Leukopenia
Conditions
Brief summary
A Phase 1, open-labeled, single-dose, one-sequence, one-period, 3-part study to investigate the absorption, metabolism, excretion, absolute bioavailability, and immunogenicity of GX-I7 in healthy volunteers
Detailed description
A Phase 1, open-labeled, single-dose, one-sequence, one-period, 3-part study to investigate the absorption, metabolism, excretion, absolute bioavailability, and immunogenicity of GX-I7 in healthy volunteers To show ABA and Mass balance of GX-I7
Interventions
DRUGGX-I7 or [14C] GX-I7
IM GX-I7 or IV/IM microdose of GX-I7
Sponsors
Seoul National University Hospital
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
19 Years to 45 Years
Healthy volunteers
Yes
Inclusion criteria
1. Subject is willing and able to give informed consent after listening character of the clinical trial 2. Must be 19-45 years of age, inclusive 3. Weight 50-100kg, BMI 18-30kg/m2 4. Subject who is adequately able to attend the study based on medical history and physical exam, no clinically significant abnormality from vital sign and clinical laboratory values 5. No clinical abnormality from ECG test 6. Non-smoker (no smoking or no use of any product containing nicotine least for one month and negative from urine test)
Exclusion criteria
1. Suspected or confirmed malignancy, or has malignancy history 2. Any clinically significant acute or chronic medical condition requiring care of a physician, in liver, biliary tract, renal, nervous system (CNS or peripheral). respiratory system, endocrine (diabetes, hyperlipidemia etc), cardiovascular (congestive heart failure, coronary artery disease, myocardial infarction etc), hematology, malignancy, urinary disease, mental disorder, musculoskeletal disorder, immune system (rheumatoid arthritis, lupus etc), otorhinolaryngologic diseases 3. Positive to HBsAg, hepatitis C virus (HCV) Ab and HIV Ab 4. Are considering or scheduled to undergo any surgical or dental procedure during the study 5. Administered other Investigational Product (IP) by attending other clinical study or biological equivalent study within recent 6 months 6. Any Serious adverse drug reaction (SAR) against vaccines or antibiotics, any medical history with serious allergic diseases 7. Positive from urine drug screen or respiratory alcohol screen at medical screening 8. History of alcohol, drug, or substance abuse in the past 12 months 9. A heavy alchol consumer (\>21 units/week, 1 unit = 10 g of pure alcohol) or Consumption of alcohol within 48 hours prior to hospitalization 10. Medications with antacid, analgesic, herbal treatment, vitamin, mineral (except maximum 4 grams of acetaminophen) hormone, steroids, insulin, hypoglycemic drug or other hormone substitute within 14 days before administration 11. Planning pregnancy or donation of sperm/disagreeing proper contraception during the study and 3 months following IP administration 12. Do not have veins suitable for cannulation or multiple venipunctures 13. Previously donate whole blood within 60 days or component blood within 14 days 14. Excessive consumption of foods containing grapefruits 15. Any other factor that the Investigator thinks will increase subject risk with participation
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Total radioactivity at feces,urine,blood to measure total recovery rate | 29 days | radioactivity in nCi |
Countries
South Korea
Outcome results
None listed