A single ascending-dose study of muscle regulator ace-031 in healthy volunteers

被引:138
作者
Attie, Kenneth M. [1 ]
Borgstein, Niels G. [1 ]
Yang, Yijun [1 ]
Condon, Carolyn H. [1 ]
Wilson, Dawn M. [1 ]
Pearsall, Amelia E. [2 ]
Kumar, Ravi [3 ]
Willins, Debbie A. [1 ]
Seehra, Jas S. [3 ]
Sherman, Matthew L. [1 ]
机构
[1] Acceleron Pharma Inc, Dept Med Res, Cambridge, MA 02139 USA
[2] Acceleron Pharma Inc, Dept Bioanalyt, Cambridge, MA 02139 USA
[3] Acceleron Pharma Inc, Dept Res, Cambridge, MA 02139 USA
关键词
ACE-031; activin; myostatin; neuromuscular disease; placebo-controlled clinical trial; RECEPTOR-TYPE IIB; MUSCULAR-DYSTROPHY; MOUSE MODEL; MYOSTATIN; MASS; GROWTH; OSTEOPOROSIS; HORMONE; CANCER; WOMEN;
D O I
10.1002/mus.23539
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction ACE-031 is a soluble form of activin receptor type IIB (ActRIIB). ACE-031 promotes muscle growth by binding to myostatin and other negative regulators of muscle mass. Methods This double-blind, placebo-controlled study evaluated the safety, pharmacokinetics, and pharmacodynamics of ACE-031 in 48 healthy, postmenopausal women randomized to receive 1 dose of ACE-031 (0.023 mg/kg SC) or placebo (3:1). Results ACE-031 was generally well-tolerated. Adverse events included injection site erythema. Mean ACE-031 AUC0 and Cmax increased linearly with dose; mean T1/2 was 1015 days. Statistically significant increases in mean total body lean mass (3.3%; P = 0.03, by DXA) and thigh muscle volume (5.1%; P = 0.03, by MRI) were observed at day 29 in the 3 mg/kg group. Statistically significant changes in serum biomarkers suggest ACE-031 also improved bone and fat metabolism. Conclusions Single-dose ACE-031 treatment was generally well-tolerated and resulted in increases in muscle mass in healthy postmenopausal women. Muscle Nerve [B]47[/B]: 416423, 2013
引用
收藏
页码:416 / 423
页数:8
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