{"title":"2005年至2011年NovumPRS资格筛选期间临床试验参与者中抗- hcv的发病率","authors":"J. Morgan, Darin B. Brimhall","doi":"10.30918/irjmms.82.13.049","DOIUrl":null,"url":null,"abstract":"Hepatitis C (HCV) is a contagious viral illness and is the most common blood borne infection in the United States. It frequently remains undiagnosed until the ominous symptoms of liver disease, cirrhosis, or hepatocellular carcinoma become evident. This is because most acute infections follow an asymptomatic course. Center for Disease Control (CDC) Viral Surveillance data revealed the incidence rate for hepatitis C in the U.S. to be around 0.3 cases per 100,000. This means that nearly 4 million Americans have been exposed to HCV. World-wide 170 million people are affected by HCV. It is also known that despite these staggering numbers that the majority of HCV infected people go undiagnosed. Novum Pharmaceutical Research Services (NovumPRS) is a private, for profit, Clinical Research Organization (CRO) that has been recruiting and screening adult volunteers for Phase 1 bioequivalence and bioavailability drug studies since the early 1970’s. Three sites collectively completed approximately 150 to 170 studies annually; and screened approximately 90,000 participants during the 2005 to 2011 period we reviewed. In this paper, we present our data regarding the 0.8% positive anti-HCV incidence found on screening laboratory evaluation for clinical trial volunteers prior to consideration for randomized trial enrollment at the three research facilities. Race/ethnicity and socioeconomic status were not considerations made in the reporting of our findings here. A positive anti-HCV test disqualified individuals from participation in all Phase I randomized trials conducted at our research organization not specifically related to hepatitis. All screened participants who tested positive were informed of these findings and appropriate reporting from our research organization to the epidemiology department at the appropriate state health agency was then carried out.","PeriodicalId":170316,"journal":{"name":"International Research Journal of Medicine and Medical Sciences","volume":"130 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Incidence of anti-HCV found among clinical trial participants during eligibility screening at NovumPRS from 2005 to 2011\",\"authors\":\"J. Morgan, Darin B. Brimhall\",\"doi\":\"10.30918/irjmms.82.13.049\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Hepatitis C (HCV) is a contagious viral illness and is the most common blood borne infection in the United States. It frequently remains undiagnosed until the ominous symptoms of liver disease, cirrhosis, or hepatocellular carcinoma become evident. This is because most acute infections follow an asymptomatic course. Center for Disease Control (CDC) Viral Surveillance data revealed the incidence rate for hepatitis C in the U.S. to be around 0.3 cases per 100,000. This means that nearly 4 million Americans have been exposed to HCV. World-wide 170 million people are affected by HCV. It is also known that despite these staggering numbers that the majority of HCV infected people go undiagnosed. Novum Pharmaceutical Research Services (NovumPRS) is a private, for profit, Clinical Research Organization (CRO) that has been recruiting and screening adult volunteers for Phase 1 bioequivalence and bioavailability drug studies since the early 1970’s. Three sites collectively completed approximately 150 to 170 studies annually; and screened approximately 90,000 participants during the 2005 to 2011 period we reviewed. In this paper, we present our data regarding the 0.8% positive anti-HCV incidence found on screening laboratory evaluation for clinical trial volunteers prior to consideration for randomized trial enrollment at the three research facilities. Race/ethnicity and socioeconomic status were not considerations made in the reporting of our findings here. A positive anti-HCV test disqualified individuals from participation in all Phase I randomized trials conducted at our research organization not specifically related to hepatitis. 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引用次数: 0
摘要
丙型肝炎(HCV)是一种传染性病毒疾病,是美国最常见的血源性感染。它经常被诊断出来,直到肝病、肝硬化或肝细胞癌的不祥症状变得明显。这是因为大多数急性感染都是无症状的。疾病控制中心(CDC)病毒监测数据显示,美国丙型肝炎的发病率约为每10万人0.3例。这意味着近400万美国人接触过丙型肝炎病毒。全世界有1.7亿人感染丙型肝炎病毒。众所周知,尽管有这些惊人的数字,但大多数丙型肝炎病毒感染者未得到诊断。Novum Pharmaceutical Research Services (NovumPRS)是一家私营的营利性临床研究组织(CRO),自20世纪70年代初以来一直在招募和筛选成人志愿者进行i期生物等效性和生物利用度药物研究。三个地点每年总共完成约150至170项研究;在2005年到2011年期间,我们对大约9万名参与者进行了筛选。在本文中,我们介绍了在三个研究机构考虑随机试验入组之前,对临床试验志愿者进行筛选实验室评估时发现的0.8%的抗- hcv阳性发生率的数据。种族/民族和社会经济地位在我们的研究报告中没有考虑到。在我们的研究机构进行的所有与肝炎无关的I期随机试验中,抗hcv检测阳性的个体被取消参加资格。所有检测呈阳性的筛选参与者都被告知这些发现,然后由我们的研究组织向适当的州卫生机构的流行病学部门进行适当的报告。
Incidence of anti-HCV found among clinical trial participants during eligibility screening at NovumPRS from 2005 to 2011
Hepatitis C (HCV) is a contagious viral illness and is the most common blood borne infection in the United States. It frequently remains undiagnosed until the ominous symptoms of liver disease, cirrhosis, or hepatocellular carcinoma become evident. This is because most acute infections follow an asymptomatic course. Center for Disease Control (CDC) Viral Surveillance data revealed the incidence rate for hepatitis C in the U.S. to be around 0.3 cases per 100,000. This means that nearly 4 million Americans have been exposed to HCV. World-wide 170 million people are affected by HCV. It is also known that despite these staggering numbers that the majority of HCV infected people go undiagnosed. Novum Pharmaceutical Research Services (NovumPRS) is a private, for profit, Clinical Research Organization (CRO) that has been recruiting and screening adult volunteers for Phase 1 bioequivalence and bioavailability drug studies since the early 1970’s. Three sites collectively completed approximately 150 to 170 studies annually; and screened approximately 90,000 participants during the 2005 to 2011 period we reviewed. In this paper, we present our data regarding the 0.8% positive anti-HCV incidence found on screening laboratory evaluation for clinical trial volunteers prior to consideration for randomized trial enrollment at the three research facilities. Race/ethnicity and socioeconomic status were not considerations made in the reporting of our findings here. A positive anti-HCV test disqualified individuals from participation in all Phase I randomized trials conducted at our research organization not specifically related to hepatitis. All screened participants who tested positive were informed of these findings and appropriate reporting from our research organization to the epidemiology department at the appropriate state health agency was then carried out.