Department of Clinical Pharmacy, School of Pharmacy, University of Colorado, Aurora, CO, USA.
Ann Pharmacother. 2013 Mar;47(3):340-9. doi: 10.1345/aph.1R501.
To review the pharmacology, efficacy, and safety of phentermine/topiramate (PHEN/TPM) in the management of obese patients.
MEDLINE (1966-July 2012) was searched using the terms weight loss, obesity, phentermine and topiramate, phentermine, topiramate, Qnexa, Qsymia, and VI-0521. Additionally, the new drug application and prescribing information for PHEN/TPM were retrieved.
STUDY SELECTION/DATA EXTRACTION: All studies considering the pharmacology, efficacy, and safety of PHEN/TPM were reviewed with a focus on efficacy and safety data from Phase 3 trials.
In 3 Phase 3 trials (EQUIP, CONQUER, and SEQUEL), treatment with PHEN/TPM consistently demonstrated statistically significant weight loss compared with placebo. After 56 weeks of treatment, percent weight loss achieved with PHEN/TPM was 10.6%, 8.4%, and 5.1% with 15/92 mg, 7.5/46 mg, and 3.75/23 mg, respectively (p < 0.0001). The 52-week extension study (SEQUEL) showed maintained weight loss over 2 years with 9.3% and 10.5% weight loss from baseline for 7.5/46 mg and 15/92 mg PHEN/TPM (p < 0.0001). A significantly higher proportion of patients achieved greater than 5%, 10%, or 15% weight loss with PHEN/TPM compared with placebo. Significant reductions in waist circumference, fasting triglycerides, and fasting glucoses were also attributable to PHEN/TPM. The drug was generally well tolerated in clinical trials. Adverse reactions occurring in 5% or more of study subjects included paresthesia, dizziness, dysgeusia, insomnia, constipation, and dry mouth.
PHEN/TPM is a new, once-daily, controlled-release, combination weight-loss product approved as an adjunct to diet and exercise for chronic weight management of obese or overweight patients with weight-related comorbidities. PHEN/TPM is modestly effective and a viable option for patients interested in losing weight, although long-term safety data are lacking.
综述苯丁胺/托吡酯(PHEN/TPM)在肥胖患者管理中的药理学、疗效和安全性。
使用减重、肥胖、苯丁胺和托吡酯、苯丁胺、托吡酯、Qnexa、Qsymia 和 VI-0521 等术语对 1966 年至 2012 年 7 月的 MEDLINE 进行检索。此外,还检索了 PHEN/TPM 的新药申请和说明书。
研究选择/数据提取:所有考虑 PHEN/TPM 的药理学、疗效和安全性的研究均进行了综述,重点是 3 期试验的疗效和安全性数据。
在 3 项 3 期试验(EQUIP、CONQUER 和 SEQUEL)中,与安慰剂相比,PHEN/TPM 治疗可显著减轻体重。治疗 56 周后,15/92mg、7.5/46mg 和 3.75/23mg 组的 PHEN/TPM 治疗体重减轻百分比分别为 10.6%、8.4%和 5.1%(p<0.0001)。52 周延长研究(SEQUEL)显示,7.5/46mg 和 15/92mg PHEN/TPM 治疗 2 年内体重持续减轻,与基线相比分别减轻 9.3%和 10.5%(p<0.0001)。与安慰剂相比,更多的患者接受 PHEN/TPM 治疗后体重减轻超过 5%、10%或 15%。PHEN/TPM 还可显著降低腰围、空腹甘油三酯和空腹血糖。该药在临床试验中通常具有良好的耐受性。发生在 5%或以上研究对象中的不良反应包括感觉异常、头晕、味觉障碍、失眠、便秘和口干。
PHEN/TPM 是一种新的、每日 1 次、控释、联合减肥产品,获批用于辅助饮食和运动治疗肥胖或超重伴有肥胖相关合并症的慢性体重管理。PHEN/TPM 疗效适度,是对减肥感兴趣的患者的可行选择,但缺乏长期安全性数据。