与注射用生物制剂相匹配的安慰剂开发——实用教程。

Q2 Medicine
Antibody Therapeutics Pub Date : 2025-05-08 eCollection Date: 2025-07-01 DOI:10.1093/abt/tbaf009
Lun Xin, Zhe Zhang, Kushan Shah, Venus Hashemi, Xuanyue Li, Grace Qin, Steven Ren, Wei Chen, Yunsong Li
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引用次数: 0

摘要

背景:在药物开发中,安慰剂对照试验对于评估治疗效果至关重要。开发一种适合注射生物制剂的安慰剂面临着独特的挑战,特别是在不含活性药物成分的情况下匹配活性药物的物理特性。方法:本研究开发了一种生物安慰剂配方的方法,重点关注相关化学基质的颜色和粘度匹配。采用自定义颜色反褶积算法进行精确配色,并采用羧甲基纤维素钠(Na-CMC)调节不同缓冲体系的粘度。研究了缓冲液、着色剂和赋形剂之间的相互作用,以确保物理性质的一致性。在冻融和热应力条件下进行了稳定性试验。结果:颜色匹配算法成功地实现了与活性药物在视觉上无法区分的结果,通过色差的经验参数(ΔE值)来测量。Na-CMC可以有效地匹配生物制剂的粘度,保持所需的物理外观。显色剂和缓冲系统之间的显著相互作用影响粘度和渗透压。稳定性测试证实,安慰剂配方保留了其颜色、pH值和渗透压,在压力测试后只有轻微的粘度变化。结论:我们的研究为生物安慰剂的开发提供了一个系统的方法,为匹配生物制剂的颜色和粘度提供了一个可靠的框架。这些方法和发现支持使用量身定制的辅料和颜色匹配算法,以确保临床试验中的盲化,提高药物疗效评估的严密性,并为未来生物药物开发中的安慰剂设计做出贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Matching placebo development for injectable biologics-a practical tutorial.

Background: In drug development, placebo-controlled trials are vital for assessing treatment efficacy. Developing a suitable placebo for injectable biologics presents unique challenges, particularly in matching the physical characteristics of the active drug without containing its active pharmaceutical ingredient.

Methods: Our study developed a methodology for biologic placebo formulations, focusing on color and viscosity matching, in relevant chemical matrixes. A custom color deconvolution algorithm was used for precise color-matching, and sodium carboxymethyl cellulose (Na-CMC) was employed to adjust viscosity in different buffer systems. The interactions between buffers, color agents, and excipients were investigated to ensure consistency in physical properties. Stability testing was conducted under freeze/thaw and thermal stress conditions.

Results: The color-matching algorithm successfully achieved visually indistinguishable results from the active drug, measured by an empirical parameter for color differences (ΔE values). Na-CMC was effective in matching the viscosity of biologic formulations, maintaining the desired physical appearance. Significant interactions between color agents and buffer systems influenced viscosity and osmolality. Stability tests confirmed that the placebo formulations retained their color, pH, and osmolality, with only minor viscosity changes after stress testing.

Conclusions: Our study presents a systematic approach to biologic placebo development, providing a reliable framework for matching the color and viscosity of biologics. The methods and findings support the use of tailored excipients and color-matching algorithms to ensure clinical blinding in trials, enhancing the rigor of drug efficacy assessments and contributing to future placebo design in biologic drug development.

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来源期刊
Antibody Therapeutics
Antibody Therapeutics Medicine-Immunology and Allergy
CiteScore
8.70
自引率
0.00%
发文量
30
审稿时长
8 weeks
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