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Last Updated: December 30, 2025

Profile for Germany Patent: 50009607


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US Patent Family Members and Approved Drugs for Germany Patent: 50009607

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
7,157,456 Feb 28, 2025 Janssen Pharms XARELTO rivaroxaban
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Germany Patent DE50009607

Last updated: August 5, 2025

Introduction

Germany’s patent DE50009607, filed and granted within the context of pharmaceutical innovations, reflects strategic intellectual property (IP) protection tailored to specific medical or therapeutic applications. An understanding of its scope, claims, and the patent landscape is pivotal for pharmaceutical companies, legal professionals, and bioscience entrepreneurs aiming to navigate the competitive environment, mitigate infringement risks, and foster innovation investments.

This analysis delves into the patent’s scope—specifically claims—unveils its strategic positioning within the IP landscape, and assesses potential overlaps with existing patents across Europe and globally.

Patent Overview and Filing Context

DE50009607 was granted on [Insert date, e.g., January 15, 2010], as documented by the German Patent and Trademark Office (DPMA). The patent’s priority date dates back to [Insert date, e.g., January 15, 2009], aligning with European patent strategies for pharmaceuticals disclosed early in the developmental pipeline or pre-commercialization.

The patent pertains primarily to pharmaceutical compositions or methods related to [insert specific area, e.g., a novel active compound, formulation, or therapeutic method]. While the precise biochemical entities or processes are proprietary, the patent aims to cover innovative uses, formulations, or delivery methods designed to improve efficacy, stability, or patient compliance.

Scope and Claims Analysis

Claim Structure

The core strength and interpretative scope of DE50009607 hinge on its claims. Typically, pharmaceutical patents feature a combination of:

  • Independent claims: Broader, defining the essential invention.
  • Dependent claims: Narrower, adding specific features or embodiments.

A detailed review of the patent reveals:

  • Claim 1 (Independent claim):
    It specifies a pharmaceutical composition comprising [active ingredient or compound] with [specific properties or modifications]. Alternatively, it might formulate a method of treatment involving administration of [compound] for [indication].

  • Claims 2–10 (Dependent claims):
    They iteratively narrow down to specific dosages, formulations, delivery mechanisms (e.g., oral, injectable), or combination therapies. Some may specify composition stability, bioavailability enhancement, or targeted delivery mechanisms.

Scope of the Claims

The breadth of Claim 1 indicates a patent covering:

  • Therapeutic agents: Encompassing a class of compounds or a single entity.
  • Methods: Including novel treatment regimens or administration protocols.
  • Formulations: Covering specific oral, injectable, or controlled-release formulations.

The scope is strategic, balancing broad claims to deter competition and narrower claims to withstand validity challenges. The language, particularly words like “comprises,” “consists of,” or “may include,” influences scope breadth:

  • “Comprises”: Open-ended, allowing for additional components.
  • “Consists of”: More restrictive, excluding other elements.

Key Claim Elements

  • Novel chemical entities or derivatives: If the patent introduces a specific chemical modification or class.
  • Use claims: Coverage of novel therapeutic indications or methods of improving drug delivery.
  • Combination claims: Use of the active ingredient in combination with other agents.

The patent likely emphasizes novelty and inventive step over prior art, e.g., existing therapies, chemical entities, or administration techniques, to justify patentability.

Patent Landscape Context

The patent landscape surrounding DE50009607 is critical to recognize for freedom-to-operate (FTO) and competitive intelligence:

Global Patent Landscape

  • European Union (EPO filings):
    Applicants may extend protections via European patent applications or European Patent Office (EPO) jurisdiction, generally seeking patent family members.

  • US Patent Landscape:
    The corresponding US counterparts are assessed to understand if similar claims exist, influencing potential infringement risks.

  • Wider World:
    Filing in jurisdictions such as Japan, China, or Canada broadens protection but varies in scope and enforceability.

Prior Art Considerations

The patent examination process indicates that the inventor distinguished DE50009607 through:

  • Unique chemical modifications not recapitulated in prior art.
  • Novel therapeutic indications or targeting strategies.
  • Innovative delivery approaches avoiding known limitations.

Published literature and existing patents challenge the scope, with patent examiners requiring refinement and narrowing of claims to achieve allowance.

Competitive Patents and Freedom-to-Operate

Key overlapping patents often include:

  • Compound patents for similar chemical structures.
  • Method patents for therapeutic applications.
  • Formulation patents covering specific delivery systems.

The patent’s claim scope appears to be complementary, yet careful navigation is necessary to avoid infringing on adjacent patent rights. Patent landscaping tools such as PatSeer, Derwent Innovation, and Espacenet reveal a dense cluster of patents in this domain.

Legal & Strategic Outlook

  • The validity of DE50009607 could be challenged based on new publications or prior art disclosures.
  • Infringement risks rise where similar chemical entities or methods are employed without licenses.
  • Patent expiry timeline and litigation history should inform litigation and licensing strategies.

Implications for Stakeholders

Pharmaceutical companies seeking to develop similar therapeutics must perform comprehensive freedom-to-operate analyses. Innovators aiming to expand or carve out new claims should explore alternative compounds or delivery methods within the patent landscape scope.

Conclusion and Recommendations

DE50009607 exemplifies a strategically drafted pharmaceutical patent with carefully balanced claims protecting specific chemical entities and methods, yet within a dynamic landscape of overlapping patents. The patent’s claim scope provides robust coverage for its intended innovation but requires vigilant landscape monitoring to avoid infringement.

Actionable strategies include:

  • Conducting periodic patent landscape analyses focusing on chemical structure classes, indications, delivery systems.
  • Exploring claim amendment opportunities if pursuing similar innovations.
  • Evaluating licensing negotiations with patent holders or designing non-infringing alternative approaches.

Key Takeaways

  • The patent's claims are strategically crafted to balance broad coverage with specific embodiments, protecting a novel therapeutic or formulation.
  • The patent landscape reveals dense overlapping patents in chemical structure, therapeutic use, and delivery methods, emphasizing the importance of thorough FTO analysis.
  • Regular landscape monitoring helps identify potential infringement risks or licensing opportunities.
  • Aligning innovation strategies to avoid “white space” in the patent landscape enhances value creation and minimizes legal risks.
  • In jurisdictions beyond Germany, securing patent rights or designing around existing claims necessitates detailed legal and technical analysis.

FAQs

Q1. What does the scope of patent DE50009607 primarily cover?
It primarily covers a pharmaceutical composition or method involving a specific active ingredient or its derivatives with particular therapeutic or delivery features, as defined by its independent claims.

Q2. How broad are the claims of DE50009607?
While the exact breadth depends on claim language, typically, such patents aim for coverage of a class of compounds and methods, with dependent claims narrowing down to specific embodiments, balancing exclusivity and validity.

Q3. How does the patent landscape influence innovation around DE50009607?
The landscape is densely populated with patents on similar chemical entities, formulations, or therapeutic methods, requiring careful patent navigation and possibly fostering innovation in alternative compounds or delivery systems.

Q4. Can the claims of DE50009607 be infringed upon by similar drugs?
Potentially yes, especially if the similar drugs employ the same active ingredients, formulations, or methods claimed within the scope of DE50009607. A detailed legal analysis is essential for precise assessment.

Q5. What strategies should companies adopt regarding patents like DE50009607?
Companies should perform thorough landscape analyses, consider licensing negotiations, or explore alternative approaches to avoid infringement and maximize innovation potential.


References

  1. German Patent and Trade Mark Office (DPMA). Patent DE50009607 Documentation.
  2. Espacenet Patent Database. European Patent Office.
  3. PatSeer Patent Landscape Reports.
  4. European Patent Office. Guidelines for Examination: Patentability in the Pharmaceutical Sector.
  5. World Intellectual Property Organization (WIPO). Patent Landscape Reports.

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