Literature DB >> 21925682

Efficacy and tolerability of the novel triple reuptake inhibitor amitifadine in the treatment of patients with major depressive disorder: a randomized, double-blind, placebo-controlled trial.

Pierre Tran1, Phil Skolnick, Pal Czobor, N Y Huang, Mark Bradshaw, Anthony McKinney, Maurizio Fava.   

Abstract

Amitifadine (EB-1010, formerly DOV 21,947) is a serotonin-preferring triple reuptake inhibitor with a relative potency to inhibit serotonin, norepinephrine, and dopamine uptake of ∼1:2:8, respectively. This 6-week, multicenter, randomized, double-blind, parallel, placebo-controlled study evaluated the efficacy and tolerability of amitifadine in 63 patients with major depressive disorder. Eligible patients (17-item Hamilton Depression Rating Scale [HAMD-17] ≥ 22 at baseline) were randomized to amitifadine 25 mg twice daily (BID) for 2 weeks, then 50 mg BID for 4 weeks or placebo. Mean baseline scores in the modified intent-to-treat population (n = 56) were 31.4 for the Montgomery-Åsberg Depression Rating Scale (MADRS), 29.6 for the HAMD-17, and 25.4 for the Derogatis Interview for Sexual Functioning - Self Report (DISF-SR). At the end of the 6-week double-blind treatment, estimated least squares mean change from baseline (mixed-model repeated measures [MMRM]) in MADRS total score was statistically significantly superior for amitifadine compared to placebo (18.2 vs. 22.0; p = 0.028), with an overall statistical effect size of -0.601 (Cohen's d). Amitifadine also was statistically significantly superior to placebo (p = 0.03) for the Clinical Global Impression of Change - Improvement. An anhedonia factor score grouping of MADRS Items 1 (apparent sadness), 2 (reported sadness), 6 (concentration difficulties), 7 (lassitude), and 8 (inability to feel) demonstrated a statistically significant difference in favor of amitifadine compared to placebo (p = 0.049). No differences were observed between treatments in DISF-SR scores. Amitifadine was well-tolerated. Two patients on each treatment discontinued the study early due to adverse events; however, no serious adverse events were reported. This initial clinical trial in patients with severe major depression demonstrated significant antidepressant activity with amitifadine, including attenuating symptoms of anhedonia, and a tolerability profile that was comparable to placebo. The efficacy and tolerability of amitifadine for major depressive disorder are being investigated in additional clinical trials.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21925682     DOI: 10.1016/j.jpsychires.2011.09.003

Source DB:  PubMed          Journal:  J Psychiatr Res        ISSN: 0022-3956            Impact factor:   4.791


  26 in total

Review 1.  Triple reuptake inhibitors as potential next-generation antidepressants: a new hope?

Authors:  Horrick Sharma; Soumava Santra; Aloke Dutta
Journal:  Future Med Chem       Date:  2015-11-30       Impact factor: 3.808

Review 2.  Impact of Antidepressant Drugs on Sexual Function and Satisfaction.

Authors:  David S Baldwin; Chris Manson; Magda Nowak
Journal:  CNS Drugs       Date:  2015-11       Impact factor: 5.749

3.  Triple monoamine uptake inhibitors demonstrate a pharmacologic association between excessive drinking and impulsivity in high-alcohol-preferring (HAP) mice.

Authors:  David S O'Tousa; Kaitlin T Warnock; Liana M Matson; Ojas A Namjoshi; Michael Van Linn; Veera Venkata Tiruveedhula; Meredith E Halcomb; James Cook; Nicholas J Grahame; Harry L June
Journal:  Addict Biol       Date:  2013-10-13       Impact factor: 4.280

4.  Evaluation of safety and tolerability, pharmacokinetics, and pharmacodynamics of BMS-820836 in healthy subjects: a placebo-controlled, ascending single-dose study.

Authors:  Robert Risinger; Zubin Bhagwagar; Feng Luo; Matthew Cahir; Laura Miler; Anisha E Mendonza; Jeffrey H Meyer; Ming Zheng; Wendy Hayes
Journal:  Psychopharmacology (Berl)       Date:  2013-12-15       Impact factor: 4.530

5.  Prolonging the Reduction of Nicotine Self-Administration in Rats by Coadministering Chronic Nicotine With Amitifadine, a Triple Monoamine Reuptake Inhibitor With CYP2B6 Inhibitory Actions.

Authors:  Edward D Levin; Corinne Wells; Susan Slade; Michelle Lee; Anthony A McKinney; Jed E Rose; Amir H Rezvani
Journal:  Nicotine Tob Res       Date:  2020-02-06       Impact factor: 4.244

6.  Amitifadine, a triple monoamine re-uptake inhibitor, reduces nicotine self-administration in female rats.

Authors:  Edward D Levin; Corinne Wells; Joshua E Johnson; Amir H Rezvani; Frank P Bymaster; Jed E Rose
Journal:  Eur J Pharmacol       Date:  2015-06-20       Impact factor: 4.432

7.  Azepines and piperidines with dual norepinephrine dopamine uptake inhibition and antidepressant activity.

Authors:  Dean G Brown; Peter R Bernstein; Ye Wu; Rebecca A Urbanek; Christopher W Becker; Scott R Throner; Bruce T Dembofsky; Gary B Steelman; Lois A Lazor; Clay W Scott; Michael W Wood; Steven S Wesolowski; David A Nugiel; Stephanie Koch; Jian Yu; Donald E Pivonka; Shuang Li; Carol Thompson; Anna Zacco; Charles S Elmore; Patricia Schroeder; JianWei Liu; Christopher A Hurley; Stuart Ward; Hazel J Hunt; Karen Williams; Joseph McLaughlin; Valerie Hoesch; Simon Sydserff; Donna Maier; David Aharony
Journal:  ACS Med Chem Lett       Date:  2012-11-12       Impact factor: 4.345

8.  Amitifadine, a triple monoamine uptake inhibitor, reduces binge drinking and negative affect in an animal model of co-occurring alcoholism and depression symptomatology.

Authors:  Kaitlin T Warnock; Andrew R S T Yang; Heon S Yi; Harry L June; Timothy Kelly; Anthony S Basile; Phil Skolnick; Harry L June
Journal:  Pharmacol Biochem Behav       Date:  2012-11       Impact factor: 3.533

Review 9.  Anhedonia: a concept analysis.

Authors:  Nancy Ho; Marilyn Sommers
Journal:  Arch Psychiatr Nurs       Date:  2013-04-24       Impact factor: 2.218

10.  SKF83959 is a novel triple reuptake inhibitor that elicits anti-depressant activity.

Authors:  Xing Fang; Lin Guo; Jia Jia; Guo-zhang Jin; Bin Zhao; Yong-yong Zheng; Jian-qi Li; Ao Zhang; Xue-chu Zhen
Journal:  Acta Pharmacol Sin       Date:  2013-07-29       Impact factor: 6.150

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