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A 6 Week Study to Determine the Effectiveness of R228060 in Adult Subjects with Major Depressive Disorder Clinical Trials Info presented on Clinical Trials Search is not intended to be a substitute for certified medical advice, visits or professional assistance using a real physician. We are not physicians. Always consult your dr. about A 6 Week Study to Determine the Effectiveness of R228060 in Adult Subjects with Major Depressive Disorder conditions. Clinical Trials Search.org is a site dedicated to listing clinical research studies in human subjects. A 6 Week Study to Determine the Effectiveness of R228060 in Adult Subjects with Major Depressive Disorder Clinical research trials and A 6 Week Study to Determine the Effectiveness of R228060 in Adult Subjects with Major Depressive Disorder health trials happen in many of localities throughout the U.S.. A clinical trial or clinical study is a research project with human volunteer subjects. Clinical drug trials and pharmaceutical clinical trials typically measure the effectualness of new drugs. The function of the studies / projects is to resolve particular human medical questions. Clinical trials are a popular manner for mDs, government agencies, and private sector corporations to discover remedies for all varieties of circumstances, like A 6 Week Study to Determine the Effectiveness of R228060 in Adult Subjects with Major Depressive Disorder. A 6 Week Study to Determine the Effectiveness of R228060 in Adult Subjects with Major Depressive Disorder Clinical Trials and other clinical trials allow volunteers to obtain healthcare treatment options before they are available to the masses. Some times the participants undergo professional assistance for free of charge, and occasionally they are paid for their time. Sometimes there is a cost for a A 6 Week Study to Determine the Effectiveness of R228060 in Adult Subjects with Major Depressive Disorder clinical trial. Human subjects often get the best healthcare available for their A 6 Week Study to Determine the Effectiveness of R228060 in Adult Subjects with Major Depressive Disorder condition. Dangers are a reality, however, and may include additional or frequent mD visits, healthcare dangers (potentially life-jeopardising), and/or the treatment being ineffectual. Trials are federally governed with rigorous guidelines to protect clinical trials patients.

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A 6 Week Study to Determine the Effectiveness of R228060 in Adult Subjects with Major Depressive Disorder



A 6 Week Study to Determine the Effectiveness of R228060 in Adult Subjects with Major Depressive Disorder

For Condition: Major Depressive Disorder
Status: Completed
Sponsor(s): Johnson & Johnson Pharmaceutical Research and Development, L.L.C. ,
Synopsis: The purpose of this research study is to determine the effectiveness of 2 target doses of R228060 in comparison with placebo during 6 weeks of treatment in moderately to severely depressed adult subjects with major depressive disorder. Approximately 488 subjects will be involved in the study.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Randomized, Double-Blind, Parallel Assignment, Efficacy Study
Minimum Age/Maximum Age: 18 Years/65 Years
Genders: Both
Protocol Entry Criteria: - Generally healthy adults on the basis of a physical examination, medical history, ECG and laboratory work-up. - Subject needs to meet criteria for diagnosis of moderate or severe major depression as defined by the protocol. - The subject also needs to be an outpatient to participate in this study.
Total Enrollment: 488

Location and Contact Information:

JJ PRD Research Center
Titusville,  New Jersey,  08560
United States
 


Additional Information:
Study ID Numbers:
  R228060-MDD-201; 
Study Start Date: 
Record last reviewed: May 2004
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00073203

Other Major Depressive Disorder Studies:
1. Therapy for Depression with Co-occurring Panic or Anxiety Symptoms

2. Major Depressive Disorder Study In Adults

3. Depression Study In Adults

4. Treatment of patients with Major Depressive disorder with an investigational compound

5. Open-Label Treatment with Duloxetine Hydrochloride Once-Daily Dosing for Evaluation of Stabilization Dose in Patients with Major Depression

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