Pharmacokinetics and safety of sacubitril/valsartan (LCZ696) in patients with mild and moderate hepatic impairment
Kenneth M. Kulmatycki1, Thomas Langenickel2, Wai Hong Ng3, Parasar Pal4, Wei Zhou3, Tsu-Han Lin3, Iris Rajman2, Priyamvada Chandra3, Gangadhar Sunkara3
1 Novartis Institutes for Biomedical Research, Cambridge, MA, USA, 2 Novartis Institutes for BioMedical Research, Basel, Switzerland,
3 Novartis Institutes for Biomedical Research, East Hanover, NJ, USA, and
4 Novartis Healthcare Pvt. Ltd., Hyderabad, Telangana, India
DOI 10.5414/CP202988
Abstract
Objectives: To assess the protein binding and pharmacokinetics of sacubitril/valsartan analytes (sacubitril, sacubitrilat, and valsartan) in an open-label, single oral dose (200 mg), parallel-group study in patients with mild and moderate hepatic impairment (Child-Pugh class A and B) and matched healthy subjects. Methods: This study enrolled 32 subjects (n = 8 in each hepatic impairment and matched healthy subjects groups). Blood samples were collected at pre-determined time points to assess pharmacokinetics of sacubitril, sacubitrilat, and valsartan. Subjects with severe hepatic impairment were excluded as valsartan exposure is expected to be substantially increased in these patients. Results: Sacubitril exposure (AUC) increased by 53% and 245% while the exposure to sacubitrilat was increased by 48% and 90% in patients with mild and moderate hepatic impairment, respectively. Sacubitril Cmax increased by 57% and 210% in mild and moderate hepatic impairment; however, for both sacubitrilat and valsartan, Cmax was unchanged. Valsartan AUC increased in patients with mild and moderate hepatic impairment by 19 – 109%, respectively. Conclusions: The increase in systemic exposures to all sacubitril/valsartan analytes correlated with the severity of liver disease. The plasma unbound fraction of sacubitrilat in patients with moderate hepatic impairment was slightly higher than in matched healthy subjects. This difference was not considered clinically significant. Safety assessments showed that sacubitril/valsartan was safe and well tolerated across all the study groups.
Author Details
Authors
Departments
- 1 Novartis Institutes for Biomedical Research, Cambridge, MA, USA,
- 2 Novartis Institutes for BioMedical Research, Basel, Switzerland,
- 3 Novartis Institutes for Biomedical Research, East Hanover, NJ, USA, and
- 4 Novartis Healthcare Pvt. Ltd., Hyderabad, Telangana, India
Address
Kenneth M. Kulmatycki, PhD
Novartis Institutes for Biomedical Research
220 Massachusetts Avenue, 342E
Cambridge, MA 02139, USA
Email:
[email protected]
Citation
Kenneth M. Kulmatycki, Thomas Langenickel, Wai Hong Ng, Parasar Pal, Wei Zhou, Tsu-Han Lin, Iris Rajman, Priyamvada Chandra, and Gangadhar Sunkara. Pharmacokinetics and safety of sacubitril/valsartan (LCZ696) in patients with mild and moderate hepatic impairment
. 2017; 55: 728-739. doi: 10.5414/CP202988.