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罗那卡列特,一种钙敏感受体拮抗剂,对桡骨骨折愈合时间无显著影响:一项随机、双盲、安慰剂对照的 II 期临床试验结果。

Ronacaleret, a calcium-sensing receptor antagonist, has no significant effect on radial fracture healing time: results of a randomized, double-blinded, placebo-controlled Phase II clinical trial.

机构信息

Medicines Development Center, GlaxoSmithKline, King of Prussia, PA 19406, USA.

出版信息

Bone. 2011 Oct;49(4):845-52. doi: 10.1016/j.bone.2011.06.017. Epub 2011 Jun 30.

Abstract

BACKGROUND

Fractures cause significant morbidity, mortality, and use of health care resources. An oral agent that enhances fracture healing could reduce costs and prevent future disabilities. In Phase I studies, ronacaleret, a novel calcium-sensing receptor antagonist, stimulated parathyroid hormone (PTH) release and increased bone formation markers, suggesting that it may act as an effective oral anabolic agent to enhance fracture healing.

METHODS

This was a randomized, double-blind, placebo-controlled, parallel-group, clinical trial in 85 male and female subjects who had sustained a closed, unilateral, extra-articular fracture of the distal radius and were receiving conservative treatment. Subjects were randomly assigned in a double-blind manner to ronacaleret 200 mg twice daily, ronacaleret 400 mg once daily or matching placebo and followed for 12 weeks. Fracture healing was assessed by radiographs and quantitative computed tomography (CT), and bone turnover markers were measured. The study was terminated early for futility based on the results of an unplanned interim analysis.

RESULTS

There were no significant differences between treatment groups in time to radiographic fracture healing (74, 65 and 68 days for placebo, 200 mg twice daily and 400 mg once daily dose groups, respectively), cortical bridging, grip strength, pain and swelling, time to cast removal, or range of motion. Markers of bone formation and levels of whole PTH, intact PTH and serum calcium increased following treatment with ronacaleret.

CONCLUSION

Ronacaleret had no significant effect on duration of healing by radiograph or CT scan, time to cast removal, clinical symptoms, grip strength, or range of motion.

摘要

背景

骨折会导致显著的发病率、死亡率和医疗资源的使用。一种能促进骨折愈合的口服药物可以降低成本并预防未来的残疾。在 I 期研究中,新型钙敏感受体拮抗剂罗卡列净刺激甲状旁腺激素 (PTH) 释放并增加骨形成标志物,表明它可能作为一种有效的口服合成代谢药物来增强骨折愈合。

方法

这是一项在 85 名男性和女性受试者中进行的随机、双盲、安慰剂对照、平行组临床试验,他们患有闭合性、单侧、关节外桡骨远端骨折,并接受保守治疗。受试者以双盲方式随机分配至罗卡列净 200mg 每日两次、罗卡列净 400mg 每日一次或匹配安慰剂组,并随访 12 周。通过 X 射线和定量 CT(CT)评估骨折愈合情况,并测量骨转换标志物。根据计划外中期分析的结果,该研究因无效而提前终止。

结果

在放射学骨折愈合时间(安慰剂组、200mg 每日两次组和 400mg 每日一次组分别为 74、65 和 68 天)、皮质桥接、握力、疼痛和肿胀、去除石膏的时间或活动范围方面,治疗组之间没有显著差异。罗卡列净治疗后,骨形成标志物和全 PTH、完整 PTH 和血清钙水平升高。

结论

罗卡列净对 X 射线或 CT 扫描的愈合持续时间、去除石膏的时间、临床症状、握力或活动范围均无显著影响。

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