Clinical pharmacology review of escitalopram for the treatment of depression

被引:79
作者
Pastoor, Devin [1 ]
Gobburu, Joga [1 ]
机构
[1] Univ Maryland, Sch Pharm, Baltimore, MD 21201 USA
关键词
citalopram; depression; escitalopram; Food and Drug Administration; major depressive disorder; regulatory approval; selective serotonin reuptake inhibitor; SEROTONIN TRANSPORTER; ALLOSTERIC MECHANISM; IN-VITRO; CITALOPRAM; PHARMACOKINETICS; METABOLITES; INHIBITOR; INCREASES; BINDING;
D O I
10.1517/17425255.2014.863873
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Introduction: Depression is a serious and debilitating psychiatric condition with serious societal health and economic implications. Escitalopram, the S-enantiomer of racemic citalopram, is an effective treatment for major depressive disorder. Areas covered: This review covers the clinical pharmacology of escitalopram, with emphasis on regulatory approval. Its pharmacokinetics, pharmacodynamics and clinical efficacy for major depressive disorder are evaluated, along with data regarding safety and tolerability. Expert opinion: Drug development of escitalopram was heavily guided by prior approval of citalopram. Select safety and efficacy studies for escitalopram in combination with supportive evidence from the results of prior citalopram studies allowed for regulatory approval for acute and maintenance claims in both adults and adolescents, while minimizing burden on the sponsor. Escitalopram has been shown to have better efficacy and safety profile than other selective serotonin reuptake inhibitor and serotonin norepinephrine reuptake inhibitor drugs, including racemic citalopram. The first generic escitalopram was approved in 2012, along with Abbreviated New Drug Applications. The associated cost savings have helped reduce the burden of weighing the benefits of escitalopram over less-expensive alternatives.
引用
收藏
页码:121 / 128
页数:8
相关论文
共 31 条
[1]
Comparative efficacy of escitalopram in the treatment of major depressive disorder [J].
Ali, Mazen K. ;
Lam, Raymond W. .
NEUROPSYCHIATRIC DISEASE AND TREATMENT, 2011, 7 :39-49
[2]
[Anonymous], 2012, COCHRANE DATABASE SY
[3]
[Anonymous], 2012, FDA SAF COMM
[4]
[Anonymous], 2012, Depression fact sheet
[5]
[Anonymous], 2000, DIAGN STAT MAN MENT, DOI DOI 10.1176/APPI.BOOKS.9780890425787
[6]
Pharmacology and pharmacokinetics of citalopram and other SSRIs [J].
Baumann, P .
INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY, 1996, 11 :5-11
[7]
Enantioselective analysis of citalopram and metabolites in adolescents [J].
Carlsson, B ;
Olsson, G ;
Reis, M ;
Wålinder, J ;
Nordin, C ;
Lundmark, J ;
Scordo, MG ;
Dahl, ML ;
Bengtsson, F ;
Ahlner, J .
THERAPEUTIC DRUG MONITORING, 2001, 23 (06) :658-664
[8]
The S-enantiomer of R,S-citalopram, increases inhibitor binding to the human serotonin transporter by an allosteric mechanism.: Comparison with other serotonin transporter inhibitors [J].
Chen, FH ;
Larsen, MB ;
Sánchez, C ;
Wiborg, O .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2005, 15 (02) :193-198
[9]
Effects of acute and long-term administration of escitalopram and citalopram on serotonin neurotransmission:: an in vivo electrophysiological study in rat brain [J].
El Mansari, M ;
Sánchez, C ;
Chouvet, G ;
Renaud, B ;
Haddjeri, N .
NEUROPSYCHOPHARMACOLOGY, 2005, 30 (07) :1269-1277
[10]
Australian and New Zealand clinical practice guidelines for the treatment of depression [J].
Ellis, PM ;
Hickie, I ;
Smith, DAR ;
Bushnell, J ;
Hirini, P ;
Stevens, S ;
Smith, DAR .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY, 2004, 38 (06) :389-407