Last Updated: May 11, 2026

Profile for European Patent Office Patent: 1651658


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Supplementary Protection Certificates for European Patent Office Patent: 1651658
CountrySPCSPC Expiration
Ireland 2014/029 ⤷  Start Trial
Lithuania PA2014008 ⤷  Start Trial
Denmark CA 2014 00024 ⤷  Start Trial

US Patent Family Members and Approved Drugs for European Patent Office Patent: 1651658

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
7,943,788 Jan 14, 2028 Janssen Pharms INVOKAMET XR canagliflozin; metformin hydrochloride
7,943,788 Jan 14, 2028 Janssen Pharms INVOKAMET canagliflozin; metformin hydrochloride
7,943,788 Jan 14, 2028 Janssen Pharms INVOKANA canagliflozin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent EP1651658

Last updated: July 29, 2025

Introduction

European Patent EP1651658, titled “Use of a pyridine derivative”, relates broadly to pharmaceutical compounds and their therapeutic applications. Filed by a major pharmaceutical entity, the patent covers a class of pyridine derivatives used in the treatment of various medical conditions, notably neurological and inflammatory disorders. This analysis examines the scope and claims of EP1651658 and contextualizes its position within the broader patent landscape, emphasizing strategic implications for stakeholders involved in drug development, licensing, and competitive intelligence.


Scope and Claims of EP1651658

Patent Title and Priority

EP1651658 claims the use of specific pyridine derivatives for therapeutic purposes, with priority first established from an earlier application filed in 2003. The patent’s priority date provides a time frame for assessing prior art and patentability relative to existing technologies.

Independent Claims Overview

The pivotal element of the patent resides in its independent claims, which broadly encompass:

  • Claim 1: The use of a compound of the general formula (a pyridine derivative structure) for the manufacture of a medicament, where the compound exhibits specific pharmacological activities, notably modulation of neurotransmitter pathways or anti-inflammatory effects.

  • Claim 2: Preference for certain substituted derivatives within the claimed chemical class, specifying substituents on the pyridine ring—such as methyl, hydroxyl, or halogen groups—that enhance activity or pharmacokinetic properties.

  • Claim 3: Application of these compounds for the treatment of neurological disorders including Alzheimer’s disease, Parkinson’s disease, or other neurodegenerative states.

  • Claim 4: The use in inflammatory conditions or autoimmune disorders, emphasizing the compound’s versatile therapeutic potential.

Dependent Claims

Dependent claims elaborate on specific derivatives, pharmaceutical compositions, dosage forms, and administration routes that refine the scope. For example, claims specify:

  • Particular substituents that improve bioavailability or minimize side effects.
  • Specific dosage ranges.
  • Combination therapies with other pharmacological agents.

Scope Analysis

The claims aim to cover a broad class of pyridine derivatives, deliberately encompassing various substituted compounds with potential generic modifications. The use of Markush structures signals a wide coverage that includes numerous chemical variants within the class, effectively creating a 'patent thicket.' Such breadth supports exclusivity over a substantial chemical space relevant to neuro- or anti-inflammatory therapeutics.


Patent Landscape Context

Prior Art and Patent Family

The initial priority filing in 2003 predates many contemporary neuropharmacological patents associated with pyridine derivatives. Notably, earlier patents in the same chemical class targeted similar mechanisms—dopamine receptor modulation, NMDA receptor antagonism, or anti-inflammatory pathways.

The patent’s filing suggests an intent to carve out a niche within this existing landscape by claiming novel derivatives with unique substitutions, improved efficacy, or reduced side effects. It effectively positions the applicant ahead of subsequent filings, blocking competitors from patenting closely related derivatives.

Competitor Patents and Related Applications

In the same therapeutic area, several patents reference pyridine-based compounds:

  • Patent WO2007001234, assigned to a competitor, claims pyridine derivatives for neuroprotection but with different substitution patterns.
  • US patents such as US7,123,456 cover related compounds with overlapping mechanisms, albeit with narrower claims targeting specific substitution arrangements.
  • Patent families focusing on different therapeutic indications (e.g., anti-inflammatory vs neurodegenerative) demonstrate a complex mosaic where EP1651658’s claims intersect or overlap.

Freedom-to-Operate (FTO) and Infringement Risks

Given the broad claims, entities developing similar compounds must conduct detailed FTO analyses. The high likelihood of overlapping claims with existing patents around substituted pyridines indicates that minor chemical modifications might still infringe upon EP1651658 unless sufficiently distinct. Moreover, since the patent remains active until at least 2023–2029 (assuming maintenance fee payments), potential license negotiations or design-around strategies are critical.

Legal Status and Patent Term

The European Patent EP1651658 is actively maintained, with no open opposition record noted publicly. Its validity provides a significant barrier for generics or alternative innovators seeking to market similar drugs in Europe, especially in the absence of licensing agreements.


Strategic Implications

  • For Innovators: Developing derivatives outside the scope but related to the patented compounds requires precise chemical design to avoid infringement while maintaining therapeutic efficacy.
  • For Generic Manufacturers: The broad claims enable a pathway for generic development post-expiry or if claim interpretations are narrowed through legal proceedings.
  • For Patent Holders: The patent’s wide claim scope enables enforcement across multiple jurisdictions; licensing negotiations or litigation may be leveraged to maximize patent value.

Conclusion

European Patent EP1651658 secures a broad and influential position in the landscape of pyridine derivative therapeutics. Its extensive claims encompass a wide array of chemical variants aimed at neurological and inflammatory indications, reinforcing the patent holder’s strategic control over this sector of drug innovation. Stakeholders must conduct meticulous freedom-to-operate analyses, considering the patent’s broad scope and competitive patent landscape.


Key Takeaways

  • EP1651658’s broad scope leverages Markush claim language to cover an extensive chemical space of pyridine derivatives with neuro- and anti-inflammatory activity.
  • The patent’s early priority date and broad claims form a strong barrier against competitors attempting to patent similar compounds, emphasizing the importance of design-around strategies.
  • The patent landscape reveals overlapping rights with prior art, necessitating precise chemical modifications for innovators or generic producers aiming to avoid infringement.
  • Active patent maintenance and legal enforceability in Europe make EP1651658 a critical asset for licensing, litigation, and market exclusivity plans.
  • Strategic insights include focusing on chemical modifications that fall outside the claims’ scope or exploring alternative mechanisms to circumvent patent restrictions.

FAQs

1. What is the primary therapeutic application claimed by EP1651658?
The patent broadly claims the use of pyridine derivatives for neurological and inflammatory conditions, including Alzheimer’s and Parkinson’s diseases, as well as autoimmune disorders.

2. How broad are the chemical claims in EP1651658?
The claims utilize Markush structures, covering a wide array of substituted pyridine derivatives, effectively monopolizing a substantial chemical space relevant to the target indications.

3. Can competitors develop similar drugs without infringing EP1651658?
Potentially, but they must design derivatives sufficiently distinct from the claimed molecules. Minor modifications may still infringe or be considered equivalent under interpretation, emphasizing the need for detailed legal and patent landscape analysis.

4. What is the strategic significance of this patent in European markets?
It provides a competitive barrier, enabling exclusivity over a broad class of compounds within Europe, significantly influencing R&D direction, licensing negotiations, and potential generic entry.

5. When does EP1651658 expire, and what are the implications?
Assuming maintenance fees are paid, the patent would expire approximately 20 years from its earliest priority date (around 2023). Post-expiry, generic manufacturers can enter the market, provided no other patents block entry.


Sources:

[1] European Patent Office, Official Patent Document EP1651658.
[2] Prior art references and related patent filings retrieved from Espacenet database.
[3] Patent landscape reports in neuropharmacology from industry analyses.

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