Stable isotope techniques in early drug development: An economic evaluation

被引:13
作者
Browne, TR
机构
[1] Boston Univ, Sch Med, Dept Neurol, Boston, MA 02118 USA
[2] Boston Univ, Sch Med, Dept Pharmacol, Boston, MA 02118 USA
[3] Boston Dept Vet Affairs Med Ctr, Neurol Serv, Boston, MA USA
关键词
D O I
10.1002/j.1552-4604.1998.tb04418.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Stable isotope labeled (SIL) drug methods are compared with standard methods for performing early (phases I and IIa) drug development studies (mass balance, bioavailability, single-dose volunteer and patient, multiple-dose volunteer and patient). Sn methods offer considerable reduction in the cost (>50%) and number of subjects (67%) required for bioavailability and multiple-dose patient studies. Moreover, a complete early drug development program is described for optimally combining SIL and standard studies, which can reduce cost by 23% and number of subjects by 36% compared with a program using standard methods. These reductions should result in development time savings of at least one year.
引用
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页码:213 / 220
页数:8
相关论文
共 33 条
[1]  
Abramson FP, 1996, DRUG METAB DISPOS, V24, P697
[2]   CRIMS - CHEMICAL-REACTION INTERFACE MASS-SPECTROMETRY [J].
ABRAMSON, FP .
MASS SPECTROMETRY REVIEWS, 1994, 13 (04) :341-356
[3]  
BJORGE SM, 1997, STABLE ISOTOPES PHAR, P233
[4]  
BROWN TR, 1997, STABLE ISOTOPES PHAR, P13
[5]  
Browne Thomas R., 1997, Neurology, V48, pA111
[6]   STUDIES WITH STABLE ISOTOPES .3. PHARMACOKINETICS OF TRACER DOSES OF DRUG [J].
BROWNE, TR ;
GREENBLATT, DJ ;
HARMATZ, JS ;
EVANS, JE ;
SZABO, GK ;
EVANS, BA ;
SCHUMACHER, GE .
JOURNAL OF CLINICAL PHARMACOLOGY, 1985, 25 (01) :59-63
[7]   STUDIES WITH STABLE ISOTOPES .1. CHANGES IN PHENYTOIN PHARMACOKINETICS AND BIOTRANSFORMATION DURING MONOTHERAPY [J].
BROWNE, TR ;
EVANS, JE ;
SZABO, GK ;
EVANS, BA ;
GREENBLATT, DJ ;
SCHUMACHER, GE .
JOURNAL OF CLINICAL PHARMACOLOGY, 1985, 25 (01) :43-50
[8]   PERFORMANCE OF HUMAN MASS BALANCE METABOLITE IDENTIFICATION STUDIES USING STABLE ISOTOPE (C-13, N-15) LABELING AND CONTINUOUS-FLOW ISOTOPE-RATIO MASS-SPECTROMETRY AS AN ALTERNATIVE TO RADIOACTIVE LABELING METHODS [J].
BROWNE, TR ;
SZABO, GK ;
AJAMI, A ;
WAGNER, D .
JOURNAL OF CLINICAL PHARMACOLOGY, 1993, 33 (03) :246-252
[9]   STUDIES WITH STABLE ISOTOPES .2. PHENOBARBITAL PHARMACOKINETICS DURING MONOTHERAPY [J].
BROWNE, TR ;
EVANS, JE ;
SZABO, GK ;
EVANS, BA ;
GREENBLATT, DJ .
JOURNAL OF CLINICAL PHARMACOLOGY, 1985, 25 (01) :51-58
[10]   STABLE ISOTOPES IN CLINICAL PHARMACOKINETIC INVESTIGATIONS - ADVANTAGES AND DISADVANTAGES [J].
BROWNE, TR .
CLINICAL PHARMACOKINETICS, 1990, 18 (06) :423-433