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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
来源:
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.
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页码:213 / 220
页数:8
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