270
views
0
recommends
+1 Recommend
1 collections
    0
    shares

      2023 CiteScore (issued by Scopus) is 5.4, SNIP 0.454, ranking 21/103 in Category "Biochemistry, Genetics and Molecular Biology (miscellaneous)".  https://www.scopus.com/sourceid/21101107165

      Interested in becoming a BIO Integration published author?

      • Platinum Open Access with no APCs.
      • Fast peer review/Fast publication online after article acceptance.

      Check out the call for papers on our website: https://bio-integration.org/call-for-papers-bio-integration-2/

      scite_
       
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      A Phase I, Randomized, Single-Ascending-Dose, Multiple-Dose, and Food-Effect Trial of the Safety, Efficacy, and Pharmacokinetics of Topiroxostat in Healthy Chinese Participants

      Published
      research-article
      Bookmark

            Abstract

            Background: As the structure of the human diet changes, the prevalence of hyperuricemia is increasing each year. Hyperuricemia and its comorbidities, such as gout, severely affect quality of life. Moreover, hyperuricemia causes renal impairment and is associated with chronic kidney disease. Topiroxostat, a selective xanthine oxidoreductase inhibitor, has been approved to treat hyperuricemia or gout in Japan. Topiroxostat has shown good tolerance and efficacy in the Japanese population. However, its pharmacokinetic (PK) characteristics, efficacy, and safety in the Chinese population remains unknown.

            Objective: This trial evaluated the PK profile, safety, efficacy, and food effects of Topiroxostat in healthy Chinese participants.

            Methods: The major endpoint was determination of the PK profile of Topiroxostat. Topiroxostat concentrations were detected with LC-MS/MS. PK parameters were calculated in Phoenix WinNonlin 8.1. Minor endpoints were safety and efficacy assessments. Assessment of adverse events and safety was performed by clinicians. Plasma uric acid concentration (ΔECmax and ΔAUEC) was determined as the pharmacodynamic index. This study consisted of three arms: single ascending dose (20, 40, and 80 mg, N = 10), multiple dose (80 mg BID, 7 days, N = 10), and food effects (40 mg single dose, fasting-fed cross-over design, N = 10).

            Results: In the single-ascending-dose arm, Topiroxostat showed rapid absorption and excretion, with Tmax <1.6 h and T1/2 2.49–3.72 h. Additionally, Topiroxostat showed a wide distribution, on the basis of moderate Vz/F (242.8–336.36 L). The main PK parameters Cmax, AUC0-t, and AUC0-C showed a linear relationship with dose (R2 = 0.5146, 0.8416, 0.8386, respectively). In the multiple-dose arm, no significant differences were observed in Cmin on days 3–6 (P = 0.265). No serious adverse events were observed. Regarding efficacy, plasma uric acid levels were controlled to low levels during multiple-dose administration. In the food-effects arm, the fed group showed a lower Cmax than the fasting group (316.00 ± 135.81 vs. 478.40 ± 175.42 ng/mL, P = 0.033) but demonstrated better efficacy (ΔECmax, P < 0.001; ΔAUEC, P < 0.001).

            Conclusions: Topiroxostat showed rapid absorption and a broad distribution in healthy Chinese adults. Additionally, it showed good safety and tolerance in the Chinese population. Moreover, the pharmacodynamic profile indicated that post cibum administration increased the efficacy of Topiroxostat.

            Main article text

            Introduction

            According to the 2006 European League Against Rheumatism guidelines, hyperuricemia is defined as an elevated serum urate level exceeding 6.0 mg/dL [1, 2]. Hyperuricemia can lead to monosodium urate formation and accumulation in joints or other tissues, and can cause gout [3]. Hyperuricemia is a risk factor for hypertension, insulin resistance, kidney disease, and cerebro-cardiovascular disease [46].

            Commonly used urate-lowering drugs in China, such as allopurinol, benzbromarone, or febuxostat, are associated with differing adverse effects. Allopurinol can cause severe cutaneous adverse reactions and hypersensitivity, because of the predisposing genetic factor HLA-B*5801, particularly in Asian populations [79]. Benzbromarone has been withdrawn from many European markets because of hepatotoxicity and deaths due to hepatic failure [7]. Febuxostat, compared with allopurinol, is associated with a greater risk of cardiovascular death in patients with gout [10]. Topiroxostat (FYX-051, CAS# 577778-58-6, Fuji Yakuhin Co., Ltd), a xanthine oxidoreductase inhibitor, has demonstrated good safety and is approved to treat hyperuricemia and gout in Japan [1113]. Topiroxostat 120 mg/day has shown non-inferior efficacy to that of allopurinol at 200 mg/day [11]. Additionally, Topiroxostat has demonstrated other effects, such as renoprotective effects [14, 15]. Given the good safety and efficacy of Topiroxostat, this drug should be introduced in China.

            Previous clinical trials in the Japanese population have revealed that Topiroxostat shows a regular pharmacokinetic (PK) profile. However, differences in genetic background between the Japanese and Chinese populations might potentially influence the PK or drug response [16, 17]. To our knowledge, no reports have described the PK and pharmacodynamic (PD) characteristics of Topiroxostat in Chinese participants. Therefore, to evaluate the PK profile, safety, and efficacy in the Chinese population, we designed and performed this phase I, single-ascending-dose, multiple-dose, and food-effect trial of Topiroxostat in healthy Chinese participants.

            Methods

            Participants

            A total of 30 healthy Chinese adults were enrolled in this study from October 28th to November 17th in 2020. The inclusion criteria were as follows: ≥18 and ≤45 years of age; weight: ≥50.0 kg for men or ≥45.0 kg for women; body mass index (BMI) ≥19.0 and ≤25 kg/m2; no abnormalities in vital signs, physical examination, hematology analysis, urinalysis, chemistry, coagulation test, electrocardiogram, and liver color Doppler ultrasound; voluntarily participation in the study, provision of signed informed consent, and willingness and ability to comply with trial procedures; and no pregnancy plans, and voluntary use of effective contraceptive measures during treatment. The major exclusion criteria were as follows: asthma, urticaria, and other allergic disease history, or allergy to Topiroxostat or related pharmaceutic adjuvants; presence of acute illness within 2 weeks prior; history of serious diseases affecting important organs or systems (including but not limited to the liver, kidneys, heart, lungs, immune, gastrointestinal tract, skin, or metabolic system); history of gout; history of taking any medicine, herbs, or other drugs within 2 weeks prior; history of taking mercaptopurine-associated drugs within 4 weeks prior; history of consumption of alcohol, caffeine, grapefruit, or other foods that might influence drug metabolism in 48 h prior; positive blood pregnancy test; and poor compliance.

            This trial was approved by the ethics committee of Sun Yat-sen University Memorial Hospital (2020-YW-061). Additionally, this trial was registered on www.chinadrugtrials.org.cn (CTR20202265). Written informed consent was obtained from all participants.

            Study Endpoint, Safety, and Efficacy Assessments

            The major endpoints of this trial were the PK profiles obtained in single-ascending-dose, multiple-dose, and food-effects studies in healthy Chinese adults, including Cmax, AUC0-t, AUC0-∞, Tmax, t1/2, MRT0-t, MRT0-∞, CL/F, Vz/F, and Kel.

            Minor endpoints were the assessment of the safety and efficacy of Topiroxostat. Efficacy was evaluated on the basis of plasma uric acid concentration (ΔECmax, change in maximum uric acid effective concentration; ΔAUEC: change in area under the uric acid concentration-time curve), determined by the Laboratory Department, Sun Yat-sen Memorial Hospital. Assessments of adverse events (AEs) and safety assessments were performed by clinicians.

            Trial design

            To evaluate the safety, PD, PK profile, and food effects of Topiroxostat (Fuji Yakuhin Co., Ltd.), we designed and performed this phase I, single-site, randomized, single-ascending-dose, multiple-dose, and food-effect trial ( Figure 1 ) by using 20 mg tablets of Topiroxostat.

            Figure 1

            Study design schematic.

            This trial consisted of three arms ( Figure 1 ), as follows.

            1st arm: single-dose arm. A single-ascending-dose, random, open-label, parallel trial was designed to evaluate a single dose of Topiroxostat. Doses of 20 mg, 40 mg, and 80 mg were administered to ten participants (fasting; male:female ratio = 1:1). Because the protocol for the 40 mg group in the single-dose arm was the same as that for the 40 mg fasting subgroup, data for the 40 mg group in the single-dose arm were collected from the food-effects arm ( Figure 1 ).

            The 40 mg group PK data were collected in the food-effects arm.

            A total of 17 time points of blood for PK analysis were sampled pre-administration, and at 0.083 h (5 min), 0.25 h (15 min), 0.50 h (30 min), 0.75 h (45 min), 1.00 h, 1.25 h, 1.50 h, 2.00 h, 2.50 h, 3.00 h, 4.00 h, 6.00 h, 8.00 h, 12.00 h, 24.00 h, and 48.00 h.

            Three time points of blood for PD analysis were sampled pre-administration, and at 12 h and 24 h.

            2nd arm: food-effects arm. A single dose, random, open label, double-cycle, cross-over trial was designed to evaluate food effects (standardized high-fat meal) on Topiroxostat (40 mg). The high-fat diet contained a total of 926.6 kcal with 50% fat. The high-fat menu included milk (250 mL), egg (approximately 110 g), toast (100 g), bacon (55 g), and butter (21 g). We enrolled ten participants, who were randomly divided into two groups. The 40 mg fasting group data were the same as those in the 1st arm ( Figure 1 ). The wash-out time between the fed and fasting intervention was more than 4 days.

            A total of 17 time points of blood for PK analysis per cycle was sampled pre-administration, and at 0.083 h (5 min), 0.25 h (15 min), 0.50 h (30 min), 0.75 h (45 min), 1.00 h, 1.25 h, 1.50 h, 2.00 h, 2.50 h, 3.00 h, 4.00 h, 6.00 h, 8.00 h, 12.00 h, 24.00 h, and 48.00 h.

            Three time points of blood for PD analysis were sampled per cycle pre-administration, and at 12 h and 24 h.

            3rd arm: multiple-dose arm. After more than 4 days of wash-out, the ten participants who received 80 mg Topiroxostat in the 1st arm were enrolled into the multiple-dose (3rd) arm. They received 80 mg Topiroxostat twice per day (q12 h) from the morning of day 1 to day 7 (a total of 13 times).

            A total of 36 time points of blood for PK analysis were sampled pre-administration, and at 0.083 h (5 min), 0.25 h (15 min), 0.50 h (30 min), 0.75 h (45 min), 1.00 h, 1.25 h, 1.50 h, 2.00 h, 2.50 h, 3.00 h, 4.00 h, 6.00 h, 8.00 h, 12.00 h, 48 h, 72 h, 96 h, 120 h, 144 h, 144.083 h, 144.25 h, 144.50 h, 144.75 h, 145.00 h, 145.25 h, 145.50 h, 146.00 h, 146.50 h, 147.00 h, 148.00 h, 150.00 h, 152.00 h, 156.00 h, 168.00 h, and 192.00 h.

            Topiroxostat tablets were taken orally by all participants with 240 mL of warm water (40–45°C).

            Quantification of Topiroxostat

            Blood samples (4 mL per time point) were collected into heparin sodium polypropylene tubes. Plasma was separated by centrifugation at 2–8°C and 1,500 g for 10 min. All samples were frozen at −80°C in 2 h. The analytes were extracted by protein precipitation.

            The plasma concentration of Topiroxostat was detected by liquid chromatography and tandem mass spectrometry with D4-Topiroxostat (CATO Research Chemicals In.) as the internal standard. The range of quantification was 1.00–1000 ng/mL. A SHIMADZU LC-20A system equipped with a ZORBAX Extend C18 (4.6×150 mm, 3.5 μm, Agilent) column and Security Guard Cartridges C18 (4×2.0 mm ID, Phenomenex) pre-column were maintained at 40°C. The mobile phase was 5 mM ammonium acetate and acetonitrile (v:v = 3:2) at 1.0 mL/min for 3.0 min. An AB SCIEX Turbo Spray/4000 Q TRAP system was used to detect the analyte. The ESI negative mode ion spray voltage was set to −4.2 kV at 500°C.

            The linear range of this method was 1.00–1000 ng/mL. The accuracy of intra-day precision (including LLOQ) ranged from 96.5% to 105.1%. Additionally, the accuracy of the inter-day precision (including LLOQ) was in the range of 98.9%–101.9%. The matrix effects, recovery, and stability results are shown in Supplement Tables 2–5. No clear hyperlipidemia matrix effect was observed in the low-concentration quality control (deviation: −3%) and the high-concentration quality control (deviation: 0.88%).

            Statistical analysis

            The PK parameter set was used for analysis of all PK data. PK and PD parameters were calculated in Phoenix WinNonlin 8.1. An analysis of variance model was used to determine the effect of food on PK. The safety set (SS) was used for AE analysis. The PD parameter set was used for the analysis of PD data. Quantitative data are described as mean ± SD and number. Qualitative data are described as frequency and constituent ratio.

            Other statistical analyses were performed in SPSS version 21.0 (IBM®). Categorical variables were analyzed with χ2 test or Fisher exact test. Continuous variables were analyzed with Mann-Whitney U-test to compare two subgroups. P values < 0.05 were considered to be statistically significant.

            Results

            Characteristics of participants

            A total of 30 healthy Chinese adults were enrolled in this study. All participants were included in the PKPS, PD parameter set, and SS analysis. The baseline characteristics of the 30 participants are summarized in Table 1 . No significant differences were observed in the characteristics of participants among the three arms.

            Table 1

            Characteristics of Participants

            Characteristics20 mg (N = 10)40 mg (N = 10)80 mg (N = 10)Total (N = 30)
            FastingFedTotal
            Age (years, mean ± SD)24.95 ± 4.2926.97 ± 5.0228.86 ± 3.8127.91 ± 4.3227.12 ± 5.2826.66 ± 4.67
            Sex: Male/female5/53/22/35/55/515/15
            Ethnicity: Han/Other10/05/04/19/19/128/2
            Height (cm, mean ± SD)162.85 ± 7.34169.60 ± 10.37168.30 ± 12.99168.95 ± 11.10161.70 ± 10.11164.50(9.86)
            Weight (kg, mean ± SD)55.04 ± 6.5264.18 ± 11.3362.06 ± 13.3763.12 ± 11.7358.73 ± 7.3258.96(9.16)
            BMI (kg/m2, mean ± SD)20.69 ± 1.2522.14 ± 1.6321.72 ± 2.2821.93 ± 1.8822.42 ± 1.2221.68(1.61)
            PK and PD characteristics in the single-ascending-dose arm

            PK parameters are summarized in Table 2 . The drug-time curve of the single-ascending-dose arm is illustrated in Figure 2A . Cmax, AUC0-t, and AUC0-∞ increased with ascending dose. The linear analysis of dose and Cmax, AUC0-t, and AUC0-∞ is shown in Figure 2B (R2 = 0.5146, 0.8416, and 0.8386, respectively). AUC0-t and the AUC0-∞ showed a linear relationship with dose.

            Table 2

            PK Parameter Summary

            PK Parameter20 mg40 mg P*80 mg P #
            FastingFastingFedFastingFirst DoseLast Dose
            MeanCV(%)MeanCV(%)MeanCV(%)MeanCV(%)MeanCV(%)MeanCV(%)
            Cmax, Css_max (ng/mL)331.0855.2478.4036.7316.0043.0 0.033 1285.9059.1673.7030.51032.4047.3 0.046
            Css_min (ng/mL)///////////6.2254.0/
            Css_av (ng/mL)///////////122.5129.3/
            AUC0-t (h·ng/mL)333.3528.9629.6020.8530.4925.40.1121734.9633.41278.5026.01563.8329.50.130
            AUC0-∞ (h·ng/mL)343.1127.7643.7722.2538.9125.40.1111753.7733.21304.2926.61620.4632.10.127
            Tmax (h)0.6594.61.1862.71.5848.50.2490.8060.41.6030.61.4534.50.507
            t1/2 (h)3.72109.56.08111.52.49139.40.1533.3131.21.7349.05.8275.8 0.010
            MRT0-t (h)1.8846.72.5133.52.4024.30.7372.4425.02.3321.23.4923.2 0.001
            MRT0-∞ (h)2.5565.03.2337.02.6729.00.2302.7323.92.5622.3//
            CL/F (L/h)62.3427.364.8521.777.7220.00.06951.5443.266.8837.659.7538.30.516
            Vz/F (L)336.36119.3491.4891.9250.21113.80.170242.8044.8154.6735.2450.8153.2 0.001
            Kel (1/h)0.3672.60.2262.30.4945.6 0.004 0.2221.60.4632.30.1764.7 <0.001
            AUC_%Extrap (%)3.0775.71.9692.01.5566.60.5411.1044.11.8180.63.0477.30.177

            PK, pharmacokinetic; *fasting group vs. fed group; #first dose vs. last dose.

            Figure 2

            PK profile of Topiroxostat. A. Mean plasma concentration-time curve of Topiroxostat single ascending dose arm; B. The linear relation of single ascending dose and main PK parameter; C. Mean plasma concentration-time curve of Topiroxostat food effects arm; D. Mean plasma concentration-time curve of Topiroxostat multiple dose arm. (Bar: SD)

            Additionally, PK parameters in the 20 mg group were associated with the characteristics of participants ( Table 3 ). Cmax was associated with age (P = 0.019). Meanwhile, AUC0-t, AUC0-∞, and CL/F were associated with height (P < 0.001) and weight (P = 0.008, 0.002, 0.002, respectively). In addition, t1/2, MRT0-t, MRT0-∞, and Kel were associated with BMI (P = 0.006, 0.048, 0.029, and 0.006, respectively). CL/F was associated with sex (P = 0.032). Vz/F was associated with sex in the 80 mg group (P = 0.032). However, no significant associations were observed in the 40 mg group.

            Table 3

            Correlation of Characteristics of Participants, PD Parameters, and PK Parameters in the Single-dose Arm

            PK Parameter20 mg (N = 10), R2 40 mg (N = 10), R2 80 mg (N = 10), R2 Total (N = 30), R2
            SexAgeHeightWeightBMISexAgeHeightWeightBMISexAgeHeightWeightBMIΔECmax ΔAUEC
            Cmax (ng/mL)0.548 0.019 0.0600.1660.6761.0000.7010.7110.7510.2600.8410.8030.6140.5800.489 0.040 0.024
            AUC0-t (h·ng/mL)0.0560.328 <0.001 0.008 0.6510.4210.9340.5300.3650.8810.3100.9600.1920.2930.829 0.001 <0.001
            AUC0-∞ (h·ng/mL)0.0320.293 <0.001 0.002 0.4890.3100.9070.4100.2930.9600.4210.9600.2500.3100.803 0.001 <0.001
            Tmax (h)0.7620.5900.9150.5640.0890.9520.6050.6020.1730.4760.6750.2270.6010.6700.3280.0940.064
            t1/2 (h)1.0000.9600.7510.283 0.006 0.3100.6760.8670.6270.7260.1510.8290.5900.8030.8290.5450.400
            MRT0-t (h)0.6900.1740.3650.841 0.048 0.6900.2440.8010.3280.2760.5950.7510.2260.2580.987 0.026 0.009
            MRT0-∞ (h)0.6900.2140.4050.934 0.029 0.5480.7260.8140.8290.9871.0000.7770.3930.3280.9600.1810.084
            CL/F (L/h) 0.032 0.293 <0.001 0.002 0.4890.3100.9070.4100.2930.9600.4210.9600.2500.3100.8030.1290.120
            Vz/F (L)0.4210.4670.2600.7760.0740.4210.6270.9070.7260.803 0.032 0.4890.0770.3280.6030.7300.995
            Kel (1/h)1.0000.9600.7510.283 0.006 0.3100.6760.8670.6270.7260.1110.9470.5650.8150.7510.5570.408
            AUC_%Extrap (%)0.3100.6030.0540.2200.7260.5480.7010.6000.5560.5800.3100.2440.6140.9870.7010.0960.110

            PK profiles showed significant associations with PD characteristics. As shown in Figure 3A , 80 mg Topiroxostat demonstrated stronger effects than 20 or 40 mg (ANOVA, P < 0.001, F = 14.42; Table 4 ). Notably, AUC0-t and AUC0-∞ showed a significant correlation of ΔECmax (P = 0.001, 0.001) and ΔAUEC (P < 0.001, 0.001; Table 3 ). In addition, a potential linear relationship was observed between dose and ΔECmax or ΔAUEC (R2 = 0.4484 and 0.4797; Figure 3C, D ).

            Table 4

            Blood Uric Acid Levels Among Groups

            PD Parameter20 mg (N = 10, mean ± SD)40 mg (N = 10, mean ± SD)80 mg (N = 10, mean ± SD) P 3 F4
            FastingFed P 1 Fed/fasting2 Single DoseMulti-Dose
            ΔECmax −30.20 ± 8.53−34.70 ± 11.82−63.10 ± 13.00 <0.001 1.82−57.10 ± 14.81−154.30 ± 24.59 <0.001 14.42
            ΔAUEC−360.60 ± 178.60−541.20 ± 213.65−953.40 ± 218.18 <0.001 1.76−940.80 ± 293.79−19104.60 ± 4178.33 <0.001 16.14

            1, 40 mg fasting group vs. 40 mg fed group; 2, BF/AF: fasting level/fed level; 3, ANOVA P value among 20 mg, 40 mg, and 80 mg fasting single dose; 4, ANOVA F value among 20 mg, 40 mg, and 80 mg fasting single dose. (ΔECmax, change in maximum of uric acid effective concentration; ΔAUEC: change in area under the uric acid concentration-time curve)

            Figure 3

            PD profile of Topiroxostat. A. ΔEC-time curve of Topiroxostat single ascending dose arm; B. ΔEC-time curve of Topiroxostat food effects arm; C, D. The linear relation of single ascending dose and main PD parameter; E. ΔEC-time curve of Topiroxostat multiple dose arm. (ΔEC, delta effective concentration; ΔAUEC: delta area under the plasma concentration–time curve). (Bar: SD)

            PK and PD characteristics in the multiple-dose arm

            Concentration-time curves of three doses are shown in Figure 2D . With respect to those in the first administration and last administration in the multiple-dose arm, Css_max (673.70 ± 205.74 vs. 1032.40 ± 488.21, P = 0.046), t1/2 (1.73 ± 0.85 vs. 5.82 ± 4.41, P = 0.010), MRT0-t (2.33 ± 0.49 vs. 3.49 ± 0.81, P = 0.001), and Vz/F (154.67 ± 54.46 vs. 450.81 ± 239.83, P = 0.001) increased, whereas Kel (0.46 ± 0.15 vs. 0.17 ± 0.11, P < 001) decreased ( Table 2 ). However, we did not find significant differences in Cmin in the mornings of days 3, 4, 5, and 6 (ANOVA analysis, P = 0.2649, F = 1.38).

            In the PD analysis, uric acid decreased in 4 days and was maintained at a low level at days 5–7 ( Figure 3E ). Uric acid increased after the interruption of administration.

            PK and PD characteristics in the food-effects arm

            Concentration-time curves of the fed and fasting groups are shown in Figure 2C . As shown in Table 1 , a standardized high-fat meal decreased Cmax (478.40 ± 175.42 vs. 316.00 ± 135.81, P = 0.033) and increased Kel (0.22 ± 0.14 vs. 0.49 ± 0.22, P = 0.004).

            Although the fed group showed lower Cmax levels, this group also showed stronger efficacy (ΔECmax: −63.10 ± 13.00 vs. −34.70 ± 11.82, P < 0.001, fed/fasting = 1.82; ΔAUEC: −953.40 ± 218.18 vs. −541.20 ± 213.65, P < 0.001, fed/fasting = 1.76; Table 4 ).

            Safety of Topiroxostat in the three arms

            To assess the safety of Topiroxostat, we recorded all AEs. As shown in Table 5 , no serious AEs occurred in this trial. Topiroxostat demonstrated good safety in the Chinese population. We analyzed the associations between AEs and PK characteristics among the three arms (Supplement Table 4) but did not find any correlations of AEs and PK profiles.

            Table 5

            Summary of AEs

            Dosage P*20 mg (N = 10)40 mg (N = 10)80 mg (N = 10)
            FastingFedSingle DoseMulti-Dose
            TimesCases (%)TimesCases (%)TimesCases (%)TimesCases (%)TimesCases (%)
            Any AE1.000137(70.00)43(30.00)11(10.00)257(70.00)218(80.00)
            Any SAENA00(0.00)00(0.00)00(0.00)00(0.00)00(0.00)
            Any ADRNA137(70.00)43(30.00)11(10.00)257(70.00)208(80.00)
            WBC count increased0.66711(10.00)00(0.00)00(0.00)11(10.00)11(10.00)
            Neutrophil count increased1.00011(10.00)00(0.00)00(0.00)11(10.00)11(10.00)
            AnemiaNA00(0.00)00(0.00)00(0.00)00(0.00)22(20.00)
            Transferrin increased0.20700(0.00)00(0.00)00(0.00)22(20.00)00(0.00)
            Urinary leukocyte0.66711(10.00)00(0.00)00(0.00)00(0.00)22(20.00)
            Protein urine present0.43922(20.00)11(10.00)00(0.00)55(50.00)00(0.00)
            Blood urine present0.41422(20.00)00(0.00)00(0.00)44(40.00)33(30.00)
            Urinary α1-microglobulin increased0.75411(10.00)11(10.00)00(0.00)22(20.00)00(0.00)
            Urinary β2-microglobulin increased1.00011(10.00)11(10.00)00(0.00)11(10.00)00(0.00)
            Urinary NAG increased0.66700(0.00)00(0.00)00(0.00)11(10.00)00(0.00)
            Blood sodium decreased0.20722(20.00)00(0.00)11(10.00)00(0.00)00(0.00)
            Serum potassium decreased0.66711(10.00)00(0.00)00(0.00)00(0.00)00(0.00)
            ECG: Abnormal QRS wave complex0.66700(0.00)00(0.00)00(0.00)11(10.00)22(20.00)
            ECG: abnormal T wave0.75411(10.00)11(10.00)00(0.00)22(20.00)32(20.00)
            Sinus bradycardia0.20700(0.00)00(0.00)00(0.00)22(20.00)00(0.00)
            Diastolic pressure decreased0.66700(0.00)00(0.00)00(0.00)21(10.00)00(0.00)
            Blood CPK increasedNA00(0.00)00(0.00)00(0.00)00(0.00)11(10.00)
            Blood triglycerides increased0.66700(0.00)00(0.00)00(0.00)11(10.00)11(10.00)
            ALT increasedNA00(0.00)00(0.00)00(0.00)00(0.00)11(10.00)
            γGTP increasedNA00(0.00)00(0.00)00(0.00)00(0.00)11(10.00)
            FlatulenceNA00(0.00)00(0.00)00(0.00)00(0.00)11(10.00)
            PyrexiaNA00(0.00)00(0.00)00(0.00)00(0.00)11(10.00)
            Bacterial test positiveNA00(0.00)00(0.00)00(0.00)00(0.00)11(10.00)

            *, P value of AE and dose; ALT, alanine aminotransferase; ADR, adverse drug reaction; AE, adverse event; CPK, creatine phosphokinase; ECG, electrocardiograph; γGTP, γ-glutamyltransferase; NA, not applicable; NAG, β-N-acetyl-D-glucosaminidase; RBC, red blood cell; SAE, serious adverse event; WBC, white blood cell.

            Discussion

            This is the first study reporting the safety, PD, and PK profile of Topiroxostat in Chinese participants. This phase I PK study indicated that Topiroxostat is safe and well tolerated in the Chinese population. Moreover, single daily and post cibum administration is suitable for Topiroxostat.

            Single-dose Topiroxostat showed moderate variability in the Chinese population, on the basis of Cmax (36.7–59.1%) and AUC0-∞ CV (22.2–33.2%). Regarding absorption, distribution, metabolism, and excretion characteristics, Topiroxostat showed rapid absorption (Tmax < 1.6 h), rapid excretion (t1/2 = 2.49–3.72 h), and a wide distribution (Vz/F = 242.8–336.36 L). Topiroxostat is insoluble in 0.1 mol/L HCl, methanol (0.57 mg/mL), ethanol (0.48 mg/mL), and water (0.007 mg/mL), and is slightly soluble in N,N-dimethylformamide [18]. Because its fat solubility is higher than its water solubility, the high Vz/F suggested a broad organ or tissue distribution of Topiroxostat. We observed that the AUC of the first dose in the multiple-dose regimen (80 mg) was lower than the expected value ( Table 2 ). This finding might have been due to psychological changes, because the multiple-dose arm was the first trial of the entire study, and participants were likely to have felt more nervous when participating in the trial for the first time. These psychological changes might have influenced function of the intestines, the main area of absorption of Topiroxostat [19]. Cmax significantly decreased after the first dose. A comparison of our study and a PK study in healthy Japanese adults who received 60 mg Topiroxostat [20] showed no clear difference in the main PK parameters between populations. This phase I PK study provided the necessary information for Topiroxostat in the Chinese population.

            In the secondary efficacy endpoint, Topiroxostat showed excellent urate-decreasing effects. A high dose (80 mg) showed stronger effects, on the basis of PD parameters (ΔEC and ΔAUEC; Figure 3A–D ). Multiple administration (80 mg, BID) steadily controlled plasma uric acid to low levels ( Figure 3E ). A previous phase III trial of Topiroxostat in hyperuricemic Japanese patients reported that Topiroxostat 120 mg/day provides non-inferior urate reduction efficacy to that of allopurinol 200 mg/day [11]. Meanwhile, the same team has also reported a dose-response relationship of Topiroxostat [21]. Our results supported that the urate-decreasing effect of Topiroxostat shows a potential dose-response relationship ( Table 4 ).

            Considering the food effects, we observed that a standard high-fat diet enhanced the urate-decreasing effects of Topiroxostat ( Figure 3B , Table 4 ). Although Topiroxostat showed a dose-response relationship in the single-ascending-dose arm, we did not observe higher drug exposure in the fed group ( Table 2 , Figure 2C ). Luo et al. have predicted the PK and PD of Topiroxostat in humans according to a physiologically based PK model [19]. Their results have indicated that Topiroxostat does not penetrate and accumulate well in most organs/tissues (tissue-to-blood partition coefficient < 1.0) [19]. However, Topiroxostat shows a broad organ/tissue distribution [19]. We presumed that this distribution led to high total Topiroxostat accumulation, thus resulting in high Vz/F. Adipose tissue has been found to show the highest tissue-to-blood partition coefficient [19]. Therefore, we presumed that the standard high-fat diet enhanced the effects of Topiroxostat by increasing its the organ/tissue accumulation. The long residence time of Topiroxostat might be the main cause of its pharmacological activity [19]. More evidence should be gathered to demonstrate this hypothesis. Overall, post cibum administration increased the efficacy of Topiroxostat in the Chinese population.

            In analyzing the safety of Topiroxostat, we did not use a placebo group in this trial; however, all AEs observed in this trial were mild. In addition, no potential dose-toxicity relationship was observed between PK and AE. However, renal or cardiac relative toxicity were the main AEs. Nevertheless, Horino et al. have reported that Topiroxostat shows renoprotective effects in patients with chronic kidney disease [14]. Additionally, Sugiyama et al. have reported that Topiroxostat may not cause QT-interval prolongation [20]. Furthermore, a large population phase III study of Topiroxostat has shown that a dose of 120 mg/day is well tolerated [11]. The incidence of overall AEs with 120 mg/day Topiroxostat were similar to those of allopurinol at 200 mg/day [11]. A long-term-safety observational study has shown no specific problems regarding the safety of Topiroxostat after its approval [22]. Other phase II studies have also indicated Topiroxostat’s good safety and tolerance [2123]. Overall, Topiroxostat is considered a safe and effective drug for treating gout and hyperuricemia in daily practice. In the future, we will confirm the safety and effects of Topiroxostat under actual conditions in the Chinese population. Febuxostat, a xanthine oxidoreductase inhibitor, is widely used in clinical practice. According to one report, Febuxostat, compared with allopurinol, poses a risk of cardiovascular death in patients with gout [10]. Topiroxostat did not demonstrate cardiovascular toxicity in our trial, in agreement with findings from previous studies [20, 23, 24]. Moreover, Topiroxostat shows a lower incidence rate of gouty arthritis than febuxostat [23, 25]. Topiroxostat might be more beneficial in patients with hyperuricemia who are experiencing gouty arthritis. In contrast, Febuxostat elicits a more rapid decrease in serum uric acid than Topiroxostat in patients with cardiovascular disease and hyperuricemia [26]. Febuxostat has stronger antioxidant effects than Topiroxostat in patients with hyperuricemia and chronic kidney disease [27]. Thus, Topiroxostat and Febuxostat have differing advantages and adaptation effects.

            This trial has two potential limitations. First, we were unable to explain the PK and PD relationships with food effects. However, a PK/PD model such as the physiologically based PK model may be considered to predict their relationship. Second, this study was based on a healthy Chinese population. Considering the differences in PK profiles between the Japanese and Chinese populations, further PK/PD trials in patients with hyperuricemia, older people, and other populations should be performed in the future.

            Conclusion

            The PK profile of Topiroxostat in the Chinese population was assessed in this study. No severe AEs were observed in any participants. Topiroxostat had good safety and tolerance in the Chinese population. Additionally, this phase I PK and PD study of Topiroxostat supports that post cibum administration is suitable for Topiroxostat in the Chinese population.

            Acknowledgments

            We thank Fuji Yakuhin Co., Ltd and Guangzhou Fushituopi Co., Ltd for supporting this trial.

            Conflicts of interest

            This trial was supported by Fuji Yakuhin Co., Ltd and Guangzhou Fushituopi Co., Ltd. There are no additional possible conflicts of interest to report.

            Author Contributions

            All authors participated and performed this trial together. Suiwen Ye performed sample collection and wrote the manuscript; Wei Zhuang performed statistics and revised the manuscript; and Xiuping Lai enrolled the participants. Yunni Lin, Jing Wang, and Junyi Chen were in charge of the nursing work. Guoping Zhong was the sub-investigator and designed the trial. Herui Yao enrolled the participants and supported the trial. Junyan Wu was the principal investigator of this trial.

            Funding

            This study was supported by the National Science and Technology Major Project (grant No. 2020ZX09201021), the National Natural Science Foundation of China (grant Nos. 81572596 and 81972471), the Basic and Applied Basic Research Fund of Guangdong Province (grant No. 2020A1515110637), the Natural Science Foundation of Guangdong Province (grant No. 2017A030313828), the Guangzhou Science and Technology Major Program (grant No. 201704020131), the Guangdong Science and Technology Department (grant No. 2020B1212060018), the Sun Yat-sen University Clinical Research 5010 Program (grant No. 2018007), the Sun Yat-sen Clinical Research Cultivating Program (grant No. SYS-C-201801), the Guangdong Medical Science and Technology Program (grant No. A2020558), and Tencent Charity Foundation (grant Nos. SYSU-81000-20200311-0001 and SYSU-05160-20200506-0001).

            Additional material

            Supplementary Tables

            References

            1. , , , , , et al. EULAR evidence based recommendations for gout. Part I: Diagnosis. Report of a task force of the Standing Committee for International Clinical Studies Including Therapeutics (ESCISIT). Ann Rheum Dis 2006;65:1301–11. Journal Article; Practice Guideline; Research Support, Non-U.S. Gov’t; Review. [PMID: 16707533 DOI: 10.1136/ard.2006.055251]

            2. , , , , , et al. 2018 updated European League Against Rheumatism evidence-based recommendations for the diagnosis of gout. Ann Rheum Dis 2020;79:31–8. [PMID: 31167758 DOI: 10.1136/annrheumdis-2019-215315]

            3. , , , . Gout. Lancet 2021;397:1843–55. Journal Article; Research Support, Non-U.S. Gov’t; Review. [PMID: 33798500 DOI: 10.1016/S0140-6736(21)00569-9]

            4. , . Definition of hyperuricemia and gouty conditions. Curr Opin Rheumatol 2014;26:186–91. [PMID: 24419750 DOI: 10.1097/BOR.0000000000000028]

            5. , , . Cardiovascular and renal effects of hyperuricaemia and gout. Reumatismo 2012;63:253–62. Journal Article; Review. [PMID: 22303532 DOI: 10.4081/reumatismo.2011.253]

            6. , , , , , et al. Hyperuricaemia and gout in cardiovascular, metabolic and kidney disease. Eur J. Intern Med 2020;80:1–11. [PMID: 32739239 DOI: 10.1016/j.ejim.2020.07.006]

            7. , , . Safety and tolerability of available urate-lowering drugs: a critical review. Expert Opin Drug Saf 2019;18:261–71. Journal Article; Review. [PMID: 30915866 DOI: 10.1080/14740338.2019.1594771]

            8. , , , , , et al. Allopurinol hypersensitivity: a systematic review of all published cases, 1950-2012. Drug Saf 2013;36:953–80. Journal Article; Research Support, Non-U.S. Gov’t; Review; Systematic Review. [PMID: 23873481 DOI: 10.1007/s40264-013-0084-0]

            9. , , , , , et al. HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol. Proc Natl Acad Sci U S A 2005;102:4134–39. Journal Article; Research Support, Non-U.S. Gov’t. [PMID: 15743917 DOI: 10.1073/pnas.0409500102]

            10. , , , , , et al. Cardiovascular safety of febuxostat or allopurinol in patients with gout. N Engl J Med 2018;378:1200–10. Comparative Study; Equivalence Trial; Journal Article; Multicenter Study; Randomized Controlled Trial; Research Support, Non-U.S. Gov’t. [PMID: 29527974 DOI: 10.1056/NEJMoa1710895]

            11. , , , , , et al. Comparison of topiroxostat and allopurinol in Japanese hyperuricemic patients with or without gout: a phase 3, multicentre, randomized, double-blind, double-dummy, active-controlled, parallel-group study. J Clin Pharm Ther 2016;41:290–7. [PMID: 27109450 DOI: 10.1111/jcpt.12391]

            12. , , , . FYX-051: a novel and potent hybrid-type inhibitor of xanthine oxidoreductase. J Pharmacol Exp Ther 2010;336:95–103. [PMID: 20952484 DOI: 10.1124/jpet.110.174540]

            13. , , , , . Perfecting a high hypoxanthine phosphoribosyltransferase activity–uricase KO mice to test the effects of purine- and non-purine-type xanthine dehydrogenase (XDH) inhibitors. Br J Pharmacol 2020;177:2274–85. [PMID: 31971609 DOI: 10.1111/bph.14978]

            14. , , , , , et al. Effects of topiroxostat in hyperuricemic patients with chronic kidney disease. Clin Exp Nephrol 2018;22:337–45. [PMID: 28752287 DOI: 10.1007/s10157-017-1452-3]

            15. , , , , , et al. Renoprotective effects of topiroxostat for Hyperuricaemic patients with overt diabetic nephropathy study (ETUDE study): a prospective, randomized, multicentre clinical trial. Nephrology 2018;23:1023–30. [PMID: 28990729 DOI: 10.1111/nep.13177]

            16. . Pharmacokinetic differences between ethnic groups. Lancet 2002;359:78. Letter; Comment. [PMID: 11809218 DOI: 10.1016/s0140-6736(02)07296-3]

            17. , , , . Pharmacogenomics and personalized medicine: a review focused on their application in the Chinese population. Acta Pharmacol Sin. 2015;36:535–43. Journal Article; Research Support, Non-U.S. Gov’t; Review. [PMID: 25891088 DOI: 10.1038/aps.2015.10]

            18. Association JHP. Pharmceuticals Medical Devices Agency. 2015. Available from: https://www.docin.com/p1-2266296066.html . 2015.

            19. , , , , , et al. Prediction of the pharmacokinetics and pharmacodynamics of topiroxostat in humans by integrating the physiologically based pharmacokinetic model with the drug-target residence time model. Biomed Pharmacother 2020;121:109660. [PMID: 31733581 DOI: 10.1016/j.biopha.2019.109660]

            20. , , , , . QT/QTc study conducted in Japanese adult healthy subjects: a novel xanthine oxidase inhibitor topiroxostat was not associated with QT prolongation. J Clin Pharmacol 2014;54:446–52. [PMID: 24214189 DOI: 10.1002/jcph.226]

            21. , , , , . Clinical efficacy and safety of topiroxostat in Japanese male hyperuricemic patients with or without gout: an exploratory, phase 2a, multicentre, randomized, double-blind, placebo-controlled study. J Clin Pharm Ther 2016;41:298–305. [PMID: 27079434 DOI: 10.1111/jcpt.12392]

            22. , , , , , et al. Long-term safety and effectiveness of the xanthine oxidoreductase inhibitor, topiroxostat in Japanese hyperuricemic patients with or without gout: a 54-week open-label, multicenter, post-marketing observational study. Clin Drug Invest 2020;40:847–59. [PMID: 32621143 DOI: 10.1007/s40261-020-00941-3]

            23. , , , , . Multicenter, open-label study of long-term topiroxostat (FYX-051) administration in Japanese hyperuricemic patients with or without gout. Clin Drug Investig 2018;38:1135–43. [PMID: 30219951 DOI: 10.1007/s40261-018-0699-0]

            24. , , . Clinical efficacy and safety of topiroxostat in Japanese hyperuricemic patients with or without gout: a randomized, double-blinded, controlled phase 2b study. Clin Rheumatol 2017;36:649–56. [PMID: 27832384 DOI: 10.1007/s10067-016-3474-8]

            25. , , , , , et al. Multicenter, open-label study of long-term administration of febuxostat (TMX-67) in Japanese patients with hyperuricemia including gout. J Clin Rheumatol 2011;17:S50–6. Comparative Study; Journal Article; Multicenter Study; Randomized Controlled Trial; Research Support, Non-U.S. Gov’t. [PMID: 21654270 DOI: 10.1097/RHU.0b013e31822541d0]

            26. , , , , . Cross-over trial of febuxostat and topiroxostat for hyperuricemia with cardiovascular disease (TROFEO Trial). Circ J 2017;81:1707–12. Journal Article; Randomized Controlled Trial. [PMID: 5283948 DOI: 10.1155/2019/5283948]

            27. , , , , , et al. Changeover trial of febuxostat and topiroxostat for hyperuricemia with cardiovascular disease: sub-analysis for chronic kidney disease (TROFEO CKD Trial). Ann Thorac Cardiovasc Surg 2020;26:202–08. Journal Article; Randomized Controlled Trial. [PMID: 31748427 DOI: 10.5761/atcs.oa.19-00162]

            Author and article information

            Journal
            BIOI
            BIO Integration
            BIOI
            Compuscript (Ireland )
            2712-0082
            2712-0074
            September 2022
            05 July 2022
            : 3
            : 3
            : 93-102
            Affiliations
            [1] 1Phase I Clinical Trial Centre, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, PR China
            [2] 2Institute of Clinical Pharmacology, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, PR China
            Author notes
            *Correspondence to: Junyan Wu, E-mail: wujunyan@ 123456mail.sysu.edu.cn ; Herui Yao, E-mail: yaoherui@ 123456mail.sysu.edu.cn

            aThese authors contributed equally.

            Article
            bioi20220006
            10.15212/bioi-2022-0006
            c2bf1377-6612-49d5-b765-154959ffe0ca
            Copyright © 2022 The Authors

            This is an open access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/). See https://bio-integration.org/copyright-and-permissions/

            History
            : 02 February 2022
            : 18 April 2022
            : 16 June 2022
            Categories
            Original Article

            Medicine,Molecular medicine,Radiology & Imaging,Biotechnology,Pharmacology & Pharmaceutical medicine,Microscopy & Imaging
            topiroxostat,pharmacokinetics,Food effect,pharmacodynamics,hyperuricemia

            Comments

            Comment on this article