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Human therapeutic cocaine vaccine: safety and immunogenicity

机译:人类可卡因治疗疫苗:安全性和免疫原性

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This randomized, double blind, placebo controlled, phase I clinical trial assessed the safety and immunogenicity of a therapeutic cocaine vaccine TA-CD in 34 former cocaine abusers: 8 at 13 mug active vaccine, 10 at 82 mug and 10 at 709 mug, with two additional subjects getting placebo in each cohort. All got intra-muscular injections at 0-2 months and were monitored for safety and antibody production for 3 months. Of the 34 subjects 27 completed the full course of three injections, of these, only 24 returned for the final scheduled visit at day 84. The vaccine was well-tolerated and had no serious drug-related adverse events, although three subjects at the highest dose experienced brief post injection twitching. Fifteen subjects on TA-CD therapeutic vaccine were followed for 1 year. Antibody levels were correlated with vaccine dose and number of injections. Anti-cocaine antibodies were detected after the second injection, peaked at 3 months and declined to baseline by 1 year. Thus, the therapeutic vaccine was well tolerated with dose related increases in antibody levels, and a high proportion of patients recruited into the study were retained.
机译:这项随机,双盲,安慰剂对照的I期临床试验评估了可卡因治疗性疫苗TA-CD在34位前可卡因滥用者中的安全性和免疫原性:13杯有效疫苗中有8杯,82杯中有10杯,709杯中有10杯,每个队列中还有两个受试者接受安慰剂治疗。所有患者均于0-2个月进行肌肉注射,并在3个月内进行安全性和抗体产生监测。在34位受试者中,有27位完成了三剂全程注射,其中只有24位在第84天返回了最终的预定就诊。该疫苗具有良好的耐受性,没有严重的与药物相关的不良事件,尽管最高的三位受试者剂量在注射后短暂抽搐。对十五名接受TA-CD治疗性疫苗的受试者进行了为期一年的随访。抗体水平与疫苗剂量和注射次数相关。第二次注射后检测到抗可卡因抗体,在3个月达到峰值,并在1年后降至基线。因此,治疗性疫苗对抗体水平的剂量相关增加具有良好的耐受性,并且保留了招募至该研究中的大部分患者。

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