Clinical Trials Directory

Trials / Completed

CompletedNCT03965858

Efficacy, Safety and Pharmacokinetic Study of Inhaled Esketamine in Treatment-resistant Depression

A Multicentre, Double-blind, Randomised, Placebo - Controlled Phase II Study to Assess Efficacy, Safety and Pharmacokinetics of Inhaled Esketamine in Subject With Treatment-resistant Depression in the Course of Major Depressive Disorder

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
88 (actual)
Sponsor
Celon Pharma SA · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to determine the efficacy, safety and pharmacokinetics of inhaled Esketamine in participants with treatment-resistant depression (TRD) in the course of Major Depressive Disorder (MDD). The study is to determine the efficacy and dose response of three Esketamine doses, compared with placebo.

Detailed description

This is a randomized, multiple dose, placebo-controlled, double-blind, multicentre study of Esketamine DPI, inhalation powder delivered via dry powder inhaler (DPI) in participants with TRD in the course of MDD. There are 3 study phases: Screening phase, a two weeks double-blind treatment phase and a 6-week follow-up phase. Participants are to be randomized in 1:1:1:1 ratio to receive placebo or one of the three doses of Esketamine DPI. Participants from each group will receive different dosing sequences, consider as a single dose, corresponding to low, medium, high Esketamine dose or placebo. Participants will undergo one cycle of treatment consisting of four doses of Esketamine DPI or placebo over 14-day period. Participants safety will be monitored throughout the study.

Conditions

Interventions

TypeNameDescription
DRUGEsketamine DPI - low doseEsketamine DPI is to be administered via dry powder inhaler. Each dose correspond to low Esketamine dose.
DRUGEsketamine DPI - medium doseEsketamine DPI is to be administered via dry powder inhaler. Each dose correspond to medium Esketamine dose.
DRUGEsketamine DPI - high doseEsketamine DPI is to be administered via dry powder inhaler. Each dose correspond to high Esketamine dose.
DRUGPlacebo DPIPlacebo DPI is to be administered via dry powder inhaler.

Timeline

Start date
2019-02-25
Primary completion
2020-03-15
Completion
2020-04-24
First posted
2019-05-29
Last updated
2020-04-28

Locations

12 sites across 1 country: Poland

Source: ClinicalTrials.gov record NCT03965858. Inclusion in this directory is not an endorsement.