Effect of Food on the Pharmacokinetics of 2 Formulations of DRL-17822, a Novel Selective Cholesteryl Ester Transfer Protein (CETP) Inhibitor, in Healthy Males

被引:2
作者
Kruithof, Annelieke C. [1 ]
Kumar, Rajinder [2 ]
Stevens, Jasper [1 ]
de Kam, Marieke L. [1 ]
Gautam, Anirudh [3 ]
Alikunju, Shanavas [2 ]
Padhi, Bijay K. [2 ]
Kulkarni, Swati [2 ]
Raghuvanshi, Rajeev S. [2 ]
Gandhi, Rajesh [2 ]
Burggraaf, Jacobus [1 ]
Kamerling, Ingrid M. C. [1 ]
机构
[1] Ctr Human Drug Res, Zernikedreef 8, NL-2333 CL Leiden, Netherlands
[2] Dr Reddys Labs Ltd, Hyderabad, India
[3] Dr Reddys Labs SA, Basel, Switzerland
关键词
amorphous solid dispersion formulation; cholesteryl ester transfer protein (CETP) inhibition; DRL-17822; food effect; nanocrystal formulation; pharmacokinetics; CORONARY-HEART-DISEASE; HIGH-RISK; DENSITY-LIPOPROTEIN; SAFETY; PHARMACODYNAMICS; TOLERABILITY; EVACETRAPIB; STATINS; TRIALS;
D O I
10.1002/cpdd.707
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
DRL-17822 is a novel selective cholesteryl ester transfer protein inhibitor that showed an increased exposure, including an increase of >20-fold of maximum concentration and area under the plasma concentration-time curve from time zero to the time of the last quantifiable concentration, following a high-fat breakfast using a nanocrystal formulation. To reduce this effect of food, we generated an amorphous solid dispersion formulation. In this study, we compared the food effect of both formulations of DRL-17822 in a 2-part randomized, open-label, 4-way crossover study involving healthy adult males 18-45 years of age. In both parts of the study, 12 subjects received both formulations of DRL-17822 in both the fasted and fed states; a low-fat breakfast was provided in the first part and a high-fat breakfast in the second part. Compared to the nanocrystal formulation, the amorphous solid dispersion formulation substantially increased DRL-17822 exposure in the fasted state, including increased maximum concentration, area under the plasma concentration-time curve from time zero to the time of the last quantifiable concentration, and area under plasma concentration-time curve from time zero to infinity. Following a high-fat breakfast, DRL-17822 exposure was increased to a lesser extent in the amorphous solid dispersion formulation compared to the nanocrystal formulation (P < .001). Moreover, compared to the nanocrystal formulation the amorphous solid dispersion formulation caused a more pronounced increase in high-density lipoprotein in the fasted state. Consuming breakfast increased the effect of DRL-17822 on high-density lipoprotein. Taken together, our results indicate that by improving its formulation, DRL-17822 has a favorable exposure profile and therefore a more predictable food effect profile.
引用
收藏
页码:1042 / 1052
页数:11
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