Efficacy and Tolerability of Generic Mirtazapine (Mirtax) for Major Depressive Disorder: Multicenter, Open-label, Uncontrolled, Prospective Study

被引:4
作者
Song, Hoo Rim [1 ,2 ]
Bahk, Won-Myong [2 ]
Woo, Young Sup [2 ]
Jeong, Jong-Hyun [2 ]
Kwon, Young-Joon [1 ]
Seo, Jeong Seok [3 ]
Kim, Won [4 ]
Kim, Moon-Doo [5 ]
Shin, Young-Chul [6 ]
Lee, Sang-Yeol [7 ]
Min, Kyung Joon [8 ]
机构
[1] Soonchunhyang Univ, Cheonan Hosp, Dept Psychiat, Cheonan, South Korea
[2] Catholic Univ Korea, Coll Med, Seoul 07345, South Korea
[3] Konkuk Univ, Chungju Hosp, Chungju, South Korea
[4] Inje Univ, Seoul Paik Hosp, Seoul, South Korea
[5] Jeju Natl Univ Hosp, Jeju, South Korea
[6] Kangbuk Samsung Hosp, Seoul, South Korea
[7] Wonkwang Univ Hosp, Iksan, South Korea
[8] Chung Ang Univ Hosp, Seoul, South Korea
关键词
Mirtazapine; Generic drugs; Efficacy; Tolerability; SEROTONIN REUPTAKE INHIBITORS; STRUCTURED INTERVIEW GUIDE; DOUBLE-BLIND; RATING-SCALE; BRAND-NAME; FLUOXETINE; PAROXETINE; REMISSION; PLACEBO; ONSET;
D O I
10.9758/cpn.2015.13.2.144
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Objective: Mirtax is a generic mirtazapine widely used since 2003. We conducted an open-label, uncontrolled 6-week study to evaluate the efficacy and safety of Mirtax for major depressive disorder (MDD). Methods: Ninety three MDD patients with the diagnosis of MDD and 17-item Hamilton Depression Rating Scale (HDRS) score >= 14 were recruited. The HDRS, Montgomery-Asberg Depression Rating Scale (MADRS), and the Clinical Global Impressions-Severity Scale (CGI-S) were administered at baseline, 1, 2, 4 and 6 weeks, Response (>= 50% decrease in the HDRS or MADRS score), remission (absolute HDRS score or MADRS score <= 10) and CGI-I score <= 2 were also calculated, Adverse event (AE) frequency and severity, weight, blood pressure, and pulse rate were checked to assess safety. Results: The starting dosage was 11.5+/-6.4 mg/day, and the maintenance dosage was 23.1+/-9.4 mg/day. During 6 weeks, HDRS, MADRS and CGI-S scores decreased from 25.1+/-5.6 to 11.9+/-8.6 (mean change -13.1+/-8.3, p<0.001), from 30.2+/-6.3 to 13.73+/-10.40 (mean change -16.5+/-9.8, p<0.001), and from 5.0+/-0.8 to 2.5+/-1.3 (mean change -2.5+/-1.3, p<0.001), respectively, The percentages of responders, remitters by HDRS and patients with a CGI-I score <= 2 were 64.6%, 35.4% and 52.7%, respectively. Significant decreases in HDRS, MADRS and CGI-S scores were confirmed at week 1, The total rate of AEs was 32.3%; the most frequently reported AEs were sedation (4.3%) and constipation (4,3%), Weight was increased from 58.8+/-10.6 to 60.3+/-9.3 kg (mean change 0.7+/-1.7 kg, p=0.004). Conclusion: This study, as the first clinical trial of generic mirtazapine, demonstrated the efficacy and tolerability of Mirtax for MDD using a single treatment design.
引用
收藏
页码:144 / 149
页数:6
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