Bauer Timothy A, Wolff Andrew A, Hirsch Alan T, Meng Lisa L, Rogers Kevin, Malik Fady I, Hiatt William R
Division of Internal Medicine, Department of Medicine, University of Colorado - School of Medicine, USA CPC Clinical Research, Aurora, CO, USA.
Cytokinetics, Inc., South San Francisco, CA, USA.
Vasc Med. 2014 Aug;19(4):297-306. doi: 10.1177/1358863X14534516. Epub 2014 May 28.
Tirasemtiv (CK-2017357), a novel small-molecule activator of the fast skeletal muscle troponin complex, slows the rate of calcium release from troponin, thus sensitizing fast skeletal muscle fibers to calcium. In preclinical studies, tirasemtiv increased muscle force and delayed the onset and reduced the extent of muscle fatigue during hypoxia in vitro and muscle ischemia in situ. This study evaluated the effect of single doses of tirasemtiv on measures of skeletal muscle function and fatigability in patients with stable calf claudication due to peripheral artery disease (PAD). Sixty-one patients with an ankle-brachial index ≤0.90 in the leg with claudication received single double-blind doses of tirasemtiv 375 mg and 750 mg and matching placebo in random order about 1 week apart. After 33 patients were treated, the 750 mg dose was decreased to 500 mg due to adverse events and these dose groups were combined for analysis. On each study day, bilateral heel-raise testing was performed before and at 3 and 6 hours after dosing; a 6-minute walk test was performed at 4 hours after dosing. Claudicating calf muscle performance was increased at the highest dose and plasma concentration of tirasemtiv; however, the 6-minute walk distance decreased with both the dose and plasma concentration of tirasemtiv, possibly due to dose-related adverse events, particularly dizziness, that could impede walking ability. In conclusion, the mechanism of fast skeletal muscle troponin activation improved muscle function but not 6-minute walking distance in patients with claudication due to PAD. CLINICALTRIALSGOV IDENTIFIER NCT01131013:
替拉西明(CK-2017357)是一种新型的快速骨骼肌肌钙蛋白复合物小分子激活剂,它可减缓肌钙蛋白释放钙的速率,从而使快速骨骼肌纤维对钙更敏感。在临床前研究中,替拉西明可增加肌肉力量,并在体外缺氧和原位肌肉缺血期间延缓肌肉疲劳的发作并减轻其程度。本研究评估了单剂量替拉西明对因外周动脉疾病(PAD)导致的稳定型小腿间歇性跛行患者骨骼肌功能和疲劳性指标的影响。61例患侧踝肱指数≤0.90的间歇性跛行患者,随机、双盲接受单剂量375mg和750mg替拉西明及匹配的安慰剂治疗,给药间隔约1周。33例患者接受治疗后,由于不良事件,750mg剂量降至500mg,将这些剂量组合并进行分析。在每个研究日,给药前以及给药后3小时和6小时进行双侧提踵试验;给药后4小时进行6分钟步行试验。替拉西明最高剂量和血浆浓度时,间歇性跛行的小腿肌肉表现有所改善;然而,6分钟步行距离随替拉西明的剂量和血浆浓度增加而减少,这可能是由于与剂量相关的不良事件,尤其是头晕,从而影响行走能力。总之,快速骨骼肌肌钙蛋白激活机制改善了因PAD导致的间歇性跛行患者的肌肉功能,但未改善6分钟步行距离。临床试验注册号NCT01131013: