Study of the Effect of Renal Impairment on the Pharmacokinetics of Isavuconazole.

NCT ID: NCT01555866

Last Updated: 2015-09-01

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 49 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-03-31
• Study Completion Date: 2013-04-30

Brief Summary

This is a 2-part, open-label study, designed to evaluate the effect of renal disease on the pharmacokinetics of BAL4815 (active isavuconazole moiety) relative to the pharmacokinetics in healthy subjects with normal renal function.

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.

Conditions

Pharmacokinetics of Isavuconazole; Healthy Volunteers; Renal Impaired

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Blinding Strategy: NONE

Study Groups

Part 1 Subjects with End Stage Renal Disease (ESRD)

Group Type: EXPERIMENTAL

isavuconazole

Intervention Type: DRUG

IV

Part 1 Healthy Subjects

Group Type: EXPERIMENTAL

isavuconazole

Intervention Type: DRUG

IV

Part 2 Subjects with Mild Renal Impairment

Group Type: EXPERIMENTAL

isavuconazole

Intervention Type: DRUG

IV

Part 2 Subjects with Moderate Renal Impairment

Group Type: EXPERIMENTAL

isavuconazole

Intervention Type: DRUG

IV

Part 2 Subjects with Severe Renal Impairment

Group Type: EXPERIMENTAL

isavuconazole

Intervention Type: DRUG

IV

Part 2 Subjects with no Renal Impairment

Group Type: EXPERIMENTAL

isavuconazole

Intervention Type: DRUG

IV

Interventions

isavuconazole

IV

Intervention Type: DRUG

Other Intervention Names

BAL4815, BAL8557

Eligibility Criteria

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

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Basilea Pharmaceutica International Ltd

INDUSTRY

Sponsor Role: collaborator

Astellas Pharma Global Development, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Medical Director

Role: STUDY_DIRECTOR

Astellas Pharma Global Development

Locations

DaVita Research

Denver, Colorado, United States

Clinical Pharmacology Miami

Miami, Florida, United States

DaVita Clinical Research

Minneapolis, Minnesota, United States

Countries

United States

Other Identifiers

9766-CL-0018

Identifier Type: -

Identifier Source: org_study_id