Healthy
Conditions
Keywords
Healthy, Volunteers
Brief summary
A randomized, double-blind, placebo-controlled, single-dose, dose escalation study (Phase I) to evaluate the tolerability and pharmacokinetics of Belviq in adult Korean volunteers.
Detailed description
The volunteers are screened through medical history, physical exam, laboratory tests etc. within 4 weeks (-28d\ -2d) prior to the day scheduled for taking the investigational product (1d). The final subjects determined eligible for this clinical trial through screening tests are randomized to the dose groups with Belviq 10 mg and 20 mg. Twelve subjects are assigned to each group (9 subjects to study drug and 3 subjects to placebo), and the study drug or placebo are administered to the corresponding administration group. The subjects are discharged on the morning of 4d after completing the set study schedule at 72 hours after administration. The subjects then visit for the final tests on the last out-patient visiting day. Belviq is progressed sequentially from the low-dose group to the high-dose group. The blood sampling time for the pharmacokinetic evaluation is as follows. Blood sampling for pharmacokinetic evaluation : Before administration(0), and 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 16, 24, 36, 48 and 72 h (17 times) after medication.
Interventions
DRUGBelviq 10mg
Belviq 10mg single dose administration
DRUGBelviq 20mg
Belviq 20mg single dose administration
DRUGPlacebo
Placebo single dose administration
Sponsors
IlDong Pharmaceutical Co Ltd
Study design
Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes
Inclusion criteria
1. Subject is a healthy adult aged 18 \ 60 years old at the time of screening. 2. Subject has body weight index (BMI) 23.0 \ 32.0. ☞ BMI(kg/m2) = weight (kg)/{height (m)}2 3. Subject does not have congenital or chronic disease and is without pathologic symptom or finding on medical exam. Vital sign Supine SBP (mmHg) 90-140 DBP (mmHg) 50-90 Heart rate (beat/min) 40-80 Respiratory rate (breaths/min) 8-18 4. Subject was determined eligible according to the results of clinical laboratory tests like serum test, hematologic test, blood chemistry test, urine test etc. and vital signs, electrocardiography, physical exam etc. performed during the screening exam. SBP(mmHg) 90-140 DBP(mmHg) 50-90 Heart rate (beat/min) 40-80 Respiratory rate (breaths/min) 8-18 5. Subject decided to participate voluntarily and gave written Informed consent to comply with the instructions after listening to and fully understanding the detailed explanation about this trial.
Exclusion criteria
1. Subject has clinically significant liver, kidney, neurologic, immunologic, respiratory, endocrine disease or hematologic·oncologic disease, cardiovascular disease or psychiatric disease (mood disorder, compulsive disorder etc.) or such medical history (including subject with hepatitis virus in case of liver disease). 2. Subject has history of gastrointestinal disease (such as Crohn's disease, ulcer, acute or chronic pancreatitis etc.) or gastrointestinal surgery (except simple appendectomy or hernia operation) that can affect the absorption of the study drug. 3. Subject has hypersensitivity reaction to drug (aspirin, antibiotics etc.) or history of clinically significant hypersensitivity reaction. 4. Subject has history of drug abuse or tested positive to abused drug in the urine drug screening test (performed during screening and on Day -1). 5. Subject took any prescribed drug or oriental medicine within 2 weeks prior to the first medication or any over-the-counter (OTC) drug or vitamins within 1 week prior to the first medication or paracetamol 48 hours prior to taking the study drug (however, the subject can be included if other criteria are met according to the discretion of the investigator). 6. Subject participated in another study and received medication within 3 months prior to the first medication day (3 months are judged to be the period in between medications). 7. Subject has history of using the following drug * Fenfluramine/dexfenfluramine or phentermine * Drug that may increase the risk of valvulopathy or primary pulmonary hypertension (Cyproheptadine, Trazodone, Nefazodone, Amoxapine, tricyclic antidepressants, mirtazapine, pergolide, ergotamine, methysergide). 8. Subject received whole blood transfusion (500 mL) within 3 months prior to the first medication or blood transfusion within 1 month prior to the first medication. 9. Subject continually drinks (in excess of 28 units/week (21 unit/week for women), 1 unit = 10 g of pure alcohol) or cannot abstain from drinking for 48 hours prior to the study drug administration through the hospitalization period. 10. Subject smokes 3 cigarettes or more in one day or cannot abstain from smoking for 48 hours prior to the study drug administration through the hospitalization period. 11. Subject took caffeine-containing food within 48 hours prior to the first medication, or cannot abstain from taking during the hospitalization period. 12. Subject has tested positive to HbsAg, HCV Ab, HIV Ab tests. 13. Subject has peculiar diet, is a vegetarian or consumes food that may affect the drug metabolism (e.g. St. John's Wort). 14. Subject had serious change in dietary habit or activity from 4 weeks prior to the study drug administration. 15. Subject or his/her partner cannot or is not willing to use appropriate contraceptives during the trial period and for 28 days after termination of the study (for women,
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| echocardiography | participants will be followed for the duration of hospital stay and post study visit, an expected average of 10 days |
| electrocardiography | participants will be followed for the duration of hospital stay and post study visit, an expected average of 10 days |
| clinical laboratory tests | participants will be followed for the duration of hospital stay and post study visit, an expected average of 10 days |
| physical exam | participants will be followed for the duration of hospital stay and post study visit, an expected average of 10 day |
| Vital signs | participants will be followed for the duration of hospital stay and post study visit, an expected average of 10 days |
| adverse event | participants will be followed for the duration of hospital stay and post study visit, an expected average of 10 days |
Secondary
| Measure | Time frame |
|---|---|
| Cmax, Cmax/D, AUClast, AUClast/D, AUCinf, AUCinf/D, tmax, t1/2 of Belviq | Before administration(0), and 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 16, 24, 36, 48 and 72 h (17 times) after medication. |
| CL/F, Vz/F of Belviq | Before administration(0), and 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 16, 24, 36, 48 and 72 h (17 times) after medication |
| Change in Belviq concentration in the blood with time | Before administration(0), and 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 16, 24, 36, 48 and 72 h (17 times) after medication. |
Countries
South Korea
Outcome results
None listed