PYRIDAZINE COMPOUNDS FOR INHIBITION OF NAV1.8

DE602019076972T2Active Publication Date: 2025-10-15LIEBER INSTITUTE INC
View PDF 0 Cites 0 Cited by

Patent Information

Application Number
DE602019076972
Authority / Receiving Office
DE · DE
Patent Type
Patents
Current Assignee / Owner
Priority Date
2018-07-09
Filing Date
2019-07-09
Publication Date
2025-10-15
Estimated Expiration
2039-07-09

AI Technical Summary

Technical Problem

Current treatments for chronic and acute pain, such as steroidal and nonsteroidal anti-inflammatory drugs, amine reuptake inhibitors, and opioids, have limitations, and selective inhibitors for voltage-gated sodium channels, particularly Na v 1.7 and Na v 1.8, have shown limited efficacy in clinical trials, while Na v 1.8 inhibitors face challenges with selectivity and pharmacokinetics.

Method used

Development of pyridazine compounds that selectively inhibit Na v 1.8 sodium channels, which are administered to modulate or inhibit the channel activity, thereby treating conditions associated with increased Na v 1.8 expression or activity, including pain, neurological disorders, and psychiatric diseases.

Benefits of technology

The pyridazine compounds effectively inhibit Na v 1.8 channels, providing therapeutic benefits for conditions like inflammatory and neuropathic pain, multiple sclerosis, and autism, with potential for improved selectivity and pharmacokinetic profiles compared to existing inhibitors.

✦ Generated by Eureka AI based on patent content.
Patent Text Reader
Need to check novelty before this filing date? Find Prior Art
No text content released.