CompletedNCT05970510
Official study titleA Multicenter, Randomized, Double-blind, Placebo-controlled Phase Ⅲ Study to Evaluate the Efficacy and Safety of Toludesvenlafaxine Hydrochloride Sustained-release Tablets in Participants With Generalized Anxiety Disorder.
This study has finished and is no longer accepting participants.
In BeijingAnxietyMedication studyAges 18–65
- Countries
- China
- Sponsor
- Luye Pharma Group Ltd.
TerminatedNCT05941442
Official study titleA Phase 2, Randomized, Double-blind, Placebo-controlled Trial to Evaluate the Efficacy, Safety, and Tolerability of Darigabat in Participants With Panic Disorder
This study ended early.
Multiple locations, including PhoenixAnxietyMedication studyAges 18–65
- Countries
- United States
- Sponsor
- AbbVie
CompletedNCT01577160
Official study titleAn Open Label, Prospective, Non-Comparative Study to Evaluate Flexible Dose of Paliperidone ER and Clinical Response in the Treatment of Subjects With Schizophrenia
This study has finished and is no longer accepting participants.
Location not clearly listedSchizophreniaMedication studyAges 18–65
- Countries
- Sponsor
- Johnson & Johnson Taiwan Ltd
WithdrawnNCT05344365
Official study titleAn Open-label, Sequential Cohorts, Flexible Dose Study to Evaluate the Tolerability, Safety and Pharmacokinetics of Iloperidone in Elderly Patients With Parkinson's Disease Psychosis (PDP)
This study was withdrawn before enrollment.
In St. PetersburgSchizophreniaMedication studyAges 65+
- Countries
- United States
- Sponsor
- Vanda Pharmaceuticals
CompletedNCT04712734
What is this study about?This study evaluated the safety of Iloperidone for people with schizophrenia.
This study has finished and is no longer accepting participants.
Multiple locations, including Garden GroveSchizophreniaMedication studyAges 18–65
- Countries
- United States
- Sponsor
- Vanda Pharmaceuticals
CompletedNCT07191483
Official study titleA Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, Pharmacokinetics (PK), and Pharmacodynamics (PD) of KYN-5356 as Adjunctive Treatment in Adults With Cognitive Impairment Associated With Schizophrenia
This study has finished and is no longer accepting participants.
Multiple locations, including Little RockSchizophreniaMedication studyAges 18–55
- Countries
- United States
- Sponsor
- Kynexis B.V.
CompletedNCT06817356
Official study titleA Phase 2, Double-Blind, Proof of Concept Study to Evaluate Mazdutide Compared With Placebo in Participants With Alcohol Use Disorder
This study has finished and is no longer accepting participants.
Multiple locations, including ScottsdaleAddictionMedication studyAges 21–65
- Countries
- United States
- Sponsor
- Eli Lilly and Company
CompletedNCT03359785
Official study titleA Phase 2 Randomized, Double-Blind, Placebo-Controlled, Cross-Over Study to Evaluate Pharmacodynamic Effects, Safety, Tolerability, and Pharmacokinetics of Multiple Oral Doses of TAK-831 in Adult Subjects With Schizophrenia
This study has finished and is no longer accepting participants.
In GaithersburgSchizophreniaMedication studyAges 18–60
- Countries
- United States
- Sponsor
- Neurocrine Biosciences (Biotech company)
CompletedNCT01010776
Official study titleA Study to Evaluate Switching From Risperidone to Paliperidone ER (Extended Release) in the Treatment of Stable But Symptomatic Schizophrenia Outpatients: Patients Satisfaction and Quality of Life
This study has finished and is no longer accepting participants.
Multiple locations, including Belo HorizonteSchizophreniaMedication studyAges 18–60
- Countries
- Brazil
- Sponsor
- Janssen-Cilag Farmaceutica Ltda.
CompletedNCT00890292
What is this study about?This study evaluated the safety of JNJ-31001074 for people with ADHD.
This study has finished and is no longer accepting participants.
Location not clearly listedADHDMedication studyAges 12–17
- Countries
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT00890240
What is this study about?This study evaluated the safety of JNJ-31001074 for people with ADHD.
This study has finished and is no longer accepting participants.
Location not clearly listedADHDMedication studyAges 6–11
- Countries
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Enrolling By InvitationNCT05814653
Official study titleEvaluating the Feasibility of a Primary Care-based Treatment for Restrictive Eating Disorders in Children and Adolescents in the Health System
This study is by invitation only.
In RochesterEating disordersBehavioural studyAges 7–18
- Countries
- United States
- Sponsor
- Mayo Clinic