Wells T G
Divisions of Pediatric, Nephrology and Pediatric Clinical Pharmacology and Toxicology, University of Arkansas for Medical Sciences and the Arkansas Children's Hospital, Little Rock, Arkansas 72202, USA.
Blood Press Monit. 1999 Jun-Aug;4(3-4):189-92.
Clinical trials assessing the safety, effectiveness and pharmacokinetics of new antihypertensive medications have been numerous as new classes of medications have been developed and brought to market over the past two decades. However, very few clinical trials have been initiated and completed in children with hypertension. Excluding diuretics, only one antihypertensive medication marketed within the past 20 years has any pediatric pharmacokinetic or dosing information published in the drug label and none have a pediatric indication. There are many reasons that these studies have not been done. Summation of the data collected in large epidemiologic studies that establish normal blood pressure and define hypertension using casual measurements have been a relatively recent event in pediatrics. Although ambulatory blood pressure measurement has been studied for the past decade there is still uncertainty with respect to the standardization of devices, measurement technique and normal values in a multi-racial pediatric population. As a result, no large scale, industry-sponsored clinical trials involving antihypertensive therapy have employed this measurement technique in children. In recognition of this problem, US Congress passed the Food and Drug Administration Modernization Act in 1997. Among the many provisions of this law, the US Food and Drug Administration (FDA) is required to publish a list of approved drugs for which additional information may prove beneficial for children. This law and subsequent action by the FDA also provides a mechanism by which manufacturers may gain six months of additional market exclusivity if adequate and well-controlled pediatric trials are completed and submitted to the FDA in response to a formal written request for these studies. Because such studies have not been previously undertaken and the new rules provide a significant financial incentive, written requests have been issued for pediatric studies involving more than a dozen antihypertensive agents. The FDA published a sample written request for oral antihypertensives in children and several potential study designs were presented.
在过去二十年中,随着新型抗高血压药物的研发和上市,评估其安全性、有效性和药代动力学的临床试验层出不穷。然而,针对儿童高血压开展并完成的临床试验却寥寥无几。除利尿剂外,过去20年内上市的抗高血压药物中,只有一种在药品标签中公布了儿科药代动力学或给药信息,且均无儿科适应症。这些研究未开展有诸多原因。在儿科学领域,汇总大型流行病学研究中收集的数据以确定正常血压并通过随机测量定义高血压是相对较新的事情。尽管过去十年一直在研究动态血压测量,但在多民族儿科人群中,关于设备标准化、测量技术和正常值仍存在不确定性。因此,没有大规模的、由行业赞助的涉及抗高血压治疗的临床试验在儿童中采用这种测量技术。认识到这一问题后,美国国会于1997年通过了《食品药品管理局现代化法案》。该法律的众多条款中,要求美国食品药品管理局(FDA)公布一份已批准药物清单,对于这些药物,更多信息可能对儿童有益。该法律以及FDA随后采取的行动还提供了一种机制,如果完成了充分且严格控制的儿科试验并应FDA对这些研究的正式书面请求提交给FDA,制造商可获得六个月的额外市场独占期。由于此前尚未开展此类研究,且新规则提供了重大经济激励,已针对涉及十几种抗高血压药物的儿科研究发出了书面请求。FDA发布了一份针对儿童口服抗高血压药物的书面请求样本,并提出了几种潜在的研究设计。