A Study to Investigate the Effect of Severe Renal Impairment on Gilteritinib Compared to Healthy Participants With Normal Renal Function
Study Details
Study Description
Brief Summary
The purpose of this study is to evaluate the pharmacokinetics of a single oral dose of gilteritinib in male and female participants with severe, mild and moderate renal impairment compared to healthy male and female participants with normal renal function. This study will also evaluate the safety and tolerability of a single oral dose of gilteritinib in male and female participants with severe, mild and moderate renal impairment and healthy male and female participants with normal renal function.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 1 |
Detailed Description
This study is comprised of 2 parts. Part 1 includes participants with severe renal impairment and normal renal function. Part 2 includes participants with mild and moderate renal impairment and normal renal function. Participants will be residential for a single period of 14 days/13 nights. Participants will be discharged from the clinical unit on day 14 on the condition that all required assessments have been performed and that there are no medical reasons for a longer stay in the clinical unit.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Part 1: Participants with Severe Renal Impairment Participants will receive a single oral dose of gilteritinib under fasting conditions on Day 1 |
Drug: Gilteritinib
Oral
Other Names:
|
| Experimental: Part 1: Participants with Normal Renal Function Participants will receive a single oral dose of gilteritinib under fasting conditions on Day 1 |
Drug: Gilteritinib
Oral
Other Names:
|
| Experimental: Part 2: Participants with Mild Renal Impairment Participants will receive a single oral dose of gilteritinib under fasting conditions on Day 1. |
Drug: Gilteritinib
Oral
Other Names:
|
| Experimental: Part 2: Participants with Moderate Renal Impairment Participants will receive a single oral dose of gilteritinib under fasting conditions on Day 1. |
Drug: Gilteritinib
Oral
Other Names:
|
| Experimental: Part 2: Participants with Normal Renal Function Participants will receive a single oral dose of gilteritinib under fasting conditions on Day 1. |
Drug: Gilteritinib
Oral
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Pharmacokinetics (PK) of gilteritinib in plasma: Area under the concentration-time curve (AUC) from the time of dosing extrapolated to time infinity (AUCinf) [Up to 23 days]
AUCinf will be recorded from the pharmacokinetic (PK) plasma samples collected.
- Pharmacokinetics (PK) of gilteritinib in plasma: Area under the concentration-time curve from the time of dosing to the last measurable concentration (AUClast) [Up to 23 days]
AUClast will be recorded from the pharmacokinetic (PK) plasma samples collected.
- Pharmacokinetics (PK) of gilteritinib in plasma: Maximum concentration (Cmax) [Up to 23 days]
Cmax will be recorded from the pharmacokinetic (PK) plasma samples collected.
- Pharmacokinetics (PK) of gilteritinib in plasma: Apparent clearance (CL/F) [Up to 23 days]
CL/F will be recorded from the pharmacokinetic (PK) plasma samples collected.
- Pharmacokinetics (PK) of gilteritinib in urine: Area under the concentration-time curve from the time of dosing extrapolated to the time infinity (AUCinf,u) [Up to 23 days]
AUCinf,u will be recorded from the pharmacokinetic (PK) urine samples collected.
- Pharmacokinetics (PK) of gilteritinib in urine: Area under the concentration-time curve from the time of dosing to the last measurable concentration (AUClast, u) [Up to 23 days]
AUClast,u will be recorded from the pharmacokinetic (PK) urine samples collected.
- Pharmacokinetics (PK) of gilteritinib in urine: Maximum concentration (Cmax,u) [Up to 23 days]
Cmax,u will be recorded from the pharmacokinetic (PK) urine samples collected.
Secondary Outcome Measures
- Number of participants with Adverse Events (AEs) [Up to Day 23]
Adverse Events will be coded using Medical Dictionary for Regulatory Activities (MedDRA). An AE is any untoward medical occurrence in a patient or clinical study participant temporally associated with the use of study investigational product (IP), whether or not considered related to the study IP. "Adverse event" means any untoward medical occurrence associated with the use of a drug in humans, whether or not considered drug related.
- Number of participants with laboratory value abnormalities and/or adverse events (AEs) [Up to Day 23]
Number of participants with potentially clinically significant laboratory values.
- Number of participants with vital sign abnormalities and/or adverse events (AEs) [Up to Day 23]
Number of participants with potentially clinically significant vital sign values.
- Number of participants with routine 12-lead electrocardiogram (ECG) abnormalities and/or Adverse Events (AEs) [Up to Day 23]
Number of participants with potentially clinically significant ECG values.
Eligibility Criteria
Criteria
Inclusion Criteria:
Participant is eligible for participation in the study if all of the following apply:
-
Participant has body mass index (BMI) range of 18.5 to 40.0 kg/m^2, inclusive and weighs at least 50 kg at screening.
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Female participant is not pregnant and the following condition apply: Not a woman of childbearing potential (WOCBP)
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Male participant with female partner(s) of childbearing potential (including breastfeeding partner) must agree to use contraception throughout the treatment period and for 120 days after Investigational Product (IP) administration.
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Male participant must not donate sperm during the treatment period and for 120 days after investigational product (IP) administration.
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Male participant with pregnant partner(s) must agree to remain abstinent or use a condom for the duration of the pregnancy throughout the study period and for 120 days after IP administration.
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Participant has renal function defined by estimated glomerular filtration rate (eGFR) using modification of diet in renal disease (MDRD) formula:
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Normal renal function with eGFR ≥ 90 mL/min per 1.73 m^2, or
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Mild renal impairment with eGFR 60 to <90 mL/min per 1.73 m^2, or
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Moderate renal impairment with eGFR 30 to <60 mL/min per 1.73 m^2, or
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Severe renal impairment as defined by the National Kidney Foundation and by eGFR <30 mL/min per 1.73 m2 and not on hemodialysis (preferably not higher than 20 mL/min per 1.73 m2, with at least 50% of participants required to have eGFR ≤ 20 mL/min per 1.73 m^2).
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Participant has adequate venous access to allow collection of study-related samples.
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Participant agrees not to participate in another interventional study while participating in the present study.
Exclusion Criteria:
Participant will be excluded from participation in the study if any of the following apply:
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Participant has received any investigational therapy within 28 days or 7 half-lives, whichever is longer, prior to day -1.
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Participant has any condition which makes the participant unsuitable for study participation.
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Female participant who has been pregnant within 6 months prior to screening or breastfeeding within 3 months prior to screening.
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Participant has a known or suspected hypersensitivity to gilteritinib or any components of the formulation used.
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Participant has had previous exposure with gilteritinib.
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Participant has any of the liver function tests (alkaline phosphatase [ALP], alanine aminotransferase [ALT], aspartate aminotransferase [AST] and total bilirubin [TBL]) ≥ 1.5 × upper limit of normal on day -1. In such a case, the assessment may be repeated once.
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Participant has any clinically significant history of allergic conditions (including drug allergies, asthma, eczema or anaphylactic reactions, but excluding untreated, asymptomatic, seasonal allergies) prior to IP administration.
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Participant has/had febrile illness or symptomatic, viral, bacterial (including upper respiratory infection) or fungal (noncutaneous) infection within 1 week prior to day -1.
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Participant has a mean corrected QT interval using Fridericia's formula (QTcF) of > 450 msec (for male and female participants) on day -1. If the mean QTcF exceeds the limits above, 1 additional triplicate 12-lead electrocardiogram (ECG) may be taken.
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Participant has a history of smoking more than 10 cigarettes (or equivalent amount of tobacco) per day within 3 months prior to day -1.
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Participant has a history of consuming > 14 units for male participants or > 7 units for female participants of alcoholic beverages per week within 6 months prior to screening or has a history of alcoholism 3 months prior to screening or drug/chemical/ substance abuse within 1 year prior to screening (note: 1 unit = 12 ounces of beer, 4 ounces of wine, 1 ounce of spirits/hard liquor) or the participant tests positive for alcohol at screening or on day -1.
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Participant has used any inducer of cytochrome P450 (CYP)3A metabolism (e.g., St. John's Wort, barbiturates and rifampin) in the 3 months prior to day -1.
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Participant has had significant blood loss, donated ≥ 1 unit (450 mL) of whole blood or donated plasma within 7 days prior to day -1 and/or received a transfusion of any blood or blood products within 60 days.
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Participant has a history of unexplained syncope, cardiac arrest, unexplained cardiac arrhythmias or torsades de pointes, structural heart disease or a family history of long QT syndrome.
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Participant has a positive serology test for hepatitis A virus immunoglobulin M antibodies, hepatitis B surface antigen, hepatitis C virus antibodies or antibodies to human immunodeficiency virus type 1 and/or type 2 at screening. Participants with isolated hepatitis B core antibody (with negative hepatitis B surface antigen and negative hepatitis B surface antibody) may be eligible if hepatitis B DNA or hepatitis C RNA is undetectable.
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Participant is an employee of Astellas, the study-related contract research organizations (CROs) or the clinical unit.
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Participant who has received any of the following drugs/products within 2 weeks prior to IP administration:
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Strong or moderate CYP3A inhibitors (e.g., grapefruit, Seville oranges, ketoconazole or fluconazole)
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Strong or moderate inhibitors and all inducers of P-glycoprotein
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Substrates of multidrug and toxin extrusion 1
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Drugs that target serotonin 5-hydroxytryptamine receptor 1 or 5-hydroxytryptamine receptor 2B
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Participant has a positive result for SARS-CoV-2 polymerase chain reaction (PCR) test during screening.
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Participant has clinical signs and symptoms consistent with COVID-19 infection, e.g., fever, dry cough, dyspnea, sore throat, muscle or body aches and gastrointestinal symptoms or confirmed infection by appropriate SARS-CoV-2 PCR test within the 4 weeks prior to screening.
Additional criteria for participants with mild, moderate and severe renal impairment:
-
Participant who has a history of any clinically significant illness (other than renal disease and conditions related to renal disease, such as stable diabetes and stable hypertension), medical condition or laboratory abnormality within 3 months prior to screening which precludes the participant from study participation.
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Participant has a mean pulse rate < 40 or > 90 bpm; mean systolic blood pressure (SBP) < 90 or > 160 mmHg; mean diastolic blood pressure (DBP) < 50 or > 100 mmHg (measurements taken in triplicate after participant has been resting in the supine position for at least 5 minutes; pulse rate will be measured automatically) on day -1. If the mean blood pressure exceeds the limits above, 1 additional triplicate may be taken.
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Participant who has had a change in dose regimen of medically required medication(s) in the 2 weeks prior to IP administration (permitted concomitant medications) and/or participant for whom dose changes are likely to occur during the study (minor dose changes are allowed in agreement with the sponsor) and/or participant has used nonpermitted concomitant medication(s) (including, but not limited to vitamins, hormonal contraceptives and natural and herbal remedies) in the 3 weeks prior IP administration, except for topical dermatological products (including corticosteroid products) and hormone replacement therapy (HRT).
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Participant who requires or is likely to require any new concomitant medications during the course of the study.
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Participant who has a renal disease secondary to malignancy.
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Participant who has a fluctuating or rapidly deteriorating renal function within 4 weeks prior to IP administration, as indicated by strongly varying or worsening clinical and/or laboratory signs of renal impairment within the screening period.
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Participant has a hemoglobin result of < 8.5 g/dL.
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Participant has a functioning kidney transplant.
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Participant has used any drugs of abuse (amphetamines, barbiturates, benzodiazepines, cannabinoids, cocaine and/or opiates) within 3 months prior to day -1 or the participant tests positive for drugs of abuse (amphetamines, barbiturates, benzodiazepines, cannabinoids,cocaine and/or opiates) at screening or on day -1, unless the positive result is due to an approved prescription medication.
Additional criteria for healthy participants with normal renal function:
-
Participant has any history or evidence of any clinically significant cardiovascular, gastrointestinal, endocrine, hematologic, hepatic, immunologic, metabolic, urologic, pulmonary, neurologic, dermatologic, psychiatric, renal and/or other major disease or malignancy.
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Participant has any clinically significant abnormality following the physical examination, ECG and protocol-defined clinical laboratory tests at screening or on day -1.
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Participant has a mean pulse rate < 45 or > 90 bpm; mean SBP > 150 mmHg; mean DBP > 90 mmHg (measurements taken in triplicate after participant has been resting in the supine position for at least 5 minutes; pulse rate will be measured automatically) on day -1. If the mean blood pressure exceeds the limits above, 1 additional triplicate may be taken.
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Participant has used any prescribed or nonprescribed drugs (including, but not limited to vitamins, hormonal contraceptives and natural and herbal remedies) in the 2 weeks prior to IP administration, except for occasional use of acetaminophen (up to 2 g/day), topical dermatological products (including corticosteroid products) and HRT.
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Participant has used any drugs of abuse (amphetamines, barbiturates, benzodiazepines, cannabinoids, cocaine and/or opiates) within 3 months prior to day -1 or the participant tests positive for drugs of abuse (amphetamines, barbiturates, benzodiazepines, cannabinoids, cocaine and/or opiates) at screening or on day -1.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | National Institute of Clinical Research | Garden Grove | California | United States | 92844 |
| 2 | Orange County Research Institute | Tustin | California | United States | 92780 |
| 3 | Orlando Clinical Research Center | Orlando | Florida | United States | 32809 |
| 4 | Site BG35901 | Sofia | Bulgaria | 1000 |
Sponsors and Collaborators
- Astellas Pharma Global Development, Inc.
Investigators
- Study Director: Medical Director, Astellas Pharma Global Development, Inc.
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 2215-CL-0114
- 2020-003993-32