Evaluating the efficacy of vilazodone in achieving remission in patients with major depressive disorder. (March 2015)
- Record Type:
- Journal Article
- Title:
- Evaluating the efficacy of vilazodone in achieving remission in patients with major depressive disorder. (March 2015)
- Main Title:
- Evaluating the efficacy of vilazodone in achieving remission in patients with major depressive disorder
- Authors:
- Citrome, Leslie
Gommoll, Carl P.
Tang, Xiongwen
Nunez, Rene
Mathews, Maju - Abstract:
- <abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <p>The aim of this study was to evaluate the efficacy of vilazodone using different definitions of remission. Post-hoc analyses were carried out using data from an 8-week, multicenter, randomized, double-blind, placebo-controlled trial of vilazodone 40 mg/day in adults with major depressive disorder (NCT01473394). The primary efficacy endpoint was a mean change in the Montgomery–Åsberg Depression Rating Scale (MADRS) total score; additional measures included the Clinical Global Impressions-Severity (CGI-S) and Hamilton Rating Scale for Anxiety (HAMA) scores. In addition to treatment response (MADRS≥50% improvement), post-hoc analyses were carried out for remission of depressive symptoms [MADRS score⩽10; MADRS⩽5 (complete remission)], anxiety symptoms (HAMA⩽7), and combined depression and anxiety symptoms (MADRS/HAMA⩽10/⩽7), as well as for overall symptom severity (CGI-S=1). Odds ratios (ORs) and numbers needed to treat (NNTs) were also calculated. Significant outcomes were obtained with vilazodone versus placebo for MADRS response (50.6 vs. 33.3%, OR=2.04, <italic>P</italic>&lt;0.001, NNT=6), remission (34.0 vs. 21.8%, OR=1.82, <italic>P</italic>=0.003, NNT=9), and complete remission (18.2 vs. 8.3%, OR=2.42, <italic>P</italic>=0.002, NNT=11). More patients receiving vilazodone rather than placebo also met remission criteria for HAMA (48.8 vs. 35.2%, OR=1.82, <italic>P</italic>=0.002, NNT=8), MADRS/HAMA<abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <p>The aim of this study was to evaluate the efficacy of vilazodone using different definitions of remission. Post-hoc analyses were carried out using data from an 8-week, multicenter, randomized, double-blind, placebo-controlled trial of vilazodone 40 mg/day in adults with major depressive disorder (NCT01473394). The primary efficacy endpoint was a mean change in the Montgomery–Åsberg Depression Rating Scale (MADRS) total score; additional measures included the Clinical Global Impressions-Severity (CGI-S) and Hamilton Rating Scale for Anxiety (HAMA) scores. In addition to treatment response (MADRS≥50% improvement), post-hoc analyses were carried out for remission of depressive symptoms [MADRS score⩽10; MADRS⩽5 (complete remission)], anxiety symptoms (HAMA⩽7), and combined depression and anxiety symptoms (MADRS/HAMA⩽10/⩽7), as well as for overall symptom severity (CGI-S=1). Odds ratios (ORs) and numbers needed to treat (NNTs) were also calculated. Significant outcomes were obtained with vilazodone versus placebo for MADRS response (50.6 vs. 33.3%, OR=2.04, <italic>P</italic>&lt;0.001, NNT=6), remission (34.0 vs. 21.8%, OR=1.82, <italic>P</italic>=0.003, NNT=9), and complete remission (18.2 vs. 8.3%, OR=2.42, <italic>P</italic>=0.002, NNT=11). More patients receiving vilazodone rather than placebo also met remission criteria for HAMA (48.8 vs. 35.2%, OR=1.82, <italic>P</italic>=0.002, NNT=8), MADRS/HAMA (32.1 vs. 20.4%, OR=1.83, <italic>P</italic>=0.004, NNT=9), and CGI-S (24.1 vs. 11.5%, OR=2.41, <italic>P</italic>&lt;0.001, NNT=8). Treatment with vilazodone 40 mg/day may help adult patients with major depressive disorder achieve remission of depression and/or anxiety symptoms.</p> </sec> </abstract> … (more)
- Is Part Of:
- International clinical psychopharmacology. Volume 30:Number 2(2015:Mar.)
- Journal:
- International clinical psychopharmacology
- Issue:
- Volume 30:Number 2(2015:Mar.)
- Issue Display:
- Volume 30, Issue 2 (2015)
- Year:
- 2015
- Volume:
- 30
- Issue:
- 2
- Issue Sort Value:
- 2015-0030-0002-0000
- Page Start:
- Page End:
- Publication Date:
- 2015-03
- Subjects:
- Psychopharmacology -- Periodicals
Psychotropic drugs -- Periodicals
Psychopharmacology -- periodicals
Psychotropic Drugs -- periodicals
615.7805 - Journal URLs:
- http://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=toc&D=yrovft&AN=00004850-000000000-00000 ↗
http://www.intclinpsychopharm.com/ ↗
http://journals.lww.com/intclinpsychopharm/Pages/default.aspx ↗
http://journals.lww.com/pages/default.aspx ↗
http://firstsearch.oclc.org ↗
http://www.lww.com/Product/0268-1315 ↗ - DOI:
- 10.1097/YIC.0000000000000056 ↗
- Languages:
- English
- ISSNs:
- 0268-1315
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4538.674500
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