Single-Dose Pharmacokinetics of Milvexian in Participants with Normal Renal Function and Participants with Moderate or Severe Renal Impairment

Abstract

Objective

The aim of this study was to assess the effect of moderate or severe renal impairment on the pharmacokinetic (PK) properties of milvexian.

Methods

This open-label, parallel-group study assessed the PK, safety, and tolerability of a single oral 60 mg dose of milvexian in participants with normal renal function (n = 8; estimated glomerular filtration rate [eGFR] ≥ 90 mL/min/1.73 m²) and participants with moderate (n = 8; eGFR ≥ 30 to ≤ 59 mL/min/1.73 m²) or severe (n = 8; eGFR < 30 mL/min/1.73 m²) renal impairment. Regression analysis was performed using linear regression of log-transformed PK parameters versus eGFR.

Results

Milvexian was well tolerated, with no deaths, serious adverse events, or serious bleeding reported. The maximum milvexian concentration (C_max) was similar for all groups. Based on a regression analysis of milvexian concentration versus eGFR, participants with eGFR values of 30 and 15 mL/min/1.73 m², respectively, had area under the curve (AUC) values that were 41% and 54% greater than in participants with normal renal function. Median time to maximum concentration (T_max) was similar for the three groups (4.5–5.0 h). The half-life increased for participants with moderate (18.0 h) or severe (17.7 h) renal impairment compared with those with normal renal function (13.8 h).

Conclusion

A single dose of milvexian 60 mg was safe and well tolerated in participants with normal renal function and moderate or severe renal impairment. There was a similar increase in milvexian exposure between the moderate and severe renal groups.

Clinical Trials Registration

This study was registered with ClinicalTrials.gov (NCT03196206, first posted 22 June 2017).

Supplementary Information

The online version contains supplementary material available at 10.1007/s40262-022-01150-1.

Key Points

This open-label study assessed the pharmacokinetics, safety, and tolerability of milvexian, an oral small molecule inhibitor of factor XIa, in participants with normal renal function and participants with moderate or severe renal impairment.

A single dose of milvexian 60 mg was safe and well tolerated in participants with normal renal function and in those with moderate or severe renal impairment.

Modest increases in milvexian exposure were observed in participants with moderate and severe renal impairment, but these are not likely to be clinically relevant.

Introduction

Patients with cardiovascular and thromboembolic diseases are at an increased risk of serious thrombotic events, which necessitates the use of antithrombotic therapies [1–5]. However, fears about an increased risk of bleeding events can lead to patients either not receiving antithrombotic therapy or being suboptimally treated with currently available agents [6–8]. Thus, there is a need for novel anticoagulants with an improved benefit/risk profile compared with current standards of care.

In the coagulation cascade, hemostasis and thrombosis are balanced through the regulation of blood factors, cellular components (e.g., platelets), and other coordinating proteins [9]. Thrombin plays a primary role in the coagulation cascade by activating platelet aggregation; Factors V, VIII, XI, and XIII; and forming fibrin [9, 10]. The zymogen Factor XI (FXI) is converted by thrombin to the activated protease Factor XIa (FXIa). FXIa leads to formation of a clot through direct activation of Factor IX, which in turn activates Factor X to convert prothrombin to thrombin, followed by the thrombin-mediated conversion of fibrinogen to fibrin [11, 12]. The downstream conversion of prothrombin to thrombin via FXIa is amplified through a positive feedback loop.

Modulation of FXIa may provide a novel mechanism for systemic anticoagulation with the potential to improve the benefit/risk profile of existing anticoagulants [13–16]. Based on findings from clinical and preclinical models, hemostasis is not solely dependent on the FXI pathway, and FXIa inhibitors have the potential to reduce thrombus formation [17–20]. Notably, spontaneous bleeding is rare in individuals with congenital FXI deficiencies and, for these individuals, mild bleeding after a serious injury or surgery is the only clinical manifestation of FXI deficiency [21–23]. Additionally, results from in vivo and clinical studies have shown that there is a reduced risk of adverse cardiovascular events and venous thromboembolism with FXI deficiency [13, 16, 24–26]. These findings support further investigation of FXIa inhibitors to prevent thrombotic events with a safer bleeding profile [11, 12, 27].

Milvexian (BMS-986177/JNJ-70033093) is a potentially first-in-class, oral, small-molecule that inhibits FXIa with high affinity and selectivity [28]. Milvexian is being developed to prevent thrombotic events in diverse patient populations. It has demonstrated antithrombotic activity while preserving hemostasis in preclinical models of arterial and venous thrombosis, and was generally safe and well tolerated in phase I studies in healthy participants and in individuals with hepatic impairment [29–32]. Milvexian is being investigated in an ongoing phase II study for the secondary prevention of major cardiovascular events in patients with acute ischemic stroke [33]. A separate study on the prevention of total venous thromboembolism events in patients undergoing total knee replacement surgery has been completed [34].

Patients with renal impairment are at heightened risk of bleeding when taking anticoagulant therapies [35]; however, it is unknown if this is purely due to increases in drug exposure, intrinsic features of this patient population, or a combination of both [36–38]. The increased risk of bleeding in patients with renal impairment has been observed even without anticoagulant therapies, with one study demonstrating a 1.5-fold increased risk of bleeding in patients with chronic kidney disease compared with those without chronic kidney disease [39]. Patients with chronic kidney disease demonstrate abnormalities in platelet physiology (e.g., α–granules) in addition to deregulation of arachidonic acid and prostaglandin metabolism that results in reduced adhesion and aggregation, increasing bleeding risk [40, 41]. Additionally, uremic patients exhibit higher concentrations of prostacyclin and increased nitric oxide generation by platelets, which both independently inhibit platelet aggregation and contribute to dysfunctional hemostasis and increased bleeding risk. Therefore, patients with renal impairment who use currently available antithrombotics may benefit from a drug with an improved safety profile, such as milvexian.

Based on results from a previous first-in-human study, renal excretion of milvexian is estimated to be below 20%, therefore renal impairment may not have a large impact on milvexian exposure [31]. However, patients with impaired renal function can display altered pharmacokinetic (PK) properties because of inhibition of several pathways of hepatic and intestinal metabolism and transport [42], and PK evaluation in certain patient populations with renal impairment is recommended by regulatory bodies [43, 44]. The future patient population for milvexian may include patients with end-stage renal disease (ESRD), necessitating investigation of the effect renal impairment has on milvexian PK properties.

This study assessed the effect of renal impairment on the PK and pharmacodynamic (PD) properties of milvexian as well as the safety and tolerability of milvexian in participants with normal renal function and moderately or severely impaired renal function.

Methods

Ethics

This study was conducted in accordance with Good Clinical Practice, as defined by the International Council for Harmonisation and in accordance with the ethical principles underlying European Union Directive 2001/20/EC and the United States Code of Federal Regulations, Title 21, Part 50 (21CFR50). The study was registered with ClinicalTrials.gov (NCT03196206, first posted 22 June 2017). The protocol, amendments, and participant informed consent received appropriate approval by the Independent Ethics Committee (IEX) and the Institutional Review Board (IRB) of IntegReview IRB (now Advarra; Columbia, MD, USA) prior to initiation of the study at the site. Prior to the beginning of the study, all participants provided written informed consent, including consent for any screening procedures conducted to establish participant eligibility for the study. The study was conducted at two clinical sites (Clinical Pharmacology of Miami LLC, Miami, FL, USA; and Orlando Clinical Research Center, Orlando, FL, USA) from 6 July 2017 to 4 March 2018.

Study Design

This was an open-label, parallel-group study to evaluate the PK, safety, and tolerability of a single dose of milvexian in participants with normal renal function and participants with moderate or severe renal impairment. As the study was nonrandomized, enrolled participants, including those not dosed, were assigned sequential participant numbers. Participants were matched by age, body weight, and sex. Participants underwent screening evaluations to determine eligibility within 21 days before study treatment administration. Eligible participants were enrolled in one of three renal function groups based on estimated glomerular filtration rate (eGFR). The eGFR was determined by the Modification of Diet in Renal Disease formula. Normal renal function was defined as an eGFR ≥ 90 mL/min/1.73 m², moderate renal impairment was defined as an eGFR ≥ 30 to ≤ 59 mL/min/1.73 m², and severe renal impairment was defined as an eGFR < 30 mL/min/1.73 m². On Day 1, all participants in the three renal function groups received an oral 60 mg dose of milvexian after consumption of a standard meal. Selection of the 60 mg dose was based on in vivo preclinical pharmacology data from the rabbit electric arterial thrombosis model, differences in the affinity of milvexian for rabbit and human FXIa, and modeling results [45]. Simcyp PBPK simulator v15 was employed using a minimal physiologically based PK (PBPK) model developed for milvexian to estimate the potential increase in exposures when simulating varying degrees of renal impairment based on eGFR. The 60 mg dose is within the dose linear range of milvexian, and therefore the results from this study can be extrapolated to infer differences with renal impairment at any other dose of milvexian within the known dose-proportional range (20–200 mg) [31].

Participants

Eligible participants included men and women not of childbearing potential, aged 18–70 years, with a body mass index of 18.0–32.0 kg/m² for participants with normal renal function or 18.0–38.0 kg/m² for participants with moderate or severe renal impairment. In all three renal function groups, eligible participants were in good health as determined by no clinically significant deviation from normal in medical or surgical history, physical examination, electrocardiograms (ECGs), and clinical laboratory determinations, except for renal insufficiency, which was predefined by renal function group. Participants were ineligible if they had an indwelling catheter in preparation for dialysis, history of coagulopathy, gastrointestinal disease, or any major surgery within 4 weeks of study treatment administration (or planned within 2 weeks of study completion). Additionally, participants in the severe renal function group could not be on dialysis.

Safety Assessments

Safety and tolerability were assessed based on medical review of adverse event (AE) reports and the results of vital sign measurements, ECG measurements, physical examinations, and clinical laboratory tests.

Pharmacokinetic and Pharmacodynamic Assessments

The PK properties of milvexian were derived from plasma concentration versus time and urinary excretion data. Assessed parameters included maximum observed plasma concentration (C_max), time of C_max (T_max), area under the plasma concentration-time curve (AUC) from time zero to time of the last quantifiable concentration (AUC_t), AUC from time zero extrapolated to infinite time (AUC_∞), terminal plasma half-life (T_½), apparent total body clearance (CLT/F), fraction of unbound drug (fu), C_max of free drug (C_max fu), AUC from time zero to time of the last quantifiable concentration of free drug (AUC_t fu), AUC from time zero extrapolated to infinite time of free drug (AUC_∞ fu), apparent total body clearance of free drug (CLT/F fu), total amount recovered in urine (Urt), percentage dose of milvexian total amount recovered in urine (%Urt), renal clearance (CL_R), and protein binding.

Activated partial thromboplastin time (aPTT) and FXI clotting activity were examined as exploratory PD biomarkers.

Clinical Laboratory Evaluations

Plasma samples were analyzed for milvexian concentration and milvexian protein binding using a validated liquid chromatography with tandem mass spectrometry (LC-MS/MS) assay at ICON Laboratory Services, Inc. (Whitesboro, NY, USA). Samples were analyzed using Analyst version 1.4.2 (Applied Biosystems, Framingham, MA, USA). LC-MS/MS assays had a lower limit of quantification of 1.0 ng/mL and an upper limit of quantification of 1000 ng/mL. Individual participant PK parameter values were derived by noncompartmental methods using a validated PK analysis program. The cumulative milvexian Urt was calculated as the summation of the product of the concentration of the analyte with the volume of urine collected over a collection interval. To determine CL_R, the cumulative amount of milvexian excreted in urine was divided by the plasma AUC over the same time interval, data permitting. The designated protein-binding blood sample was analyzed for milvexian protein binding by LC-MS/MS. Validated assays were performed at Labcorp Colorado Coagulation to measure aPTT and FXI clotting activity (Englewood, CO, USA).

Sample Collection

Blood and/or urine samples were obtained at screening and on Days −1 and 4 for clinical laboratory evaluations in all three renal function groups. Additional blood and/or urine samples were obtained from participants in the moderate and severe renal impairment groups on Day 2.

Details on the timing of sample collection for PK and PD assessments are shown in Online Resource 1.

Statistical Analyses

The population for safety analysis included all participants who received one dose of milvexian. The evaluable PK population included all participants who received milvexian and from whom valid PK parameter data were obtained. The PD population included all participants who received milvexian and had any available PD biomarker data. Determination of the study sample size was not based on statistical power considerations. However, it was calculated that data from eight healthy participants and eight participants with various levels of impaired renal function would provide 80% probability for the 90% confidence interval (CI) of the geometric mean ratio (GMR) for milvexian to be within (78.58%, 127.25%), (88.69%, 112.75%), and (88.69%, 112.75%) of the GMR point estimate for C_max, AUC_t, and AUC_∞, respectively.

All milvexian PK data were summarized using descriptive statistics. A regression analysis was performed using linear regression of log-transformed C_max, AUC_t, and AUC_∞ versus eGFR or creatinine clearance (CrCL; estimated using the Cockcroft–Gault equation). In the regression analysis, the dependent variables were the log-transformed PK parameters, and baseline eGFR or CrCL values were the independent variables. Predicted values for each of the PK parameters and associated 90% CIs were calculated for eGFR and CrCL equal to 15, 30, and 90 (mL/min/1.73 m² for eGFR and mL/min for CrCL), representing the lower bound cut-off for severe renal impairment, moderate renal impairment, and normal renal function, respectively. In addition, GMRs of each PK parameter’s predicted values were calculated for eGFR and CrCL values of 30: 90 (moderate renal impairment: normal renal function) and 15: 90 (severe renal impairment: normal renal function). All statistical analyses and calculations were performed using SAS^® software version 9.3 (SAS Institute Inc., Cary, NC, USA).

Results

Participants

A total of 43 participants were enrolled in this study, of whom 24 participants (55.8%) entered the treatment period, received one dose of study treatment, and completed the study. Of the patients who did not enter the treatment period, the majority (n = 18) no longer met the study eligibility criteria; the remaining participant withdrew consent. Eight participants were enrolled in each renal function group (normal renal function, eGFR ≥ 90 mL/min/1.73 m²; moderate renal impairment, eGFR ≥ 30 to ≤ 59 mL/min/1.73 m²; and severe renal impairment, eGFR < 30 mL/min/1.73 m²). All 24 participants were included in the safety, PK, and PD analyses. Table 1 outlines the demographics and characteristics of the participants enrolled in each renal function group.

Table 1.

Baseline characteristics of the study participants

Characteristica	Normal renal functionb [n = 8]	Moderate renal impairmentc [n = 8]	Severe renal impairmentd [n = 8]	Total [N = 24]
Male sex [n (%)]	7 (87.5)	6 (75.0)	5 (62.5)	18 (75.0)
Age, years [median (range)]	53.5 (30–67)	63.0 (46–70)	61.5 (27–70)	60.0 (27–70)
Race [n (%)]
White	6 (75.0)	7 (87.5)	5 (62.5)	18 (75.0)
Black or African American	1 (12.5)	0	3 (37.5)	4 (16.7)
Asian	0	1 (12.5)	0	1 (4.2)
Biracial	1 (12.5)	0	0	1 (4.2)
BMI, kg/m2 [median (range)]	30.90 (19.6–31.5)	34.60 (24.3–37.5)	32.75 (20.4–37.9)	31.45 (19.6–37.9)
eGFR, mL/min/1.73 m2 [median (range)]	104.5 (91–157)	49.0 (36–59)	20.5 (9–26)	–
CrCL, mL/min [median (range)]	125.0 (104–174)	67.0 (44–83)	32.0 (11–37)	–

BMI body mass index, eGFR estimated glomerular filtration rate, CrCL creatinine clearance

^aAll values presented as median (minimum–maximum) unless otherwise stated

^bNormal renal function was an eGFR ≥ 90 mL/min/1.73 m²

^cModerate renal impairment was an eGFR ≥ 30 to ≤ 59 mL/min/1.73 m²

^dSevere renal impairment was an eGFR < 30 mL/min/1.73 m²

Safety and Tolerability

Administration of a single dose of milvexian 60 mg was generally safe and well tolerated across the three renal function groups. There were no deaths or serious AEs (SAEs) leading to discontinuation during the study. One SAE was reported in one participant during the screening period, and this participant was not assigned to a renal function group and did not receive milvexian. The incidence of AEs was low and was equally distributed across renal function groups. Three participants (12.5%) reported one AE following administration of milvexian. Two participants (8.3%) reported headache, and one participant (4.2%) reported somnolence. An overall summary of AEs is presented in Table 2. All AEs were mild in intensity and considered by the investigator to be related to study treatment. No treatment was required for AEs, and all AEs resolved without sequelae. No bleeding events were reported. In addition, there were no clinically relevant findings or trends in clinical laboratory test, ECG, vital sign, or physical examination results.

Table 2.

Adverse events

AE	Normal renal functiona [n = 8]	Moderate renal impairmentb [n = 8]	Severe renal impairmentc [n = 8]	Total [N = 24]
Any AE	1 (12.5)	1 (12.5)	1 (12.5)	3 (12.5)
Headache	0	1 (12.5)	1 (12.5)	2 (8.3)
Somnolence	1 (12.5)	0	0	1 (4.2)

Data are expressed as n (%)

AE adverse event, eGFR estimated glomerular filtration rate

^aNormal renal function was an eGFR ≥ 90 mL/min/1.73 m²

^bModerate renal impairment was an eGFR ≥ 30 to ≤ 59 mL/min/1.73 m²

^cSevere renal impairment was an eGFR < 30 mL/min/1.73 m²

Pharmacokinetics

Mean milvexian plasma concentration-time profiles are shown in Fig. 1, and PK parameters are summarized in Table 3. Mean concentrations of milvexian were higher in participants with moderate or severe renal impairment compared with participants with normal renal function following a single dose of milvexian. A regression analysis indicated that C_max was similar for all renal function groups, while AUC_t and AUC_∞ increased with decreasing eGFR and CrCL. From the slopes estimated in the eGFR-based regression analysis, on average, participants with eGFR values of 30 and 15 mL/min/1.73 m² would have a 39% and 50% increase in AUC_t and a 41% and 54% increase in AUC_∞, respectively, compared with participants with normal renal function (eGFR 90 mL/min/1.73 m²) (Fig. 2). From the estimated slopes in the CrCL-based regression analysis, on average, participants with CrCL values of 30 and 15 mL/min would have a 38% and 49% increase in AUC_t and a 40% and 52% increase in AUC_∞, respectively, compared with a participant with normal renal function (CrCL 90 mL/min) (Fig. 2).

Fig. 1.

Mean (± SD) milvexian plasma concentration versus time profile. SD standard deviation.

Table 3.

Summary statistics of milvexian plasma and urine PK parameters by renal function group

Parametera	Normal renal functionb [n = 8]	Moderate renal impairmentc [n = 8]	Severe renal impairmentd [n = 8]
Cmax, ng/mL	462 (30)	406 (46)	462 (42)
%fu	8.85 (8)	8.81 (11)	8.40 (15)
Cmax fu, ng/mL	40.9 (29)	35.8 (44)	38.8 (44)
AUCt, ng·h/mL	3860 (36)	5004 (34)	7094 (33)
AUCt fu, ng·h/mL	341 (33)	441 (32)	596 (41)
AUC∞, ng·h/mL	3916 (36)	5154 (32)	7411 (37)
AUC∞ fu, ng·h/mL	347 (34)	454 (30)	623 (44)
AUC96, ng·h/mL	3883 (36)	5015 (34)	7167 (35)
Tmax, h	4.50 (4.00–5.00)	4.75 (4.00–7.00)	5.00 (4.50–8.00)
T½, h	13.8 (3.45)	18.0 (5.37)	17.7 (4.75)
CLT/F, L/h	15.3 (36)	11.6 (32)	8.10 (37)
CLT/F fu, L/h	173 (33)	132 (30)	96.4 (44)
CLR, mL/h	1617 (52)	914 (40)	263 (65)
%Urt	10.5 (45)	7.64 (33)	3.14 (75)
%Protein binding	91.1 (1)	91.1 (1)	91.5 (1)

PK pharmacokinetic, C_max maximum observed plasma concentration, fu fraction of unbound drug, C_max fu maximum observed plasma concentration of free drug, AUC_t area under the plasma concentration-time curve from time zero to time of the last quantifiable concentration, AUC_t fu AUC from time zero to time of the last quantifiable concentration of free drug, AUC_∞ AUC from time zero extrapolated to infinite time, AUC_∞ fu AUC from time zero extrapolated to infinite time of free drug, AUC₉₆ AUC from time zero to 96 h, T_max time of maximum observed plasma concentration, T_½ terminal plasma half-life, CLT/F apparent total body clearance, CLT/F fu apparent total body clearance of free drug, CL_R renal clearance, %Urt percentage dose of milvexian total amount recovered in urine, %CV percentage coefficient of variation, SD standard deviation

^aC_max, %fu, C_max fu, AUC_t, AUC_t fu, AUC_∞, AUC_∞ fu, AUC₉₆, CLT/F, CLT/F fu, CL_R, %Urt, and %protein binding are presented as adjusted geometric mean (%CV); T_max is presented as median (minimum–maximum); and T_½ is presented as mean (SD)

^bNormal renal function was an eGFR ≥ 90 mL/min/1.73 m²

^cModerate renal impairment was an eGFR ≥ 30 to ≤59 mL/min/1.73 m²

^dSevere renal impairment was an eGFR < 30 mL/min/1.73 m²

Fig. 2.

Predicted values of milvexian PK parameters based on renal impairment from the regression analysis of eGFR^a and CrCL^b in a moderate and b severe renal impairment. ^aPredicted values for each PK parameter and associated 90% CI for eGFR (mL/min/1.73 m²) equal to 15, 30, and 90 were obtained from the linear regression model. GMRs of each PK parameter predicted values were calculated for eGFR values of 30: 90 (moderate renal impairment: normal renal function) and 15: 90 (severe renal impairment: normal renal function). ^bPredicted values for each PK parameter and associated 90% CI for CrCL (mL/min) equal to 15, 30, and 90 were obtained from the linear regression model. GMRs of each PK parameter predicted values were calculated for CrCL values of 30: 90 (moderate renal impairment: normal renal function) and 15: 90 (severe renal impairment: normal renal function). PK pharmacokinetic, eGFR estimated glomerular filtration rate, CrCL creatinine clearance, GMR geometric mean ratio, CI confidence interval, C_max maximum observed concentration, AUC_t area under the plasma concentration-time curve from time zero to time of the last quantifiable concentration, AUC_∞ area under the plasma concentration-time curve from time zero extrapolated to infinite time

Median T_max was similar across all renal function groups. As a result of decreasing CLT/F with decreasing renal function (15.3, 11.6, and 8.10 L/h in participants with normal renal function, moderate renal impairment, and severe renal impairment, respectively), the T_½ was slightly longer for the moderate (17.7 h) and severe (18.0 h) renal impairment groups compared with the normal renal function group (13.8 h). The CL_R was lower for both the moderate and severe renal impairment groups compared with the normal renal function group. Correspondingly, excretion in the urine, as measured by %Urt, was lower in the moderate and severe renal impairment groups compared with those with normal renal function. Protein binding was similar for all renal function groups and the unbound parameters showed similar results across the different renal function groups.

Pharmacodynamics

Mean baseline (predose Day 1) aPTT values were similar across renal function groups and ranged from 23.9 to 25.3 s. Administration of a single oral dose of milvexian resulted in a concentration-dependent prolongation of aPTT that was similar across all renal function groups (Fig. 3). Mean peak aPTT values were achieved at 5, 5, and 6 h postdose, corresponding to percentage changes from baseline of 127%, 97%, and 100% for the normal renal function, moderate renal impairment, and severe renal impairment groups, respectively.

Fig. 3.

Mean (± SD) aPTT versus time profile. SD standard deviation, aPTT activated partial thromboplastin time

Mean baseline (predose Day 1) FXI clotting activity values were similar across renal function groups and ranged from 105.4 to 115.7%. Administration of a single oral dose of milvexian resulted in a concentration-related decrease in FXI clotting activity (Fig. 4). The magnitude of decrease appeared to be similar across renal function groups. Mean nadir FXI clotting activity values were achieved at 5, 5, and 7 h postdose for participants with normal renal function, and moderate and severe renal impairment corresponding to percentage changes from baseline of 39.4%, 31.9%, and 31.8%, respectively.

Fig. 4.

Mean (± SD) FXI clotting activity versus time profile. SD standard deviation, FXI Factor XI

Discussion

This study evaluated the PK, safety, and tolerability of a single, 60 mg dose of milvexian in participants with normal renal function and participants with moderate or severe renal impairment. Milvexian is a potentially first-in-class, oral, small-molecule FXIa inhibitor being developed to prevent and treat thrombotic events across diverse patient populations [28]. FXIa inhibitors have the potential to improve the benefit/risk profile of existing anticoagulants by reducing thrombus formation without causing an increase in bleeding [13–20]. There is additional unmet need for safer anticoagulants in renal impairment patients with concomitant cardiovascular disease as these patients have a higher intrinsic risk of bleeding [39], and this risk may further increase with currently available anticoagulants [36–38].

Administration of a single dose of 60 mg milvexian was generally safe and well tolerated in participants with normal renal function and participants with moderate or severe renal impairment. The incidence of AEs was low and was equally distributed independent of renal function. Of note, no bleeding events were reported. Bleeding risk in patients receiving currently available anticoagulants is variable [46], but patients with renal impairment are at a higher risk of bleeding events generally and may benefit from dose adjustments of anticoagulants [47, 48]. Safety and tolerability results from the current study of milvexian add to evidence from a phase I study in healthy volunteers as well as a phase I study in participants with hepatic impairment that also demonstrated the safety and tolerability of milvexian [31, 32].

Previous studies demonstrated low renal excretion of milvexian (< 20%), which suggested that renal impairment may not have a significant impact on exposure [31]. Results from the regression analysis in the current study indicate that C_max and T_max will be similar across all renal function groups, with an increase in overall exposure in the moderate and severe renal impairment groups of approximately 40% and 50%, respectively. The corresponding predicted increase in milvexian drug exposure in patients with renal impairment is similar to results reported for other anticoagulants [46]; for example, rivaroxaban has shown a 56% increase in exposure in patients undergoing dialysis compared with healthy participants [49]. Similarly, apixaban has shown a 44% increase in exposure in patients with severe renal impairment (CrCL of 15 mL/min) compared with healthy participants [50]. Overall, the magnitude of increases in milvexian exposure may not be clinically relevant in patients with renal impairment, pending assessment of exposure–response.

Administration of a single dose of milvexian resulted in a concentration-dependent aPTT prolongation that was similar across the three renal function groups. Similarly, administration of milvexian led to a concentration-related decrease in FXI clotting activity across the three renal function groups. Results from the PD assessments suggest that renal function does not alter the PK/PD relationship with either aPTT or FXI clotting activity.

A limitation of this study is that the PK data were obtained from a small sample of participants. However, as noted earlier, the sample size for this study was based on the precision estimate of the GMRs of specific PK measurements of milvexian for a group with renal impairment versus a healthy group. Despite a modest sample size, regression analyses from the current study, which included eight healthy participants and 16 participants with various levels of impaired renal function, provided 90% CIs within the specified range. In addition, baseline characteristics were generally balanced across groups for age, sex, race, and body mass index, and as such would not contribute to any significant changes in PK across renal groups. Future studies could include participants with ESRD to further investigate the impact of renal impairment on the PK and PD properties of milvexian.

Conclusions

The results of this study demonstrated that a single dose of 60 mg milvexian was generally safe and well tolerated in participants with normal renal function and participants with moderate or severe renal impairment. The PK analysis indicated that C_max and T_max were similar across renal function groups, and the PD analysis suggested that concentration-dependent prolongation of aPTT and concentration-dependent decreases in FXI clotting activity were similar across renal function groups. Although there was a modest increase in exposure, as measured by AUC, in the renal impairment groups, these values are not likely to be clinically relevant.

Supplementary Information

Below is the link to the electronic supplementary material.

Declarations

Ethics approval

This study was conducted in accordance with Good Clinical Practice, as defined by the International Council for Harmonisation and in accordance with the ethical principles underlying European Union Directive 2001/20/EC and the United States Code of Federal Regulations, Title 21, Part 50 (21CFR50). The study was registered with ClinicalTrials.gov (NCT03196206, first posted 22 June 2017). The protocol, amendments, and participant informed consent received appropriate approval by the IEX and the IRB of IntegReview IRB (now Advarra; Columbia, MD, USA) prior to initiation of the study at the site. The study was conducted at two clinical sites (Clinical Pharmacology of Miami LLC, Miami, FL, USA; and Orlando Clinical Research Center, Orlando, FL, USA) from 6 July 2017 to 4 March 2018.

Consent to participate

Prior to the beginning of the study, all participants provided written informed consent, including consent for any screening procedures conducted to establish participant eligibility for the study.

Consent for publication

Not applicable.

Availability of data and materials

The data that support the findings of this study are not publicly available due to privacy or ethical restrictions. Please contact the corresponding author, Vidya Perera, for additional information.

Code availability

Not applicable.

Conflict of interest

VP, GA, DL, ZW, SL, AB, and BM are full-time employees of Bristol Myers Squibb. LZ is a full-time employee of Janssen.

Funding

This study was sponsored by Bristol Myers Squibb.

Author contributions

VP, GA, DL, ZW, LZ, SL, AB, and BM contributed to the study design and concept, data analysis and review, or data interpretation; critically reviewed the manuscript for intellectual content; and approved the final manuscript for publication.