Randomized, Double-Blind, Placebo-Controlled Phase II Trial of AYP-101 (Soybean Phosphatidylcholine) for Submental Fat Reduction in Asian Adults.

IF 3.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Sun Young Choi, A M Abd El-Aty, Beom Joon Kim
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引用次数: 0

Abstract

Purpose: Submental fat (SMF) accumulation can affect self-image and psychological well-being, leading to a demand for nonsurgical treatment. AYP-101, which contains soybean phosphatidylcholine (SPC), is under investigation for SMF reduction. This study aimed to compare 2 concentrations of AYP-101 to placebo injections to determine the optimal concentration and evaluate safety and efficacy in reducing moderate to severe SMF in an Asian population.

Methods: This single-center, randomized, double-blind, placebo-controlled phase II trial enrolled 96 participants with moderate to severe SMF. Participants were randomly assigned to receive either a placebo or AYP-101 at either a low concentration (25 mg/mL) or a high concentration (50 mg/mL), administered every 2 weeks for up to 6 sessions. The primary endpoint was the proportion of participants achieving at least a 1-grade improvement in both the Evaluator-Reported Submental Fat Rating Scale (ER-SMFRS) and the Subject-Reported Submental Fat Rating Scale (SR-SMFRS) at 4 and 12 weeks after the final injection.

Findings: At 4 weeks post-treatment, 69.70% of the low-concentration group and 48.39% of the high-concentration group exhibited improvement in the ER-SMFRS, compared to 22.58% in the placebo group. Significant differences were noted between the low-concentration and placebo groups (P = 0.0002), with similar results at 12 weeks.

Implications: AYP-101, administered biweekly at a concentration of 25 mg/mL, appears to be a safe and effective nonsurgical option for reducing SMF in Asians.

随机、双盲、安慰剂对照的大豆磷脂酰胆碱(AYP-101)治疗亚洲成人脑下脂肪减少的II期试验。
目的:心理下脂肪(SMF)的积累会影响自我形象和心理健康,导致对非手术治疗的需求。含有大豆磷脂酰胆碱(SPC)的AYP-101正在进行SMF还原研究。本研究旨在比较两种浓度的AYP-101与安慰剂注射,以确定最佳浓度,并评估在亚洲人群中减少中重度SMF的安全性和有效性。方法:这项单中心、随机、双盲、安慰剂对照的II期试验招募了96名患有中度至重度SMF的参与者。参与者被随机分配接受安慰剂或低浓度(25mg /mL)或高浓度(50mg /mL)的AYP-101,每2周给药,最多6次。主要终点是在最终注射后4周和12周,在评估者报告的下精神脂肪评定量表(ER-SMFRS)和受试者报告的下精神脂肪评定量表(SR-SMFRS)中达到至少1级改善的参与者比例。结果:在治疗后4周,低浓度组69.70%和高浓度组48.39%的ER-SMFRS改善,而安慰剂组为22.58%。低浓度组和安慰剂组之间存在显著差异(P = 0.0002), 12周时的结果相似。意义:每两周给予浓度为25mg /mL的AYP-101似乎是一种安全有效的减少亚洲人SMF的非手术选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical therapeutics
Clinical therapeutics 医学-药学
CiteScore
6.00
自引率
3.10%
发文量
154
审稿时长
9 weeks
期刊介绍: Clinical Therapeutics provides peer-reviewed, rapid publication of recent developments in drug and other therapies as well as in diagnostics, pharmacoeconomics, health policy, treatment outcomes, and innovations in drug and biologics research. In addition Clinical Therapeutics features updates on specific topics collated by expert Topic Editors. Clinical Therapeutics is read by a large international audience of scientists and clinicians in a variety of research, academic, and clinical practice settings. Articles are indexed by all major biomedical abstracting databases.
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