Pharmacokinetics and pharmacodynamics of liposomal mifamurtide in adult volunteers with mild or moderate hepatic impairment

被引:20
|
作者
Venkatakrishnan, Karthik [1 ]
Liu, Yi [2 ]
Noe, Dennis [1 ]
Mertz, Jaime [1 ]
Bargfrede, Michael [1 ]
Marbury, Thomas [3 ]
Farbakhsh, Kambiz [4 ]
Oliva, Cristina [5 ]
Milton, Ashley [1 ]
机构
[1] Takeda Pharmaceut Int Co, Clin Pharmacol, Cambridge, MA 02139 USA
[2] Takeda Pharmaceut Int Co, Biostat, Cambridge, MA 02139 USA
[3] Orlando Clin Res Ctr, Orlando, FL USA
[4] DaVita Clin Res, Minneapolis, MN USA
[5] Takeda Global Res & Dev Europe, Clin Res, London, England
关键词
hepatic impairment; liposomes; MEPACT (R); mifamurtide; pharmacodynamics; pharmacokinetics; MURAMYL TRIPEPTIDE PHOSPHATIDYLETHANOLAMINE; NF-KAPPA-B; L-MTP-PE; TUMORICIDAL PROPERTIES; CANCER-PATIENTS; PHASE-I; OSTEOSARCOMA; MONOCYTES; ACTIVATION; CHEMOTHERAPY;
D O I
10.1111/bcp.12261
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aims To evaluate the pharmacokinetics and pharmacodynamics after a single dose of liposomal mifamurtide (liposomal muramyl tripeptide phospatidyl ethanolamine; MEPACT (R)) in adult subjects with mild (Child-Pugh Class A) or moderate (Child-Pugh Class B) hepatic impairment in comparison with age-, weight- and sex-matched healthy subjects with normal hepatic function. Methods Subjects received a 4mg dose of liposomal mifamurtide via 1h intravenous infusion. Blood samples were collected over 72h for pharmacokinetic and pharmacodynamic assessments (changes in serum interleukin-6, tumour necrosis factor- and C-reactive protein). Results Thirty-seven subjects were enrolled: nine with mild hepatic impairment, eight with moderate hepatic impairment and 20 matched healthy subjects. Geometric least-square mean ratios of total mifamurtide AUCinf for the mild hepatic impairment and moderate hepatic impairment groups vs. matched healthy subjects were 105% (90% confidence interval, 83.6-132%) and 119% (90% confidence interval, 94.1-151%), respectively, which are below the protocol-specified threshold (150%) to require development of dose-modification recommendations. Pharmacodynamic parameters for changes in serum interleukin-6 and tumour necrosis factor- concentrations were generally similar across hepatic function groups. Mifamurtide-induced increases in serum C-reactive protein were attenuated in the moderate hepatic impairment group, consistent with the liver being the major organ of C-reactive protein synthesis. No grade 3 adverse events were seen in subjects administered mifamurtide (4mg). Conclusions These results support the conclusion that mild or moderate hepatic impairment does not produce clinically meaningful effects on the clinical pharmacokinetics or pharmacodynamics of mifamurtide; no dose modifications are needed in these special patient populations based on clinical pharmacological considerations.
引用
收藏
页码:998 / 1010
页数:13
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