Switchability of neoral and equoral according to food and drug administration rules and regulations

被引:12
|
作者
Masri, MA [1 ]
Haberal, M
Rizvi, A
Stephan, A
Bilgin, N
Naqvi, A
Barbari, A
Kamel, G
Zafar, N
Emiroglu, R
Çolak, T
Manzoor, K
Matha, V
Kamarad, V
Rost, M
Rizk, S
Hazime, A
Perlik, F
机构
[1] Rizk Hosp, Beirut, Lebanon
[2] Baskent Univ, TR-06490 Ankara, Turkey
[3] SIUT, Karachi, Pakistan
[4] IVAX CZ, Prague, Czech Republic
[5] Charles Univ Prague, Prague, Czech Republic
[6] Rayak Hosp, Rayak, Lebanon
关键词
D O I
10.1016/j.transproceed.2005.07.055
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
According to the US Food and Drug Administration (FDA), if a drug product contains a drug substance that is chemically identical and is delivered to the site of action at the same rate and extent as another drug product, then it is equivalent and can be substituted (switchable) for that drug product. Methods used to define bioequivalence as stated by the FDA rules (FDA 21 CFR 320, 24) are (1) pharmacokinetic (PK) studies in healthy volunteers, (2) comparative clinical trials, and (3) pharmacodynamic (PD) studies (bioactivity). We evaluated the switch-ability of Equoral (IVAX-USA) with Neoral (Novartis Switzerland using all FDA rules. In a single oral dose, we undertook a comparative bioavailability study of Equoral (IVAX, USA) Neoral (Novartis, USA), and Neoral (Novartis UK). The pharmacokinetics of Equoral and Neoral were determined with blood levels at 0, 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 10, 12, 16, 24, 30, 36, 42, and 48 hours. The area under curve (AUC), AUC extrapolated to infinity (AUCO(-inf)), rate of absorption (T-max), extent of absorption (C-max), half time (t(1/2)) of Equoral and Neoral were all within the 90% confidence interval of 80% to 125% boundaries. A comparative multinational multicenter clinical trial in stable renal transplant patients included 70 patients (22 women and 48 men) of mean age of 33 years (range, 26 to 43) was performed in Turkey, Lebanon, and Pakistan. In this study the ratios of LSM and the 90% confidence intervals for the Nontransformed/Parameters (AUC(0-t), AUC(inf), T-max, and C-max) of Equoral and Neoral SGC were 98% and 95%, respectively, which are within the 80% to 125% FDA acceptance range. For immunosuppressive drugs, the site of action is the lymphocyte and the measurable response is the decrease in lymphocyte count caused by the relative concentration of the drug in the lymphocyte. In a controled switch, fixed-dose study, both Equoral and Neoral achieved the same concentration in the lymphocytes and caused the same degree of lymphocyte count reduction. The results of the testing (bioavailability-bioequivalence, clinical studies, and pharmacodynamic-bioactivity) required by FDA for interchangeability ("switchability") of inummosuppressive agents suggests that Neoral and Equoral are switchable.
引用
收藏
页码:2988 / 2993
页数:6
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