Department of Medicine, St. Luke's Hospital, St. Louis, MO, USA.
Rheumatol Int. 2012 Jun;32(6):1831-5. doi: 10.1007/s00296-011-2027-3. Epub 2011 Jul 19.
The aims of this study are to describe the characteristics of clinical trials in rheumatoid arthritis (RA) listed in ClinicalTrials.gov and examine existing trends in study design, funding sources, outcomes, and drugs under investigation. We conducted a survey of ongoing clinical trials in RA registered in the ClinicalTrials.gov website. We used the advanced search option and applied the following inclusion criteria, "rheumatoid arthritis", "open studies", "interventional", and "adults 18 years or older". Of 127 eligible trials, 53.5% of the studies were either phase 3 or 4, and 40.2% were phase 1, 2, and 2/3. Two-thirds of the trials were randomized (70.9%), and over half were, in addition, double-blinded (53.5%) and placebo-controlled (53.5%). Universities were listed as the primary sponsor for 18.9% of the trials and pharmaceutical industry for 73.2%. Majority of the trials were multi-center studies (93%) conducted outside the United States (54.3%). The most frequently used endpoint was drug efficacy (54.3%) followed by drug safety (25.2%). Most industry-funded trials were open for less than 12 months, whereas most university-funded trials were open for more than 24 months (58% each). Biologic therapies were the focus of most trials in the registry (78.5%). Randomized, double-blinded, placebo-controlled, phase 3 and 4 trials form the majority of ongoing clinical trials in RA. The preponderance of industry funding of RA trials and the short duration of such trials are troubling trends which need to be addressed.
本研究旨在描述 ClinicalTrials.gov 中列出的类风湿关节炎(RA)临床试验的特点,并检查研究设计、资金来源、结局和研究药物方面的现有趋势。我们对 ClinicalTrials.gov 网站上注册的正在进行的 RA 临床试验进行了调查。我们使用了高级搜索选项,并应用了以下纳入标准:“类风湿关节炎”、“开放研究”、“干预性”和“18 岁或以上的成年人”。在 127 项合格试验中,53.5%的研究处于 3 期或 4 期,40.2%处于 1 期、2 期和 2/3 期。三分之二的试验是随机的(70.9%),超过一半的试验是双盲(53.5%)和安慰剂对照(53.5%)。大学是 18.9%试验的主要赞助商,制药行业是 73.2%。大多数试验是多中心研究(93%),在美国境外进行(54.3%)。最常用的终点是药物疗效(54.3%),其次是药物安全性(25.2%)。大多数行业资助的试验开放时间不到 12 个月,而大多数大学资助的试验开放时间超过 24 个月(各占 58%)。生物疗法是该注册中心大多数试验的重点(78.5%)。随机、双盲、安慰剂对照、3 期和 4 期试验构成了正在进行的 RA 临床试验的大多数。RA 试验中行业资金的优势和此类试验的短期性是令人担忧的趋势,需要加以解决。