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Efficacy and Safety of NYX-2925 in Subjects With Neuropathic Pain Associated With Diabetic Peripheral Neuropathy (DPN)

Diabetic Peripheral Neuropathic Pain Clinical Trial

Official title:
A Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of NYX-2925 in Subjects With Neuropathic Pain Associated With Diabetic Peripheral Neuropathy

Clinical Trial Summary

To evaluate the efficacy of NYX-2925 versus placebo in treating the neuropathic pain associated with diabetic peripheral neuropathy.

Clinical Trial Description

This is a randomized, double-blind, placebo-controlled study to assess the efficacy and safety of NYX-2925 in subjects with neuropathic pain associated with diabetic peripheral neuropathy. The study will be a 13- to 16-week study, including a 1- to 4-week Screening Period, followed by a 12- week double-blind, randomized, placebo-controlled Treatment Period. ;

Study Design

Related Conditions & MeSH terms

  • Diabetic Peripheral Neuropathic Pain
  • Neuralgia
  • Peripheral Nervous System Diseases
Clinical Trial Details
NCT number NCT04146896
Study type Interventional
Source Aptinyx
Contact
Status Completed
Phase Phase 2
Start date November 12, 2019
Completion date February 23, 2022
View Details
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