Active Not RecruitingACTRN12623000838617
Official study titleAn open label study to investigate the safety and feasibility of delivering 3,4-methylenedioxymethamphetamine (MDMA)-assisted psychotherapy to patients with posttraumatic stress disorder
This study is no longer accepting new participants.
In AustraliaPTSDInterventional studyAges 18–70
- Countries
- Australia
- Sponsor
- Emyria Ltd
CompletedNCT02902601
Official study titleA Randomized, Double-blind, Placebo-controlled, Parallel-group Study to Investigate the Safety, Tolerability, and Pharmacodynamics of JNJ-54175446 in Subjects With Major Depressive Disorder
This study has finished and is no longer accepting participants.
Multiple locations, including BerlinDepressionMedication studyAges 18–64
- Countries
- Germany, Netherlands
- Sponsor
- Janssen Research & Development, LLC
CompletedNCT06225115
Official study titleA First in Human Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Ascending Oral Doses of KYN-5356 in Adult, Healthy Subjects
This study has finished and is no longer accepting participants.
In GlendaleSchizophreniaMedication studyAges 18–55
- Countries
- United States
- Sponsor
- Kynexis B.V.
CompletedNCT04943796
Official study titlePrevalence of ADHD and Health Outcomes in Adult Outpatients With Psychiatric Disorders: a Multi-country, Two-part, Observational Study
This study has finished and is no longer accepting participants.
Multiple locations, including BurnabyADHDObservational studyAges 18+
- Countries
- Canada, United Kingdom, Switzerland, + 3 others
- Sponsor
- Takeda
CompletedNCT07047820
Official study titleProspective, Observational Survey Study Assessing Effectiveness of Zuranolone in Improving PPD Symptoms in the Real-world Setting
This study has finished and is no longer accepting participants.
In WoonsocketDepressionObservational studyAges 18+
- Countries
- United States
- Sponsor
- Biogen
CompletedNCT01959594
Official study titlePhase 1, Double Blind, Sponsor Open, Randomized, Placebo Controlled, Dose Escalation, Parallel Group Study To Investigate The Safety, Tolerability And Pharmacokinetics Of Repeat Doses Of PF-06412562 In Healthy Subjects
This study has finished and is no longer accepting participants.
In New HavenSchizophreniaMedication studyAges 18–55
- Countries
- United States
- Sponsor
- Pfizer
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.
Multiple locations, including AnaheimPersonality disordersMedication studyAges 18–65
- Countries
- United States, Australia, France, + 12 others
- Sponsor
- Boehringer Ingelheim
CompletedNCT06558344
What is this study about?Researchers compared 5 mg BI 1569912, 10 mg BI 1569912, 20 mg of BI 1569912 and placebo to find out how the approaches affected depression symptoms in people with depression.
This study has finished and is no longer accepting participants.
Multiple locations, including BellflowerDepressionMedication studyAges 18–65
- Countries
- United States, Japan
- Sponsor
- Boehringer Ingelheim
CompletedNCT06280235
Official study titleA Phase II, 6-week, Multicenter, Randomized, Double Blind (Patient and Investigator) or Masked, Placebo Controlled, Dose-finding Trial to Evaluate the Efficacy, Tolerability, and Safety of Different Doses of Oral BI 1569912 as Adjunctive Therapy in MD
This study has finished and is no longer accepting participants.
Multiple locations, including TucsonDepressionMedication studyAges 18–65
- Countries
- United States, Belgium, Bulgaria, + 4 others
- Sponsor
- Boehringer Ingelheim
CompletedNCT05278104
Official study titleDouble-blind, Randomized, Parallel Group, Placebo Controlled Clinical Trial to Evaluate the Effects of Atomoxetine on Impulsivity in Behavioral Laboratory Tasks in Adult ADHD Patients
This study has finished and is no longer accepting participants.
Multiple locations, including AachenADHDMedication studyAges 18–45
- Countries
- Germany
- Sponsor
- Boehringer Ingelheim