小儿肺动脉高压临床试验的演变:是否满足了患者及其护理人员的需求?

IF 3.6 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Julie Wacker, Raphael Joye, Leon Genecand, Frederic Lador, Maurice Beghetti
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引用次数: 0

摘要

简介小儿肺动脉高压是一种罕见病。在目前的治疗时代,存活率仍然很低。有关小儿肺动脉高压医疗管理的数据匮乏,大多数肺血管扩张剂在儿童中的使用都是非标的:小儿肺动脉高压临床试验的设计和实现面临许多障碍,包括招募不足、不同年龄儿童的药物和生理数据有限、伦理问题以及缺乏有效的试验终点。创新的临床试验设计已经出现,或许能让我们克服其中的一些问题。将成人数据外推至儿童,并提供更多的药代动力学和安全性数据,对于认为儿童和成人病理生理学相似的病因仍极为重要和有效:赞助商、监管机构、患者、护理人员、医生和研究人员之间的紧密合作对于开发有效、安全的小儿肺动脉高压药物十分必要。患者和护理人员越来越多地参与到临床试验的开发过程中,这应有助于形成对患者可行且有意义的未来研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The evolution of clinical trials for pediatric pulmonary hypertension: are the needs of patients and their caregivers being met?

Introduction: Pediatric pulmonary hypertension is a rare condition. Survival remains poor in the current management era. There is a lack of data regarding the medical management of pediatric pulmonary hypertension and most pulmonary vasodilators are used off-label in children.

Areas covered: Pediatric pulmonary hypertension clinical trials' design and realization face many hurdles, including poor recruitment, limited available pharmacologic and physiologic data in children of various ages, ethical issues, and the lack of validated trial endpoint. Innovative clinical trial designs have emerged and may allow us to overcome some of these issues. Extrapolation of adult data to children, with additional pharmacokinetic and safety data, remains extremely important and valid in etiologies where the pediatric and the adult pathophysiologies are believed to be similar.

Expert opinion: Close collaboration between sponsors, regulators, patients, caregivers, physicians and researchers is necessary to develop efficacious and safe drugs for pediatric pulmonary hypertension. The increasing involvement of patients' and caregivers' participation in the development of clinical trials should help shape future research that is feasible and meaningful to the patients.

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来源期刊
Expert Review of Clinical Pharmacology
Expert Review of Clinical Pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
7.30
自引率
2.30%
发文量
127
期刊介绍: Advances in drug development technologies are yielding innovative new therapies, from potentially lifesaving medicines to lifestyle products. In recent years, however, the cost of developing new drugs has soared, and concerns over drug resistance and pharmacoeconomics have come to the fore. Adverse reactions experienced at the clinical trial level serve as a constant reminder of the importance of rigorous safety and toxicity testing. Furthermore the advent of pharmacogenomics and ‘individualized’ approaches to therapy will demand a fresh approach to drug evaluation and healthcare delivery. Clinical Pharmacology provides an essential role in integrating the expertise of all of the specialists and players who are active in meeting such challenges in modern biomedical practice.
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