Pharmacokinetics and Safety of Amenamevir in Healthy Subjects: Analysis of Four Randomized Phase 1 Studies.

INTRODUCTION: Amenamevir (ASP2151) is a nonnucleoside antiherpesvirus compound available for the treatment of varicella-zoster virus infections. In this article we summarize the findings of four phase 1 studies in healthy participants.
METHODS: Four randomized phase 1 studies investigated the safety and pharmacokinetics of single and multiple doses of amenamevir, including the assessment of age group effect (nonelderly vs elderly), food effect, and the relative bioavailability of two formulations. Amenamevir was administered orally at various doses as a single dose (5-2400 mg) or daily (300 or 600 mg/day) for 7 days.
RESULTS: Following single and multiple oral doses, amenamevir demonstrated a less than dose proportional increase in the pharmacokinetic parameters area under the plasma drug concentration versus time curve from time zero to infinity (AUCinf) and C max. After single and multiple oral 300-mg doses of amenamevir, no apparent differences in pharmacokinetics were observed between nonelderly and elderly participants. In contrast, with the amenamevir 600-mg dose both the area under the plasma drug concentration versus time curve from time zero to 24 h and C max were slightly increased and renal clearance was decreased in elderly participants. The pharmacokinetics of amenamevir was affected by food, with AUCinf increased by about 90%. In the bioavailability study, AUCinf and C max were slightly lower following tablet versus capsule administration (decreased by 14 and 12%, respectively), with relative bioavailability of 86%. The different amenamevir doses and formulations were safe and well tolerated; no deaths or serious adverse events were reported.
CONCLUSION: Amenamevir had less than dose proportional pharmacokinetic characteristics. Age may have an influence on amenamevir pharmacokinetics; however, the effect was considered minimal. The pharmacokinetics of amenamevir were affected by food, with AUCinf almost doubling when amenamevir was administered with food. The concentration versus time profile of the tablet was slightly lower than that of the capsule; the relative bioavailability of the tablet versus the capsule was 86%. Amenamevir was safe and well tolerated in the dose range investigated. FUNDING: Astellas Pharma. TRIAL REGISTRATION: ClinicalTrials.gov identifiers NCT02852876 (15L-CL-002) and NCT02796118 (15L-CL-003).

RCT Entities:   Population Interventions Outcomes

Introduction

Herpes zoster, or shingles, is the painful eruption of a rash caused by the varicella–zoster virus (VZV). Herpes zoster is more common in elderly people, patients with lymphoma, patients receiving chemotherapy or steroids, and people with HIV [1]. Antiviral therapy for herpes zoster is recommended in certain immunocompetent patients and all immunocompromised patients [2]. Nucleoside analogues such as acyclovir, valacyclovir, and famciclovir have been approved for the treatment of herpes simplex virus (HSV)-1, HSV-2, and VZV infections [3-5]. These drugs have the same mechanism of action and are widely used for the treatment of herpes zoster and herpes simplex.

Acyclovir-resistant virus has been isolated from patients with HSV. Acyclovir resistance is mediated by mutations in the thymidine kinase gene [6, 7] or the DNA polymerase gene [8]. Consequently, in clinical HSV isolates, resistance to acyclovir has been shown to be regularly linked to cross-resistance against penciclovir, whose prodrug is famciclovir [9-11]. Although acyclovir resistance of VZV is virtually unobserved in immunocompetent patients, it can be a major problem among immunosuppressed hosts, mainly those who have received prolonged acyclovir therapy [12-15].

A drug with a new mechanism of action with a lack of cross-resistance to current nucleoside analogues is desired. Amenamevir (ASP2151) is a nonnucleoside antiherpesvirus compound available for the treatment of VZV infections. Amenamevir targets the herpesvirus helicase-primase complex. This viral enzyme complex is the target for the next generation of antiherpes drugs [16, 17], as the helicase-primase complex of human Alphaherpesvirinae viruses is known to be essential for viral DNA replication and, hence, viral replication [16-20].

Preclinical pharmacology studies of amenamevir have demonstrated that amenamevir inhibits the replication of acyclovir-resistant strains of HSV-1, HSV-2, and VZV, with half-maximal effective concentrations similar to those exhibited against acyclovir-sensitive strains [21]. Initial pharmacokinetic results from two phase 1 studies (studies 15L-CL-002 and 15L-CL-003) have shown that amenamevir exhibits less than dose proportional pharmacokinetics after single and multiple doses [22]. Here we summarize the findings of four phase 1 studies (including further data from studies 15L-CL-002 and 15L-CL-003) to evaluate the safety and pharmacokinetics of single and multiple doses of amenamevir, including the assessment of age effect (nonelderly vs elderly), food effect, and the relative bioavailability of two formulations (capsule vs tablet).

Methods

Study Design, Participants, and Dosing

The designs of the four phase 1 studies in healthy participants are included in the supplementary material (Table S1). The first study was a randomized, double-blind, placebo-controlled, dose-escalation study conducted in Japan (study 15L-CL-001). Sequential cohorts of healthy male participants (aged 20–44 years) were randomized to receive a single capsule dose of amenamevir or placebo under fasting conditions. The doses of amenamevir were 5, 25, 100, 300, or 600 mg. This study was not registered at a registry website as there was no requirement in the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) “Guideline for Good Clinical Practice” to register phase 1 trials at the time it was conducted.

The second study, conducted in France (15L-CL-002; ClinicalTrials.gov identifier NCT02852876) in healthy male participants (aged 18–55 years), had two parts. Part 1 was a randomized, double-blind, placebo-controlled, single dose escalation study that evaluated the safety, tolerability, and pharmacokinetics of amenamevir 5-, 25-, 100-, 300-, 600-, 1200-, 1800-, and 2400-mg capsules under fasting conditions. Part 2 was an open-label crossover study that evaluated the effect of food on the safety, tolerability, and pharmacokinetics of a single capsule dose of 300 mg amenamevir.

The third study was a randomized, double-blind, placebo-controlled, multiple ascending dose study conducted in Japan (15L-CL-003; ClinicalTrials.gov identifier NCT02796118). Healthy male nonelderly (aged 20–44 years) and elderly (aged 65–79 years) participants were randomized to receive amenamevir capsule, 300 mg/day, or placebo capsules, or amenamevir capsule, 600 mg/day, or placebo capsules, all administered under fed conditions for 7 days. The safety and pharmacokinetics of amenamevir were assessed over a 7-day period.

The final study was a randomized, open-label, three-period crossover study conducted in the USA (15L-CL-006). Healthy male and female participants received a single capsule dose of 800 mg amenamevir under fasting conditions, a single tablet dose of 800 mg amenamevir under fasting conditions, and a single tablet dose of 800 mg amenamevir under fed conditions. Each participant underwent a 6-day washout between each period. The safety and pharmacokinetics of amenamevir were evaluated, including the relative bioavailability of amenamevir capsule and tablet formulations and the effect of food with the tablet formulation. This study was not registered at a registry website as there was no requirement in the ICH “Guideline for Good Clinical Practice” to register phase 1 trials at the time it was conducted.

The study protocols were approved by the institutional review boards at each study site (15L-CL-001 and 15L-CL-003 by OPHAC Hospital Institutional Review Board, Osaka, Japan; 15L-CL-002 by Comité Consultatif de Protection des Personnes dans la Recherche Biomédicale, Hôpital Rovert Ballanger—Centre Daniel Eisenmann, Aulnay-sous-Bois, France; 15L-CL-006 by Independent Investigational Review Board, Plantation, FL, USA), and the studies were conducted in accordance with the ethical standards of the ICH “Guideline for Good Clinical Practice.” All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1964, as revised in 2000. Written informed consent was obtained from all participants for their being included in these studies.

Pharmacokinetic Assessments

For all four studies, plasma and urine drug concentrations were determined by validated liquid chromatography–tandem mass spectrometry methods [22], and plasma drug concentration–time data were used to calculate the following pharmacokinetic parameters of amenamevir: peak drug concentration (C max), half-life (t ½), time to peak drug concentration (t max), and apparent oral clearance. For studies 15L-CL-001, 15L-CL-002, and 15L-CL-006, these parameters were all calculated after a single dose of amenamevir. For study 15L-CL-003, these parameters were assessed on days 1 and 7. The area under the plasma drug concentration versus time curve from time zero to infinity (AUCinf) was also assessed in studies 15L-CL-001, 15L-CL-002, and 15L-CL-006, and the time that the amenamevir drug concentration was above 200 ng/mL (t 200) and the area under the plasma drug concentration versus time curve from time zero to 24 h (AUC24) were also assessed in study 15L-CL-003. Urine pharmacokinetics, including the cumulative amount of the unchanged drug excreted into the urine at 24 h, the percentage of drug excreted in urine, and renal clearance were assessed in studies 15L-CL-003 and 15L-CL-006.

For study 15L-CL-001, fasting participants received amenamevir with 200 mL of water in the morning. Participants continued to refrain from having any food and drink until 4 h after dosing. Serial blood samples for amenamevir were collected before the dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 36, and 48 h after the dose.

For part 1 of study 15L-CL-002, fasting participants received amenamevir with 240 mL of water in the morning. Participants continued to refrain from having any food and drink until 4 h after dosing. For part 2 of study 15L-CL-002, amenamevir was administered either 30 min after an FDA high-fat breakfast or under the same fasting conditions as in part 1 of the study. Serial blood samples for amenamevir were collected before the dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 5, 6, 7, 8, 10, 12, 16, 24, 36, and 48 h after the dose.

For study 15L-CL-003, participants received amenamevir with 200 mL of water within 30 min after breakfast. Participants refrained from having any food and drink until 4 h after dosing. Serial blood samples for amenamevir were collected before the dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, and 12 h after the dose on day 1, before the dose on day 2 to day 6, and before the dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 36, and 48 h after the dose on day 7. Urine samples for assessment of cumulative urinary excretion of amenamevir were collected at the following intervals: before the dose and 0–4 h, 4–8 h, 8–12 h, and 12–24 h after the dose on day 1 and before the dose and 0–4 h, 4–8 h, 8–12 h, 12–24 h, 24–36 h, and 36–48 h after the dose on day 7.

For study 15L-CL-006, participants who received their dose under fasting conditions received amenamevir with 240 mL of water. Participants continued to refrain from having any food and drink until 4 h after dosing. In participants who received their dose under fed conditions, amenamevir was administered 30 min after an FDA high-fat breakfast. Serial blood samples for amenamevir were collected before the dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 16, 24, 36, and 48 h after the dose. Urine samples for assessment of cumulative urinary excretion of amenamevir were collected at the following intervals: before the dose and 0–4 h, 4–8 h, 8–12 h, 12–24 h, 24–36 h, and 36–48 h after the dose.

Safety Assessment

In all four studies, safety was evaluated by our assessing treatment emergent adverse events, 12-lead electrocardiogram (ECG) recordings, clinical laboratory parameters (biochemistry, hematology, serology, and urinalysis), vital signs (blood pressure and pulse), and physical examination findings.

Statistical Analysis

Pharmacokinetic calculations were performed with actual sampling times by noncompartmental methods with use of WinNonlin® Professional version 5.0 or higher (Pharsight, Mountain View, CA, USA) or SAS® version 8.2 or higher (SAS Institute, Cary, NC, USA). In all four studies, descriptive statistics included the number of participants reflected in the calculation (n), arithmetic mean, standard deviation, median, minimum, and maximum for continuous variables, and frequency and percentage for categorical end points.

For part 2 of study 15L-CL-002, the effect of food on the pharmacokinetics of the amenamevir capsule was assessed with the two one-sided t test procedure. A mixed effects model with treatment, sequence, and period as fixed effects and participant as a random effect was used. The same two one-sided t test procedure was used in study 15L-CL-003 to assess the effect of age on the pharmacokinetics of the amenamevir capsule and in study 15L-CL-006 to assess the relative bioavailability of the tablet and capsule formulations of amenamevir as well as the effect of food on the pharmacokinetics of amenamevir tablets. For study 15L-CL-003, a fixed effects model was used with age as an effect. For study 15L-CL-006, a mixed effects model with treatment, sequence, period, and sex as fixed effects and participant as a random effect was used. For all analyses within each model, the geometric least squares mean ratios (fed/fasting for assessing food effect; tablet/capsule for assessing relative bioavailability; elderly/nonelderly for assessing an age group effect) and their corresponding 90% confidence intervals for plasma AUCinf and C max were obtained.

Results

Participants

The baseline characteristics and demographics of the participants included in each study are reported in Table 1. The participants enrolled in the four studies were generally comparable, with the exception that study 15L-CL-006 enrolled both male and female participants and study 15L-CL-003 included elderly participants and that studies 15L-CL-001 and 15L-CL-003 enrolled Japanese participants whereas studies 15L-CL-002 and 15L-CL-006 had mainly White participants. The flow of participants through each study is shown in Figs S1, S2, S3, and S4.

Table 1

Baseline characteristics

	Study
	15L-CL-001 (n = 40)	15L-CL-002 part 1 (n = 64)	15L-CL-002 part 2 (n = 8)	15L-CL-003 nonelderly (n = 18)	15L-CL-003 elderly (n = 18)	15L-CL-006 (n = 24)
Age (years)	23.3 ± 2.2	33.1 ± 9.2	33.9 ± 9.5	23.3 ± 4.8	69.8 ± 3.5	40.0 ± 10.7
Male	40 (100%)	64 (100%)	8 (100%)	18 (100%)	18 (100%)	12 (50%)
Race
White	0	44 (68.8%)	7 (87.5%)	0	0	21 (87.5%)
Black or African American	0	15 (23.4%)	0	0	0	3 (12.5%)
Asian	40 (100%)	2 (3.1%)	0	18 (100%)	18 (100%)	0
Other	0	3 (4.7%)	1 (12.5%)	0	0	0
Weight (kg)	62.6 ± 8.0	74.9 ± 8.1	76.0 ± 12.7	61.1 ± 6.7	63.3 ± 7.7	71.1 ± 11.6
Height (m)	1.73 ± 0.06	1.77 ± 0.06	1.78 ± 0.05	1.74 ± 0.05	1.65 ± 0.06	1.66 ± 0.11
BMI (kg/m2)	20.8 ± 1.9	24.0 ± 2.2	23.9 ± 2.7	20.2 ± 1.9	23.2 ± 1.9	25.6 ± 2.5

All values are presented as the mean ± standard deviation unless otherwise stated

BMI body mass index

Pharmacokinetics

The mean concentration versus time curves following a single administration of amenamevir capsule by dose cohort in participants enrolled in study 15L-CL-001 and part 1 of study 15L-CL-002 are shown in Fig. 1. Furthermore, the pharmacokinetic parameter estimates for single-dose capsule administration of amenamevir in study 15L-CL-001 are presented in Table 2. These studies show that the mean AUCinf and C max increased in a less than dose proportional way, whereas the median t max and mean t ½ were similar for each dose.

Fig. 1

Mean plasma concentration versus time profile of amenamevir in a study 15L-CL-001 and b part 1 of study 15L-CL-002 after a single capsule dose of amenamevir at 5 mg (open circles), 25 mg (closed circles), 100 mg (open triangles), 300 mg (closed triangles), 600 mg (open squares), 1200 mg (closed squares), 1800 mg (open diamonds), and 2400 mg (closed diamonds)

Table 2

Summary of amenamevir plasma pharmacokinetics after a single dose

Study	Amenamevir dose (mg)	No.	AUCinf (ng h/mL)	C max (ng/mL)	t max (h)a	t ½ (h)	CL/F (L/h)
15L-CL-001	5	6	474 ± 113	42.9 ± 3.99	1.75 (1.00–3.00)	7.75 ± 1.58	11.1 ± 2.88
	25	6	1980 ± 303	177 ± 21.9	2.50 (1.00–4.00)	7.42 ± 0.59	12.9 ± 2.04
	100	6	5870 ± 1670	526 ± 76.9	2.00 (1.00–3.00)	7.09 ± 1.40	18.4 ± 5.71
	300	6	11,700 ± 1920	1040 ± 264	3.00 (2.00–4.00)	6.88 ± 0.56	26.2 ± 4.49
	600	6	18,700 ± 2960	1680 ± 218	3.00 (2.00–4.00)	6.86 ± 0.62	32.7 ± 4.78
	Dose proportionalityb	–	0.766 (0.718–0.814)	0.759 (0.720–0.799)	–	–	–
15-CL-002 part 1	Dose proportionalityb	–	0.750 (0.714–0.785)	0.773 (0.740–0.806)	–	–	–
15-CL-002 part 2	300 (fasting)	8	11,200 ± 3420	937 ± 389	2.00 (1.5–5.0)	8.20 ± 1.79	29.2 ± 9.8
	300 (fed)	8	20,700 ± 4130	1580 ± 257	5.00 (3.0–5.0)	8.45 ± 1.25	15.0 ± 2.8
	GMRc	–	1.90 (1.55–2.32)	1.82 (1.34–2.48)	–	–	–

All values are presented as the mean ± standard deviation unless otherwise stated

AUC area under the plasma concentration versus time curve from time zero to infinity, CL/F apparent oral clearance, C peak drug concentration, GMR geometric least squares mean ratio (fed/fasting), t terminal half-life, t time to peak drug concentration

aThe median is presented (with the range in parentheses)

bPower model assessment of dose proportionality. The values presented are the slope (with the 95% confidence interval in parentheses)

cFor the fed/fasting condition (with the 90% confidence interval in parentheses)

The geometric least squares mean ratios of elderly to nonelderly participants for C max and AUC24 in study 15L-CL-003 are presented in Table 3. In participants receiving the amenamevir 300-mg dose, there were no consistent differences in the amenamevir pharmacokinetics between nonelderly and elderly participants. After a single 300-mg dose of amenamevir, elderly participants had a slight increase in AUC24 and C max compared with nonelderly participants, whereas after multiple 300-mg doses of amenamevir, AUC24 and C max were both slightly decreased in elderly participants. In contrast, in participants receiving amenamevir at 600 mg/day, C max and AUC24 of amenamevir were both slightly increased in elderly participants after single and multiple doses. In this study, the mean t 200 was around 24 h on day 7 for amenamevir at both 300 mg/day and 600 mg/day in both age groups (Table 4), which is assumed to be a relevant parameter for clinical efficacy [23].

Table 3

Geometric least squares mean ratio of elderly/nonelderly participants for amenamevir plasma pharmacokinetics after multiple doses in study 15L-CL-003

Dose (mg)	Day	AUC24 (ng h/mL)	C max (ng/mL)
300	1	1.09 (0.85–1.38)	1.05 (0.81–1.35)
	7	0.96 (0.75–1.24)	0.89 (0.67–1.19)
600	1	1.28 (0.92–1.77)	1.18 (0.93–1.50)
	7	1.16 (0.90–1.49)	1.10 (0.90–1.36)

The values presented are the geometric least squares mean ratio (with the 90% confidence interval in parentheses) for elderly/nonelderly participants

AUC area under the plasma concentration versus time curve from time zero to 24 h, C peak drug concentration

Table 4

Summary of amenamevir urine pharmacokinetics and plasma t 200 after multiple doses in study 15L-CL-003

Age group	Amenamevir dose (mg)	Day	No.	Ae24 (mg)	Ae%	CLR (L/h)	t 200 (h)
Nonelderly	300	1	6	33.22 ± 9.50	11.07 ± 3.17	2.45 ± 0.53	21.1 ± 2.0
		7	6	30.80 ± 10.40	10.27 ± 3.47	2.22 ± 0.61	21.5 ± 2.9
	600	1	6	49.56 ± 10.82	8.26 ± 1.80	2.30 ± 0.43	22.8 ± 0.5
		7	6	42.13 ± 12.84	7.02 ± 2.14	2.15 ± 0.64	24.4 ± 2.7
Elderly	300	1	6	30.06 ± 3.77	10.02 ± 1.26	2.11 ± 0.53	22.2 ± 1.8
		7	6	28.79 ± 7.82	9.60 ± 2.61	2.17 ± 0.58	23.8 ± 4.8
	600	1	6	50.78 ± 13.66	8.46 ± 2.28	1.80 ± 0.25	22.9 ± 1.1
		7	6	39.30 ± 13.72	6.55 ± 2.29	1.67 ± 0.43	26.7 ± 3.8

All values are presented as the mean ± standard deviation

Ae cumulative amount of the unchanged drug excreted into the urine at 24 h, Ae% percentage of drug excreted in urine, CL renal clearance, t time above 200 ng/mL, t time to peak drug concentration

In study 15L-CL-003, renal clearance of amenamevir ranged from 2.11 to 2.45 L/h with 300 mg/day and from 1.67 to 2.30 L/h with 600 mg/day. The percentage of drug excreted in urine was lower in participants receiving amenamevir at 600 mg/day compared with participants receiving amenamevir at 300 mg/day in both the nonelderly and the elderly participants. Renal clearance was lower in elderly participants compared with nonelderly participants after single and multiple doses of 600 mg (Table 4).

The pharmacokinetics of amenamevir were affected by food. In part 2 of study 15L-CL-002, the AUCinf and C max of a single capsule dose of 300 mg amenamevir were increased when amenamevir was administered with food (Table 2, Fig. 2), t ½ remained the same, whereas apparent oral clearance was reduced. There was a 90% increase in AUCinf and an 82% increase in C max when amenamevir was administered with food relative to fasting conditions. Similar results were seen in study 15L-CL-006 (Table 5). Furthermore, in study 15L-CL-006, the percentage of amenamevir excreted unchanged in the urine in participants receiving the tablet formulation under fasting and fed conditions showed that the urine excretion increased when amenamevir was administered with food (Table 6).

Fig. 2

Mean plasma concentration versus time profile of amenamevir after a single capsule dose under fasting (open circles) and fed (closed circles) conditions in part 2 of study 15L-CL-002

Table 5

Summary of amenamevir capsule and tablet plasma pharmacokinetics after a single dose in study 15L-CL-006

Formulation	Condition	Sex	No.	AUCinf (ng h/mL)	Cmax (ng/mL)	t max (h)a	t ½ (h)	CL/F (L/h)
Capsule	Fasting	Male	12	26,900 ± 8800	2050 ± 713	2.0 (2.0–4.0)	7.8 ± 1.1	32.2 ± 8.5
		Female	12	31,800 ± 9340	2720 ± 721	2.0 (1.5–4.0)	7.2 ± 1.1	27.2 ± 7.8
		Male and female	24	29,300 ± 9220	2390 ± 779	2.0 (1.5–4.0)	7.5 ± 1.2	29.7 ± 8.4
Tablet	Fasting	Male	12	23,700 ± 10,400	1900 ± 851	2.0 (1.0–6.0)	7.9 ± 1.0	40.7 ± 19.9
		Female	12	30,200 ± 15,600	2570 ± 1060	2.0 (1.5–8.0)	7.1 ± 0.8	34.1 ± 18.8
		Male and female	24	27,000 ± 13,400	2230 ± 998	2.0 (1.0–8.0)	7.5 ± 1.0	37.4 ± 19.2
	Fed	Male	10	45,760 ± 11,914	3000 ± 501	4.0 (4.0–8.0)	7.9 ± 1.2	18.7 ± 5.6
		Female	12	50,573 ± 15,170	3420 ± 662	4.0 (3.0–8.0)	7.0 ± 1.1	17.0 ± 4.7
		Male and female	22	48,400 ± 13,700	3230 ± 619	4.0 (3.0–8.0)	7.4 ± 1.2	17.8 ± 5.1
GMR capsule/tabletb			–	0.86 (0.77–0.95)	0.88 (0.78–1.00)	–	–	–
GMR tablet fed/fastingb			–	1.92 (1.67–2.22)	1.55 (1.34–1.81)	–	–	–

Values are presented as the mean ± standard deviation unless otherwise stated

AUC area under the plasma concentration versus time curve from time zero to infinity, CL/F apparent oral clearance, C peak drug concentration, GMR geometric least squares mean ratio, t terminal half-life, t time to peak drug concentration

aThe median is presented (with the range in parentheses)

bThe 90% confidence interval is given in parentheses

Table 6

Summary of amenamevir urine pharmacokinetics in study 15L-CL-006

Formulation	Condition	No.	Aelast (mg)	Ae%	CLR (L/h)
Capsule	Fasting	24	54.89 ± 14.05	6.86 ± 1.76	2.00 ± 0.56
Tablet	Fasting	24	49.08 ± 20.57	6.13 ± 2.57	1.94 ± 0.49
	Fed	22	86.64 ± 20.04	10.83 ± 2.51	1.93 ± 0.60

All values are presented as the mean ± standard deviation

Ae cumulative amount of the unchanged drug excreted into the urine, Ae% percentage of drug excreted in urine, CL renal clearance

The pharmacokinetics of the amenamevir tablet and capsule in fasting participants enrolled in study 15L-CL-006 are shown in Fig. 3 and Tables 5 and 6. AUCinf and C max were slightly lower following tablet versus capsule administration in the fasted state, which reflected a relative bioavailability of 86%.

Fig. 3

Mean plasma concentration versus time profiles of amenamevir after a single capsule (open circles) or tablet (open triangles) dose under fasting conditions as well as after a single tablet dose under fed conditions (open squares) in study 15L-CL-006

Safety

Amenamevir was safe and well tolerated. No deaths or serious adverse events were reported in any study. In studies 15L-CL-001, 15L-CL-002, and 15L-CL-003, all adverse events reported with amenamevir were mild in severity, and no adverse events resulted in participants discontinuing their participation in the study. Two participants discontinued their participation in study 15L-CL-006 because of an adverse event, although the events were not considered related to treatment.

In study 15L-CL-001, four of 30 participants (13.3%) who received single doses of amenamevir experienced an adverse event: one participant each receiving amenamevir at a dose of 5, 100, 300, or 600 mg. Only one adverse event was considered possibly related to the amenamevir dose of 300 mg (increase in aspartate aminotransferase level).

In part 1 of study 15L-CL-002, four of 48 participants (8.3%) who received single doses of amenamevir experienced an adverse event: one receiving 100 mg amenamevir, one receiving 300 mg amenamevir, and two receiving 600 mg amenamevir. Of these, three events were considered related to study treatment: headache (unlikely), headache (possibly), and shoulder pain (possibly). No adverse events were reported in part 2 of study 15L-CL-002.

In study 15L-CL-003, adverse events were reported in four of six nonelderly participants (66.7%) receiving 600 mg amenamevir, three of six elderly participants (50.0%) receiving placebo, and one elderly participant of six participants (16.7%) receiving 600 mg amenamevir. Five participants experienced an adverse event that was considered possibly related to treatment: two nonelderly participants receiving 600 mg amenamevir (headache), one elderly participant receiving 600 mg amenamevir (blood amylase level increased), and two elderly participants receiving placebo (headache and blood cholesterol level increased, respectively).

In study 15L-CL-006, 13 of 24 participants (54.2%) reported 25 adverse events. The adverse events occurring in more than one participant were alopecia (n = 5), constipation (n = 3), upper respiratory tract infection (n = 2), and vomiting (n = 2). In all five cases of alopecia, the alopecia was mild in severity and occurred in female participants on day 15. It was described as finding hair on the pillow or increased hair loss on brushing. Examination of these participants did not reveal bald patches or scalp changes. Three adverse events were moderate in severity (pharyngitis, upper respiratory tract infection, and pain in an extremity; all n = 1), and the remainder were mild.

In all four studies, there were no clinically significant changes from the baseline in vital signs, ECGs, or clinical laboratory assessments.

Discussion

The helicase-primase inhibitor amenamevir offers an alternative therapeutic approach for patients with VZV infection. Data from the four human studies described here highlight the pharmacokinetics of amenamevir in various clinical settings (single and multiple dosing, food effect, age effect, and relative bioavailability of capsule versus tablet), as well as its safety and tolerability. Following single and multiple oral doses, amenamevir demonstrated a less than dose proportional increase in the pharmacokinetic parameters AUCinf and C max. Amenamevir was rapidly absorbed, and t max and t ½ of amenamevir were similar across all doses.

The pharmacokinetics of amenamevir were affected by food, with results showing that AUCinf almost doubled when amenamevir was administered with food. C max also increased with food (1.5–1.8-fold increase), and there was also a delay in t max after eating. Food is known to affect the bioavailability of multiple oral drugs by various means, including delaying gastric emptying, stimulating bile flow, changing gastrointestinal pH, increasing splanchnic blood flow, changing luminal metabolism of a drug substance, and physically or chemically interacting with a dosage form or a drug substance [24]. Although the cause of the changes in the pharmacokinetics of amenamevir with food is unknown, it is likely due to the low solubility of amenamevir. After food is consumed, bile acid is released. Bile acid is likely to increase the solubility of amenamevir and, therefore, the increase in exposure to amenamevir with food may be due to the increased levels of bile acid. In any case, the effect of food on the pharmacokinetics of amenamevir should be taken into consideration when one is selecting the appropriate time of the day to administer amenamevir as well as the appropriate dose.

Age may have a minimal influence on the pharmacokinetics of amenamevir, as demonstrated in study 15L-CL-003. In this study, in participants receiving the amenamevir 300-mg dose, there were no consistent differences in amenamevir pharmacokinetics between nonelderly and elderly participants. In participants receiving amenamevir at 600 mg/day, C max and AUC24 of amenamevir were both slightly increased and renal clearance was decreased in elderly participants after single and multiple doses. However, the 90% confidence interval of the geometric least squares mean ratios for both pharmacokinetic parameters across the dose range was wide and included 1; therefore, the age effect was considered to be minimal.

Two of the studies described here were conducted in Japanese participants and two were conducted in predominantly White populations. Although a direct comparison was not possible across the separate studies, the pharmacokinetic parameters of amenamevir in the two single ascending dose studies were similar [22], suggesting that there were no substantial differences between Japanese and non-Japanese participants.

In study 15L-CL-006, there were slight differences in the pharmacokinetics of the amenamevir tablet and capsule in fasting male and female participants. In this study, AUCinf and C max were slightly lower following tablet versus capsule administration in the fasted state, and this is reflected by a relative bioavailability of 86%. Subsequent studies of amenamevir used the tablet formulation as the final product.

In study 15L-CL-003, the mean t 200 of amenamevir on day 7 was around 24 h (range 21.5–26.7 h) for all doses investigated. In a murine pharmacokinetic/pharmacodynamic analysis of amenamevir, it was determined that t 100, the length of time the amenamevir concentration in plasma exceeds 100 ng/mL, was the most reasonable way to predict the efficacy of amenamevir with respect to the complete inhibition of HSV-1 replication [23]. As the activity of amenamevir against VZV is approximately twofold lower than that against HSV-1 [23], it was speculated that VZV growth can be suppressed with a dosage regimen resulting in a t 200 of close to 24 h per day. As such, the results of study 15L-CL-003 suggest that amenamevir may be effective against VZV.

Amenamevir was safe and well tolerated across all doses investigated in these studies. No deaths or serious adverse events were reported, and no clinically significant effects on vital signs, ECG, and clinical laboratory parameters were observed. These results are consistent with the phase 2 clinical study of amenamevir in patients with recurrent genital herpes [25].

Like most phase 1 studies, the sample sizes were relatively small, which is a limitation of these studies and may affect the interpretation of the results.

Conclusion

In conclusion, amenamevir was safe and well tolerated at single (up to 2400 mg) and multiple (up to 600 mg/day for 7 days) doses and showed less than dose proportional pharmacokinetic characteristics.

Below is the link to the electronic supplementary material.

Supplementary material 1 (PDF 487 kb)