A Drug-drug Interaction Trial of Rifampicin Pharmacokinetics Effect on Fluzoparib

NCT ID: NCT04011124

Last Updated: 2020-02-26

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 16 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-07-24
• Study Completion Date: 2019-09-16

Brief Summary

The primary objective of the study was to assess the effect of repeated oral doses of Rifampicin on the pharmacokinetic profile of a single dose of Fluzoparib.

The secondary objective of the study was to assess the safety of Fluzoparib given alone versus Fluzoparib coadministered with Rifampicin.

Conditions

Healthy Male Subjects

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Rifampicin + Fluzoparib

Group Type: EXPERIMENTAL

Fluzoparib

Intervention Type: DRUG

single dose on Day 1 and Day 12

Rifampicin

Intervention Type: DRUG

QD on Day 5-14 for 10 days

Interventions

Fluzoparib

single dose on Day 1 and Day 12

Intervention Type: DRUG

Rifampicin

QD on Day 5-14 for 10 days

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Sign the informed consent form before the trial and fully understand the trial content, process and possible adverse reactions;

2. Ability to complete the study as required by the protocol;

3. Age on the date of signing the informed consent form is 18 to 50 years old (including both ends) and is limited to male subjects only;

4. Male subjects are willing to have no birth plans in the next 6 months and voluntarily take effective contraception;

5. The fasting weight is not less than 50kg, and the body mass index (BMI) is in the range of 18 kg/m2 to 28 kg/m2 (including both ends);

6. Health status: no medical history of heart, liver, kidney, digestive tract, nervous system, mental abnormalities and metabolic abnormalities;

7. Accepted physical examination results (vital signs, physical examination) and routine laboratory examination (blood routine, blood biochemistry, urine routine, etc.), 12-lead ECG, X-chest, abdominal B-ultrasound, etc. or no clinical significance if abnormal.

8. Creatinine clearance (CLCr) ≥ 80 mL/min, and creatinine is less than or equal to the upper limit of normal

Exclusion Criteria

1. Participate in blood donation within 3 months before screening and donate blood volume ≥400mL or blood loss ≥400mL, participate in blood donation within 1 month before screening and donate blood volume ≥200mL or blood loss ≥200mL, or receive blood transfusion;

2. Allergic constitution, including a history of severe drug allergy or drug allergy; a history of allergies to fluzoparib capsule or its excipients;

3. with drug and/or alcohol abuse history, or alcohol, nicotine and drug screening positives, or drug abuse in the past five years or used drugs 3 months before the trial; and could not prohibit smoking and alcohol during the trial period ;

4. with medical history of cardiovascular disease such as myocarditis, coronary heart disease, pathological arrhythmia, and stroke;

5. Pulmonary diseases, including invasive lung disease, pneumonia, dyspnea, etc.;

6. Chronic kidney disease, renal insufficiency, history of renal anemia;

7. have a history of dysphagia or any history of gastrointestinal disease that affects drug absorption;

8. any uncontrolled peptic ulcer, colitis, pancreatitis, etc.;

9. Anyone who has undergone any surgery within the first 6 months of screening; has undergone any surgery that affects gastrointestinal absorption (including gastrectomy, bowel resection, stomach reduction, etc.);

10. with acute disease that has been clinically determined by the investigator occurred within 1 month before screening;

11. Other important organ diseases such as the nervous system, cardiovascular system, urinary system, digestive system, respiratory system, metabolic and musculoskeletal system with clear medical history (such as uncontrolled diabetes, high blood pressure, etc.), enabling investigators considered unsuitable for participation in the study;

12. Those who have taken any clinical trial drugs within 3 months;

13. Take any drug that affects liver metabolism within 28 days before taking the investigational drug;

14. Take any prescription or over-the-counter medication within 14 days before taking the investigational drug;

15. Take any vitamin products or herbs within 14 days before taking the investigational drug;

16. Clinical laboratory tests are abnormal and clinically significant, or other clinical findings indicate the following diseases, including but not limited to gastrointestinal, kidney, liver, nerve, blood, endocrine, tumor, lung, immune, mental or cardiovascular disease;

17. combined with other viral infections (anti-HCV, anti-HIV positive, HBsAg positive) or combined with syphilis infection;

18. The subject refused to discontinue any beverage containing methylxanthine, such as caffeine (coffee, tea, cola, chocolate, etc.) or alcoholic beverages or any juice, 48 hours before the investigational drug was administered until the end of the study;

19. Strenuous exercise, or other factors affecting drug absorption, distribution, metabolism, excretion, etc.;

20. The investigator believes that the subjects are not eligible to participate in this trial.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

Jiangsu HengRui Medicine Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

First Affiliated Hospital of Zhejiang University School of Medicine

Hangzhou, Zhejiang, China

Countries

China

Other Identifiers

FZPL-I-110

Identifier Type: -

Identifier Source: org_study_id