CompletedNCT03627195
Official study titleA Randomized, Double Blind, Placebo Controlled, Single Ascending Dose Study With Lurasidone Injectable Suspension to Evaluate Safety, Tolerability and Pharmacokinetics in Subjects With Schizophrenia
This study has finished and is no longer accepting participants.
In Long BeachSchizophreniaMedication studyAges 18–65
- Countries
- United States
- Sponsor
- Sumitomo Pharma America, Inc.
CompletedNCT02624167
Official study titleA Phase IIA, Prospective, Randomized, Double-blind, Multiple-dose Study of NW-3509A in Chronic Schizoprhenia Patients Not Responding to Their Current Anti-psychotic Medication
This study has finished and is no longer accepting participants.
Multiple locations, including Garden GroveSchizophreniaMedication studyAges 18–65
- Countries
- United States, India
- Sponsor
- Newron Pharmaceuticals SPA
CompletedNCT00880217
What is this study about?Researchers compared JNJ-31001074 1 mg/d, JNJ-31001074 3 mg/d, JNJ-31001074 10 mg/d, Atomoxetine 80 mg/d, OROS methylphenidate HCl 54 mg/d and placebo to find out how the approaches affected ADHD symptoms in adults with ADHD.
This study has finished and is no longer accepting participants.
Multiple locations, including Little RockADHDMedication studyAges 18–55
- Countries
- United States
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT03382639
Official study titleA Phase 2, 12-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel Study to Evaluate Efficacy, Safety, Tolerability, and Pharmacokinetics of 3 Dose Levels of TAK-831 in Adjunctive Treatment of Adult Subjects With Negative Symptoms of Schizophrenia
This study has finished and is no longer accepting participants.
Multiple locations, including Garden GroveSchizophreniaMedication studyAges 18–60
- Countries
- United States, Bulgaria, Czechia, + 5 others
- Sponsor
- Neurocrine Biosciences (Biotech company)
CompletedNCT03107026
What is this study about?Researchers compared dasotraline 4mg, dasotraline 6mg and placebo, tracking side effects to assess safety and tolerability in adults with binge eating.
This study has finished and is no longer accepting participants.
Multiple locations, including PhoenixEating disordersMedication studyAges 18–55
- Countries
- United States
- Sponsor
- Sumitomo Pharma America, Inc.
CompletedNCT01655680
What is this study about?Researchers compared ABT-126 and placebo to find out how the approaches affected memory, attention and other thinking skills in people with schizophrenia.
This study has finished and is no longer accepting participants.
Multiple locations, including AnaheimSchizophreniaMedication studyAges 20–65
- Countries
- United States, United Kingdom, Russia
- Sponsor
- AbbVie (prior sponsor, Abbott)
CompletedNCT00396565
About this title
A Study to Evaluate Effectiveness and Safety of ER OROS Paliperidone in Patients With Schizophrenia
Read the official source — NCT00396565What is this study about?Researchers compared ER OROS paliperidone, placebo and Olanzapine to find out how the approaches affected psychotic symptoms in people with schizophrenia.
This study has finished and is no longer accepting participants.
Multiple locations, including Aizu-WakamatsuSchizophreniaMedication studyAges 20+
- Countries
- Japan
- Sponsor
- Janssen Pharmaceutical K.K.
CompletedNCT00714688
Official study titleA Multicentre, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Dose-Response Study to Evaluate Efficacy and Safety of Prolonged Release (PR) OROS Methylphenidate (54 and 72 mg/Day) in Adults With Attention Deficit/Hyperactivity Disorder
This study has finished and is no longer accepting participants.
Multiple locations, including AntwerpADHDMedication studyAges 18–65
- Countries
- France, United Kingdom, Switzerland, + 8 others
- Sponsor
- Janssen-Cilag International NV
CompletedNCT01192880
Official study titleA Phase III, Multi-Center, Randomized, 24 Week, Double-Blind, Parallel-Group, Placebo-Controlled Study to Evaluate Efficacy and Safety of RO4917838 in Stable Patients With Persistent, Predominant Negative Symptoms of Schizophrenia Treated With Antipsychotics Followed by a 28 Week, Double-Blind Treatment Period
This study has finished and is no longer accepting participants.
Multiple locations, including Costa MesaSchizophreniaMedication studyAges 18+
- Countries
- United States, Bulgaria, China, + 4 others
- Sponsor
- Hoffmann-La Roche
CompletedNCT06796868
Official study titleA Multicenter, Randomized , Double-blind, Parallel, Placebo-controlled Design Clinical Trial of GW117 Tablets
This study has finished and is no longer accepting participants.
Multiple locations, including BaodingDepressionMedication studyAges 18–65
- Countries
- China
- Sponsor
- Beijing Greatway Pharmaceutical Technology Co.,Ltd.
CompletedNCT02942004
Official study titleA Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-547 Injection in the Treatment of Adult Female Subjects With Severe Postpartum Depression and Adult Female Subjects With Moderate Postpartum Depression
This study has finished and is no longer accepting participants.
Multiple locations, including ChandlerDepressionMedication studyAges 18–45
- Countries
- United States
- Sponsor
- Supernus Pharmaceuticals, Inc. (Pharmaceutical company)