Relative Bioavailability of CE-Iohexol (Captisol-enabled™ Iohexol) Injection and Omnipaque™ Injection

CyDex Pharmaceuticals

Status

Completed

Conditions

Coronary Angiography

Contrast-induced Nephropathy

Treatments

Other: Omnipaque™ (iohexol) Injection

Other: CE-Iohexol

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT03869983

Study Number-1802282 (Other Identifier)

CE-Iohexol Protocol -101

Details and patient eligibility

About

This study is designed to compare the bioavailability of the test Product(CE-Iohexol Injection) and the reference product Iohexol Injection (Omnipaque™) following intravenous injection in normal healthy volunteers. The secondary objective is to assess the safety and tolerability of the treatments administered. Captisol® is present to improve stability and to potentially reduce the risk of contrast-induced acute kidney injury(CI-AKI) associated with iohexol administration.

Full description

This is a single center, randomized, double-blind, 2-period, crossover study. A total of 24 subjects will be enrolled in the study; subjects will be dosed as 2 groups of 12 subjects each. Additional subjects may be enrolled into the study to obtain the statistical power of 90%. Subjects will attend a screening visit within 28 days prior to Period 1, and eligible subjects will then return to the clinic on the evening prior to Day -1. On Day 1, prior to dosing, subjects will be randomized to receive either CE-Iohexol Injection or the reference product during the first treatment period and the alternate product during the second treatment period. In each period, the study drug will be administered after a fasting period ≥8 hours. Each dose of intravenous iohexol will be separated by a minimum of a 7-day washout period. The test or reference product (iohexol 350 mg Iodine/mL, 80 mL) will be infused at a high flow rate of 4 mL/second for a dose of 400 mgI/kg for 70 kg subject. The test or reference product will be administered using a power injector. Plasma samples for determination of iohexol concentrations will be obtained from arm #2 (the arm not used for dosing) at 0 (pre-dose), 30 seconds, 5, 10, 15, 20, 30 and 45 minutes, and 1, 2, 3, 4, 6, 8, 12, 24, and 48 hours after infusion start; the 30-second sample obtained at the end of infusion. Subjects will be discharged from the clinic on Day 3 following collection of the 48-hour blood sample.

Enrollment

24 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Women of childbearing potential who are sexually active with a non-sterile male partner must be using a medically acceptable form of birth control for the duration of the trial and for 30 days after the last dose of study drug
BMI within the range of 18.5-35 kg/m2, inclusive, and body weight > 45 kg
No significant disease or abnormal laboratory values
Normal vital signs, without any clinically significant abnormalities
Normal 12-lead electrocardiogram, without any clinically significant abnormalities of rate, rhythm or conduction
Nonsmokers defined as not having smoked in the past 3 months prior to dosing
Estimated glomerular filtration rate (eGFR) of > 60 mL/min/1.73 m2

Exclusion criteria

Known hypersensitivity or allergy to iohexol, CAPTISOL®, Omnipaque™ or its excipients
Known hypersensitivity or allergy to iodine or radio-opaque dyes
Women who are pregnant or breast feeding
History or presence of asthma or other pulmonary disease, thyroid disease (hypo- or hyperthyroidism), hepatitis or other liver disease
Any disease or condition (medical or surgical) which, in the opinion of the investigator, might compromise a major system; or other conditions that may interfere with the absorption, distribution, metabolism or excretion of study drug, or would place the subject at increased risk
Abnormal laboratory values which are considered clinically significant
Positive screen for Hepatitis B (HbsAg, Hepatitis B Surface Antigen), Hepatitis C (anti HCV, Hepatitis C Antibody), or HIV (anti-HIV 1/2)
Participation in a clinical research study involving the administration of an investigational or marketed drug or device within 30 days prior to the first dose
Use of medication other than topical products without significant systemic absorption, hormonal contraceptives and hormone replacement therapy
Unwilling to refrain from consumption of alcohol within 48 hours prior to each dose administration and during any in-patient period.
Positive urine drug screen, positive alcohol breath test or positive cotinine test at screening and upon check-in to the study facility
History of significant alcohol abuse within one year prior to screening or regular use of alcohol within six months prior to the screening visit
Illicit drug use,significant mental illness, physical dependence to any opioid, or any history of drug abuse or addiction
A history of difficulty with donating blood or with the insertion of large-calibre catheter
Donation of plasma (500 mL) within 7 days prior to drug administration.
Hemoglobin < 128 g/L (males) and < 115 g/L (females) and hematocrit < 0.36 L/L (males) and < 0.32 L/L (females) at screening
Any history of photosensitivity