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作 者:张翼飞[1] 杜鹏飞[1] 徐敏[1] 张毅[1] 张连珍[1] 王卫庆[1] 赵咏桔[1] 宁光[1]
机构地区:[1]上海第二医科大学附属瑞金医院内分泌科,上海市内分泌代谢病临床医学中心,上海200025
出 处:《中国新药与临床杂志》2005年第5期373-375,共3页Chinese Journal of New Drugs and Clinical Remedies
摘 要:目的:评价重组人生长激素(rhGH)注射液(2种规格:T1和T2)与注射用rhGH冻干粉针剂(参比制剂,R)的人体生物等效性。方法:运用随机、单盲、三阶段交叉方法分别对24名健康男性志愿者单次皮下注射0.2IU·kg-1的R,T1和T2。测定不同时间点生长激素血药浓度,并进行相关药动学参数分析。结果:T1,T2的AUC0~24的90%置信区间分别落在R的103.4%~116.5%和105.7%~119.6%范围内,T1的AUC0~24的90%置信区间落在T2的91.9%~103.7%范围内;T1和T2的cmax的90%置信区间分别落在R的91.9%~114.0%和103.7%~127.2%范围内,T1的cmax的90%置信区间亦落在T2的81.6%~97.4%的范围内。tmax在R及T1,T2间无统计学差异(P>0.05)。结论:T1,T2与R具有生物等效性。AIM: To evaluate the bioequivalence between recombinant human growth hormone (rhGH) injection(2 standard: T1 and T2)and rhGH for injection(R). METHODS: The study drugs were tested in a randomized, single-blind and three-period crossover study in 24 healthy males. The three drugs were administered by subcutaneous injection at a single dose of 0.2 IU·kg^(-1) per body weight. The venous blood samples were collected at different time points to test the serum concentrations of growth hormone(GH). RESULTS:The 90 % confidence intervals(CI) of T1,T2 AUC_(0-24) between three products were as follows: 103.4 %-116.5 % and 105.7 %-119.6 %, that of T1 AUC_(0-24) was 91.9 %-103.7 % of T2 extent. The CIs of T1,T2 c_(max) between three products were as follows: 91.9 %-114.0 % and 103.7 %-127.2 %, and CI of T1 c_(max) was in 81.6 %-97.4 % of the T2 extent. There was no significant difference of t_(max) between all the three products statistically (P>0.05). CONCLUSION:There is bioequivalent between rhGH for reconstitution and two liquid formulations of rhGH.
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