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
| Type | Name | Description |
|---|---|---|
| DRUG | Esketamine DPI - low dose | Esketamine DPI is to be administered via dry powder inhaler. Each dose correspond to low Esketamine dose. |
| DRUG | Esketamine DPI - medium dose | Esketamine DPI is to be administered via dry powder inhaler. Each dose correspond to medium Esketamine dose. |
| DRUG | Esketamine DPI - high dose | Esketamine DPI is to be administered via dry powder inhaler. Each dose correspond to high Esketamine dose. |
| DRUG | Placebo DPI | Placebo 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.