- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01555866
Study of the Effect of Renal Impairment on the Pharmacokinetics of Isavuconazole.
A Phase 1 Open Label, 2 Part, Parallel Group Study to Investigate the Effect of Renal Impairment on the Pharmacokinetics of Isavuconazole
Study Overview
Status
Intervention / Treatment
Detailed Description
In Part 1, eligible subjects will be enrolled into one of 2 groups based on their renal function. All subjects will receive a single 1-hour infusion of isavuconazole and will remain confined for 4 days. Subjects with normal renal function will return to the clinic for several outpatient visits over 15 days after dosing. Subjects with renal disease will complete the same outpatient visits which correspond to scheduled dialysis dates and then be readmitted to the clinic on study Day 15 to receive a second 1-hour infusion of isavuconazole followed by their normal dialysis procedure and then remain confined for 4 days. ECGs, vital signs, blood draws will be obtained throughout the study for safety and to assess the amount of study drug in the body as well as study drug removed in subjects undergoing dialysis.
In Part 2, eligible subjects will be enrolled into one of 4 groups based on their renal function. All subjects will receive a single 1-hour infusion of isavuconazole and remain confined for 4 days. Subjects will return to the clinic for several outpatient visits over 15 days after dosing. ECGs, vital signs, blood draws will be obtained throughout the study for safety and to assess the amount of study drug in the body.
Study Type
Enrollment (Actual)
Phase
- Phase 1
Contacts and Locations
Study Locations
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-
Colorado
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Denver, Colorado, United States, 80228
- DaVita Research
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Florida
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Miami, Florida, United States, 33014
- Clinical Pharmacology Miami
-
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Minnesota
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Minneapolis, Minnesota, United States, 55404
- DaVita Clinical Research
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Subject must weigh at least 45 kg and have a body mass index of 18-35 kg/m2
- If female, the subject agrees to sexual abstinence, is surgically sterile, postmenopausal or using a medically acceptable double-barrier method to prevent pregnancy and agrees to continue using this method during the study and until 28 days after final study dug administration. Female subjects must not be lactating or pregnant as documented by a negative pregnancy test at Screening and Day -1
- If male, the subject agrees to sexual abstinence, is surgically sterile, or is using a medically acceptable method to prevent pregnancy and agrees to continue using this method during the study and until 90 days after the end of the study
- The subject has good venous access
- Female subject must not donate ova starting at Screening and throughout the study period, and for 28 days after final study drug administration.
Exclusion Criteria:
- The subject has a previous history of any clinically significant gastro-intestinal, neurological, hepatic, pulmonary, metabolic, dermatologic, immunologic, cardiovascular, psychiatric, genitourinary, endocrine, hematological disorder or disease, malignancy excluding non-melanoma skin cancer or any other medical condition that would preclude participation in the study
- The subject has evidence of any cardiac conduction abnormalities
- The subject has a history of unexplained syncope, cardiac arrest, unexplained cardiac arrhythmia, torsade de pointes, structural heart disease, or family history of Long QT syndrome
- The subject has a supine systolic blood pressure less than 90 or greater than 160 mmHg, and diastolic blood pressure less than 50 or greater than 90 mmHg, or pulse rate less than 40 or greater than 100 beats per minute, either at Screening and Day -1
- The subject has a history of consuming more than 14 units of alcoholic beverages per week, has a history of alcohol abuse within the past 2 years prior to Screening, or has a positive screen for alcohol at Screening or Day -1. (NOTE: one unit = 12 ounces of beer, 4 ounces of wine or 1 ounce of spirits/hard liquor.)
- The subject has a positive test for alcohol or drugs of abuse at Screening or Day-1, unless it is an expected result due to an approved concomitant medication for subjects with renal impairment
- The subject has used nicotine patches or any tobacco-containing products within 1 month prior to Day-1 or is a smoker, defined as greater than 10 cigarettes per week
- The subject has had treatment with prescription drugs or complementary and alternative medicines within 14 days prior to Screening, or over-the-counter medication within 14 days prior to Screening (with the exception of acetaminophen up to 2 grams/day)
- The subject anticipates an inability to abstain from caffeine or alcohol for 48 hours prior to Day -1 and throughout the duration of the study
- The subject anticipates an inability to abstain from grapefruit, Seville oranges, star fruit, or any products containing these items from 72 hours prior to Day -1 and throughout the duration of the study
- The subject has/had febrile illness or symptomatic, viral, bacterial (including upper respiratory infection), or fungal (non-cutaneous) infection within 7 days prior to Day -1
- The subject has been vaccinated within the last 30 days prior to Screening
- The subject has a positive test for hepatitis C antibody or hepatitis B surface antigen at Screening or a known history of human immunodeficiency virus
- The subject has a known or suspected hypersensitivity to isavuconazole, the azole class of compounds, or any components of the study drugs
- The subject has received an experimental agent within 30 days or ten half-lives, whichever is longer, prior to Screening
- The subject has had any significant blood loss, donated one or more units (450 mL) of blood or received a transfusion of any blood or blood products within 60 days or donated plasma within 7 days prior to Day -1
- The subject has any other condition, which in the opinion of the investigator, precludes the subject's participation in the trial
Study Plan
How is the study designed?
Design Details
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Part 1 Subjects with End Stage Renal Disease (ESRD)
|
IV
Other Names:
|
Experimental: Part 1 Healthy Subjects
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IV
Other Names:
|
Experimental: Part 2 Subjects with Mild Renal Impairment
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IV
Other Names:
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Experimental: Part 2 Subjects with Moderate Renal Impairment
|
IV
Other Names:
|
Experimental: Part 2 Subjects with Severe Renal Impairment
|
IV
Other Names:
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Experimental: Part 2 Subjects with no Renal Impairment
|
IV
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pharmacokinetics variables for BAL4815 (in plasma): AUC72 and Cmax
Time Frame: Day 1, Part 1
|
Area under the concentration-time curve from 0 to 72 hours (AUC72) and Maximum concentration (Cmax)
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Day 1, Part 1
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Pharmacokinetics variables for BAL4815 (in plasma): AUCinf, AUClast, and Cmax
Time Frame: Day 1, Part 2
|
Area under the concentration-time curve from time 0 extrapolated to infinity (AUCinf), Area under the plasma concentration-time curve from time of dosing to the last quantifiable concentration (AUClast)
|
Day 1, Part 2
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pharmacokinetics variables for BAL4815 (in plasma): AUCinf and AUClast
Time Frame: Day 1, Part 1
|
Day 1, Part 1
|
|
Pharmacokinetics variables for BAL4815 (in plasma): tmax, t1/2, Vz, and CLtot , Ae, Ae% , CLR
Time Frame: Day 1, Parts 1 and 2
|
Time to attain maximum concentration (tmax), Apparent terminal elimination half-life (t ½), Apparent volume of distribution during terminal phase (Vz), Total clearance (CLtot), Cumulative amount of unchanged drug excreted in urine (Ae), Percent of drug excreted in urine (Ae%), Renal clearance of the drug from plasma (CLR)
|
Day 1, Parts 1 and 2
|
Pharmacokinetics unbound (u) variables for BAL4815 (in plasma and in urine): AUC inf,u, AUC72,u, AUClast,u, Cmax,u, Vz,u, CLtot,u, CLR,u
Time Frame: Day 1, Parts 1 and 2
|
Day 1, Parts 1 and 2
|
|
Pharmacokinetics variables for End Stage Renal Disease (ESRD) subjects for BAL4815: AUC72, Cmax, and tmax
Time Frame: Day 15, Part 1
|
Day 15, Part 1
|
|
Pharmacokinetics variables for BAL8728 (in plasma and urine): AUCinf, AUClast, AUC72, Cmax, tmax , t1/2, Vz, CLtot, Ae, Ae% , CLR
Time Frame: Day 1, Parts 1 and 2
|
Day 1, Parts 1 and 2
|
|
Pharmacokinetics variables for End Stage Renal Disease (ESRD) subjects for BAL8728: AUC72, Cmax, and tmax
Time Frame: Day 15, Part 1
|
Day 15, Part 1
|
|
Safety assessed by recording adverse events, laboratory assessments, vital signs, electrocardiograms (ECGs)
Time Frame: Part 1: Continuous, up to Day 24; Part 2: Continuous, up to Day 15
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Part 1: Continuous, up to Day 24; Part 2: Continuous, up to Day 15
|
Collaborators and Investigators
Collaborators
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 9766-CL-0018
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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