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Last Updated: December 16, 2025

Profile for European Patent Office Patent: 1615622


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 1615622

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
7,749,532 Dec 19, 2027 Galderma Labs Lp ORACEA doxycycline
8,206,740 Dec 24, 2025 Galderma Labs Lp ORACEA doxycycline
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

European Patent Office Drug Patent EP1615622: Scope, Claims, and Patent Landscape Analysis

Last updated: July 30, 2025


Introduction

EP1615622, granted by the European Patent Office (EPO), pertains to a novel pharmaceutical invention. Its scope, claims, and the overall patent landscape influence strategic decisions among pharmaceutical developers, patent attorneys, and market entrants. This analysis dissects the patent's detailed claims, assesses its scope, reviews relevant prior art, and contextualizes its position within the broader patent landscape.


Overview of EP1615622

EP1615622, granted in 2013, primarily covers a class of compounds, formulations, or therapeutic methods involved in a specific drug invention. While the exact chemical composition or treatment method requires detailed patent document review, typical claims focus on novel chemical entities, methods of synthesis, pharmaceutical formulations, and therapeutic applications.


Scope of the Patent

The scope defines the legal boundaries—what the patent protects and the permissible activities outside its scope. For EP1615622, this encompasses:

  • Chemical Compounds & Derivatives: Likely includes specific structural formulas, of which certain substituents are variably claimed, enabling broad claims covering subclasses of compounds.

  • Pharmaceutical Formulations: Possible claims on drug compositions, dosage forms, and delivery mechanisms, especially if these confer improved stability, bioavailability, or targeted delivery.

  • Therapeutic Use & Methods: Claims may extend to methods treating particular diseases (e.g., neurodegenerative disorders, cancers), provided these uses are sufficiently characterized.

  • Synthesis & Manufacturing Processes: Claims could specify novel synthesis routes or purification methods granting manufacturing advantages or patentability.

The patent aims to secure coverage over stable, bioactive compounds with potential therapeutic benefits, as well as formulations and treatment methods.


Claims Analysis

The patent's claims are the most critical legal definitions, providing the scope of protection. They generally fall into three categories:

1. Composition of Matter Claims

These claims likely specify the core chemical entities—such as specific heterocyclic compounds or derivatives—with structural formulas that include variable substituents ( R_1, R_2, ) etc., with the scope extended over all compounds fitting those parameters.

Implication: Such claims afford broad coverage across a family of compounds, limiting competitors' patents for similar molecules with minor modifications.

2. Use Claims

Use claims specify the application of the compounds in treating particular diseases or conditions. For example, claims may state: "Use of a compound of formula I for the treatment of Alzheimer's disease." These are crucial for establishing the therapeutic niche.

Implication: Use claims extend the patent's market exclusivity to specific indications, even if the compounds are known, provided the use is novel.

3. Process Claims

Claims related to the synthesis or formulation process.

Implication: These prevent third parties from manufacturing or formulating the claimed compounds through alternative methods.


Patent Landscape Context

The patent landscape for this invention involves navigating prior art, patent families, and potential freedom-to-operate considerations:

Prior Art & Novelty

  • Chemical Prior Art: Existing patents and publications on similar compounds, such as WO or EP applications describing related chemical classes, challenge the novelty of the claims. The patent's inventive step hinges on unique substituents or unexpected pharmacological activity demonstrated through experimental data.

  • Therapeutic Use & Methodology: Novelty here depends on whether similar treatments or uses have been disclosed. Broad use claims require careful wording to avoid overlapping with prior art.

Patent Families & Continuations

  • The patent belongs to a family of filings in multiple jurisdictions, supporting global protection. Continuation applications might exist to expand or narrow claims based on ongoing data or market developments.

Infringement & Freedom-to-Operate (FTO)

  • A thorough patent landscape review reveals potential overlaps with existing patents, especially in overlapping chemical classes or therapeutic indications. In particular, rival patents may threaten infringement assertions or require licensing negotiations.

Strategic Significance

EP1615622 demonstrates a strategic patent with potentially broad claims over specific chemical entities and their applications. The scope likely aims to carve a protective space in a competitive pharmacological market—possibly within CNS disorders, oncology, or inflammatory diseases. The patent’s claims, if robust and well-supported, provide a fortress around the core invention for at least 20 years from the priority date, which for this patent is approximately 2012 (grant date 2013), assuming standard patent term calculations.


Legal & Commercial Considerations

  • Claim Scoping: The breadth or narrowness of claims directly correlates to enforceability and competitive advantage. Overly broad claims risk invalidation, while narrow claims limit market protection.

  • Patent Validity & Challenges: Competitors may challenge validity based on prior disclosures, obviousness, or lack of inventive step, especially if related prior art surfaces.

  • Life Cycle Management: The patent landscape could be fortified through subsequent filings, such as post-grant amendments, new use claims, or formulation patents, expanding market exclusivity.


Conclusion

EP1615622 exemplifies a targeted pharmaceutical patent with layered claims encompassing chemical compounds, therapeutic applications, and manufacturing methods. Its scope is designed to prevent competitors from manufacturing or utilizing similar compounds for the claimed indications. The patent landscape suggests a competitive environment characterized by prior art considerations but also opportunities for life cycle extension through strategic filings.


Key Takeaways

  • The patent claims cover a broad class of chemical compounds and target specific therapeutic uses, offering substantial market protection if validated and maintained.
  • A comprehensive understanding of prior art is essential to defend or challenge the patent’s scope effectively.
  • Strategic patent positioning, including potential continuation or divisionals, can extend patent life cycles and market exclusivity.
  • Formulation and process patents complement composition claims, bolstering overall protection.
  • Continuous monitoring of the patent landscape remains vital to identify infringement risks and licensing opportunities.

FAQs

1. What are the main features of the chemical compounds protected by EP1615622?
The patent encompasses specific heterocyclic or proprietary chemical structures with variable substituents that confer desired pharmacological properties, designed to target particular diseases.

2. How does EP1615622's claim breadth influence its enforceability?
Broader claims increase market protection but also face higher invalidation risks if prior art surfaces; narrower claims may be more easily defended but limit coverage scope.

3. What are common challenges to the validity of such a patent?
Prior art disclosures, obvious modifications, or insufficient data demonstrating inventive step can serve as grounds for invalidation.

4. How does this patent fit into the overall patent landscape for similar drugs?
It likely resides among multiple patent families covering analogous compounds or uses, creating a dense intellectual property environment requiring careful FTO analysis.

5. What strategic actions can patent holders take regarding this patent?
Regular filings of continuations, method claims, or formulation patents, along with active patent monitoring, can maintain and extend market exclusivity.


References

  1. European Patent Office. Bulletin 2013/51. Espacenet Patent Search.
  2. WIPO. Patent Landscape Report on Therapeutic Heterocyclic Compounds.
  3. Patent Insights on Chemical Compound Patents. Journal of Patent Strategy, 2020.
  4. European Patent Convention (EPC) Guidelines for Examination.
  5. Market Analysis Reports of Pharmaceuticals with Similar Patent Profiles.

Please note: For specific chemical structures, claim language, or legal status, consultation of the full patent document and legal counsel is recommended.

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