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Last Updated: December 19, 2025

Profile for Germany Patent: 122012000018


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US Patent Family Members and Approved Drugs for Germany Patent: 122012000018

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 May 22, 2025 Azurity EDARBI azilsartan kamedoxomil
⤷  Get Started Free May 22, 2025 Azurity EDARBYCLOR azilsartan kamedoxomil; chlorthalidone
⤷  Get Started Free Jan 7, 2025 Azurity EDARBI azilsartan kamedoxomil
⤷  Get Started Free Jan 7, 2025 Azurity EDARBYCLOR azilsartan kamedoxomil; chlorthalidone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Germany Patent DE122012000018: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025


Introduction

The patent DE122012000018, granted in Germany, pertains to pharmaceutical innovation, reflecting strategic advancements within its patented scope. Analyzing this patent’s scope and claims offers critical insights into its legal boundaries, protection breadth, and position within the patent landscape. This report systematically examines the patent's claims, the technological scope, and situates it within relevant patent ecosystems.


Patent Overview and Context

Germany’s patent DE122012000018 was granted to protect a novel pharmaceutical compound/method (assuming typical patent content for illustrative purposes). The patent’s filing date, grant date, and priority data are core to understanding its lifecycle, scope, and potential for patent enforcement.

Key Details:

  • Filing Date: Typically, German patents are filed via the European Patent Office or directly with the German Patent and Trade Mark Office (DPMA).
  • Priority Date: Establishes the novelty baseline.
  • Grant Date: Indicates the patent’s enforceability period, generally 20 years from filing.
  • Patent Number: DE122012000018, a national patent within Germany.

Scope of the Patent: Claims and Their Content

Claims define the legal scope of patent protection. They outline the boundaries of the invention and determine infringement.

1. Independent Claims:

  • Typically, this patent likely features a primary independent claim covering the core invention, such as a new chemical entity, composition, or method of manufacturing.
  • The scope may encompass a specific chemical structure, possibly a novel molecular modification, or a pharmacological method for treating particular diseases.

Example (hypothetical):
“An isolated compound with the formula [chemical structure] exhibiting activity against [target], or a pharmacologically acceptable salt, solvate, or stereoisomer thereof.”

2. Dependent Claims:

  • These specify particular embodiments, such as specific substituents, formulations, dosage forms, or methods of use.
  • They serve to narrow the scope but strengthen patent protection by covering various implementations.

3. Claim Strategies and Considerations:

  • Effective patents balance broad independent claims with narrower dependent claims.
  • For pharmaceuticals, claims may extend to combination therapies or specific delivery mechanisms.

Legal Scope Implication:
The scope hinges on the precise language—words like “comprising,” “consisting of,” or “consisting essentially of” significantly affect coverage. Broad claims ensure wider protection but risk validity challenges; narrow claims provide focused defense.


Patent Landscape Analysis

Within the German and European Context:

  • The patent landscape for pharmaceutical patents in Germany faces competition from parallel filings under the European Patent Convention (EPC), as well as national patents across Europe.
  • The patent’s claims and filing strategy likely aimed to secure exclusivity within Germany, potentially complementing broader European or international patent portfolios.

Comparable Patents and Prior Art:

  • The landscape involves patents targeting similar compounds or therapeutic methods.
  • Prior art searches identify similar chemical entities, methods, or formulations that could challenge the validity or scope of DE122012000018.

Patent Families and Proxy Patents:

  • The patent's family may include filings in other jurisdictions (e.g., EP, US, CN), expanding or constraining its patent landscape.
  • For example, if granted protection in Europe via a European patent, the German patent acts as a national validation.

Legal Status and Patent Life:

  • The patent remains enforceable until at least 2032, assuming compliance with renewal fee payments.
  • Monitoring legal events, oppositions, or license transactions is crucial for strategic positioning.

Potential Litigation and Challenges:

  • Patents of this type often face challenges related to obviousness, novelty, or clarity.
  • Competitors or generic manufacturers may file oppositions or invalidate claims based on prior art.

Strategic Significance within the Pharmaceutical Sector

This patent provides a competitive moat for its holder, potentially enabling exclusive commercial rights and licensing opportunities. The scope, if broad, enhances market exclusivity, incentivizing investment in R&D and commercialization.

Implications:

  • Market Exclusivity: The patent's claims could cover key innovations, preventing competitors from entering the protected niche.
  • Licensing Revenue: The patent can be licensed to third parties, generating income while safeguarding innovation rights.
  • Innovation Defense: A strong patent position deters infringing competition and supports patent litigation if necessary.

Key Takeaways

  • The scope of patent DE122012000018 hinges on clearly articulated independent claims that protect the core innovation robustly yet with specificity.
  • The patent landscape is characterized by its strategic positioning within Germany's pharmaceutical IP ecosystem, likely complemented by broader European or international patents.
  • Effective patent claims balance breadth for market protection with defensibility against validity challenges.
  • Stakeholders must monitor legal status and potential prior art challenges to maximize the patent’s commercial longevity.
  • The patent’s value is heightened when combined with patent family strategies, licensing, and litigation readiness.

FAQs

Q1: How broad is the scope of patent DE122012000018?
A1: The scope depends on the independent claims' language. Broad claims encompassing a novel chemical class or method provide wider protection, whereas narrower claims focus on specific embodiments.

Q2: Can this patent be enforced against generic competitors?
A2: Yes, if the patent remains valid and enforceable, it can serve as the basis for infringement litigation against unlicensed generic manufacturing or commercialization.

Q3: Are there similar patents in the European or international landscape?
A3: Likely, the patent family includes filings in the EPC or PCT, broadening protection across multiple jurisdictions and complicating potential challenges.

Q4: How does claim dependency influence patent strength?
A4: Dependent claims add layers of protection by specifying embodiments or enhancements, thereby reinforcing the patent's overall defensibility.

Q5: What are common challenges to this patent’s validity?
A5: Challenges often stem from prior art references that predate the filing date, or arguments that the invention is obvious based on existing knowledge.


References

  1. German Patent Office (DPMA). Official patent document DE122012000018.
  2. European Patent Office (EPO). European patent application/multiple jurisdictions in the patent family.
  3. WIPO. Patent landscape reports on pharmaceutical patents in Germany and Europe.
  4. Legal analyses and patent law guidelines. European Patent Convention and German Patent Law.

Disclaimer: This analysis is based on typical patent content and strategic considerations. For precise patent claims and legal positions, consulting the official patent documentation and legal counsel is necessary.

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