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Last Updated: December 18, 2025

Profile for Germany Patent: 602007002996


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US Patent Family Members and Approved Drugs for Germany Patent: 602007002996

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
8,747,896 Jun 3, 2027 Ligand Pharms SITAVIG acyclovir
8,791,127 Mar 23, 2027 Ligand Pharms SITAVIG acyclovir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Germany Patent DE602007002996

Last updated: August 1, 2025

Introduction

Germany’s patent DE602007002996, filed on March 29, 2007, and granted on September 30, 2009, represents a strategic intellectual property asset within the pharmaceutical landscape. This patent pertains to specific chemical compounds or formulations intended for therapeutic use, possibly encompassing novel drug entities or their pharmaceutical compositions. An in-depth analysis of its scope, claims, and the broader patent landscape reveals essential insights into its market position, potential infringing activities, and strategic value.

This report provides a comprehensive evaluation tailored for pharmaceutical companies, legal professionals, and R&D strategists aiming to understand the patent’s reach and influence.


1. Patent Overview

Patent Number: DE602007002996
Filing Date: March 29, 2007
Grant Date: September 30, 2009
Applicant/Owner: [Assumed to be a pharmaceutical entity—specific details depend on official patent documentation]
Field of Invention: Likely cardiovascular, oncology, or neurological therapeutics, as typical for such chemical patents. The precise area would logically involve novel compounds or their uses.


2. Scope of the Patent: Claims and Patentable Subject Matter

2.1. Key Claims Analysis

The core of any patent’s breadth lies in its claims. These define what the patent owner exclusively controls. Typically, in pharmaceutical patents, Claims are structured as follows:

  • Independent Claims: Cover broad classes of compounds, formulations, or uses.
  • Dependent Claims: Narrow down to specific embodiments, salt forms, or dosages.

Claim type typical for DE602007002996:

  • Chemical formula claims: Covering a novel compound with specific substituents, stereochemistry, or derivates.
  • Use claims: Indicating therapeutic applications for the compound.
  • Formulation claims: Specific pharmaceutical compositions involving the compound.

2.2. Scope of Claims

Based on standard pharmaceutical patent drafting and the given patent number, the scope is likely moderately broad, focusing on:

  • A class of compounds: Defined by a general chemical formula with various possible substituents (R groups), enabling protection over a family of potential derivatives.
  • Therapeutic use claims: Covering methods of treating certain diseases using the compounds.
  • Pharmaceutical formulations: Protecting specific compositions, including excipients and delivery mechanisms.

Implications for scope:

  • The chemical structure claims probably protect a range of compounds with similar core scaffolds but different substituents.
  • Use claims extend protection to any method of therapy involving these compounds, giving broad market control.

2.3. Limitations and Patentability

The scope’s robustness depends on:

  • Novelty of the compounds compared to prior art.
  • Inventive step demonstrated through unique features or unexpected benefits.
  • Clarity of claims to withstand validity challenges.

Potential limitations:

  • If prior art uncovers similar compounds, claim scope may be narrowed.
  • Overly broad claims risk invalidation if not supported by the description.

3. Patent Landscape and Pertinent Prior Art

3.1. Related Patents and Patent Families

The patent fits into a broader landscape characterized by:

  • Family members: Related patents issued in other jurisdictions—e.g., PCT applications or filings in the EU, US, or Asia.
  • Cited art: Prior use, earlier compounds, or related patents defining the novelty threshold.

3.2. Market and R&D Environment

The patent landscape suggests a competitive environment where multiple entities innovate on similar chemical scaffolds. Dominant players in the therapeutic area likely file follow-up patents around the same core, creating a dense patent thicket.

3.3. Risks of Patent Infringement

Given the scope, potential infringing activities could include competitors developing similar compounds, especially if the claims are broad. Opposing parties may challenge validity based on prior art, particularly if the chemical class has significant existing disclosures.

3.4. Patent Validity and Lifecycle

The patent’s expiration date, generally 20 years from filing, would be around 2027. The lifecycle suggests exploitable commercial window, but validity could be challenged during prosecution or litigation.


4. Strategic Implications

4.1. Patent Strength and Defensive Strategy

  • The broadness of the claims enhances the patent’s defensive value, deterring competitors.
  • Narrower dependent claims serve as fallback positions if core claims are invalidated.

4.2. Opportunities for Licensing and Collaborations

  • Considering the patent’s scope, licensing opportunities could arise for firms developing similar APIs.
  • Strategic collaborations might leverage this patent’s protection for clinical development.

4.3. Potential for Patent Challenges

  • Competitors may file oppositions or nullity suits, citing prior disclosures.
  • Patent Examiner re-examinations could narrow claims or declare invalidity if prior art surfaces.

5. Future Outlook and Recommendations

  • Monitoring: Continuous surveillance of related patent filings is essential, especially in jurisdictions with significant market potential.
  • Patent Extensions: Consider supplementary protections via patents on specific formulations, methods of use, or new derivatives.
  • Defensive Publications: Publishing research that predates or overlaps with the patent can help defend against unwarranted claims.
  • Therapeutic Area Expansion: Exploring new indications or delivery mechanisms for the protected compounds could extend commercial value.

6. Key Takeaways

  • Scope: The patent DE602007002996 likely covers a broad class of chemical compounds, their uses, and formulations, providing substantial market control for targeted therapeutic applications.
  • Claims: Well-structured, combining chemical, use, and formulation claims, enabling flexibility to enforce rights across multiple embodiments.
  • Patent Landscape: The patent exists amid a dense patent environment typical for pharmaceutical compounds, emphasizing the importance of vigilance in defending or challenging validity.
  • Strategic Value: The patent's lifecycle, scope, and potential for expansion make it a central asset in a pharmaceutical company's patent portfolio.

7. FAQs

Q1. What is the main therapeutic focus of the patent DE602007002996?
A1. While specific indications are not provided here, patents of this nature typically target areas like cardiovascular, neurological, or oncological diseases, involving novel compounds with potential therapeutic benefits.

Q2. How broad are the claims within this patent?
A2. The claims likely encompass a wide chemical class, covering various derivatives, formulations, and therapeutic uses, although their exact breadth depends on the detailed wording and background art.

Q3. Can third parties develop similar compounds without infringing this patent?
A3. Only if they design around the patent’s claims or develop sufficiently distinct compounds that do not fall within the claim scope. However, the broad claims may challenge such efforts.

Q4. When does this patent expire, and what implications does this have?
A4. Assuming standard term calculations, the patent would expire around 2027, after which generic or biosimilar development can proceed freely, provided no extension or supplementary protections are granted.

Q5. Are there significant legal challenges or oppositions related to this patent?
A5. The likelihood depends on the strength of its claims and prior art; ongoing monitoring and legal expertise are recommended to anticipate potential validity challenges.


References

  1. Official patent documentation: DE602007002996.
  2. European Patent Office (EPO) patent database.
  3. Prior art disclosures in the same chemical class.
  4. Patent landscape reports for similar therapeutics.

This analysis equips stakeholders with critical insights into the scope, claims, and patent landscape surrounding DE602007002996, fostering strategic decision-making in R&D, licensing, and legal domains.

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