A 6-week randomized, placebo-controlled trial of CP-316,311 (a selective CRH1 antagonist) in the treatment of major depression

被引:185
作者
Binneman, Brendon [1 ]
Feltner, Douglas [1 ]
Kolluri, Sheela [1 ]
Shi, Yuanjun [1 ]
Qiu, Ruolun [1 ]
Stiger, Thomas [1 ]
机构
[1] Pfizer Inc, Pfizer Global Res & Dev, Groton, CT 06340 USA
关键词
D O I
10.1176/appi.ajp.2008.07071199
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: The corticotropin-releasing hormone (CRH) system is implicated in the pathogenesis of several psychiatric disorders, including major depressive disorder. This study was designed to evaluate the safety and efficacy of CP-316,311, a selective nonpeptide antagonist of corticotropin-releasing hormone type 1 (CRH1) receptors, in the treatment of recurrent major depressive disorder. Method: Of a total of 167 patients with recurrent major depression who were screened, 123 were randomly assigned to receive 400 mg of CP-316,311 twice daily, or 100 mg of sertraline daily, or placebo in a 6-week fixed-dose, double-blind, double-dummy, parallel-group, placebo- and sertraline-controlled trial. The primary efficacy analysis compared the change in score from baseline to end-point on the 17-item Hamilton Depression Rating Scale (HAM-D) between the CP-316,311 and placebo groups. A group sequential design was used to support early trial termination based on efficacy or futility at a planned interim analysis. Results: The evaluable data set for the interim analysis included 28 patients in the CP-316,311 group, 31 patients in the placebo group, and 30 patients in the sertraline group. In the interim analysis, the change from baseline in the HAM-D score at the final visit was not significantly different between the CP-316,311 and placebo groups, while change from baseline between the sertraline and placebo groups was significantly different. Given these results, futility was declared for CP-316,311 and the trial was terminated. Conclusions: Although CP-316,311 was safe and well tolerated in this study population, it failed to demonstrate efficacy in the treatment of major depression.
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页码:617 / 620
页数:4
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