NAFARELIN CONTROLLED RELEASE INJECTABLE - THEORETICAL CLINICAL PLASMA PROFILES FROM MULTIPLE DOSING AND FROM MIXTURES OF MICROSPHERES CONTAINING 2-PERCENT, 4-PERCENT AND 7-PERCENT NAFARELIN

被引:13
作者
BURNS, RA
VITALE, K
SANDERS, LM
机构
[1] Syntex Research, Palo Alto, CA, 94304
关键词
D O I
10.3109/02652049009021849
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Nafarelin controlled release injectable (CRI) releases a decapeptide drug for target one month therapy. Nafarelin, a luteinizing hormone releasing hormone agonistic analogue, is microencapsulated in biodegradable poly(lactide-co-glycolide) microspheres and given by intramuscular injection. Clinical data from a human single dose Phase I clinical study are modelled to develop theoretical multiple dose profiles and theoretical single dose profiles from mixtures of two or three formulations. Single dose injections of nafarelin CRI microspheres (4mg nafarelin) containing 2, 4, or 7 per cent nafarelin all achieve useful plasma drug levels throughout the target 30 day interval. Therapeutic suppression of testosterone levels was observed in all subjects participating in the phase I clinical study. Highest plasma nafarelin levels are achieved in the 0-10 and 20-35 day post-injection intervals. Theoretical multiple dosing profiles generated from the single dose clinical results show significant oscillations in plasma nafarelin levels depending on the particular dosing interval selected. Thirty or forty day dosing intervals yield significant variability in plasma nafarelin levels at steady state; 15 day dosing intervals show less variability. Therapeutic testosterone suppression was observed in the single dose study, so the nafarelin dose per injection can be reduced in multiple dosing therapies. Theoretical plasma nafarelin profiles from certain mixtures of 2 and 4 per cent nafarelin microspheres or 2 and 7 per cent nafarelin microspheres indicate that a 60 day product could be achieved. In general, all three formulations yield their lowest plasma drug levels during the 10-20 day post-injection interval. Therefore any mixture of these formulations will likewise exhibit low plasma drug levels during this interval. © 1990 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted.
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页码:397 / 413
页数:17
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