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Clinical Trial to Evaluate Safety, Tolerability and Efficacy of NFX88 in SCI

Spinal Cord Injuries Clinical Trial

Official title:
Randomized, Double-blind, Placebo Controlled, Parallel, Multicentric, Phase IIa Clinical Trial to Evaluate Safety, Tolerability, Therapeutic Efficacy of Daily Oral Treatment NFX88 on Neuropathic Pain in Patients With Spinal Cord Injury

Clinical Trial Summary

In summary, this small-scale study is designed to demonstrate that the NFX88 is safe and well tolerated, as well as preliminary evidence of improvement in the score of VAS, PD-Q, and PGIC scales.

Clinical Trial Description

This is a Phase IIa (proof of concept), randomized, double-blind, placebo controlled, parallel group, multicentric, clinical trial to evaluate the safety, tolerability and efficacy of daily oral treatment with NFX88 in SCI patients who are not receiving opiates or cannabinoids and present neuropathic pain with an average pain score ≥ 4 measured with a VAS scale during the last week at screening ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04148573
Study type Interventional
Source Neurofix S.L.
Contact
Status Completed
Phase Phase 2
Start date October 1, 2019
Completion date July 20, 2022
View Details
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