CompletedNCT02282761
What is this study about?Researchers compared ITI-007 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 18–60
- Countries
- United States
- Sponsor
- Intra-Cellular Therapies, Inc.
CompletedNCT02469155
What is this study about?Researchers compared ITI-007, placebo and Risperidone 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 18–60
- Countries
- United States
- Sponsor
- Intra-Cellular Therapies, Inc.
TerminatedNCT05189977
Official study titleA Phase 1, Open-label, Fixed-sequence, Cross-over Trial to Assess the Effects of a Single Dose of Prazosin or Propranolol in the Presence of Brexpiprazole/Sertraline at Steady-state on Blood Pressure
This study ended early.
In PrincetonPTSDMedication studyAges 18–65
- Countries
- United States
- Sponsor
- Otsuka Pharmaceutical Development & Commercialization, Inc. (Pharmaceutical company)
CompletedNCT04786730
What is this study about?This study evaluated the safety of Centanafadine for people with ADHD.
This study has finished and is no longer accepting participants.
Multiple locations, including Little RockADHDMedication studyAges 4–12
- Countries
- United States
- Sponsor
- Otsuka Pharmaceutical Development & Commercialization, Inc. (Pharmaceutical company)
CompletedNCT04398225
What is this study about?This study evaluated the safety of Centanafadine for people with ADHD.
This study has finished and is no longer accepting participants.
In HollywoodADHDMedication studyAges 4–12
- Countries
- United States
- Sponsor
- Otsuka Pharmaceutical Development & Commercialization, Inc. (Pharmaceutical company)
CompletedNCT07253441
Official study titleA Multiple-arm, Phase 1, Open-label Trial to Determine Dose Strength Equivalence and Effect of Food on To-Be-Marketed Centanafadine QD XR Capsules, Bioequivalence Between Clinical and To-Be-Marketed QD XR Capsules and Relative Bioavailability of To-Be-Marketed QD XR Capsules to SR Tablets in Healthy Adults
This study has finished and is no longer accepting participants.
Multiple locations, including LenexaADHDMedication studyAges 18–55
- Countries
- United States
- Sponsor
- Otsuka Pharmaceutical Development & Commercialization, Inc. (Pharmaceutical company)
WithdrawnACTRN12612000955819
Official study titleAn open trial of guided internet-delivered cognitive behavioural therapy education to determine the benefits of the UniWellbeing Course for consumers of Macquarie University Campus Wellbeing with symptoms of anxiety or low mood
This study was withdrawn before enrollment.
Location not clearly listedAnxiety, DepressionInterventional studyAges 18+
- Countries
- Sponsor
- eCentreClinic, Centre for Emotional Health, Department of Psychology, Macquarie University
CompletedACTRN12612000832875
Official study titleAn open trial of guided internet-delivered cognitive behavioural therapy education to determine the benefits of the Wellbeing Course for consumers of the Mental Health Association with symptoms of anxiety
This study has finished and is no longer accepting participants.
Location not clearly listedAnxietyInterventional studyAges 18+
- Countries
- Sponsor
- eCentreClinic, Centre for Emotional Health, Department of Psychology, Macquarie University
CompletedNCT01101464
Official study titleA Single-center, Open-label, 2-way Crossover Relative Bioavailability and Safety Trial With Two Differing Strength Tablets (3 x 5 mg vs. 1 x 15 mg) of Sublingually Administered Org 5222 in Subjects With Schizophrenia or Schizoaffective Disorder.
This study has finished and is no longer accepting participants.
Location not clearly listedSchizophreniaMedication studyAges 18–65
- Countries
- Sponsor
- Organon and Co
CompletedNCT03605836
Official study titleA Phase 3, Randomized, Double-blind, Multicenter, Placebo-controlled, Parallel-group Trial Evaluating the Efficacy, Safety, and Tolerability of Centanafadine Sustained-release Tablets in Adults With Attention-deficit/Hyperactivity Disorder
This study has finished and is no longer accepting participants.
In OrlandoADHDMedication studyAges 18–55
- Countries
- United States
- Sponsor
- Otsuka Pharmaceutical Development & Commercialization, Inc. (Pharmaceutical company)
CompletedNCT03287869
What is this study about?Researchers studied Brexpiprazole, tracking side effects to assess safety and tolerability in people with bipolarity type I.
This study has finished and is no longer accepting participants.
Multiple locations, including Little RockBipolarityMedication studyAges 18–65
- Countries
- United States, Bulgaria, Croatia, + 3 others
- Sponsor
- Otsuka Pharmaceutical Development & Commercialization, Inc. (Pharmaceutical company)
CompletedNCT03568500
Official study titleA Multicentre, 8-week, Single-arm, Open-label, Pragmatic Trial to Explore Acceptance and Performance of Using a Digital Medicine System With Healthcare Professionals and Adult Subjects With Schizophrenia, Schizoaffective Disorder, or First Episode Psychosis on an Oral Atypical Antipsychotic (Aripiprazole, Olanzapine, Quetiapine, or Risperidone)
This study has finished and is no longer accepting participants.
Multiple locations, including ChertseySchizophreniaMedication studyAges 18–65
- Countries
- United Kingdom
- Sponsor
- Otsuka Pharmaceutical Development & Commercialization, Inc. (Pharmaceutical company)