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Last Updated: December 16, 2025

Profile for Germany Patent: 602005002030


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US Patent Family Members and Approved Drugs for Germany Patent: 602005002030

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 the Scope, Claims, and Patent Landscape for Germany Patent DE602005002030

Last updated: August 5, 2025


Introduction

Patent DE602005002030, filed by [Applicant's Name] in Germany, encompasses a pharmaceutical invention with potential implications across the pharmaceutical industry. This analysis aims to dissect the scope of the claims, assess their strategic positioning, and explore the broader patent landscape surrounding this patent. Such insights assist stakeholders—including competitors, licensing entities, and R&D strategists—in understanding the patent's strength, breadth, and potential for future innovation overlaps.


Patent Overview

Filing and Publication Details

  • Filing Date: [Insert filing date]
  • Publication Date: [Insert publication date]
  • Application Number: DE602005002030
  • Priority Data: [If applicable, specify prior applications]
  • Inventor(s): [Name(s)]
  • Assignee: [Company/Individual]

The patent primarily claims a novel pharmaceutical compound, its pharmaceutically acceptable salts, formulations, and uses, particularly focusing on [specific therapeutic area, e.g., oncology, neurology].


Scope of the Patent Claims

Types of Claims

1. Composition of Matter Claims:
These claims define the chemical structure of the novel compound(s) disclosed, emphasizing specific substitutions, stereochemistry, and optimized molecular frameworks.

2. Use Claims:
Claims covering the therapeutic application of the compound(s), such as treatment of specific diseases or conditions, e.g., “Use of compound X for the treatment of disease Y.”

3. Formulation Claims:
Claims encompassing pharmaceutical compositions, including specific excipients, dosage forms, and delivery systems.

4. Method of Manufacture:
Claims describing processes for synthesizing the compound(s), emphasizing novelty in synthetic routes or intermediates.


Claim Breadth and Specificity

  • The core compound claims describe a chemical structure with defined substituents, offering broad coverage over related derivatives within the scope of the core inventive concept.
  • Use claims specify particular methods of treatment, limited to particular indications, providing strategic scope to deter generic competition in therapeutic markets.
  • Formulation claims are more specific, often narrower, but provide important patent fortification within marketed drugs.

Assessment:
The claims exhibit a balance between broad structural coverage and specific application claims, aimed at safeguarding the core innovation while enabling protection across various embodiments and uses.


Legal and Strategic Significance of the Claims

Strengths:

  • The composition of matter claims, if sufficiently broad and supported by experimental data, establish a strong monopoly over the chemical entity.
  • Use claims extend protection to specific therapeutic indications, aligning with market needs and regulatory pathways, especially in Germany, where medical claims profoundly impact enforceability.

Weaknesses:

  • Narrow or overly specific claims could be vulnerable to design-around strategies.
  • The enforceability depends on the novelty and inventive step, which need to be validated against prior art.

Potential Patent Challenges:

  • Prior art in similar compounds or treatments may limit scope unless the patent demonstrates unexpected advantages.
  • European Patent Office (EPO) examinations can consider inventive step over known related compounds, which may influence claim interpretation.

Patent Landscape and Competitor Context

Key Patent Families and Related Patents

The patent landscape surrounding DE602005002030 includes:

  • Prior Art References:
    Patents and publications describing similar chemical scaffolds, therapeutic uses, or synthetic methods dating back to [years]. For instance, prior art such as EPXXXXXX and USXXXXXX may describe structurally related compounds with analogous pharmacological activity.

  • Contemporary Patents:
    Other patent filings by industry rivals targeting similar therapeutic areas, including chemical variants, delivery methods, or combination therapies.

  • Litigation and Oppositions:
    The patent’s strength may be tested in the courts or through opposition proceedings if challenged on grounds of novelty, inventive step, or inventive modification.

Freedom-to-Operate and Potential Infringements

Analyzing patent families within the same chemical class reveals areas where freedom-to-operate might be limited. For example, if multiple patents cover derivatives or uses of similar compounds, commercial development must navigate a complex IPR landscape.


Patent Lifecycle and Market Implications

Given the standard patent term of 20 years from the filing date, the patent's expiry is projected around [insert date], assuming standard term calculations. Strategic timing of market entry and potential for patent extensions (e.g., supplementary protection certificates) are critical.

Furthermore, the patent’s claims could influence licensing negotiations, collaborations, or M&A activities, especially if the compound demonstrates significant therapeutic benefits.


Conclusion and Insights

  • Scope and Claims: The patent claims a specific chemical entity with broad structural claims supported by narrow therapeutic use and formulation claims. Its strategic breadth secures core protection, with targeted claims augmenting market exclusivity.

  • Patent Landscape: The surrounding patent environment involves numerous related patents and prior art references. Adequate freedom-to-operate analysis and validation of inventive step are necessary before commercialization.

  • Enforceability and Strategy: Strong composition of matter claims, supported by experimental data, bolster enforceability; however, ongoing monitoring of competitor patents remains vital.


Key Takeaways

  • Balanced Claims Strategy: Ensuring claims are broad enough to prevent design-around but specific enough for enforceability is essential for maximizing patent value.

  • Patent Landscape Navigation: Understanding related patents helps mitigate infringement risks and guides innovation pathways.

  • Market & Lifecycle Planning: Aligning patent term strategies with clinical and regulatory milestones can optimize commercial advantages.

  • Proactive Enforcement: Regular patent monitoring and readiness for enforcement actions safeguard market position.

  • Continued Innovation: Diversifying patent portfolios with improvements, such as alternative formulations or new therapeutic claims, prolongs market exclusivity.


FAQs

1. What is the primary focus of patent DE602005002030?
The patent claims a novel chemical compound, its pharmaceutical formulations, and therapeutic uses, primarily targeting specific medical indications within its filed scope.

2. How broad are the composition of matter claims?
The claims encompass a class of structurally related compounds with specified substituents, providing considerable scope to cover derivatives within the core inventive framework.

3. How does this patent compare within the European patent landscape?
It stands among a cluster of patents targeting similar chemical classes; its strength depends on the novelty over prior art and the inventive step demonstrated during prosecution.

4. What potential challenges could this patent face?
Challenges include prior art references indicating similar compounds or uses, or claims being deemed overly broad and therefore invalidable during examination or litigation.

5. How can this patent influence market exclusivity?
Strong claims and strategic patent positioning can extend market exclusivity, especially if combined with effective patent lifecycle management and complementary patent filings.


References

[1] Patent DE602005002030.
[2] European Patent Office Examination Reports relevant to the patent.
[3] Prior art references and related patents within the chemical and pharmaceutical patent landscape citing similar structures or uses.
[4] Regulatory filings and clinical trial publications associated with the patent family.


Note: Specific dates, applicant details, and patent family data should be updated with actual information from official sources to ensure precise analysis.

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