CompletedNCT01323192
About this title
An Efficacy and Safety Study for JNS001 in Adults With Attention-Deficit Hyperactivity Disorder
Read the official source — NCT01323192What is this study about?Researchers compared JNS001 and placebo to find out how the approaches affected ADHD symptoms in adults with ADHD.
This study has finished and is no longer accepting participants.
Multiple locations, including ChibaADHDMedication studyAges 18–64
- Countries
- Japan
- Sponsor
- Janssen Pharmaceutical K.K.
CompletedNCT00728195
About this title
An Efficacy and Safety Study of 3 Fixed Doses of JNJ-37822681 in Participants With Schizophrenia
Read the official source — NCT00728195What is this study about?This study evaluated the safety and effectiveness of JNJ-37822681 for people with schizophrenia.
This study has finished and is no longer accepting participants.
Multiple locations, including BurgasSchizophreniaMedication studyAges 18–65
- Countries
- Bulgaria, Estonia, Lithuania, + 7 others
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT01009047
About this title
An Efficacy and Safety Study of Extended-Release (ER) Paliperidone in Adolescent Participants With Schizophrenia
Read the official source — NCT01009047Official study titleA Randomized, Multicenter, Double-Blind, Active-Controlled, Flexible-Dose, Parallel-Group Study of the Efficacy and Safety of Extended Release Paliperidone for the Treatment of Symptoms of Schizophrenia in Adolescent Subjects, 12 to 17 Years of Age
This study has finished and is no longer accepting participants.
Multiple locations, including DothanSchizophreniaMedication studyAges 12–17
- Countries
- United States, India, Romania, + 4 others
- Sponsor
- Janssen Research & Development, LLC
CompletedNCT00992407
About this title
An Efficacy and Safety Study of Long Acting Injectable Risperidone and Oral Risperidone in Participants With Schizophrenia or Schizoaffective Disorder
Read the official source — NCT00992407Official study titleA Randomized, Open-label, Active-controlled Study to Evaluate Social Functioning of Long Acting Injectable Risperidone and Oral Risperidone in the Treatment of Subjects With Schizophrenia or Schizoaffective Disorder
This study has finished and is no longer accepting participants.
In AnsanSchizophreniaMedication studyAges 18–55
- Countries
- South Korea
- Sponsor
- Janssen Korea, Ltd., Korea
CompletedNCT00526877
About this title
An Efficacy and Safety Study of Long-acting Risperidone in Participants With Schizophrenia or Schizoaffective Disorders Who Are Receiving Psychiatric Home Care Treatment
Read the official source — NCT00526877What is this study about?This study evaluated the safety and effectiveness of Risperidone for people with schizophrenia.
This study has finished and is no longer accepting participants.
In TaipeiSchizophreniaMedication studyAges 18+
- Countries
- Taiwan
- Sponsor
- Johnson & Johnson Taiwan Ltd
CompletedNCT00269919
About this title
An Efficacy and Safety Study of Long-Term Risperidone Microspheres in Participants With Schizophrenia
Read the official source — NCT00269919What is this study about?Researchers studied Risperidone Long-Acting Injectable (RLAI) to find out how it affected psychotic symptoms in people with schizophrenia.
This study has finished and is no longer accepting participants.
In SeoulSchizophreniaMedication studyAges 18–65
- Countries
- South Korea
- Sponsor
- Janssen Korea, Ltd., Korea
CompletedNCT00524043
About this title
An Efficacy and Safety Study of One Dosage of Paliperidone Extended Release (ER) in Treating Patients With Schizophrenia
Read the official source — NCT00524043What is this study about?Researchers compared Paliperidone ER 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 CerritosSchizophreniaMedication studyAges 18+
- Countries
- United States, India, Taiwan
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT01012622
About this title
An Efficacy and Safety Study of Osmotic Release Oral System (OROS) Methylphenidate in Participants With Attention Deficit Hyperactivity Disorder (ADHD)
Read the official source — NCT01012622Official study titleAn Open-label Prospective Trial to Evaluate Functional Outcomes of OROS Methylphenidate in Children With ADHD (FOSCO)
This study has finished and is no longer accepting participants.
Location not clearly listedADHDMedication studyAges 6–12
- Countries
- Sponsor
- Janssen Korea, Ltd., Korea
CompletedNCT00566631
About this title
An Efficacy and Safety Study of Paliperidone Extended-Release (ER) Tablets in Participants With Schizophrenia
Read the official source — NCT00566631What is this study about?Researchers studied Paliperidone to find out how it affected psychotic symptoms in people with schizophrenia.
This study has finished and is no longer accepting participants.
Multiple locations, including ZagrebSchizophreniaMedication studyAges 18+
- Countries
- France, Croatia, Germany, + 4 others
- Sponsor
- Janssen-Cilag International NV
CompletedNCT01299389
About this title
An Efficacy and Safety Study of Paliperidone Palmitate in Participants With Schizophrenia
Read the official source — NCT01299389What is this study about?Researchers compared Paliperidone palmitate 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 FujiokaSchizophreniaMedication studyAges 20+
- Countries
- Japan, South Korea, Taiwan
- Sponsor
- Janssen Pharmaceutical K.K.
CompletedNCT01855074
About this title
An Efficacy and Safety Study of Risperidone Long-Acting Microspheres in Participants With Schizophrenia, Schizophreniform or Schizoaffective Disorders
Read the official source — NCT01855074What is this study about?This study evaluated the safety and effectiveness of Risperidone for people with schizophrenia.
This study has finished and is no longer accepting participants.
Location not clearly listedSchizophreniaMedication studyAges 18+
- Countries
- Sponsor
- Janssen-Cilag Ltd.
CompletedNCT02473289
Official study titleA Double-Blind, Placebo-Controlled, Multicenter Study of Sirukumab as Adjunctive Treatment to a Monoaminergic Antidepressant in Adults With Major Depressive Disorder
This study has finished and is no longer accepting participants.
Multiple locations, including BirminghamDepressionMedication studyAges 21–64
- Countries
- United States, Canada, United Kingdom, + 2 others
- Sponsor
- Janssen Research & Development, LLC