At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 197 enrolled
Drug / intervention
Liafensine +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Biomarker-Guided, Randomized, Double-Blind, Placebo-Controlled Efficacy and Safety Study of Liafensine in Patients With Treatment-Resistant Depression
In Brief
A Phase 2 clinical trial evaluating Liafensine and Placebo for Treatment Resistant Depression. Completed, enrolled 197 participants across 45 sites in 2 countries.
Detailed Summary
This study was conducted as a randomized, double-blind, placebo-controlled, multi-center Phase 2b study. Approximately 180 subjects with treatment resistant depression who meet all eligibility criteria will be enrolled. The primary endpoint is to demonstrate liafensine is superior to placebo in DGM4 positive patients with TRD.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsTreatment Resistant Depression
CountriesCanada, United States
Collaborators--
Timeline
Phase 2CompletedFinished
20222023202420252026
First PostedNov 2021
Enrollment StartJun 2022
Primary CompletionFeb 2024
Study CompletionMar 2024
TodayJul 2026
First PostedNov 9, 2021
Enrollment StartJun 29, 2022
Primary CompletionFeb 6, 2024
Study CompletionMar 5, 2024
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 4.6 years ago
Interventions
Liafensinedrug
Liafensine
Placebodrug
Placebo