Pharmacokinetics and Safety of Single-Dose Esaxerenone in Japanese Subjects with Mild to Moderate Hepatic Impairment.

INTRODUCTION: The mineralocorticoid receptor (MR) blocker esaxerenone is a new treatment for hypertension in Japan and under development for treatment of diabetic nephropathy. Hepatic impairment is known to impact the pharmacokinetics (PKs) of other MR blocking drugs. The aim of the present study was to characterise the PKs and safety of a single oral dose of esaxerenone in Japanese subjects with mild-moderate hepatic impairment.
METHODS: In this open-label, parallel-group study, subjects with mild (Child-Pugh grade A) or moderate (grade B) hepatic impairment, and healthy controls with normal hepatic function matched by age and BMI (all groups n = 6), received a single 2.5-mg oral dose of esaxerenone. Plasma concentrations were measured by liquid chromatography-tandem mass spectrometry, and PK parameters were calculated using non-compartmental analysis.
RESULTS: Geometric least-squares mean (GLSM) ratios (90% confidence intervals [CIs]) for area under the plasma concentration-time curve (up to the last quantifiable time, up to infinity) in subjects with mild hepatic impairment versus normal hepatic function were 0.837 (0.637, 1.099) and 0.824 (0.622, 1.092), respectively. Corresponding values for moderate hepatic impairment versus normal hepatic function were 1.078 (0.820, 1.415) and 1.098 (0.829, 1.454). GLSM ratios (90% CIs) for peak plasma concentration (Cmax) were 0.959 (0.778, 1.182) for mild hepatic impairment versus normal hepatic function and 0.804 (0.653, 0.992) for moderate hepatic impairment versus normal hepatic function. Time to Cmax and clearance values were comparable between groups. The incidence of adverse events (AEs) was 16.7% in the moderate hepatic impairment and normal hepatic function groups. One serious AE (hepatic encephalopathy) occurred in one subject with moderate hepatic impairment.
CONCLUSIONS: Mild to moderate hepatic impairment had no clinically relevant effect on esaxerenone exposure. Esaxerenone dosage adjustment based on PKs is unlikely to be needed in patients with mild to moderate hepatic impairment. TRIAL REGISTRATION: JapicCTI-163339. FUNDING: Daiichi Sankyo Co., Ltd.

Key Summary Points

Introduction

Mineralocorticoid receptor (MR) blockers are used to treat hypertension and oedematous conditions such as heart failure and hepatic cirrhosis [1, 2]. Currently available MR agents include spironolactone and eplerenone, both of which improve prognoses in patients with heart failure [3-5]. However, use of these MR agents is limited by adverse events (AEs) such as hyperkalaemia [6, 7], suggesting a need for new treatment options.

Esaxerenone (CS-3150) is a novel, oral, non-steroidal MR blocker approved for the treatment of hypertension and currently in development for the treatment of diabetic nephropathy in Japan [8]. In a pharmacokinetic (PK) study in healthy Japanese subjects [9, 10], esaxerenone plasma concentrations were generally proportional to dose, with steady-state levels achieved at day 4 of once-daily dosing. The time (tmax) to peak plasma concentration (Cmax) of esaxerenone was approximately 2.5–3.5 h, and the half-life (t1/2) of esaxerenone was approximately 20 h. Phase 1 studies have shown that esaxerenone is suitable for daily dosing without safety and tolerability concerns [9, 10].

Optimal functioning of the liver is important for drug elimination, and chronic liver disease is linked to various factors that lower drug-metabolising activity [11]. Hepatic impairment reduces hepatic blood flow, leading to reduced plasma clearance of drugs and altered plasma protein binding, which in turn influences the PKs of drugs [12]. Portal systemic shunting, as seen in advanced hepatic impairment, can considerably increase drug exposure by reducing the first-pass effect [12]. Changes in metabolising enzyme activity can also influence drug clearance and cause PK variations when hepatic function is impaired [12].

Several studies have examined the effect of hepatic impairment on the PKs of existing MR blockers [13-15]. When a single oral 200-mg dose of spironolactone was administered to five patients with chronic liver disease, the mean t1/2 of the active metabolite canrenone was 59.4 h, which was about three times longer than the t1/2 in healthy adults [15]. In individuals with moderate hepatic impairment, the area under the plasma concentration–time curve (AUC0–24) for eplerenone at steady state was 42% higher than in healthy adults [14]. Therefore, the prescribing information for eplerenone advises caution in patients with mild or moderate hepatic impairment [16]. A previous study has shown that esaxerenone has good bioavailability (approximately 90%) [10] and is primarily excreted as metabolites into the urine and faeces [17]. The route of esaxerenone clearance is primarily via metabolism involving oxidation by cytochrome P450 (CYP) 3A4/3A5, glucuronidation by several isozymes of uridine diphosphate-glucuronosyltransferase (UGT), and hydrolysis [17]. On the basis of these data, it is important to evaluate the effect of hepatic impairment on esaxerenone clearance. Therefore, this study investigated the PKs and safety of a single oral 2.5-mg dose of esaxerenone in Japanese subjects with mild or moderate hepatic impairment.

Methods

Study Design and Treatments

This multicentre, single-arm, open-label, parallel-group study examined the effects of mild and moderate hepatic impairment on the PK profile of a single oral 2.5-mg dose of esaxerenone (2 × 1.25-mg tablets; Daiichi Sankyo Co., Ltd, Tokyo, Japan).

Eligible subjects were identified at a screening examination 2–30 days before esaxerenone administration. Subjects were admitted to hospital the day before esaxerenone administration and then remained at the study site for three additional days after dosing for a total of 5 days and 4 nights. Assessments were performed at admission, before esaxerenone administration, and after administration but before discharge. Esaxerenone was administered on the second day of hospitalisation. Subjects were required to fast for at least 10 h on the day of dosing, then consume a standard meal [18]. Thirty minutes after eating, each subject took a single oral dose of esaxerenone with 200 mL of water. No other beverages were permitted for 1 h before or 2 h after dosing. Caffeinated drinks were prohibited during hospitalisation, and subjects were only permitted food provided at a predetermined time and prepared at the study centre. Two subsequent assessments were performed, the first on day 5 at discharge, and the second 10–14 days after esaxerenone administration (post-study examination).

The study was conducted in accordance with Good Clinical Practice guidelines, as defined by the International Conference on Harmonisation, and ethical principles outlined in the Declaration of Helsinki. The study was registered with JAPIC Clinical Trials Information (http://www.clinicaltrials.jp; JapicCTI-163339). The study received institutional review board approvals from ETHIPRO, Montreal, QC, Canada (IORG0000689); the Clinical Trials Review Committee of Hakata Clinic (1464P3S-6); and the Clinical Trials Review Committee of Kurume Clinical Pharmacology Clinic (approved on 22 August 2016; reference number not stated). All subjects provided written informed consent before inclusion in the study.

Study Subjects

Japanese male and female subjects who met the following criteria were included in the study: age 20 years or more; body mass index (BMI) less than 30 kg/m2 at screening; ability of smokers to quit smoking during hospitalisation and at each study visit; and no confirmed pregnancy for female subjects. Subjects were classified into three groups based on hepatic function at the screening examination, as determined by aspartate transaminase (AST) and alanine transaminase (ALT) levels, and Child–Pugh classification [19]: normal hepatic function (AST and ALT less than two times the upper limit of normal [ULN]); mild hepatic impairment (Child–Pugh grade A [score 5–6]); or moderate hepatic impairment (Child–Pugh grade B [score 7–9]). Healthy adult subjects with normal hepatic function were matched by age and BMI to the patients with hepatic impairment.

Exclusion criteria included any subject who had undergone whole blood collection, plasmapheresis, or platelet apheresis after screening (except blood collection for retesting); who was breastfeeding; who could not take medically reliable contraception from the time of screening to 12 weeks after the last study visit; who had an estimated glomerular filtration rate (eGFR) less than 60 mL/min/1.73 m2 at admission; who had used or planned to use prohibited concomitant drugs; who had consumed grapefruit (juice or pulp) within 7 days before esaxerenone administration; who had any previous serious disease affecting thyroid, central nervous system, respiratory, blood/haematopoietic, gastrointestinal, pituitary, or adrenal function; who had laboratory values outside reference ranges (except for hepatic function) or clinically relevant symptoms; or who had an abnormal electrocardiogram on admission. Additional exclusion criteria for subjects with mild or moderate hepatic impairment included the presence of ascites that required invasive treatment, cholestatic liver disease, or any change in medication from admission to the post-study examination.

Subjects with normal hepatic function were prohibited from taking other drugs or supplements from 14 days before esaxerenone administration until completion of the post-study assessments. Subjects with mild or moderate hepatic impairment could not receive the following medications from 2 days before dosing until completion of the post-study assessments: K+-sparing diuretics, K+ preparations, insulin preparations, ion-exchange resins, and blood products. Additionally, drugs associated with inhibition or induction of CYP3A were contraindicated from 14 days before esaxerenone administration until after the post-study assessments. Other investigational drugs were prohibited from 120 days before dosing until completion of the post-study assessments.

PK Assessments

Full details of plasma esaxerenone concentration measurement have been described previously [9]. Blood samples were collected into a vacuum tube containing ethylenediaminetetraacetic acid dipotassium salt, before, and at 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 48, 72, and 120 h after esaxerenone administration. Drug concentrations were measured by liquid chromatography–tandem mass spectrometry (LC–MS/MS). Chromatographic separation was performed using a CAPCELL PAK C18 MGIII (Shiseido Co., Ltd.; Tokyo, Japan) column (2.0 × 150 mm, 5 μm). Detection was performed using an API 4000 (AB SCIEX, Framingham, Massachusetts, USA) tandem mass spectrometer with TurboIonSpray source by electrospray ionisation in the negative ion mode and multiple-reaction monitoring of esaxerenone (m/z 465–365) and its internal standard (m/z 472–370) as described previously [9]. For esaxerenone test samples of 0.3, 4.0, and 80.0 ng/mL, intra-study assay precision was 3.7%, 3.7%, and 3.5%, respectively. Accuracy of the assay ranged from 0.3% to 1.0%, with a lower limit of quantification of 0.1 ng/mL.

The primary endpoint of the study was esaxerenone PKs, based on plasma concentrations using a non-compartmental method: Cmax, AUC up to the last quantifiable time (AUClast), AUC up to infinity (AUCinf), tmax, t1/2, apparent volume of distribution based on the terminal phase (Vz/F), and apparent total body clearance (CL/F).

Phoenix® WinNonlin® (version 6.3, Certara USA Inc., Princeton, NJ, USA) was used for PK parameter calculation.

Safety Assessments

Safety assessments were performed at various time points throughout the study and included vital signs (blood pressure, pulse rate, and body temperature), laboratory tests, body weight, and electrocardiogram findings. AEs were categorised in accordance with the Medical Dictionary for Regulatory Activities (MedDRA/J Ver. 14.0) System Organ Class and Preferred Terms for the individual AEs. MedDRA® the Medical Dictionary for Regulatory Activities terminology is the international medical terminology developed under the auspices of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH).

Statistical Analyses

The planned sample size of 18 subjects, six in each subgroup, was based on guidance from the United States Food and Drug Administration [20] and the European Medicines Agency [21]. The PK analysis set comprised subjects who received a single dose of the study drug, who had no serious study protocol violation, and who had samples and measurements available for each assessment. The safety analysis set comprised subjects who received a single dose of the study drug.

Baseline values were defined as the last non-missing measurement (including repeated and unscheduled measurements) before the study drug dose, unless otherwise specified. To assess the effect of hepatic impairment (mild or moderate) versus normal hepatic function, an analysis of variance (ANOVA) was used with hepatic impairment as a fixed effect. Geometric least-squares mean (GLSM) ratio and 90% confidence interval (CI) values for AUCinf, AUClast, and Cmax were calculated. Scatter plots were created for CL/F with respect to hepatic function (Child–Pugh score and albumin concentration).

Statistical analysis was performed using SAS (version 9.2, SAS Institute, Cary, NC, USA).

Results

Subject Disposition

A total of 18 subjects were enrolled in the study, six in each group. Except for hepatic function, baseline characteristics did not differ significantly between the study groups (Table 1). All subjects enrolled in the mild or moderate hepatic impairment groups had liver cirrhosis caused by hepatitis virus infection, hepatic steatosis, or other conditions. All subjects completed the study and were included in the PK analysis and safety analysis sets.

Table 1

Baseline demographics and clinical characteristics

Parameters	Normal hepatic function (n = 6)	Hepatic impairment
		Mild (n = 6)	Moderate (n = 6)
Age, years	58.2 ± 7.8	56.0 ± 9.6	63.5 ± 7.4
Sex, male/female	4/2	5/1	5/1
Weight, kg	69.2 ± 2.7	69.5 ± 5.2	72.1 ± 11.4
Body mass index, kg/m2	25.6 ± 2.3	24.4 ± 2.0	27.4 ± 3.4
SBP, mmHg	122.8 ± 10.8	130.8 ± 8.2	115.8 ± 10.3
DBP, mmHg	71.0 ± 11.3	79.2 ± 10.1	73.0 ± 2.4
Albumin, g/L	40.9 ± 3.3	40.3 ± 2.2	37.4 ± 4.9
AST, U/L	16.5 ± 4.0	25.5 ± 6.9	30.7 ± 9.9
Below ULN, n (%)	6 (100.0)	4 (66.7)	4 (66.7)
ULN to < 2 × ULN, n (%)	0	2 (33.3)	2 (33.3)
≥ 2 × ULN, n (%)	0	0	0
ALT, U/L	16.7 ± 6.9	29.3 ± 18.8	25.7 ± 7.6
Below ULN, n (%)	5 (83.3)	3 (50.0)	6 (100.0)
ULN to < 2 × ULN, n (%)	1 (16.7)	3 (50.0)	0
≥ 2 × ULN, n (%)	0	0	0
Child–Pugh score, n (%)a
Grade A (score 5)	–	5 (83.3)	0
Grade A (score 6)	–	1 (16.7)	0
Grade B (score 7)	–	0	4 (66.7)
Grade B (score 8)	–	0	1 (16.7)
Grade B (score 9)	–	0	1 (16.7)
Encephalopathy grade, n (%)a
None	–	6 (100.0)	0
1 or 2	–	0	6 (100.0)
3 or 4	–	0	0

Values are means ± standard deviations, or numbers of subjects (%)

ALT alanine transaminase, AST aspartate transaminase, DBP diastolic blood pressure, SBP systolic blood pressure, ULN upper limit of normal

aEvaluated in subjects with mild and moderate hepatic impairment only

PKs

The time course of plasma esaxerenone concentrations is shown in Fig. 1a, b. The PK profile of esaxerenone did not differ across hepatic function groups; thus, PK parameters were relatively similar in subjects with different degrees of hepatic impairment (Table 2). Although mean Cmax values were similar in the mild hepatic impairment group (25.5 ng/mL) and normal hepatic function group (26.0 ng/mL), AUClast (514 vs 602 ng h/mL) and AUCinf (521 vs 620 ng h/mL) were lower in the mild hepatic impairment than normal hepatic function group. The value for mean Cmax was lower (21.2 vs 26.0 ng/mL) in the moderate hepatic impairment versus normal hepatic function group, whereas the mean value for AUClast was slightly greater (659 vs 602 ng h/mL), as was the mean value for AUCinf (692 vs 620 ng h/mL). No major differences were evident between the three hepatic function groups regarding tmax, t1/2 and Vz/F. Moreover, no trend was evident between the three study groups regarding differences in exposure to esaxerenone, and CL/F was similar between the three groups (Table 2).

Fig. 1

Plasma concentration–time profiles of esaxerenone in Japanese subjects with normal or impaired hepatic function: a linear plot; b semi-log plot. LLOQ lower limit of quantification, SD standard deviation

Table 2

Pharmacokinetic parameters for esaxerenone

Parameters	Normal hepatic function (n = 6)	Hepatic impairment
		Mild (n = 6)	Moderate (n = 6)
Cmax, ng/mL	26.0 ± 2.98	25.5 ± 7.03	21.2 ± 4.50
AUClast, ng h/mL	602 ± 127	514 ± 153	659 ± 178
AUCinf, ng h/mL	620 ± 141	521 ± 156	692 ± 195
tmax, h	4.00 (2.00, 6.00)	4.00 (1.50, 6.00)	3.50 (2.00, 8.00)
t1/2, h	22.0 ± 3.71	18.2 ± 1.57	24.7 ± 6.47
CL/F, L/h	4.19 ± 0.847	5.19 ± 1.55	3.90 ± 1.23
Vz/F, L	130 ± 12.7	135 ± 38.3	131 ± 18.9

Values are mean ± standard deviation, or median (minimum, maximum)

AUC area under the plasma concentration–time curve up to infinity, AUC area under the concentration–time curve up to the last quantifiable time, CL/F apparent total body clearance, C maximum plasma concentration, t terminal elimination half-life, t time to reach maximum plasma concentration, V/F apparent volume of distribution based on the terminal phase

The GLSM ratios for Cmax, AUClast, and AUCinf are shown in Table 3. For subjects with mild hepatic impairment versus normal hepatic function, the GLSM ratios (90% CI) for AUClast and AUCinf were 0.837 (0.637, 1.099) and 0.824 (0.622, 1.092), respectively, and 0.959 (0.778, 1.182) for Cmax. For subjects with moderate hepatic impairment versus normal hepatic function, GLSM ratios (90% CI) for AUClast and AUCinf were 1.078 (0.820, 1.415) and 1.098 (0.829, 1.454), respectively, and 0.804 (0.653, 0.992) for Cmax. CL/F values were distributed within a fixed range (approximately 3–7 L/h) in all groups and did not show any clear trends as Child–Pugh score increased (Fig. 2a) or as baseline albumin levels decreased (Fig. 2b).

Table 3

Ratios for esaxerenone pharmacokinetic parameters in subjects with hepatic impairment versus normal hepatic function

	Geometric least-squares mean		Ratio (hepatic impairment/normal)	90% CI
	Hepatic impairment	Normal function
Mild hepatic impairment
Cmax, ng/mL	24.785	25.842	0.959	0.778, 1.182
AUClast, ng h/mL	495.071	591.809	0.837	0.637, 1.099
AUCinf, ng h/mL	500.942	607.886	0.824	0.622, 1.092
Moderate hepatic impairment
Cmax, ng/mL	20.790	25.842	0.804	0.653, 0.992
AUClast, ng h/mL	637.698	591.809	1.078	0.820, 1.415
AUCinf, ng h/mL	667.411	607.886	1.098	0.829, 1.454

CI confidence interval, AUC area under the plasma concentration–time curve up to infinity, AUC area under the concentration–time curve up to the last quantifiable time, CI confidence interval, C maximum plasma concentration

Fig. 2

Scatter plots of a Child–Pugh score and b albumin at baseline versus apparent total body clearance of esaxerenone in Japanese subjects with normal or impaired hepatic function

Safety

Overall, two subjects experienced three AEs (Table 4). One patient with moderate hepatic impairment had severe hepatic encephalopathy, as judged by the investigator, 3 days after esaxerenone administration—this event was judged as a serious AE by the investigator—and mild headache; these events were considered possibly related to esaxerenone. The hepatic encephalopathy resolved after hospitalisation and pharmacological treatment, and the headache resolved after treatment. This subject had a history of hepatic encephalopathy and constipation; indeed, their blood ammonia level was high before and after administration, with 224 μg/dL 1 month before administration and 223 μg/dL after AE onset (normal range 30–80 μg/dL), and the subject had ongoing constipation. The subject underwent colonic hydrotherapy and their blood ammonia concentration decreased to 98 μg/dL 2 days after AE onset, and improvement of hepatic encephalopathy was observed. Therefore, the possibility that this event was worsened by constipation was considered. Esaxerenone PKs in this subject (Cmax 15.5 ng/mL, AUClast 783 ng h/mL) did not differ from that of other study subjects.

Table 4

Adverse events in subjects with varying degrees of hepatic function treated with a single dose of esaxerenone

Adverse events	Normal hepatic function (n = 6)	Hepatic impairment		Total (n = 18)
		Mild (n = 6)	Moderate (n = 6)
Any adverse event	1 (16.7)	0	1 (16.7)	2 (11.1)
Nervous system disorders	0	0	1 (16.7)	1 (5.6)
Headache	0	0	1 (16.7)	1 (5.6)
Hepatic encephalopathy	0	0	1 (16.7)	1 (5.6)
Laboratory test abnormalities	1 (16.7)	0	0	1 (5.6)
Aspartate transaminase increase	1 (16.7)	0	0	1 (5.6)

Values are number of subjects (%)

One subject with normal hepatic function had an increased AST level, considered by the investigator to be unrelated to esaxerenone. This change was transient and resolved without pharmacological treatment; at follow-up, the change was determined to have been owing to an altered living environment.

There were no deaths or discontinuations and no abnormal changes in vital signs, electrocardiogram, and other laboratory tests (including K+) during the study.

Discussion

This study evaluated the effect of hepatic impairment on esaxerenone PKs and safety after single-dose administration in Japanese subjects. The results indicate that esaxerenone PKs after a single 2.5-mg oral dose are not influenced by mild or moderate hepatic impairment. The scatter plot of Child–Pugh scores at baseline and esaxerenone CL/F values showed that the CL/F for each subject was distributed within a fixed range and that there was no clear trend of decreased clearance as Child–Pugh score increased, with considerable overlap between mean CL/F values in the different groups. When plasma albumin levels decrease owing to impaired hepatic function, the PKs of highly protein-bound drugs are affected [22]. Although esaxerenone has a high protein-binding rate (98.2–99.0%; unpublished data on file, Daiichi Sankyo, Tokyo, Japan), only two subjects with hepatic impairment had blood albumin levels below 35 g/L in our study, which may explain why no correlation was identified between blood albumin level and esaxerenone clearance (Fig. 2b). Thus, between-group differences in esaxerenone clearance indicate no consistent trend associated with the extent of hepatic impairment, and no clear influence of hepatic impairment on the PK profile of esaxerenone.

In a previous mass balance study of esaxerenone in healthy volunteers, excretion of unchanged esaxerenone in faeces and urine was 18.7% and 1.6%, respectively, of the administered dose (total excretion of radioactivity was 92.5% in faeces and urine); thus, clearance of esaxerenone was primarily via metabolism [17]. From the analysis of urinary and faecal metabolites after administration of radiolabelled esaxerenone to humans and from in vitro metabolic studies, esaxerenone metabolism is considered to involve oxidation by CYP3A4/3A5, glucuronidation by several isozymes of UGT, and hydrolysis [17]. Hepatic impairment reportedly influences various CYP enzymes, including CYP3A; however, UGT activity may be generally less susceptible to mild to moderate hepatic impairment than oxidation by CYP [12]. Because multiple pathways are involved in esaxerenone elimination, it seems likely that mild and moderate hepatic impairment will have only a minor influence on esaxerenone PKs.

The impact of hepatic function on the PKs of MR blockers was studied previously in patients receiving eplerenone [14]. Because the main route of eplerenone elimination is considered to be via CYP3A metabolism, non-Asian patients with moderate hepatic impairment who were receiving eplerenone had an AUC value approximately 1.4-fold higher than that in healthy adults [13], thus creating increased potential for AEs such as hyperkalaemia [6, 7]. In contrast, our study showed that esaxerenone AUC increased to a smaller extent by about 1.1-fold in moderate hepatic impairment versus normal hepatic function. Therefore, the PKs of esaxerenone are considered to be less affected by hepatic function than the PKs of eplerenone.

Esaxerenone was generally well tolerated in the current study, in agreement with existing data from two other phase 1 studies [9, 10]. A previous, multiple-dose study of esaxerenone safety in healthy Japanese men reported that all AEs were mild or moderate: two resolved with treatment and the others resolved without treatment [9].

Hyperkalaemia is a well-recognised AE of MR blockers, especially in patients with diabetes or kidney dysfunction. In a repeated-dose study of 10–100 mg esaxerenone for 10 days [9], serum K+ concentration increased with esaxerenone dosage. However, in our trial, no clinically significant changes in K+-related laboratory test values were found, and only one AST increase was observed in one subject. As our study was a small, single-dose study, we were unable to quantify the potential risk of hyperkalaemia in esaxerenone-treated patients with more advanced hepatic failure, such as liver cirrhosis complicated with ascites. A case of serious hepatic encephalopathy developed in the moderate hepatic impairment group in our study, but because blood ammonia concentration in this subject was high before esaxerenone administration, it is very likely that this event was due to chronic constipation; indeed, the event resolved with treatment and was considered unrelated to the overall safety profile of esaxerenone.

The limitations of this study include that it only investigated PK after a single esaxerenone dose and did not include a multiple-dose arm. Furthermore, the study sample size was only six subjects per group, which is the minimum required by FDA and EMA guidance [20, 21], and the study did not evaluate patients with severe hepatic impairment.

Conclusions

The current findings indicate that mild or moderate hepatic impairment has no clinically relevant effect on esaxerenone PKs and that dose adjustment is considered unnecessary from the PK viewpoint.

Why carry out this study?

Safety concerns related to increased exposure to eplerenone, a mineralocorticoid receptor (MR) blocker used to treat hypertension and heart failure, have been identified in patients with mild to severe hepatic impairment, which has led to advised caution or limitation of its use in these patients.

Esaxerenone, a novel non-steroidal MR blocker, has a favourable pharmacokinetic (PK) profile for daily oral treatment in healthy subjects.

This study aimed to examine the PK and safety profile of a single oral dose of esaxerenone in Japanese subjects with mild to moderate hepatic impairment.

What was learned from the study?

Mild to moderate hepatic impairment did not have any clinically relevant effect on esaxerenone exposure and the drug was safe in this subject population.

Esaxerenone can be administered at unadjusted dosages to subjects with mild to moderate hepatic impairment.

Because of this, side effects observed with other drugs in this class of MR blockers can likely be avoided during treatment.