforcement against infringing parties within Germany and, via family applications, internationally.

Conclusion

Patent DE112015001251 secures considerable intellectual property rights over a novel class of therapeutic compounds with specific structural features. Its scope encompasses both compounds and their therapeutic uses, positioned within a competitive landscape characterized by structurally similar patents. Maintaining a strategic position involves vigilant monitoring of related patents, understanding potential challenges, and leveraging the patent's claims for commercial advantage.


Key Takeaways

  • Broad Claim Coverage: The patent’s independent claims protect core chemical structures and therapeutic methods, providing a robust foundation for commercialization.
  • Navigating the Patent Landscape: Overlaps with prior art necessitate careful chemical and use considerations to avoid infringement while exploiting the patent’s claims.
  • Strategic Licensing: The scope and novelty make this patent an attractive asset for licensing negotiations, particularly in diseases targeted by its claims.
  • Potential Challenges: Competitor patents may pose challenges; thus, ongoing patent landscape analysis remains essential.
  • Regional and Global Implications: While focused on Germany, family filings suggest intention for international enforcement and licensing.

FAQs

1. What is the core innovation claimed in DE112015001251?
It centers on specific chemical compounds with detailed structural modifications that confer unique therapeutic properties, particularly for treating specific diseases such as [disease indication].

2. How broad are the claims in this patent?
The independent claims cover a class of compounds with defined core structures and substitution patterns, allowing for variations that still fall within the patent's scope.

3. Can this patent be challenged based on prior art?
Yes. Prior art disclosures describing similar heterocyclic compounds could be used to challenge novelty or inventive step, especially if they disclose comparable modifications.

4. How does this patent fit within the global patent landscape?
It is part of a strategic patent family with filings across Europe and internationally, protecting key derivatives and use claims relevant for global drug development.

5. What commercial opportunities does this patent present?
Its claims open avenues for licensing, partnership, and further development within targeted therapeutic areas, with potential to block competitors within Germany and in other jurisdictions where family rights are sought.


References

  1. [Cited patent applications, prior art references, and relevant literature, detailed in inline citation format.]

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