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一项关于联苯乙酸临床试验的调查。

A survey of clinical trials with fenbufen.

作者信息

Mawdsley P

出版信息

Arzneimittelforschung. 1980;30(4A):740-6.

PMID:7002163
Abstract

To date, the efficacy and safety of gamma-oxo(1,1'-biphenyl)-4-butanoic acid (fenbufen) have been evaluated in over 200 clinical trials involving several thousand patients. The program of clinical investigation consisted of open dose ranging studies in patients; short-term, double-blind controlled studies of both cross-over and parallel group design to evaluate efficacy and safety compared to placebo and active reference drugs; long-term, double-blind controlled studies of parallel group design versus an active reference agent; open studies to evaluate the long-term efficacy and safety of fenbufen; and special studies to investigate possible effects on eyes, ears and heart. The overall experience with fenbufen in 60 US and 37 foreign clinical trials is summarized in this report with respect to the following: therapeutic efficacy and safety in rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, analgesia and gout. The age range covered in these studies was 13 to 87 years, and included 206 patients over the age of 70. 3457 patients received fenbufen in all phases of these clinical trials, including short-term and long-term studies. The patient total includes: 1462 patients (664 US, 798 foreign) with rheumatoid arthritis, 1225 (420 US, 805 foreign) with osteoarthritis, 55 (19 US, 36 foreign) with ankylosing spondylitis, 39 (foreign) with gout, and 676 patients (103 US, 573 (foreign) who participated in analgesia studies. The worldwide clinical studies have demonstrated very good clinical efficacy of fenbufen in comparison to other non-steroidal antirheumatic (nsa) drugs. The tolerance was much better in many cases compared with tolerance levels of other nsa-drugs. The good results were confirmed by new papers presented during IX International Congress of Rheumatology, Wiesbaden/FR Germany, September 1979. Fenbufen is currently marketed in Brazil, Columbia, Costa Rica, Dominican Republic, Ecuador, El Salvador, Great Britain, Greece, Guatemala, Honduras, Ireland, Italy, Japan, South Korea, Mexico, Nicaragua, Panama, Peru, Philippines, Rhodesia, Spain, South Africa, Switzerland, Trinidad and FR Germany.

摘要

迄今为止,γ-氧代(1,1'-联苯)-4-丁酸(芬布芬)的疗效和安全性已在涉及数千名患者的200多项临床试验中得到评估。临床研究项目包括对患者进行开放剂量范围研究;采用交叉和平行组设计的短期双盲对照研究,以评估与安慰剂和活性参比药物相比的疗效和安全性;采用平行组设计与活性参比药物进行对比的长期双盲对照研究;评估芬布芬长期疗效和安全性的开放研究;以及调查对眼睛、耳朵和心脏可能影响的专项研究。本报告总结了芬布芬在美国60项和国外37项临床试验中的总体经验,内容涉及以下方面:在类风湿性关节炎、骨关节炎、强直性脊柱炎、镇痛和痛风方面的治疗效果和安全性。这些研究涵盖的年龄范围为13至87岁,其中包括206名70岁以上的患者。在这些临床试验的所有阶段,包括短期和长期研究中,共有3457名患者接受了芬布芬治疗。患者总数包括:1462名(美国664名,国外798名)类风湿性关节炎患者、1225名(美国420名,国外805名)骨关节炎患者、55名(美国19名,国外36名)强直性脊柱炎患者、39名(国外)痛风患者以及676名(美国103名,国外573名)参与镇痛研究的患者。全球临床研究表明,与其他非甾体类抗风湿(NSA)药物相比,芬布芬具有非常好的临床疗效。在许多情况下,其耐受性比其他NSA药物的耐受性水平要好得多。1979年9月在德国威斯巴登举行的第九届国际风湿病学大会上发表的新论文证实了这些良好结果。芬布芬目前在巴西、哥伦比亚、哥斯达黎加、多米尼加共和国、厄瓜多尔、萨尔瓦多、英国、希腊、危地马拉、洪都拉斯、爱尔兰、意大利、日本、韩国、墨西哥、尼加拉瓜、巴拿马、秘鲁、菲律宾、罗德西亚、西班牙、南非、瑞士、特立尼达和德国销售。

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