临床研究的当前观点:计算机辅助药物设计、伦理和良好临床实践

V. Kandi, Anusha Vundecode, Tanmai Reddy Godalwar, Sindhusree Dasari, Sabitha Vadakedath, Vikram Godishala
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引用次数: 1

摘要

在新出现的微生物和非传染性疾病以及重新出现的微生物感染的时代,医学界和公众都受到准备不足的困扰。从冠状病毒病(COVID-19)大流行的严重性可以明显看出,新型微生物疾病是一项挑战,而且正在挑战控制。这主要是由于缺乏对这种新型微生物的生物学和发病机制的完整认识,以及无法获得治疗和控制这种疾病的治疗药物和疫苗。临床研究是唯一的解决方法,它可以处理大多数这些情况。在这篇综述中,我们强调了计算机辅助药物设计(CADD)以及分子对接、分子叠加、3d药团技术、伦理和良好临床实践(GCP)在治疗药物、设备和疫苗开发中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Current Perspectives in Clinical Research: Computer-Assisted Drug Designing, Ethics, and Good Clinical Practice
In the era of emerging microbial and non-communicable diseases and re-emerging microbial infections, the medical fraternity and the public are plagued by under-preparedness. It is evident by the severity of the Coronavirus disease (COVID-19) pandemic that novel microbial diseases are a challenge and are challenging to control. This is mainly attributed to the lack of complete knowledge of the novel microbe’s biology and pathogenesis and the unavailability of therapeutic drugs and vaccines to treat and control the disease. Clinical research is the only answer utilizing which can handle most of these circumstances. In this review, we highlight the importance of computer-assisted drug designing (CADD) and the aspects of molecular docking, molecular superimposition, 3D-pharmacophore technology, ethics, and good clinical practice (GCP) for the development of therapeutic drugs, devices, and vaccines.
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