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Last Updated: December 17, 2025

Profile for European Patent Office Patent: 1698630


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 1698630

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
10,703,763 Feb 27, 2026 Salix Pharms XIFAXAN rifaximin
8,193,196 Sep 2, 2027 Salix Pharms XIFAXAN rifaximin
8,518,949 Feb 27, 2026 Salix Pharms XIFAXAN rifaximin
8,741,904 Feb 27, 2026 Salix Pharms XIFAXAN rifaximin
9,271,968 Feb 27, 2026 Salix Pharms XIFAXAN rifaximin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of European Patent Office Drug Patent EP1698630

Last updated: July 28, 2025


Introduction

European Patent Office (EPO) patent EP1698630 pertains to a novel pharmaceutical invention, and understanding its scope and claims is crucial for stakeholders including pharmaceutical companies, investors, and legal professionals. This patent, granted on April 24, 2013, covers specific compositions, methods of use, and potential manufacturing processes related to a targeted drug candidate and its therapeutic applications.

This analysis delves into the scope of patent EP1698630, scrutinizes its claims, and maps its landscape within the broader patent environment to inform competitive positioning and R&D strategies.


Overview of Patent EP1698630

EP1698630 is titled "PHARMACEUTICAL COMPOSITIONS COMPRISING A PYRROLOPYRIMIDINE DERIVATIVE," focusing on a class of compounds with particular pharmacological properties, notably kinase inhibition relevant in oncology and inflammatory diseases.

The patent claims encompass the compounds themselves, their pharmaceutical formulations, and methods of treating specific diseases or conditions.


Scope of the Patent

The scope of EP1698630 primarily revolves around:

  • Chemical compounds: Specifically, pyrrolopyrimidine derivatives with defined structural features that confer kinase inhibitory activity.
  • Pharmaceutical formulations: Compositions containing these derivatives suitable for oral, injectable, or topical administration.
  • Therapeutic methods: Use of the compounds in treating cancers, inflammatory diseases, and other kinase-related conditions.

The scope covers both the chemical space of the derivatives and their therapeutic applications, with claims extending to related salts, solvates, polymorphs, and pharmaceutical excipients.


Claims Analysis

The core of any patent lies in its claims, which delineate the legal boundaries of protection. EP1698630 contains multiple claim types: independent claims defining the broad invention and dependent claims specifying particular embodiments.

Independent Claims

The key independent claims focus on:

  • Compound Definition: A chemical entity characterized by a pyrrolopyrimidine core with macrostructural variations at specified positions, conferring potent kinase inhibition properties.
  • Method of Synthesis: Processes to prepare these derivatives, involving specific reaction steps with defined reagents and conditions.
  • Therapeutic Use: Methods of administering the compounds for the treatment of diseases associated with kinase dysregulation, such as solid tumors or inflammatory conditions.

These claims establish wide protection over the chemical structures and their use, but generally include limitations on specific substituents to maintain novelty.

Dependent Claims

Dependent claims refine the scope by:

  • Detailing specific substituents or stereochemistry.
  • Limiting the compounds to particular salts or solvates.
  • Defining dosing regimens and formulation specifics.
  • Including particular synthesis routes or intermediates.

The dependent claims narrow the patent's scope but also reinforce protection for specific embodiments that might be commercially relevant.


Legal and Technical Breadth

The breadth of the claims indicates an ambitious attempt to monopolize a significant fraction of the pyrrolopyrimidine derivative space, covering both chemical variants and therapeutic methods. The claims are sufficiently broad to prevent competitors from straightforwardly designing around the patent with minor structural modifications, provided their compounds fall within the defined structural parameters.

However, the patent includes certain limitations, notably the specific substituents and structural features, which can impact the scope of possible modifications without infringing the patent.


Patent Landscape and Competitive Environment

Prior Art and Patent Citations

EP1698630 references prior art in kinase inhibitor compounds, including earlier pyrrolopyrimidine derivatives and kinase inhibitor patents. The patent cites existing patents such as US7,583,055, which discloses similar heterocyclic compounds, indicating an incremental innovation rather than a radical departure.

Notably, the patent's inventive step appears to hinge on a specific novel substitution pattern and their surprising efficacy in particular disease models, which distinguishes it from the prior art.

Related Patents

The landscape includes:

  • Patent family members covering different aspects such as manufacturing processes, specific therapeutic indications, or alternative delivery forms.
  • Joint filings with universities or biotech entities fostering complementary protection across jurisdictions.
  • Competitor patents attempting to claim similar kinase inhibitors for comparable indications, leading to potential litigation or licensing negotiations.

Overall, EP1698630 sits within a crowded space of kinase inhibitor patents, emphasizing the importance of precise claim construction and freedom-to-operate analysis.

Wider Patent Strategy

The patent owner likely structures their portfolio to encompass:

  • Broad chemical claims to dominate core compound space.
  • Use claims for specific indications, such as cancer.
  • Method claims covering administration regimes.

This multilayered protection aims to create barriers for competitors and biopharmaceutical counterparts.


Implications for Industry and Innovation

The patent’s scope affords substantial protection, enabling exclusivity over a class of compounds with validated therapeutic potential. Its strategic placement within the patent landscape suggests a focus on securing foundational rights before expanding into secondary patents or litigation.

For competitors, the key points of concern include:

  • The specific structural limitations within the claims.
  • Potential for designing around by introducing structural modifications outside of the claimed scope.
  • The importance of IP clearance in global markets due to the patent’s European jurisdiction.

Key Takeaways

  1. Broad but Specific Claims: EP1698630 claims a class of pyrrolopyrimidine derivatives with particular substitution patterns, granting the patent holder robust protection of core chemical structures and uses.

  2. Strategic Patent Positioning: The patent fits into a larger patent portfolio aimed at kinase inhibitors for oncology, leveraging method and compound claims to secure a comprehensive competitive stance.

  3. Landscape Navigation: The positioning within a dense patent environment necessitates careful freedom-to-operate analysis; competitors must identify structural or therapeutic gaps to innovate around the patent’s claims.

  4. Innovative Clarity: The patent’s inventive step relies on particular substitutions or pharmacological effects, underlining the importance of detailed structural modifications to safely navigate around existing IP.

  5. Global Considerations: While granted in Europe, similar patents or patent applications targeting the same chemical space are likely in the US, China, and other jurisdictions, necessitating a global IP strategy.


FAQs

Q1: What is the core chemical feature protected by EP1698630?

A1: It covers pyrrolopyrimidine derivatives with specific substitutions at designated positions, conferring kinase inhibitory activity.

Q2: Does the patent claim therapeutic methods or only chemical compounds?

A2: The patent includes both compound claims and methods of use for treating kinase-related diseases, such as cancer and inflammation.

Q3: How does this patent compare to prior art?

A3: It builds upon prior kinase inhibitor patents but claims specific structural modifications and their associated therapeutic effects, establishing inventive novelty.

Q4: Can competitors develop similar drugs without infringing EP1698630?

A4: Yes, provided their compounds fall outside the scope of the claims, such as alternative substitution patterns or different chemical scaffolds.

Q5: What should patent applicants consider to avoid infringing similar patents?

A5: They should carefully analyze the structural parameters, substitution ranges, and specific method claims, aiming for tangible structural or functional distinctions.


References

  1. European Patent Specification EP1698630, granted April 24, 2013.
  2. Prior art references relating to kinase inhibitors and pyrrolopyrimidine derivatives identified during prosecution and oppositions, accessible via EPO Espacenet database (source: https://worldwide.espacenet.com).

This comprehensive analysis aims to assist strategic patent management and R&D planning by elucidating the scope and positioning of EP1698630 within the pharmaceutical patent landscape.

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