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A Study to Evaluate the Effect of Rifampicin on the Pharmacokinetics of Abiraterone in Healthy Male Participants

Phase 1
Completed
Conditions
Healthy
Interventions
Registration Number
NCT01655147
Lead Sponsor
Janssen Research & Development, LLC
Brief Summary

The purpose of this study is to assess the effects of repeated daily administration of rifampicin on the pharmacokinetics (what the body does to the medication) of abiraterone following single-dose administration of abiraterone acetate tablets in healthy male participants.

Detailed Description

This is an open-label (all people know the identity of the intervention), single-center (study conducted at one site), 2-period, sequential-design (studies that combine both longitudinal and cross sectional methods), to evaluate the effects of rifampicin on the pharmacokinetics of abiraterone acetate in healthy male participants. The study consists of a screening phase, an open-label treatment phase, and a follow up phase. The screening phase will be within 14 days before the first study medication administration. The treatment phase will consist of 2 treatment periods, Period 1: a single oral dose of abiraterone acetate tablets, and Period 2: a daily oral dose of rifampicin capsules alongwith a single oral dose of abiraterone acetate tablets. The 2 periods will be separated by a washout period of at least 7 days. Blood sample collection for pharmacokinetic assessments will be done for determination of abiraterone and rifampicin concentrations. The follow up phase will be of 14 days. Safety evaluations for adverse events, clinical laboratory tests, electrocardiogram, vital signs, and physical examinations will be monitored throughout the study. The total study duration will be approximately 31 days.

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
19
Inclusion Criteria
  • Must have blood pressure between 90 and 140 mmHg systolic, inclusive, and no higher than 90 mmHg diastolic
  • Must have a 12-lead electrocardiogram consistent with normal cardiac conduction and function
  • Must sign an informed consent document indicating they understand the purpose of and procedures required for the study and are willing to participate in the study
  • Must agree to use an adequate contraception method and to not donate sperm during the study and for 3 months after receiving the last dose of study medication
  • Have willingness to participate in the optional pharmacogenomic component of this study, participants (or their legally acceptable representative) must have signed the informed consent form
Exclusion Criteria
  • History of or current clinically significant medical illness including cardiac arrhythmias or other cardiac disease, hematologic disease, coagulation disorders, lipid abnormalities, and others
  • Clinically significant abnormal values for hematology or clinical chemistry at screening or at admission to the study center
  • Serum testosterone level of < 200 ng/dL (at screening)
  • Clinically significant renal laboratory findings including specifically, creatinine, and creatinine clearance
  • Clinically significant hepatic laboratory findings or signs

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Abiraterone acetate + RifampicinAbiraterone acetateAbiraterone acetate 1,000 mg (4 x 250 mg) on Day 1 of Period 1. Rifampicin 600 mg (2 x 300 mg) on Days 8 to 13, and Abiraterone acetate 1,000 mg (4 x 250 mg) on Day 14 of Period 2.
Abiraterone acetate + RifampicinRifampicinAbiraterone acetate 1,000 mg (4 x 250 mg) on Day 1 of Period 1. Rifampicin 600 mg (2 x 300 mg) on Days 8 to 13, and Abiraterone acetate 1,000 mg (4 x 250 mg) on Day 14 of Period 2.
Primary Outcome Measures
NameTimeMethod
Maximum plasma concentration (Cmax) of abiraterone in Period 1 and Period 2Period 1: Day 1 to Day 4; Period 2: Day 14 to Day 17

Pharmacokinetic parameter Cmax of abiraterone was measured when abiraterone acetate was administered in Period 1 and Period 2.

Area under the plasma concentration-time curve (AUC) of abiraterone in Period 1 and Period 2Period 1: Day 1 to Day 4; Period 2: Day 14 to Day 17

Pharmacokinetic parameter AUC of abiraterone was measured when abiraterone acetate was administered in Period 1 and Period 2.

Time to reach the maximum plasma concentration (tmax) of abiraterone in Period 1 and Period 2Period 1: Day 1 to Day 4; Period 2: Day 14 to Day 17

Pharmacokinetic parameter tmax of abiraterone was measured when abiraterone acetate was administered in Period 1 and Period 2.

Eliminaton half-life (t1/2) of abiraterone in Period 1 and Period 2Period 1: Day 1 to Day 4; Period 2: Day 14 to Day 17

Pharmacokinetic parameter t1/2 of abiraterone was measured when abiraterone acetate was administered in Period 1 and Period 2.

Secondary Outcome Measures
NameTimeMethod
Number of participants with adverse eventsUp to 31 days
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