FormalPara Key Points

A low pharmacokinetic interaction potential of vericiguat was estimated from in vitro data and confirmed in ten clinical phase I drug–drug interaction studies

The pharmacokinetic drug–drug interaction profile of vericiguat is well suited to the treatment of a heart failure population using multiple concomitant medications

Vericiguat was well tolerated in all studies

1 Introduction

Vericiguat is a stimulator of soluble guanylate cyclase (sGC) currently under investigation as a first-in-class therapy for worsening chronic heart failure (HF) with reduced ejection fraction (HFrEF; VICTORIA [NCT02861534]) and preserved ejection fraction (HFpEF; VITALITY-HFpEF [NCT03547583]) [1, 2]. Vericiguat was administered orally once daily and titrated from 2.5 up to 10 mg in the phase III VICTORIA study, and is being up-titrated to 15 mg in the phase II VITALITY-HFpEF study. Vericiguat restores the nitric oxide (NO)-sGC-cyclic guanosine monophosphate pathway by directly stimulating sGC independently of NO and sensitizing sGC to NO, thus restoring cyclic guanosine monophosphate production even under low NO conditions and oxidative stress [1, 3]. The first sGC approved for clinical use was riociguat [4], which was developed as a treatment for pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension [5, 6]. The clinical benefit profile of riociguat is different to vericiguat [7], and both sGCs have distinct pharmacokinetic (PK) properties.

Patients with HF often present with multiple comorbidities and receive multiple concomitant medications [8, 9]. In the European Heart Failure Pilot Survey, 74% of patients with HF experienced one or more comorbidities [10]. Current guideline-recommended therapies propose a stepwise approach to treatment, which frequently involves multiple drugs to treat underlying causative factors, such as hypertension, myocardial ischemia, atrial fibrillation, diabetes mellitus, and dyslipidemia, further increasing the number of prescribed drugs [8, 11,12,13]. Thus, an understanding of the clearance mechanisms, elimination, and potential for drug–drug interactions (DDIs) of vericiguat is important to define allowable co-medications and is a prerequisite for further dose recommendations.

Vericiguat is a low-soluble, highly permeable, and weakly basic Biopharmaceutics Classification System class II drug [14]. Studies in healthy volunteers have demonstrated that vericiguat exhibits linear pharmacokinetics and investigated vericiguat’s pharmacodynamic interaction potential [15, 16]. Higher bioavailability and lower variability of vericiguat after administration with food compared to without has also been reported [14]. Vericiguat is a low-clearance drug (1.6 L/h in healthy volunteers and 1.3 L/h in patients with HFrEF) [17]. The plasma protein binding of vericiguat is approximately 98%, with serum albumin being the main binding component (data on file). The plasma protein binding is not affected by renal or hepatic impairment. Beyond the titration regimen, no further dose adjustment was recommended for patients with renal impairment (estimated glomerular filtration rate ≥ 15 mL/min/1.73 m2) or for patients with mild-to-moderate hepatic impairment in the VICTORIA study [1].

Following metabolite profiling in human hepatocytes, the primary biotransformation pathway of vericiguat was identified as phase II uridine diphosphate-glucuronosyltransferase (UGT)-mediated conjugation with glucuronic acid (glucuronidation) [18]. Herein, we report results identifying the UGT isoforms contributing to glucuronidation of vericiguat and the contribution of organs to the overall glucuronidation process. Further in vitro studies with human liver microsomes indicate that vericiguat has no inhibitory effects on major cytochrome P450 (CYP) isoforms [18]. Additional preclinical characterization was conducted to identify relevant vericiguat and metabolite M-1 (a pharmacologically inactive major plasma N-glucuronide metabolite) transporter proteins and the inhibitor/inducer properties of vericiguat and M-1 towards various enzymes. In addition, the different excretion pathways of vericiguat in humans and its metabolite profile were investigated in a human mass balance study. Ten healthy volunteer phase I studies further investigated the DDI profile of vericiguat based on its absorption/solubility, metabolism, preclinical findings, as well as with potential concomitant medications.

2 Methods

2.1 In Vitro Studies

Identification of the UGT isoforms involved in the glucuronidation of vericiguat, as well as transport proteins for vericiguat, was performed by several in vitro studies (see Methods section and Table 1 of the Electronic Supplementary Material [ESM]). In addition, the potential of vericiguat to act as a perpetrator by inhibiting metabolizing enzymes or transporters as well as inducing CYPs was investigated.

2.2 Phase I Studies

The conduct of all clinical studies met their local legal and regulatory requirements. All studies were conducted in Germany except for the human mass balance study, which was conducted in the Netherlands. The studies were conducted in accordance with the ethical principles that have their origin in the Declaration of Helsinki and the International Conference on Harmonisation guideline E6: Good Clinical Practice. Informed consent was obtained from all individual participants included in the studies. Quantitative measurements of vericiguat and all other drugs were performed using validated methods and in accordance with relevant guidelines (see Table 2 of the ESM for further details) [19, 20].

Healthy white male individuals were eligible in line with accepted criteria for healthy volunteer studies [21]. Across the studies, the general inclusion criteria for healthy volunteers were (with some variability depending on the study): aged 18–65 years, body mass index 18–30 kg/m2, resting heart rate 45–100 beats per minute, systolic blood pressure 90–145 mmHg, diastolic blood pressure 45–95 mmHg, and an absence of clinically relevant changes in electrocardiogram findings. Participants were excluded if they were taking regular medications, consuming foods or beverages that could influence the study objectives, unable to abide by study-specific smoking restrictions, or taking supplements with known interaction potential.

2.3 Study Design

One phase I study investigated the clearance mechanisms and elimination of vericiguat and ten phase I studies investigated the potential for DDIs with vericiguat in healthy male volunteers (Table 1). As vericiguat has been demonstrated to exhibit linear pharmacokinetics [16], the use of different doses of vericiguat across the phase I studies is not considered a limitation. In addition, the investigated doses include the target therapeutic dose range of vericiguat in HF [1, 2]. While the studies were conducted in relatively small population sizes and in healthy volunteers, all studies were performed to guideline recommendations and designed to investigate specific DDIs. Further details can be viewed in the Methods section of the ESM.

Table 1 Phase I vericiguat study design details
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2.4 Pharmacokinetic and Statistical Analyses

Pharmacokinetic parameters were estimated using non-compartmental methods by WinNonlin software (Pharsight Corporation, Mountain View, CA, USA). Area under the plasma concentration–time curve (AUC) from 0 to infinity was calculated from the AUC from time 0 to the last quantifiable concentration using the linear-logarithmic trapezoidal method and from the last predicted plasma concentration and apparent terminal rate constant (calculated from the slope of a log-linear regression). The linear-logarithmic trapezoidal method was also used to calculate partial AUCs (e.g., AUC0–24 [AUC from time 0 to 24 h after administration]) and the AUC within the dosing interval after multiple dosing (AUCτ,md). The maximum concentration (Cmax) and the trough concentration within a dosing interval were directly determined from the concentration–time data for each participant. Summary descriptive statistics were provided for the cumulative excretion of total radioactivity in urine, feces, and urine plus feces in the human mass balance study.

For the DDI studies, PK parameters with and without co-medications were compared. Depending on the design of the study, selected PK parameters were analyzed if applicable and assumed to be log-normally distributed. These included AUC, AUC0–24, AUC0–24,md (AUC0–24 after multiple-dose administration), AUC0–22 (AUC from time 0 to 22 h), AUC0–12,md (AUC from time 0 to 12 h after multiple-dose administration), AUCτ,md, Cmax, Cmax,md (Cmax within a dosing interval after multiple-dose administration), and trough concentration within a dosing interval. The logarithms of these parameters were analyzed using analysis of variance, including sequence, healthy volunteer (sequence), period, and treatment effects, except for the rifampicin, sacubitril/valsartan, and sildenafil DDI studies, which only included healthy volunteer and treatment effects. Based on these analyses, point estimates (least-squares mean) of the geometric mean ratios and 90% confidence intervals for the treatment ratios were calculated by retransformation of the logarithmic data.

2.5 Safety and Tolerability

Adverse events, vital signs, electrocardiogram, and laboratory parameters (i.e., hematology, coagulation, clinical chemistry, and urinalysis) in relation to the study drug were captured for all phase I studies.

3 Results

3.1 In Vitro Studies

In vitro studies showed that glucuronidation of vericiguat was catalyzed primarily by UGT1A9 and UGT1A1. Human liver, kidney, and intestinal microsomes fortified with uridine 5ʹ-diphospho-glucuronic acid mediate glucuronidation of vericiguat. In human liver microsomes of single donors (n = 20), the formation of M-1 correlated slightly better with propofol glucuronidation (r2 = 0.73), a highly selective UGT1A9-mediated pathway, than with estradiol 3-glucuronidation (r2 = 0.61), a highly selective UGT1A1-mediated pathway. Niflumic acid, a potent UGT1A9 inhibitor, showed stronger inhibition on vericiguat glucuronidation than a potent UGT1A1 inhibitor (atazanavir), suggesting that glucuronidation of vericiguat could be preferentially catalyzed via UGT1A9 than via UGT1A1. Further results are presented in Tables 3 and 4 of the ESM.

Additional in vitro studies have determined that vericiguat is a substrate of the transporter proteins P-glycoprotein and breast cancer resistance protein. Vericiguat is not a substrate of organic anion transporting polypeptide (OATP) 1B1, OATP1B3, or organic cation transporter 1. Metabolite M-1 is not a substrate of efflux (P-glycoprotein, breast cancer resistance protein) or uptake transporters (OATP1B1, OATP1B3). The design and interpretation of the in vitro studies were in line with official guidance [22, 23].

Furthermore, no inhibition was observed for vericiguat and its metabolite (M-1) at the highest tested concentration for efflux transporters P-glycoprotein and bile salt export pump (half maximal inhibitory concentration [IC50] > 100 µM), multidrug and toxin extrusion protein (MATE) 1 and MATE2K (IC50 > 10 µM), as well as for uptake of organic cation transporter 1 (IC50 > 50 µM), organic anion transporter (OAT) 1, OAT3, and organic cation transporter 2 (all IC50 > 5 µM). Both vericiguat and M-1 did not inhibit major UGT isoforms (UGT1A1, 1A4, 1A6, 2B4, and 2B7; all IC50 > 50 µM), except for UGT1A9 inhibition by vericiguat (IC50 = 10.6 µM, inhibitory constant [Ki] = 6.6 µM). In addition, vericiguat is an inhibitor of breast cancer resistance protein (IC50 = 20 µM) as well as OATP1B1 and 1B3 (approximate IC50 of 16 and 30 µM, respectively). Metabolite M-1 is an inhibitor of OATP1B1 and OATP1B3 (IC50 = 25.6 and 16.6 µM, respectively). However, considering the clinical exposure of vericiguat (total Cmax approximately 0.8 µM, unbound Cmax approximately 0.02 µM, and projected unbound inlet Cmax 0.03 µM; data on file) and M-1 (total Cmax 2.7 µM and unbound Cmax 0.04 µM; data on file) following a 10-mg dose once daily, the DDI risk assessment according to the US Food and Drug Administration and European Medicines Agency guidelines indicated a low potential for vericiguat and M-1 to cause DDIs when co-administered with substrates of major CYP and UGT isoforms as well as transporters.

The CYP induction potential of vericiguat and M-1 was evaluated in cultured human hepatocytes from three different donors. Vericiguat showed no significant induction of CYP1A2 and CYP2B6 up to the highest tested concentration of 10,000 μg/L (23.5 µM). For CYP3A4, a 2.7-fold increase in CYP3A4 messenger RNA was observed in one of the three donors at the highest tested concentration (4% of the rifampicin [positive control] response). The potential risk for CYP3A4 induction in the clinic was further assessed using the relative induction score method according to the US Food and Drug Administration and European Medicines Agency DDI guidance [22, 23]. The in vitro induction data in human hepatocytes (CYP3A4 messenger RNA data) and the clinical exposure data from multiple-dose oral administration of 10 mg of vericiguat once daily in patients with HFrEF (total Cmax approximately 1 µM and unbound Cmax approximately 0.02 µM; data on file) were used as input data. The relative induction score model predicted a 15% decrease in the AUC of midazolam, indicating that vericiguat is likely not a clinically meaningful inducer of CYP3A4 in vivo.

3.2 Demographics of Healthy Volunteers in all Phase I Studies

The characteristics of the healthy volunteers enrolled in each of the studies who were valid for PK analyses are shown in Tables 2, 3. Studies were conducted between 2012 and 2017.

Table 2 Demographics of healthy volunteers (pharmacokinetic analysis set) in six phase I studies investigating the clearance mechanisms, elimination, and potential for drug–drug interactions (DDIs) of vericiguat as a victim or perpetrator
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Table 3 Demographics of healthy volunteers (pharmacokinetic analysis set) in five phase I studies investigating the potential for drug–drug interactions (DDIs) of vericiguat with drugs prescribed in cardiovascular disease or acting on the nitric oxide signaling pathway
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3.3 Human Mass Balance Study

A total of six healthy volunteers received a single oral solution containing 14C-labeled vericiguat 5 mg. Mean total radioactivity (range) recovered in urine and feces within 336 h was 98.3% (95.6–99.8%) of the dose administered. Of the administered dose, 53.1% (49.9–56.1%) and 45.2% (40.1–49.9%; mean values [range]) were excreted via urine and feces, respectively.

N-glucuronide metabolite M-1, a pharmacologically inactive major plasma metabolite with no known off-target activities, represented the majority of the radioactivity in urine (Fig. 1, Fig. 1 of the ESM, and Table 4; 40.8% of the dose) together with vericiguat (9.0% of the dose). Metabolite M-15, resulting from oxidative metabolism (presumably by demethylation/decarboxylation/acetylation), was detected as a minor component in urine and feces (1.9% and 1.6%, respectively). Vericiguat represented most of the radioactivity in feces (42.6% of the dose). Metabolite M-1 was the predominant component in human plasma, accounting for 72% of total radioactivity AUC, compared with 27% for the parent drug.

Fig. 1
figure 1

Excretion and clearance of vericiguat. GIT gastrointestinal tract, UGT uridine diphosphate-glucuronosyltransferase

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Table 4 Excretion pattern of vericiguat and its metabolitesa
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3.4 Drug–Drug Interaction Studies

The clinical interaction studies confirmed and extended findings from the in vitro studies (Fig. 2, Tables 5 and 6, and Tables 5 and 6 of the ESM).

Fig. 2
figure 2

Summary of clinical interactions and pharmacokinetic changes investigating the perpetrator and victim potential of vericiguat. AUC area under the concentration–time curve, AUC0–12,md AUC from time 0 to 12 h after multiple dose administration, AUC(0–22) AUC from time 0 to 22 h, AUC(0–24) AUC from time 0 to 24 h, AUC(0–24),md AUC0–24 after multiple-dose administration, AUCτ,md AUC within the dosing interval after multiple dosing, CI confidence interval, Cmax maximum concentration within a dosing interval, Cmax,md Cmax within a dosing interval after multiple dose administration, Ctrough trough concentration within a dosing interval

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Table 5 Effects of other drugs on the pharmacokinetics of vericiguat
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Table 6 Effects of vericiguat on the pharmacokinetics of other drugs
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3.4.1 Effects of Drugs Affecting Intestinal pH on the Pharmacokinetics of Vericiguat

Pre- and co-administration of omeprazole with vericiguat reduced the AUC and Cmax of vericiguat by 32% and 49%, respectively, compared with administration of vericiguat alone. Similar results were observed with co-administration of magnesium/aluminum hydroxide with vericiguat (Table 5).

3.4.2 Effects of Drugs on the Pharmacokinetics of Vericiguat

Co-administration with ketoconazole (a multi-pathway CYP and transporter inhibitor) increased vericiguat exposure to a minor extent (by 13%). Pre- and co-treatment with rifampicin (multi-pathway UGT, CYP, and transporter inducer) led to a decrease in the AUC and Cmax of vericiguat by 29% and 9%, respectively. Inhibition of UGT1A9 by mefenamic acid led to a non-relevant increase in the AUC of vericiguat by 20% (Table 5).

Changes in the pharmacokinetics of vericiguat when given in combination with drugs prescribed in cardiovascular disease or those affecting the NO signaling pathway compared with no co-administration are also shown in Table 5. No differences between the PK parameters of vericiguat when given alone in comparison with its co-administration with warfarin, digoxin, or aspirin were observed. The analysis of variance results for the AUC0–24 and Cmax showed decreases in the exposure of vericiguat of about 7% and 9%, respectively, when vericiguat was administered with sacubitril/valsartan. While the 90% confidence intervals for both parameters excluded unity, the magnitude of change in exposure was small and not considered clinically relevant. Sildenafil co-administration at different doses had no relevant effect on vericiguat PK parameters. Of note, vericiguat exposure was decreased following co-administration with sildenafil 50 mg, but the differences in these PK parameters were small (less than 9%), did not increase at a higher sildenafil dose (100 mg), and hence were considered irrelevant. A mean difference in maximum decrease in seated blood pressure of ≤ 4–5 mmHg between multiple doses of vericiguat 10 mg with single doses of sildenafil (25, 50, or 100 mg) and placebo with single doses of sildenafil (25, 50, or 100 mg) was observed. No dose-dependent trend was observed with the different sildenafil doses.

3.4.3 Effects of Vericiguat on the Pharmacokinetics of Other Drugs

A slight reduction in midazolam exposure (by 18%) was observed after 3 days pre-treatment and 1 day co-treatment with vericiguat 10 mg (Table 6). The AUC and Cmax of 1ʹ-hydroxy midazolam, the main metabolite of midazolam, also decreased by 12% and 16%, respectively. It is noted that the molecular weight-adjusted metabolite-to-parent ratio was comparable (0.27 after administration of midazolam alone vs 0.29 after co-administration of midazolam with vericiguat), suggesting no effect on CYP3A4-mediated metabolism by vericiguat.

Vericiguat did not alter the pharmacokinetics of R- and S-warfarin or digoxin with point estimates for the treatment ratios (co-medication plus vericiguat/co-medication) of AUC and Cmax near 1. Vericiguat at steady state resulted in increases in the AUC0–12,md and Cmax,md of sacubitril by 8% and 18%, respectively, and the AUC0–12,md and Cmax,md of valsartan by 12% and 13%, respectively. Exposure and peak concentration of the active sacubitril metabolite (LBQ657) were unchanged by vericiguat. Co-administration of vericiguat increased exposure and maximum concentration of sildenafil 100 mg with vericiguat in comparison with co-administration of sildenafil with placebo by 13% and 17%, respectively (Table 6).

3.5 Safety and Tolerability

Vericiguat was well tolerated in all studies, and most treatment-emergent adverse events were of mild-to-moderate severity and as expected from the mechanism of action of vericiguat. A total of seven treatment-emergent adverse event-related discontinuations were reported across the DDI studies; however, only one (moderate headache) was related to treatment with vericiguat in the sildenafil DDI study. The treatment-emergent adverse event of moderate headache was considered to be related to both vericiguat and sildenafil.

4 Discussion

These in vitro experiments and clinical pharmacology studies characterized the biotransformation, elimination, and DDI potential of vericiguat.

4.1 Biotransformation and Elimination of Vericiguat

The glucuronidation of vericiguat is mediated by UGT1A1 and UGT1A9. The preclinical biotransformation experiments demonstrated the dominant role of UGT1A9. Considering the different abundances of these UGT isoforms in tissues, UGT1A9 is predominantly responsible for M-1 formation in the kidneys, whereas both UGT1A9 and UGT1A1 are involved in the liver [24, 25]. In the human mass balance study, M-1 represented the majority of the radioactivity in urine (41% of the dose), while vericiguat represented the majority of the radioactivity in feces (43% of the dose). Given the high oral bioavailability (93%; with food) [14], the unchanged drug recovered in feces is not due to non-absorption. Metabolite M-1 was not detected in human feces; ex vivo incubation with human feces under anaerobic conditions showed that M-1 could undergo hydrolytic cleavage to form vericiguat by microbial flora (Fig. 2 of the ESM). Based on a preclinical mass balance study in bile-duct cannulated rats, metabolite M-1 can be excreted via bile (data on file). Therefore, the parent drug observed in feces could result from biliary/intestinal secretion of the parent, as well as possible hydrolysis of M-1 in the gut lumen. Thus, although 41% of the total vericiguat dose is found in the urine as M-1, glucuronidation may contribute to a greater percentage of the overall clearance.

4.2 Pharmacokinetic Drug–Drug Interaction Potential of Vericiguat

Ten phase I DDI studies in healthy volunteers investigated the PK interactions between vericiguat and drugs that are known to affect: intestinal pH and NO signaling; inhibit/induce metabolic pathways; and drugs that are commonly administered to patients with cardiovascular disease. Polypharmacy is common in patients with HF and therefore drugs intended to be used in HF are required to possess a low potential for DDIs as these may result in uncontrolled changes in drug plasma concentrations [11,12,13].

Previous studies have shown an increase in AUC and Cmax by approximately 44% and 41%, respectively, and lower variability (geometric coefficient of variation in AUC was 19% vs 41%) of vericiguat (alone) after administration with food compared to without [14, 16]. Here, a reduction by about 30% in the bioavailability of vericiguat was observed following co-administration in fasting conditions of omeprazole (40 mg once daily) and magnesium/aluminum hydroxide (600/900 mg) relative to vericiguat alone. This is primarily driven by the increase in gastric pH, as vericiguat is a basic compound with a pKa of 4.7 and its solubility is lower in neutral conditions compared with acidic conditions. The increased exposure following administration with food is believed to be due to enhanced wettability and solubility of vericiguat by stimulation of bile salt secretion and the presence of food components enabling better solubilization. Therefore, vericiguat is recommended to be taken with food, irrespective of food type and the concomitant administration of proton pump inhibitors, as well as antacids, were allowed in phase II and III studies.

No relevant PK interaction was observed with the strong CYP3A and broad-spectrum transporter inhibitor ketoconazole (200 mg twice daily; vericiguat AUC increased by 13%) or the inducer rifampicin (600 mg once daily; vericiguat AUC decreased by 29%). Therefore, similar concomitant medications were not excluded in the clinical studies. In addition, inhibition of the major metabolizing enzyme of vericiguat, UGT1A9, by mefenamic acid (500 mg four times daily) led to a non-relevant increase in the AUC of vericiguat (by 20%), thereby allowing UGT inhibitors as concomitant medications in further clinical studies.

The lack of a DDI with midazolam (7.5 mg, single dose) in the clinic is consistent with the in vitro data indicating that vericiguat is not a CYP3A4 inhibitor [18]. Moreover, results from the relative induction score model indicate that vericiguat is likely not a clinically meaningful inducer of CYP3A4 in vivo.

Consistent with the preclinical data, vericiguat had no effect on the pharmacokinetics of narrow therapeutic index drugs commonly prescribed in cardiovascular disease (warfarin 25 mg and digoxin 0.375 mg). Similarly, warfarin, digoxin, aspirin (500 mg; single dose), and sacubitril/valsartan (co-administered at 97/103 mg twice daily) had no effect on the pharmacokinetics of vericiguat.

To rule out that a potential pharmacodynamic interaction is driven by an underlying PK interaction in the sacubitril/valsartan interaction study with vericiguat, the plasma concentrations of both compounds were measured. Exposure and peak concentration of the active sacubitril metabolite LBQ657 were unaffected by vericiguat. For valsartan, increases in exposure and peak concentration were similar following co-administration with vericiguat and co-administration with placebo. Therefore, a PK interaction between vericiguat and sacubitril/valsartan was ruled out. Furthermore, multiple oral doses of vericiguat 2.5 mg administered 2 h prior to sacubitril/valsartan had no additional effect on seated blood pressure [15].

The sildenafil DDI study indicated an increase in exposure for sildenafil co-administered with vericiguat of 22.4% or less, compared with sildenafil co-administered with placebo; however, all 90% confidence intervals included one. No meaningful change in the pharmacokinetics of vericiguat in response to sildenafil treatment was observed. No PK dose-dependent trend was observed with sildenafil (25, 50, or 100 mg).

Vericiguat was generally well tolerated and had a favorable safety profile across all phase I studies when given for a short duration or as a single dose in healthy volunteers. Most treatment-emergent adverse events were mild or moderate in severity and in line with those previously reported for vericiguat [26, 27]. However, as the studies were performed in healthy volunteers, the findings may not reflect how the combination of vericiguat and other co-medications will be tolerated in patients. The concomitant use of vericiguat and phospodiesterase-5 inhibitors, such as sildenafil, is not recommended because of the lack of clinical experience in patients with HF and the potential increased risk for symptomatic hypotension.

Overall, this series of DDI studies demonstrates that vericiguat has a low potential for PK DDIs across the intended therapeutic dose range. Vericiguat has predictable pharmacokinetics, which can be described by a one-compartment model parameterized by apparent clearance and apparent volume of distribution [17]. Based on this population PK model from patients with HFrEF [17], variability in steady-state AUC is estimated to be about 30%. Therefore, the observed maximum changes in exposure in the reported studies were within the range of reported PK vericiguat variability in patients with HFrEF and are considered not clinically relevant. The concurrent or anticipated use of drugs affecting gastric pH and known metabolic pathways, as well as drugs with a narrow therapeutic index or commonly prescribed in patients with cardiovascular disease were permitted in the phase III VICTORIA study.

5 Conclusions

A low PK interaction profile was estimated from in vitro studies and confirmed in healthy volunteer studies; changes in vericiguat exposure were in the range of 30% or less in the phase I DDI studies. Given the low potential for PK interactions, no dose adjustment beyond the dose titration algorithm as per the protocol was required in the phase III VICTORIA study [1]. These results indicate that vericiguat is suitable for the treatment of a patient population with multiple comorbidities requiring polypharmacy, such as patients with HF.