In adults with major depressive disorder, adding aripiprazole to antidepressant therapy (ADT) resulted in significant improvement in the primary endpoint, the Montgomery-Asberg Depression Rating Scale (MADRS) Total Score. In this six-week, randomized, placebo-controlled study presented here at the 160th Annual Meeting of the American Psychiatric Association, the Bristol-Myers Squibb Company (NYSE: BMY) and Otsuka Pharmaceutical Co., Ltd. atypical antipsychotic aripiprazole was added to antidepressants in patients who did not have an adequate response to ADT alone. (1)(Berman, 2007, APA Poster) These findings are from one of two completed studies evaluating adjunctive aripiprazole with ADT.
Investigational studies are important because many patients with major depressive disorder do not achieve adequate symptom response, said study investigator Arif Khan, M.D., Medical Director, Northwest Clinical Research Center, Bellevue, Wash., and Adjunct Professor, Psychiatry, Duke University, Durham, N.C. The findings from this study contribute more information about the potential use of add-on medications to antidepressant therapy in patients who inadequately respond to antidepressants alone.
Study Design and Findings
This double-blind, randomized, placebo-controlled, multi-center, six-week study enrolled adults diagnosed with major depressive disorder who had an inadequate response to one or more ADTs. After a seven to 28-day screening phase, adults in this study underwent an eight-week prospective treatment phase with one ADT plus single-blind placebo to confirm their inadequate response to ADT. The ADTs included escitalopram, fluoxetine, paroxetine controlled release, sertraline or venlafaxine extended release, dosed per label guidelines. A total of 362 adults with inadequate response then entered the six-week randomized treatment phase during which they continued their ADT plus double-blind adjunctive placebo or adjunctive aripiprazo
'"/>
Contact: David Rosen
david.m.rosen@bms.com
609-252-5675
Bristol-Myers Squibb
22-May-2007
Page: 1 2 Related medicine news :1.
Efficacy of glucosamine, chondroitin sulfate may depend on level of osteoarthritis pain2.
Efficacy of glucosamine and chondroitin sulfate may depend on level of osteoarthritis pain3.
National quality agenda, payment reform, care integration keys to improving quality, patient safety4.
LSUHSC awarded designation resulting in improved patient safety and outcomes5.
New survey uncovers how insomnia affects job performance and safety6.
Extended duration work shifts risky to the safety, well-being of medical interns, patients7.
UW study to clarify safety, effectiveness of hormone therapy during menopause8.
Ulcerative colitis remission rates from long-term safety study of LIALDA presented at DDW9.
U of M faculty honored by US FDA for contributions to national food safety and defense10.
Hospital errors rise 3 percent -- HealthGrades patient-safety study11.
MERLIN TIMI-36 study provides new safety and efficacy data for unique anti-anginal therapy