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.
In FranceADHDMedication studyAges 18–65
- Countries
- France, United Kingdom, Switzerland, + 8 others
- Sponsor
- Janssen-Cilag International NV
CompletedNCT00490971
What 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.
In FranceBipolarityMedication studyAges 18–65
- Countries
- France, United States, Bulgaria, + 13 others
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT03227224
Official study titleA Multicenter, Double-Blind, Randomized, Parallel-Group, Placebo-Controlled, Adaptive Dose-Finding Study to Evaluate the Efficacy and Safety of JNJ-42847922 as Adjunctive Therapy to Antidepressants in Adult Subjects With Major Depressive Disorder Who Have Responded Inadequately to Antidepressant Therapy
This study has finished and is no longer accepting participants.
In FranceDepressionMedication studyAges 18–70
- Countries
- France, United States, Bulgaria, + 5 others
- Sponsor
- Janssen Research & Development, LLC
CompletedNCT02417064
What is this study about?This study evaluated the safety and effectiveness of Esketamine for people with depression.
This study has finished and is no longer accepting participants.
In FranceDepressionMedication studyAges 18–64
- Countries
- France, United States, Canada, + 6 others
- Sponsor
- Janssen Research & Development, LLC
CompletedNCT02422186
What is this study about?This study evaluated the safety and effectiveness of Esketamine for people with depression.
This study has finished and is no longer accepting participants.
In FranceDepressionMedication studyAges 65+
- Countries
- France, United States, United Kingdom, + 9 others
- Sponsor
- Janssen Research & Development, LLC
CompletedEUCTR 2019-000063-24
This study has finished and is no longer accepting participants.
Historical country statuses are shown below. They describe the trial's progress and do not confirm open recruitment.
In FranceSchizophreniaHistorical research record
- Countries
- France, Bulgaria
- Sponsor
- Teva Branded Pharmaceutical Products R&D, Inc.
CompletedNCT04566601
What is this study about?Researchers compared BI 1358894 and placebo, tracking side effects to assess safety in people with borderline personality difficulties.
This study has finished and is no longer accepting participants.
In FrancePersonality disordersMedication studyAges 18–65
- Countries
- France, United States, Australia, + 12 others
- Sponsor
- Boehringer Ingelheim
CompletedNCT03893825
What is this study about?This study evaluated the safety of TV-46000 for people with schizophrenia.
This study has finished and is no longer accepting participants.
In FranceSchizophreniaMedication studyAges 13–65
- Countries
- France, United States, Canada, + 2 others
- Sponsor
- Teva Branded Pharmaceutical Products R&D, Inc.
CompletedNCT04521478
What is this study about?Researchers compared BI 1358894, placebo and Quetiapine to find out how the approaches affected depression symptoms in people with depression.
This study has finished and is no longer accepting participants.
In FranceDepressionMedication studyAges 18–65
- Countries
- France, United States, Australia, + 11 others
- Sponsor
- Boehringer Ingelheim
CompletedNCT03809325
Official study titleCross-sectional Survey to Collect Treatment Experience Feedback From Patients, Physicians, Nurses and Carers After Switching to Paliperidone Palmitate 3-monthly
This study has finished and is no longer accepting participants.
In FranceSchizophreniaObservational studyAges 18+
- Countries
- France, United Kingdom, Belgium, + 4 others
- Sponsor
- Janssen-Cilag International NV
CompletedNCT00232687
Official study titleA Comparative, Randomized, Open-Label, Multicenter Study on the Efficacy and Safety of Switch Treatment With Aripiprazole in Schizophrenic Out-patients Who Are Experiencing Insufficient Efficacy With Risperidone and/or Safety and Tolerability Issues, While on Risperidone
This study has finished and is no longer accepting participants.
In FranceSchizophreniaMedication studyAges 18–65
- Countries
- France, United Kingdom, Belgium, + 7 others
- Sponsor
- Otsuka Pharmaceutical Development & Commercialization, Inc. (Pharmaceutical company)