TerminatedNCT00907985
Official study titleDouble Blind, Double-dummy, Randomised, Placebo Controlled Study to Evaluate the Effect of Single Doses of Drug A (Lamotrigine) and Drug B (Vofopitant) Alone and in Combination on Resting Motor Threshold in Healthy Subjects
This study ended early.
In GöttingenBipolarityMedication studyAges 18–65
- Countries
- Germany
- Sponsor
- GlaxoSmithKline
CompletedNCT00210548
About this title
A Study to Evaluate the Effectiveness and Safety of 3 Doses of Paliperidone Palmitate in Treating Subjects With Schizophrenia
Read the official source — NCT00210548What is this study about?This study evaluated the safety and effectiveness of paliperidone palmitate for people with schizophrenia.
This study has finished and is no longer accepting participants.
Location not clearly listedSchizophreniaMedication studyAges 18+
- Countries
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT00490971
About this title
A Study to Evaluate the Effectiveness and Safety of Extended-Release (ER) Paliperidone Compared With Placebo in Delaying the Recurrence of Symptoms in Bipolar I Disorder
Read the official source — NCT00490971What is this study about?Researchers compared Paliperidone ER, placebo and Olanzapine to find out how the approaches affected how long people remain free of a new mood episode in people with bipolarity type I.
This study has finished and is no longer accepting participants.
Multiple locations, including ScottsdaleBipolarityMedication studyAges 18–65
- Countries
- United States, France, Bulgaria, + 13 others
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT01527305
What is this study about?Researchers studied Paliperidone palmitate to find out how it affected psychotic symptoms in people with schizophrenia.
This study has finished and is no longer accepting participants.
Multiple locations, including HuzhouSchizophreniaMedication studyAges 18–65
- Countries
- China, Malaysia, South Korea, + 1 other
- Sponsor
- Janssen Research & Development, LLC
CompletedNCT02919579
Official study titleA Placebo- and Active-Controlled Study to Evaluate the Effects of a Single-Dose and Repeat-Administration of Intranasal Esketamine on On-Road Driving in Subjects With Major Depressive Disorder (DriveSaFe2)
This study has finished and is no longer accepting participants.
In LeidenDepressionMedication studyAges 22–60
- Countries
- Netherlands
- Sponsor
- Janssen Research & Development, LLC
CompletedNCT02953639
What is this study about?This study evaluated the safety and effectiveness of Basmisanil for people with schizophrenia.
This study has finished and is no longer accepting participants.
Multiple locations, including Little RockSchizophreniaMedication studyAges 18–50
- Countries
- United States
- Sponsor
- Hoffmann-La Roche
CompletedNCT01730768
Official study titleA 12 Week, Randomized, Double-blind, Placebo-controlled, Parallel Group Study to Evaluate the Effects of Once Daily Doses of AQW051 on Cognition, in Stable Schizophrenia Patients
This study has finished and is no longer accepting participants.
Multiple locations, including Garden GroveSchizophreniaMedication studyAges 18–55
- Countries
- United States
- Sponsor
- Novartis Pharmaceuticals
CompletedNCT02824055
Official study titleA Study to Evaluate The Effects of RO5545965 in Participants With Negative Symptoms of Schizophrenia Treated With Antipsychotics
This study has finished and is no longer accepting participants.
Multiple locations, including Garden GroveSchizophreniaMedication studyAges 18–50
- Countries
- United States
- Sponsor
- Hoffmann-La Roche
CompletedNCT04693351
Official study titleA Randomized, Double-Blind, Placebo- Controlled Trial of Adjunctive Troriluzole in Obsessive Compulsive Disorder
This study has finished and is no longer accepting participants.
Multiple locations, including PhoenixOCDMedication studyAges 18–65
- Countries
- United States, Canada, United Kingdom, + 4 others
- Sponsor
- Biohaven Pharmaceuticals, Inc.
CompletedNCT00309686
About this title
A Study to Evaluate the Efficacy and Safety of Adjustable Doses of Extended-release (ER) Paliperidone Compared With Placebo, in Combination With Lithium or Valproate, to Treat Manic and Mixed Episodes in Patients With Bipolar I Disorder
Read the official source — NCT00309686Official study titleA Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter Study to Evaluate the Efficacy and Safety of Flexibly-Dosed Extended-Release Paliperidone as Adjunctive Therapy to Mood Stabilizers in the Treatment of Acute Manic and Mixed Episodes Associated With Bipolar I Disorder
This study has finished and is no longer accepting participants.
Location not clearly listedBipolarity, SchizophreniaMedication studyAges 18–65
- Countries
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT01469039
What is this study about?Researchers compared ALKS 9072 and placebo 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 Little RockSchizophreniaMedication studyAges 18–70
- Countries
- United States, Bulgaria, Malaysia, + 5 others
- Sponsor
- Alkermes, Inc.
CompletedNCT01072929
Official study titleA Double-Blind, Placebo-Controlled, Parallel-Group, Fixed-Dosage Study to Evaluate the Efficacy and Safety of Armodafinil Treatment (150 and 200 mg/Day) as Adjunctive Therapy in Adults With Major Depression Associated With Bipolar I Disorder
This study has finished and is no longer accepting participants.
Multiple locations, including BirminghamBipolarity, DepressionMedication studyAges 18–65
- Countries
- United States
- Sponsor
- Cephalon