Efficacy and Safety of TAK-653 in Treatment-Resistant Depression
NCT03312894 · Status: WITHDRAWN · Phase: PHASE2 · Type: INTERVENTIONAL
Last updated 2018-02-22
Summary
The purpose of this study is to evaluate the efficacy of TAK-653 compared with placebo in maintaining the effect of ketamine treatment on depressive symptoms.
Conditions
- Treatment-Resistant Depression
Interventions
- DRUG
-
TAK-653
TAK-653 tablets
- DRUG
-
Placebo-matching tablets
Sponsors & Collaborators
-
Millennium Pharmaceuticals, Inc.
lead INDUSTRY
Principal Investigators
-
Medical Director · Takeda
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-02-15
- Primary Completion
- 2019-02-28
- Completion
- 2019-09-30
- FDA Drug
- Yes
More Related Trials
-
Observation of Safety and Tolerability Within 1 Year of the Use of R-ketamine / Placebo in Drug-resistant Depression
NCT06232291 ·Status: COMPLETED
-
Ketamine Frequency Treatment for Major Depressive Disorder
NCT00646087 ·Status: WITHDRAWN ·Phase: PHASE4
-
Ketamine in Adolescents With Treatment-Resistant Depression
NCT02078817 ·Status: COMPLETED ·Phase: PHASE2
-
Ketamine Trial for the Treatment of Depression
NCT02401139 ·Status: COMPLETED ·Phase: PHASE1
-
Clinical Trial of TJ0113 Capsules in the Treatment of Patients With Depressive Disorder
NCT07018245 ·Status: RECRUITING ·Phase: PHASE2
-
Antidepressant Effects of TS-161 in Treatment-Resistant Depression
NCT04821271 ·Status: TERMINATED ·Phase: PHASE2
-
A Double-blind Study to Assess the Efficacy and Safety of Intranasal Esketamine for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Participants Who Are Assessed to be at Imminent Risk for Suicide
NCT02133001 ·Status: COMPLETED ·Phase: PHASE2
-
Study of Depression-Ketamine-Brain Function
NCT01135758 ·Status: TERMINATED ·Phase: PHASE2
-
Study to Evaluate the Efficacy, Safety and Tolerability of an Oral Aripiprazole/Escitalopram Combination Therapy in Participants With Major Depressive Disorder (MDD)
NCT01111539 ·Status: TERMINATED ·Phase: PHASE3
-
Efficacy and Safety Study of ABT-436 in Major Depressive Disorder
NCT01741142 ·Status: TERMINATED ·Phase: PHASE2
-
Efficacy and Safety of MK-1942 When Added to Stable Antidepressant Therapy in Participants With Treatment-Resistant Depression (TRD) (MK-1942-006)
NCT04663321 ·Status: TERMINATED ·Phase: PHASE2
-
Repeated Neurocognitive Measurements in Depressed Patients
NCT04916548 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Safety, Tolerability, PK and Efficacy of Single Doses of NV-5138 in Healthy Volunteers and Subjects With Treatment-Resistant Depression
NCT03606395 ·Status: COMPLETED ·Phase: PHASE1
-
Trial of Centanafadine Efficacy and Safety as Monotherapy or as Adjunct to SSRI in Adults With Major Depressive Disorder
NCT05536414 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Assess the Safety and Effect of TC-5214 in Patients With Major Depressive Disorder.
NCT01288079 ·Status: TERMINATED ·Phase: PHASE2
-
Using a Low Dose of Ketamine vs. Active Placebo in Treating Severe Depression and Suicide
NCT03666390 ·Status: UNKNOWN ·Phase: NA
-
Neuropharmacologic Imaging and Biomarker Assessments of Response to Acute and Repeated-Dosed Ketamine Infusions in Major Depressive Disorder
NCT03065335 ·Status: RECRUITING ·Phase: PHASE1
-
Adherence to Antidepressant Treatment in Subjects With Depression
NCT03388164 ·Status: TERMINATED ·Phase: PHASE2
-
Investigate the Clinical Responses of Ethosuximide in Patients With Treatment-Resistant Depression.
NCT03887624 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
A Study to Assess the Efficacy and Safety of TC-5214 as an Adjunct Therapy in Patients With Major Depressive Disorder
NCT01153347 ·Status: COMPLETED ·Phase: PHASE3
-
Intranasal Ketamine for Late-Life Depression and Suicidal Ideation
NCT02295787 ·Status: WITHDRAWN ·Phase: PHASE4
-
Patient Tolerability Study of GSK163090
NCT00559299 ·Status: COMPLETED ·Phase: PHASE1
-
Vortioxetine for the Treatment of Major Depression and Co-morbidities After Traumatic Brain Injury (TBI)
NCT02845349 ·Status: WITHDRAWN ·Phase: PHASE3
-
Intranasal Esketamine to Maintain the Antidepressant Response to IV Racemic Ketamine
NCT04856124 ·Status: COMPLETED
-
Trial to Determine the Maximum Tolerated Dose (MTD) Based on Safety and Tolerability, of Org 26576 in Participants With Major Depressive Disorder (174001/P05704/MK-8777-001)
NCT00610649 ·Status: COMPLETED ·Phase: PHASE2