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用于减少侧腹脂肪的他喷那铵(RZL-012):一项概念验证研究。

Tapencarium (RZL-012) for Flank Fat Reduction: A Proof-of-Concept Study.

作者信息

Shridharani Sachin M, Kennedy MacKenzie L, Gueta Racheli, Walker Patricia

出版信息

Aesthet Surg J Open Forum. 2023 Oct 27;5:ojad094. doi: 10.1093/asjof/ojad094. eCollection 2023.

Abstract

BACKGROUND

RZL-012 is a novel cytolytic drug that has shown promise in reducing localized fat deposits in a single treatment session.

OBJECTIVES

To assess the safety and efficacy of injecting RZL-012 to the flanks.

METHODS

A double-blind, placebo-controlled, proof of concept study randomized 12 patients to receive RZL-012 injections in 1 flank and placebo injections in the contralateral flank. After 12 weeks of follow-up, patients could receive RZL-012 in the placebo-treated flank and undergo follow-up for 12 weeks in the open-label phase.

RESULTS

At 12 weeks, Investigator Global Aesthetic Improvement Scale assessments showed improvement for 90.9% of RZL-012-treated flanks and 0% of placebo-treated flanks ( < .0001), 81.8% of patients were satisfied with the RZL-012-treated flanks, and 9.1% were satisfied with the placebo-treated flanks ( = .0019). Volume reduction measured on 3-dimensional images was a mean 37.27 mL, which was significantly greater than placebo ( = .0052). The product was well tolerated, with no clinically significant trends in laboratory values, electrocardiograms, or vital signs. Pharmacokinetic analyses demonstrated that RZL-012 is quickly absorbed, reaches maximum concentration in approximately 1.67 h, and has a half-life of 9.1 h. The mean maximal concentration of RZL-012 found in the blood was <1 µg/mL.

CONCLUSIONS

RZL-012 is a promising option for injectable fat reduction of the flanks in a single treatment session. The drug was well tolerated in this small patient population, with no concerning safety signals, and it had indications of efficacy. Further research is needed in large Phase 2 studies with robust efficacy measurements to confirm these early findings.

摘要

背景

RZL - 012是一种新型溶细胞药物,已显示出在单次治疗中减少局部脂肪堆积的潜力。

目的

评估向双侧胁腹注射RZL - 012的安全性和有效性。

方法

一项双盲、安慰剂对照的概念验证研究将12名患者随机分组,一侧胁腹注射RZL - 012,对侧胁腹注射安慰剂。随访12周后,患者可在接受安慰剂治疗的胁腹注射RZL - 012,并在开放标签阶段进行12周的随访。

结果

12周时,研究者整体美学改善量表评估显示,接受RZL - 012治疗的胁腹有90.9%得到改善,而接受安慰剂治疗的胁腹改善率为0%(P <.0001);81.8%的患者对接受RZL - 012治疗的胁腹满意,9.1%的患者对接受安慰剂治疗的胁腹满意(P =.0019)。三维图像测量的体积减少平均为37.27 mL,显著大于安慰剂组(P =.0052)。该产品耐受性良好,实验室检查值、心电图或生命体征均无临床显著变化趋势。药代动力学分析表明,RZL - 012吸收迅速,约1.67小时达到最大浓度,半衰期为9.1小时。血液中RZL - 012的平均最大浓度<1 μg/mL。

结论

RZL - 012是单次治疗双侧胁腹注射减脂的一个有前景的选择。在这个小样本患者群体中,该药物耐受性良好,没有令人担忧的安全信号,并有疗效迹象。需要在大型2期研究中进行更有力的疗效测量,以进一步研究证实这些早期发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1652/10631968/1b2395f34ebb/ojad094f1.jpg

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