Ishizaki T, Kamo E, Boehme K
Bull World Health Organ. 1979;57(5):787-91.
The first clinical trials of praziquantel against Schistosoma japonicum infections in Japan were planned to assess tolerance only. Three double-blind studies against placebo involving a total of 51 patients were conducted with dosages of praziquantel of 1 x 20 mg/kg body weight, 2 x 20 mg/kg, 3 x 20 mg/kg given on one day.The frequency of unwanted side effects was higher in the group of patients given praziquantel at a dose of 3 x 20 mg/kg than in all other drug- or placebo-treated patients. In general, the side effects, which included drowsiness, headache, lumbago, abdominal fullness, or epigastric discomfort, lasted for several hours but disappeared spontaneously. The results of laboratory tests showed no significant changes caused by treatment.The overall assessment showed excellent or good tolerance in all patients treated with praziquantel at the lower dose levels. In those given 3 x 20 mg/kg, tolerance was excellent in 1 of 12 patients, good in 9, and fair in 2, whereas the respective placebo-treated group showed excellent tolerance in 3 of 12, good in 7, and fair in 2.
日本针对日本血吸虫感染开展的吡喹酮首次临床试验仅计划评估耐受性。开展了三项针对安慰剂的双盲研究,共涉及51名患者,吡喹酮剂量为1×20毫克/千克体重、2×20毫克/千克、3×20毫克/千克,均于一日内给药。给予3×20毫克/千克剂量吡喹酮的患者组中,不良副作用的发生率高于所有其他接受药物治疗或安慰剂治疗的患者。一般来说,副作用包括嗜睡、头痛、腰痛、腹部胀满或上腹部不适,持续数小时但会自行消失。实验室检查结果显示治疗未引起显著变化。总体评估表明,所有接受较低剂量吡喹酮治疗的患者耐受性良好或优秀。在给予3×20毫克/千克剂量的患者中,12名患者中有1名耐受性优秀,9名良好,2名一般;而相应的安慰剂治疗组中,12名患者中有3名耐受性优秀,7名良好,2名一般。