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Mental health studies with practical context.

Public study records, presented in a clearer and more patient-friendly format for mental health research discovery.

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27277studies shown
Showing 7,633-7,644 of 27,277
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CompletedNCT03627195

Maximum Tolerated Dose of an Investigational Drug in Subjects With Schizophrenia

Official study title

A 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 Beach
SchizophreniaMedication studyAges 18–65
Countries
United States
Sponsor
Sumitomo Pharma America, Inc.
Drug study icon
CompletedNCT02624167

Safety, Tolerability and Efficacy NW-3509A in people with Chronic Schizophrenia

Official study title

A 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 Grove
SchizophreniaMedication studyAges 18–65
Countries
United States, India
Sponsor
Newron Pharmaceuticals SPA
Drug study icon
CompletedNCT00880217

3 Different Doses of JNJ-31001074 for ADHD

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 Rock
ADHDMedication studyAges 18–55
Countries
United States
Sponsor
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Drug study icon
CompletedNCT03382639

3 Dose Levels of Luvadaxistat of Adults With Negative Symptoms of Schizophrenia

Official study title

A 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 Grove
SchizophreniaMedication studyAges 18–60
Countries
United States, Bulgaria, Czechia, + 5 others
Sponsor
Neurocrine Biosciences (Biotech company)
Drug study icon
CompletedNCT03107026

Effectiveness of drug (Dasotraline) on the Safety, Effectiveness and How Well the Body Tolerates it, in Eating disorders

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 Phoenix
Eating disordersMedication studyAges 18–55
Countries
United States
Sponsor
Sumitomo Pharma America, Inc.
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CompletedNCT01655680

ABT-126 for schizophrenia

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 Anaheim
SchizophreniaMedication studyAges 20–65
Countries
United States, United Kingdom, Russia
Sponsor
AbbVie (prior sponsor, Abbott)
Drug study icon
CompletedNCT00396565

Extended-release paliperidone for schizophrenia

About this title

A Study to Evaluate Effectiveness and Safety of ER OROS Paliperidone in Patients With Schizophrenia

Read the official source — NCT00396565
What 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-Wakamatsu
SchizophreniaMedication studyAges 20+
Countries
Japan
Sponsor
Janssen Pharmaceutical K.K.
Drug study icon
CompletedNCT00714688

Effectiveness of Effectiveness and Safety of Prolonged Release OROS Methylphenidate in ADHD

Official study title

A 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 Antwerp
ADHDMedication studyAges 18–65
Countries
France, United Kingdom, Switzerland, + 8 others
Sponsor
Janssen-Cilag International NV
Drug study icon
CompletedNCT06685965

Safety study of Effects on Sleep and Safety of RE03 in PTSD

What is this study about?

Researchers compared RE03 and placebo, tracking side effects to assess safety in people with PTSD.

This study has finished and is no longer accepting participants.

In Zurich
PTSDMedication studyAges 18–64
Countries
Switzerland
Sponsor
Reconnect Labs
Drug study icon
CompletedNCT01192880

Bitopertin for schizophrenia

Official study title

A 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 Mesa
SchizophreniaMedication studyAges 18+
Countries
United States, Bulgaria, China, + 4 others
Sponsor
Hoffmann-La Roche
Drug study icon
CompletedNCT06796868

GW117 Tablets for depression

Official study title

A 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 Baoding
DepressionMedication studyAges 18–65
Countries
China
Sponsor
Beijing Greatway Pharmaceutical Technology Co.,Ltd.
Drug study icon
CompletedNCT02942004

SAGE-547 for depression

Official study title

A 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 Chandler
DepressionMedication studyAges 18–45
Countries
United States
Sponsor
Supernus Pharmaceuticals, Inc. (Pharmaceutical company)

Registry coverage

We gather information about mental health clinical trials from the public registries we index. Coverage is still expanding, so some studies may not appear yet.