Safety and Pharmacokinetics of Fluzoparib in Healthy Subjects and Those With Impaired Kidney Function
Primary Purpose
Renal Impairment
Status
Unknown status
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Fluzoparib
Fluzoparib
Fluzoparib
Sponsored by
About this trial
This is an interventional basic science trial for Renal Impairment
Eligibility Criteria
Inclusion Criteria:
-
Inclusion Criteria for subjects with impaired kidney function:
- Sign the informed consent before the trial, and fully understand the content, process, and possible adverse reactions of the trial;
- Male or female subjects aged 18 to 70 (including 18 and 70);
- Body mass index (BMI) ranges from 18 kg/m2 to 28 kg/m2 (including 18 and 28);
- The glomerular filtration rate should meet the following criteria (GFR, mL/min):Subjects with mild renal impairment (CKD2): 60-89 mL/min (including 60-89);Subjects with moderate renal impairment (CKD3): 30-59 mL/min (including 30-59 ends);
- Renal function should be stable, and the GFR results should be tested twice before administration (at least 3 days apart) within the same CKD stage.
Inclusion Criteria for subjects with normal kidney function:
- Sign the informed consent before the trial and fully understand the content, process, and possible adverse reactions of the trial;
- Male or female subjects aged 18 to 70 (including 18 and 70);
- Body mass index (BMI) ranges from 18 kg/m2 to 28 kg/m2 (including 18 and 28);
- Glomerular filtration rate (GFR) ≥90 mL/min.
Exclusion Criteria:
-
Exclusion Criteria for subjects with impaired kidney function:
- History of kidney transplant;
- Need Renal dialysis during the study;
- Urinary incontinence or anuria;
- Clinically significant heart disease, including but not limited to: congestive heart failure, symptomatic coronary artery disease, myocardial infarction, QTcF≥470 ms (female) or QTcF≥450 ms (male) within 12 months before the start of treatment;
- Received any investigational drug within 3 months before the study started;
- Taking any drugs which can affect the metabolic enzyme CYP3A within 14 days before the study started;
- Smokers and alcoholics, or those screened positive for alcohol;
- History of drug use, or drug abuse screening positive.
Exclusion Criteria for subjects with normal kidney function:
- History of kidney transplant;
- Clinically significant heart disease, including but not limited to: congestive heart failure, symptomatic coronary artery disease, myocardial infarction, QTcF≥470 ms (female) or QTcF≥450 ms (male) within 12 months before the start of treatment;
- Received any investigational drug within 3 months before the study started;
- Taking any drugs which can affect the metabolic enzyme CYP3A within 14 days before the study started;
- Smokers and alcoholics, or those screened positive for alcohol;
- History of drug use, or drug abuse screening positive.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Experimental
Arm Label
Group A
Group B
Group C
Arm Description
Outcomes
Primary Outcome Measures
Pharmacokinetics parameters of Fluzoparib: Cmax
Pharmacokinetics parameters of Fluzoparib: AUC0-t
Pharmacokinetics parameters of Fluzoparib: AUC0-∞ (if available)
Pharmacokinetics parameters of main metabolite (SHR165202) of Fluzoparib: Cmax
Pharmacokinetics parameters of main metabolite (SHR165202) of Fluzoparib: AUC0-t
Pharmacokinetics parameters of main metabolite (SHR165202) of Fluzoparib: AUC0-∞ (if available)
Secondary Outcome Measures
Other pharmacokinetics parameters of Fluzoparib: Tmax
Other pharmacokinetics parameters of main metabolite (SHR165202) of Fluzoparib: Tmax
Plasma protein binding rate of Fluzoparib
Plasma protein binding rate of main metabolite (SHR165202) of Fluzoparib
The incidence and severity of adverse events/serious adverse events (based on NCI-CTCAE 5.0)
Full Information
NCT ID
NCT05032235
First Posted
August 27, 2021
Last Updated
August 27, 2021
Sponsor
Jiangsu HengRui Medicine Co., Ltd.
1. Study Identification
Unique Protocol Identification Number
NCT05032235
Brief Title
Safety and Pharmacokinetics of Fluzoparib in Healthy Subjects and Those With Impaired Kidney Function
Official Title
A Multi-centre, Open-label and Parallel-control Study to Investigate the Pharmacokinetics of Fluzoparib in Healthy Subjects and Those With Impaired Kidney Function
Study Type
Interventional
2. Study Status
Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
September 15, 2021 (Anticipated)
Primary Completion Date
October 15, 2022 (Anticipated)
Study Completion Date
October 28, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Jiangsu HengRui Medicine Co., Ltd.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The primary objective is to evaluate pharmacokinetics of Fluzoparib and its main metabolite in subjects with impaired kidney function in comparison with healthy subjects, to develop dose recommendations for patients with renal impairment.
The secondary objective is to evaluate the safety of Fluzoparib in subjects with mild and moderate renal impairment and in healthy subjects.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Impairment
7. Study Design
Primary Purpose
Basic Science
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Model Description
Single dose of oral administration of Fluzoparib
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
24 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Group A
Arm Type
Experimental
Arm Title
Group B
Arm Type
Experimental
Arm Title
Group C
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Fluzoparib
Intervention Description
Normal Renal Function:A single oral dose of Fluzoparib will be administered.
Intervention Type
Drug
Intervention Name(s)
Fluzoparib
Intervention Description
Mild Renal Impairment:A single oral dose of Fluzoparib will be administered.
Intervention Type
Drug
Intervention Name(s)
Fluzoparib
Intervention Description
Moderate Renal Impairment:A single oral dose of Fluzoparib will be administered.
Primary Outcome Measure Information:
Title
Pharmacokinetics parameters of Fluzoparib: Cmax
Time Frame
96 hours post dose
Title
Pharmacokinetics parameters of Fluzoparib: AUC0-t
Time Frame
96 hours post dose
Title
Pharmacokinetics parameters of Fluzoparib: AUC0-∞ (if available)
Time Frame
96 hours post dose
Title
Pharmacokinetics parameters of main metabolite (SHR165202) of Fluzoparib: Cmax
Time Frame
96 hours post dose
Title
Pharmacokinetics parameters of main metabolite (SHR165202) of Fluzoparib: AUC0-t
Time Frame
96 hours post dose
Title
Pharmacokinetics parameters of main metabolite (SHR165202) of Fluzoparib: AUC0-∞ (if available)
Time Frame
96 hours post dose
Secondary Outcome Measure Information:
Title
Other pharmacokinetics parameters of Fluzoparib: Tmax
Time Frame
96 hours post dose
Title
Other pharmacokinetics parameters of main metabolite (SHR165202) of Fluzoparib: Tmax
Time Frame
96 hours post dose
Title
Plasma protein binding rate of Fluzoparib
Time Frame
Day 01 post dose
Title
Plasma protein binding rate of main metabolite (SHR165202) of Fluzoparib
Time Frame
Day 01 post dose
Title
The incidence and severity of adverse events/serious adverse events (based on NCI-CTCAE 5.0)
Time Frame
19 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
-
Inclusion Criteria for subjects with impaired kidney function:
Sign the informed consent before the trial, and fully understand the content, process, and possible adverse reactions of the trial;
Male or female subjects aged 18 to 70 (including 18 and 70);
Body mass index (BMI) ranges from 18 kg/m2 to 28 kg/m2 (including 18 and 28);
The glomerular filtration rate should meet the following criteria (GFR, mL/min):Subjects with mild renal impairment (CKD2): 60-89 mL/min (including 60-89);Subjects with moderate renal impairment (CKD3): 30-59 mL/min (including 30-59 ends);
Renal function should be stable, and the GFR results should be tested twice before administration (at least 3 days apart) within the same CKD stage.
Inclusion Criteria for subjects with normal kidney function:
Sign the informed consent before the trial and fully understand the content, process, and possible adverse reactions of the trial;
Male or female subjects aged 18 to 70 (including 18 and 70);
Body mass index (BMI) ranges from 18 kg/m2 to 28 kg/m2 (including 18 and 28);
Glomerular filtration rate (GFR) ≥90 mL/min.
Exclusion Criteria:
-
Exclusion Criteria for subjects with impaired kidney function:
History of kidney transplant;
Need Renal dialysis during the study;
Urinary incontinence or anuria;
Clinically significant heart disease, including but not limited to: congestive heart failure, symptomatic coronary artery disease, myocardial infarction, QTcF≥470 ms (female) or QTcF≥450 ms (male) within 12 months before the start of treatment;
Received any investigational drug within 3 months before the study started;
Taking any drugs which can affect the metabolic enzyme CYP3A within 14 days before the study started;
Smokers and alcoholics, or those screened positive for alcohol;
History of drug use, or drug abuse screening positive.
Exclusion Criteria for subjects with normal kidney function:
History of kidney transplant;
Clinically significant heart disease, including but not limited to: congestive heart failure, symptomatic coronary artery disease, myocardial infarction, QTcF≥470 ms (female) or QTcF≥450 ms (male) within 12 months before the start of treatment;
Received any investigational drug within 3 months before the study started;
Taking any drugs which can affect the metabolic enzyme CYP3A within 14 days before the study started;
Smokers and alcoholics, or those screened positive for alcohol;
History of drug use, or drug abuse screening positive.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yuya Wang, Ph.D
Phone
13918749176
Email
yuya.wang@hengrui.com
First Name & Middle Initial & Last Name or Official Title & Degree
Jing Rao, M.M
Phone
17612186457
Email
jing.rao@hengrui.com
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Safety and Pharmacokinetics of Fluzoparib in Healthy Subjects and Those With Impaired Kidney Function
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