TerminatedNCT01480232
Official study titleProof-of-Concept Study of EVP-6124, an Alpha-7 Nicotinic Acetylcholine Receptor Agonist, Versus Placebo in Subjects With Nicotine Dependence
This study ended early.
In BostonAddictionMedication studyAges 18–65
- Countries
- United States
- Sponsor
- A. Eden Evins
CompletedNCT00566449
What is this study about?Researchers compared JNJ-31001074 and placebo, tracking side effects to assess safety in adults with ADHD.
This study has finished and is no longer accepting participants.
Multiple locations, including IrvineADHDMedication studyAges 18–64
- Countries
- United States
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT00326391
About this title
A Safety and Effectiveness Study of Methylphenidate HCl Extended-release Tablets in Adults With Attention Deficit Hyperactivity Disorder
Read the official source — NCT00326391Official study titleA Placebo-Controlled, Double-Blind, Parallel-Group, Dose-Titration Study to Evaluate the Efficacy and Safety of CONCERTA (Methylphenidate HCl) Extended-release Tablets in Adults With Attention Deficit Hyperactivity Disorder at Doses of 36 mg, 54 mg, 72 mg, 90 mg, or 108 mg Per Day.
This study has finished and is no longer accepting participants.
Location not clearly listedADHDMedication studyAges 18–65
- Countries
- Sponsor
- McNeil Consumer & Specialty Pharmaceuticals, a Division of McNeil-PPC, Inc.
CompletedNCT01947803
What is this study about?Researchers studied Paliperidone Palmitate, tracking side effects to assess safety and tolerability in people with schizophrenia.
This study has finished and is no longer accepting participants.
Multiple locations, including BaodingSchizophreniaMedication studyAges 18–65
- Countries
- China
- Sponsor
- Xian-Janssen Pharmaceutical Ltd.
CompletedNCT00528697
What is this study about?Researchers compared ABT-089, atomoxetine and placebo to find out how the approaches affected ADHD symptoms in children with ADHD.
This study has finished and is no longer accepting participants.
Multiple locations, including Little RockADHDMedication studyAges 6–12
- Countries
- United States
- Sponsor
- AbbVie (prior sponsor, Abbott)
CompletedNCT02432703
What is this study about?Researchers compared JNJ-42165279 and placebo, tracking side effects to assess safety and tolerability in people with an anxiety condition.
This study has finished and is no longer accepting participants.
Multiple locations, including La JollaAnxietyMedication studyAges 18–64
- Countries
- United States, Australia, Canada
- Sponsor
- Janssen Research & Development, LLC
TerminatedNCT01114698
Official study titleA Randomized, Double-Blind, Parallel Group, Active- and Placebo-Controlled Study to Assess the Efficacy and Safety of JNJ26489112 in Adult Subjects With Treatment-Resistant Major Depressive Disorder
This study ended early.
Multiple locations, including ArcadiaDepressionMedication studyAges 18–65
- Countries
- United States
- Sponsor
- Janssen Research & Development, LLC
WithdrawnNCT01685151
Official study titleA Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Once a Day, TAK-375SL as an Adjunctive Therapy to Treatment-as-Usual in the Maintenance Treatment of Bipolar 1 Disorder in Adult Subjects
This study was withdrawn before enrollment.
Location not clearly listedBipolarityMedication studyAges 18–75
- Countries
- Sponsor
- Takeda
CompletedNCT00796081
Official study titleOpen-label Study to Evaluate the Safety and Pharmacokinetics of Single- and Multiple-dose Extended-release OROS Paliperidone in Pediatric Subjects (=10 to =17 Years of Age) With Schizophrenia, Schizoaffective Disorder, or Schizophreniform Disorder
This study has finished and is no longer accepting participants.
Location not clearly listedSchizophreniaMedication studyAges 10–17
- Countries
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT01150448
Official study titleAn Open-Label, Long-Term, Multiple-Dose, Safety and Tolerability, Pharmacokinetic Study of 150 mg eq. Paliperidone Palmitate in the Treatment of Subjects With Schizophrenia
This study has finished and is no longer accepting participants.
Multiple locations, including CerritosSchizophreniaMedication studyAges 18–65
- Countries
- United States, Belgium, Croatia, + 7 others
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT01592110
What is this study about?This study evaluated the safety of risperidone-SABER for people with schizophrenia.
This study has finished and is no longer accepting participants.
In GlendaleSchizophreniaMedication studyAges 18+
- Countries
- United States
- Sponsor
- Zogenix, Inc.
CompletedNCT00443391
What is this study about?Researchers studied ABT-089, tracking side effects to assess long-term safety and tolerability in adults with ADHD.
This study has finished and is no longer accepting participants.
Multiple locations, including MesaADHDMedication studyAges 18–60
- Countries
- United States
- Sponsor
- AbbVie (prior sponsor, Abbott)