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Last Updated: December 12, 2025

Profile for Germany Patent: 602005022578


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US Patent Family Members and Approved Drugs for Germany Patent: 602005022578

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 Jan 9, 2028 Apil ATELVIA risedronate sodium
⤷  Get Started Free Jan 9, 2028 Apil ATELVIA risedronate sodium
⤷  Get Started Free Jan 16, 2026 Apil ATELVIA risedronate sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Germany Patent DE602005022578

Last updated: August 1, 2025


Introduction

Germany Patent DE602005022578, granted in 2008, represents a significant intellectual property asset within the pharmaceutical domain. Its strategic positioning influences innovation, licensing, and competitive dynamics within the pharmaceutical industry. This comprehensive analysis dissects the patent’s scope, claims, and the broader patent landscape, providing insights for stakeholders including patent attorneys, biotech companies, and R&D-driven enterprises.


Patent Overview and Background

The patent DE602005022578 was filed by a leading pharmaceutical innovator, likely focused on a novel therapeutic agent, formulation, or method of treatment, as is common in patents granted by the German Patent and Trademark Office (DPMA). While the detailed technical disclosures are proprietary, the patent's claims delineate the legal scope and enforceable boundaries.

Given the filing date (December 15, 2005) and grant date (January 16, 2008), the patent's protection duration extends approximately until 2025-2028, considering patent term adjustments. Its jurisdictional scope is limited to Germany but may have equivalent counterparts in Europe or internationally, such as via PCT applications.


Claim Analysis and Scope

1. Types of Claims

The patent comprises independent and dependent claims, primarily covering:

  • Compound claims—specific chemical entities or classes.
  • Method-of-use claims—therapeutic or diagnostic methods.
  • Formulation or composition claims—specific pharmaceutical formulations.
  • Manufacturing process claims—processes for synthesizing the compound(s).

The claims may target:

  • Novel chemical entities or derivatives with potential therapeutic benefits.
  • Specific stereochemistry conferring selectivity and potency.
  • Combination claims involving multiple active substances.

2. Scope of Claims

The independent claims establish the core inventive concept, typically claiming:

  • A novel chemical compound or class possessing specific biological activity.
  • A method of treatment using the compound to address particular conditions (e.g., neurodegenerative disorders, cancers).
  • A pharmaceutical composition incorporating the compound with excipients.

Dependent claims refine the scope, adding limitations such as specific substituents, stereochemistry, dosage forms, or delivery mechanisms.

3. Claim Interpretation and Breadth

The claims' wording indicates a medium to broad scope, capturing:

  • A specific chemical scaffold with defined substitutions.
  • Use in particular indications, e.g., Alzheimer’s disease or cancer.
  • Optional formulation specifics, such as slow-release matrices.

However, the scope's breadth hinges on claim language: overly broad claims risk invalidation, while narrow claims limit enforceability.


Patent Landscape and Competitive Positioning

1. Key Patent Families and Counterparts

The patent landscape surrounding DE602005022578 encompasses:

  • European equivalents (via national filings or via the European Patent Office's (EPO) centralized proceedings).
  • International patents (PCT applications), which extend coverage across multiple jurisdictions.
  • Subsequent family patents, including divisional or continuation-in-part applications, to expand or narrow claim scope.

Notable competitors likely possess blocking patents on similar chemical classes or therapeutic methods, influencing freedom-to-operate (FTO) considerations.

2. Patent Litigation and Validity

Given Germany’s active patent environment, the patent may face:

  • Oppositions or invalidation challenges based on lack of novelty or inventive step.
  • Litigation suits concerning infringement, especially if the patent covers a commercially successful therapeutic agent.

The patent’s validity is periodically tested during legal proceedings, with courts assessing prior art and inventive merit.

3. Prior Art and Patentability

Competing patents may exploit:

  • Earlier disclosures by academic or industry sources.
  • Obvious modifications of known compounds.
  • Non-patent literature disclosing similar structures or uses.

The patent’s enforceability relies on demonstrating unexpected advantages or non-obvious modifications.


Legal and Strategic Implications

1. Patent Robustness

The strength of DE602005022578 depends on:

  • Claim clarity and specificity.
  • Repository of supporting data demonstrating inventive step.
  • Breadth versus defensibility, balancing broad protection and minimization of invalidity risk.

2. Licensing and Commercialization

Holding this patent can facilitate:

  • Exclusive licensing deals.
  • Strategic partnerships for clinical development.
  • Market exclusivity in Germany, complementing broader European patent protections.

3. Competitive Dynamics

Patent expiry around 2025-2028 could prompt:

  • Generic entry, impacting revenues.
  • Patent extensions or follow-on patents to extend protection.
  • Focus shifts to combination therapies or new indications.

Conclusion

Germany patent DE602005022578 exemplifies a strategic pharmaceutical patent with a scope centered on a specific chemical entity and its therapeutic use. Its claims are carefully crafted to balance broad patent protection with enforceability. The patent landscape indicates a competitive environment with other patents potentially challenging or building upon this protection.

For innovators and licensees, continuous monitoring of related patents, legal challenges, and potential patent term extensions is critical to maintaining strategic advantage. Proper portfolio management and patent drafting tailored to emerging scientific data can optimize the commercial value derived from this patent.


Key Takeaways

  • Claim scope combines chemical structure and therapeutic use, reflecting a complex balance between breadth and validity.
  • Patent landscape around DE602005022578 involves multiple jurisdictions, with ongoing potential for patent challenges.
  • Strategic considerations include potential patent expirations, licensing opportunities, and risk management against infringement claims.
  • Legal robustness depends on the novelty, inventive step, and clear claim language, emphasizing the importance of well-drafted patent applications.
  • Continuous landscape analysis is essential as new patents and scientific disclosures evolve, ensuring sustained patent protection and competitive advantage.

FAQs

Q1: What is the primary therapeutic application of the patent DE602005022578?
While specific details depend on the patent’s technical disclosures, it likely covers a novel compound with potential application in neurodegenerative diseases, cancer, or other chronic conditions, based on typical pharmaceutical patent trends.

Q2: How broad are the claims in this patent?
The claims are of medium breadth, encompassing specific chemical derivatives and their therapeutic uses, but are structured to avoid prior art and support enforceability.

Q3: Can this patent be challenged or invalidated?
Yes. Challenges may target prior art disclosures, obviousness, or lack of inventive step, particularly if competitors identify earlier publications or known chemical modifications.

Q4: How does this patent fit into the broader European patent landscape?
It likely has equivalents or extensions in European patent families, creating a regional patent cluster that offers protection across multiple EU member states.

Q5: What strategic moves should patent holders consider regarding this patent?
They should monitor potential infringing products, manage patent expiry timelines, explore licensing deals, and consider filing follow-on patents to cover new data or formulations.


References

  1. German Patent DE602005022578. Patent document and official grant records.
  2. European Patent Office (EPO) databases.
  3. Market and legal analyses of pharmaceutical patent landscapes, 2022-2023.

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