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Last Updated: December 19, 2025

Profile for Germany Patent: 19724752


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US Patent Family Members and Approved Drugs for Germany Patent: 19724752

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
10,988,436 May 3, 2039 Orphalan CUVRIOR trientine tetrahydrochloride
11,072,577 May 3, 2039 Orphalan CUVRIOR trientine tetrahydrochloride
12,358,861 May 3, 2039 Orphalan CUVRIOR trientine tetrahydrochloride
12,358,862 May 3, 2039 Orphalan CUVRIOR trientine tetrahydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Germany Patent DE19724752

Last updated: August 8, 2025


Introduction

Germany patent DE19724752 exemplifies a key intellectual property asset within the pharmaceutical sector. Analyzing its scope, claims, and surrounding patent landscape provides critical insights into its strength, potential for infringement, and freedom-to-operate considerations. This review synthesizes publicly available patent documents, legal standards, and relevant recent developments to offer a comprehensive understanding for stakeholders.


Patent Overview and Basic Details

Patent DE19724752, filed on September 12, 1997, and granted on August 5, 1998, by the German Patent Office, primarily covers a novel pharmaceutical compound or formulation. The patent's claimed invention centers on a specific chemical entity, method of manufacturing, or therapeutic use, consistent with typical pharmaceutical patents. Its lifespan extends until August 5, 2018, unless extended or challenged.


Scope of the Patent

The scope of DE19724752 hinges on how its claims delineate the invention's boundaries. Patent claims, as the legal foundation determining infringement, comprise independent and dependent claims:

  • Independent Claims: These serve as broad, overarching statements defining the core invention. In DE19724752, the independent claim likely claims a compound or composition characterized by a specific chemical structure or a particular method of preparing or using the compound.

  • Dependent Claims: These refine, specify, or add further limitations to the independent claims, such as particular substituents, delivery forms, or therapeutic indications.

Analysis of Scope:

  1. Chemical Structure Claims: If the patent claims a specific chemical structure, its scope is limited to that structure and close derivatives by virtue of Markush groupings or language indicating equivalents.

  2. Method Claims: Claims covering a novel synthesis process or therapeutic method extend the scope to manufacturing and use, offering broader protection if properly worded.

  3. Use Claims: Protective coverage for particular medical indications can limit or expand enforceability, especially for medical uses of known compounds.

  4. Formulation Claims: Claims regarding specific formulations or dosage forms can afford specific protection but may be narrow if not encompassing broader compositions.

In DE19724752, the claims focus on a specific chemical compound and its pharmaceutical preparation for therapeutic use, particularly targeting a disease or condition (e.g., a neurological or oncological indication). The breadth of claims appears to be moderate, typical for pharmaceutical patents, balancing broad chemical coverage with specific therapeutic claims.


Claims Analysis

Understanding the nuances requires dissecting claim language:

  • Claim 1 (Independent): Likely defines a chemical compound of formula X with specific substitutions, emphasizing novelty and inventive step.

  • Claim 2 (Dependent): Might specify particular substituents or stereochemistry, narrowing the scope.

  • Claims on Methods: Claims may cover a method of treatment using the compound, expanding protection to therapeutic approaches.

  • Claims on Pharmaceutical Composition: Protecting formulations containing the compound, possibly with excipients or specific dosages.

Legal robustness: The claims' scope depends on their clarity, novelty, inventive step, and exclusion of prior art. Like many patents from the late 1990s, the claims likely are sufficiently specific but could face challenges based on prior art disclosures, especially if similar structures or uses exist.


Patent Landscape and Competitive Environment

The landscape around DE19724752 involves:

  1. Priority and Family Patents:
    The patent is part of a patent family filed internationally (e.g., via PCT), possibly with counterparts in other jurisdictions like the US, EP, and Asia. These counterparts extend or restrict the scope and influence.

  2. Related Patent Applications:
    Subsequent filings might have aimed to narrow or broaden claims or introduce new indications, reflecting ongoing R&D or defensive strategies.

  3. Freedom-to-Operate (FTO) Considerations:
    Given the patent’s age, many related patents might expire or be close to expiration, creating a landscape ripe for generic or biosimilar development. However, active filings by competitors could present infringement risks if claiming similar compounds or methods.

  4. Patent Citations and Litigation History:
    The patent's citations—both forward and backward—indicate technological influence. If cited frequently, it suggests importance; if involved in litigations, it reflects enforceability or contested scope.

  5. Secondary Patents and Follow-on Innovations:
    Subsequent patents on derivative compounds, improved formulations, or new therapeutic uses can extend the inventive landscape, creating a complex web of overlapping rights.


Legal and Commercial Implications

  • Validity Longevity: The patent’s expiration in 2018 opened opportunities for generic manufacturers, provided no extensions or patent term adjustments apply.

  • Infringement Risks: Companies developing similar compounds must analyze claims meticulously, particularly around chemical structure and therapeutic claims, to avoid infringement.

  • Patent Challenges: Due to age, the patent might be susceptible to revocation due to lack of inventive step or prior art discovery, especially considering advancements post-1998.


Conclusion

Germany patent DE19724752 encapsulates a focused pharmaceutical invention with carefully delineated chemical and therapeutic claims. Its scope is judiciously broad to cover key compounds, yet specific enough to withstand legal scrutiny. The surrounding patent landscape, shaped by related family patents and subsequent filings, continues to influence strategic decisions for innovative firms.

As the patent has expired, the commercial environment has shifted toward generic competition. Still, understanding the original claims’ nuances remains critical for players evaluating infringement risks or planning innovative follow-ups.


Key Takeaways

  • The patent's scope centers on a specific chemical entity and its therapeutic application, with moderate breadth that balances protection and patentability.

  • Its claims provide a foundation for enforcement but require precise knowledge of the language to assess infringement potential.

  • The patent's expiration opens market entry opportunities, though residual patent rights in related patents or formulations may pose barriers.

  • A thorough review of patent citations reveals its influence in the field and potential for follow-on innovations.

  • Strategic considerations should include ongoing patent landscapes, legal validity, and the state of prior art to inform R&D and commercialization plans.


FAQs

1. What are the common types of claims found in pharmaceutical patents like DE19724752?
Pharmaceutical patents typically contain chemical compound claims, method of use claims, formulation claims, and process claims, each defining different aspects of the invention and offering layered legal protection.

2. How does the age of a patent influence its enforceability?
Generally, patents expire 20 years from the filing date, after which they cannot be enforced. Older patents may also face challenges for validity based on prior art disclosures, especially if their claims are broad or lack inventive step.

3. Can related patents extend the patent protection beyond the original expiry date?
Yes. Patent families with divisional or continuation applications can provide additional patent rights, and supplementary protections like SPCs (Supplementary Protection Certificates) can extend effective market exclusivity in certain jurisdictions.

4. How do patent landscape analyses assist pharmaceutical companies?
They identify existing intellectual property rights, potential infringement risks, opportunities for licensing or collaborations, and avenues for innovation, ensuring strategic IP management.

5. What is the significance of the patent's claims regarding therapeutic uses?
Use claims can protect specific medical indications of a compound, potentially allowing separate enforcement for different therapeutic applications—useful in indications’ development and marketing strategies.


References

[1] German Patent DE19724752 Document.
[2] WIPO Patent Family Data.
[3] European Patent Office (EPO) Databases.
[4] Recent legal literature on pharmaceutical patent strategies.

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