Acceleron Pharma, 128 Sidney Street, Cambridge, Massachusetts, 02139, USA.
Celerion, Lincoln, Nebraska, USA.
Muscle Nerve. 2018 Jun;57(6):921-926. doi: 10.1002/mus.26113. Epub 2018 Mar 15.
ACE-083 is a locally acting follistatin-based therapeutic that binds myostatin and other muscle regulators and has been shown to increase muscle mass and force in neuromuscular disease mouse models. This first-in-human study examined these effects.
In this phase 1, randomized, double-blind, placebo-controlled, dose-ranging study in healthy postmenopausal women, ACE-083 (50-200 mg) or placebo was administered unilaterally into rectus femoris (RF) or tibialis anterior (TA) muscles as 1 or 2 doses 3 weeks apart.
Fifty-eight postmenopausal women were enrolled, 42 ACE-083 and 16 placebo. No serious adverse events (AE), dose-limiting toxicities, or discontinuations resulting from AEs occurred. Maximum (mean ± SD) increases in RF and TA muscle volume were 14.5% ± 4.5% and 8.9% ± 4.7%, respectively. No significant changes in mean muscle strength were observed.
ACE-083 was well tolerated and resulted in significant targeted muscle growth. ACE-083 may have the potential to increase muscle mass in a wide range of neuromuscular disorders. Muscle Nerve 57: 921-926, 2018.
ACE-083 是一种局部作用的基于卵泡抑素的治疗药物,可与肌肉生长抑制素和其他肌肉调节剂结合,并已被证明可增加神经肌肉疾病小鼠模型中的肌肉质量和力量。这项首次人体研究检查了这些效果。
在这项针对健康绝经后女性的 1 期、随机、双盲、安慰剂对照、剂量范围研究中,ACE-083(50-200mg)或安慰剂每隔 3 周单侧肌肉注射到股直肌(RF)或胫骨前肌(TA)中,剂量为 1 或 2 次。
共纳入 58 名绝经后女性,42 名接受 ACE-083 治疗,16 名接受安慰剂治疗。无严重不良事件(AE)、剂量限制毒性或因 AE 而停药。RF 和 TA 肌肉体积的最大(平均±SD)增加分别为 14.5%±4.5%和 8.9%±4.7%。肌肉力量的平均变化无显著差异。
ACE-083 耐受性良好,导致目标肌肉显著生长。ACE-083 可能有潜力增加广泛的神经肌肉疾病中的肌肉质量。肌肉神经 57:921-926,2018 年。