Pharmacokinetics and Bioequivalence of Abiraterone Acetate Tablets in Healthy Chinese Volunteers: An Open, Randomized, Single-Dose, Three-Period, Three-Sequence Crossover Study

The ethical approval process of this trial was in accordance with the requirements of Good Clinical Practice (GCP) [8], the Helsinki Declaration [9], and relevant domestic laws and regulations. The study plan and informed consent were approved by the Medical Ethics Committee of the Affiliated Hospital of Qingdao University. All volunteers signed informed consent to be involved in the study before receiving the study drug.

The abiraterone acetate tablet test product was obtained from Qilu Pharmaceutical Co., Ltd (batch number 17F0023DD9), and the reference product Zecke^® (abiraterone acetate tablet) was purchased from Patheon Inc. (batch number VYCB).

The selection criteria for volunteers were (1) healthy male volunteers ≥18 years of age; (2) weight not less than 50 kg and body mass index between 19 and 28 kg/m²; (3) no unhealthy habits, such as smoking or alcohol consumption, and no history of drug abuse; and (4) participants who volunteered to participate in the clinical trial, understood the study procedures and signed written informed consent and were able to complete the study according to the test protocol.

The exclusion criteria were (1) abnormal results of vital sign assessments, physical examination, electrocardiogram and other laboratory examinations were clinically significant; (2) diseases of the central nervous system, the cardiovascular system, liver and kidney function, the digestive system (including acute gastroenteritis and diarrhea 2 weeks prior to drug delivery) and the respiratory system (not including upper respiratory infection 2 weeks prior to drug delivery), metabolic or skeletal system diseases, or any other diseases or physiological conditions that may have affected the results of the study; (3) a history of hospitalization or surgery within 3 months prior to the trial; (4) known active hepatitis B, human immunodeficiency virus (HIV), hepatitis C virus (HCV) or Treponema pallidum infection; (5) a history of specific allergic reactions (such as atopic dermatitis, and asthma), a history of allergy to drugs or biological agents, or a history of known allergy to the ingredients of this drug; (6) positive tests for alcohol during urine drug screening; (7) regular drinkers who consumed more than 14 units of alcohol per week (1 unit is 360 mL beer or 45 mL liquor of 40% alcohol, or 150 mL wine) during the 3 months prior to the trial; (8) smoking more than five cigarettes per day within 3 months before the trial; (9) participation as a subject in any drug clinical trial within 3 months prior to the trial; (10) people who had donated blood or lost more than 400 mL of blood during the 3 months before the experiment; (11) a history of prescription drug use during the 14 days prior to the trial; (12) a history of over-the-counter medicine use or consumption of any functional vitamins or herbal products within 48 h prior to the trial; (13) consumption of any xanthine-rich beverage or food, or grapefruit or products containing grapefruit, within 48 h prior to the test; (14) consumption of any food or drink containing caffeine (such as tea or coffee) and any alcoholic products within 48 h before the trial; (15) special requirements on diet and failure to follow the diet and corresponding regulations provided; and (16) volunteers who were considered by the investigator to exhibit poor compliance or any factors making them unsuitable for participating in the study.

A single-center, open, randomized, single-dose, three-period, three-sequence, half-repeat (only repeated reference formulation), and reference formulation-corrected fasting reference-scaled average bioequivalence (RSABE) trial was conducted in the phase I Clinical Research Center of the Affiliated Hospital of Qingdao University. Thirty-seven healthy volunteers were enrolled in this study (one subject was replaced before initial administration). SAS v9.3 software was used to generate a random table, and the volunteers were randomly divided into three groups according to a 1:1:1 ratio. Subjects were randomly assigned to one of the three groups according to the random table (Table 1) generated before the subjects were enrolled. There was a minimum 7-day washout interval between dosing, and subjects took the study drug, according to a randomized schedule, on days 1, 8, and 15 of the trial. Qualified subjects were screened to enter the phase I ward 1 day before the first periods of administration, to participate in the baseline examination. Qualified subjects were admitted to the phase I ward and fasted overnight. Subjects were forbidden to drink water from 1 h before to 1 h after taking the medicine, and could drink water freely at other times. They fasted within 4 h after taking the medicine.

During the three-period test, 4 mL of whole venous blood was collected at 0 h (within 1 h before administration) and 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 6, 8, 12, 24 and 48 h after administration and placed into an EDTA-K₂ anticoagulant tube. The plasma concentration of abiraterone acetate tablets in plasma was determined by centrifugation. Blood samples were immediately placed in crushed ice or other refrigeration equipment after collection, placed in a precooled low temperature (2–8℃) centrifuge within 60 min, and centrifuged at 3500 rpm for 10 min. The time between the blood sample being collected and the plasma sample being placed in the refrigerator was < 120 min. Plasma samples from intensive blood collection sites were temporarily stored in a refrigerator at − 20 °C and transferred to a refrigerator at − 80 °C within 24 h. Plasma samples from non-intensive blood collection sites were stored directly in a − 80 °C refrigerator until being transported to the sample testing laboratory. Plasma samples were analyzed using the proven high-performance liquid chromatography-tandem mass spectrometry (LC‒MS/MS) method of Shanghai WuXi AppTec New Drug Development Co., Ltd. The LC‒MS/MS system consisted mainly of Shimadzu’s Shimadzu LC-30AD system and Applied Biosystems/SCIEX API 6500. Mobile phase A consisted of 0.1% FA aqueous solution containing 2 mM ammonium acetate, and mobile phase B consisted of 95% acetonitrile solution containing 2 mM ammonium acetate and 0.1% FA. The flow rate was set at 0.500 mL/min. The maximum intra- and interbatch accuracies of abiraterone detection were 4.7% and 4.3%, respectively, and the intrabatch accuracies ranged from 3.2 to 6.6%. The linear range of abiraterone concentration was 0.500–200 ng/mL and the lower limit of quantification was 0.500 ng/mL.

During the three periods, the vital signs of the enrolled subjects were measured (body temperature, pulse and blood pressure) before and 2, 8, 24 and 48 h after administration, as were the levels of electrolytes (potassium, sodium and phosphorus) 24 and 48 h after administration. Subjects were also asked about their subjective feelings to evaluate whether there were adverse reactions. Safety tests, including assessments of vital signs, physical examination, 12-lead electrocardiogram, routine blood tests, routine urine tests, and blood biochemical tests, were performed before subjects withdrew from the study. The clinical characteristics and the occurrence time, duration, treatment measures and severity of adverse reactions of subjects during the trial were recorded in detail.

Pharmacokinetic metrics of abiraterone were estimated using non-compartmental methods based on plasma concentrations using SAS v9.3. The pharmacokinetic metrics estimated included time to reach C_max (T_max), maximum plasma concentration (C_max), area under the concentration-time curve from time zero to time t (AUC_t) or AUC from time zero to infinity (AUC_∞), and elimination half-life (T_½), etc.

SAS v9.3 software was used for statistical analysis. After logarithmic transformation of the major pharmacokinetic metrics (C_max, AUC_t and AUC_∞), bidirectional and unidirectional T tests were performed to calculate the geometric mean ratios (GMRs) and 90% confidence intervals (CIs) of these major pharmacokinetic metrics. When the individual coefficient of variation (CV_WR) of the pharmacokinetic metrics (AUC_t, AUC_∞ and C_max) of reference formulations was < 30%, two formulations were considered bioequivalent if the 90% CIs of the GMRs of their main pharmacokinetic parameters were within a predefined acceptable range of 80–125%. When the CV_WR of the pharmacokinetic metrics (AUC_t, AUC_∞ and C_max) of the reference formulation was ≥ 30%, the reference formulation was used to correct for RSABE: if the Critbound of the pharmacokinetic metrics (AUC_t, AUC_∞ and C_max) of the test and reference formulations was < 0 and the geometric average ratio was not beyond the range of 0.8000–1.2500, this method can be used to determine whether the test and reference formulations have bioequivalence.

Figure 1 shows the features of the study subjects. A total of 79 subjects were screened for the study and a total of 37 healthy volunteers were enrolled in this clinical study, of whom 35 volunteers completed the whole study. One subject withdrew from the study and was replaced by another subject due to difficulties in blood collection before the first administration, and one subject withdrew voluntarily. All volunteers in this study were male. The patient demographic characteristics are shown in Table 2.

Tables 3 and 4 show the specific pharmacokinetic metrics or variance analysis results of the test and reference formulations of abiraterone acetate tablet under a fasting state. The mean concentration-time curves of plasma abiraterone acetate tablets after one fasting oral administration of the test formulation and two fasting oral reference formulations are shown in Fig. 2. Individual plasma concentration-time data on abiraterone acetate tablets are presented in the electronic supplementary file. The 90% CIs of the GMR of AUC_t to AUC_∞ of the test and reference formulations were in the range of 0.8000–1.2500; the CV_WR of C_max for the reference formulation was > 30%, the Critbound result was − 0.0522, and the GMR was between 0.8000 and 1.2500 (Table 5).

A total of 18 adverse events (AEs) occurred in 11 subjects in this study. Of the 36 subjects enrolled in the safety analysis dataset, 17 AEs occurred in 10 subjects, all of which were mild AEs. After analysis, nine AEs in seven volunteers were found to be ‘probably related’ or ‘very likely related’ to the test drug and were considered adverse reactions. Eight AEs in six subjects were found to be ‘definitely not’ or ‘probably not’ related to the test drug (see Table 6 for details).