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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06112678
Other study ID # A86_13BE2314
Secondary ID
Status Completed
Phase Phase 1
First received
Last updated
Start date January 4, 2024
Est. completion date March 18, 2024

Study information

Verified date March 2024
Source Chong Kun Dang Pharmaceutical
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A phase I clinical trial to evaluate the tolerability and the pharmacokinetics of CKD-348(6).


Recruitment information / eligibility

Status Completed
Enrollment 63
Est. completion date March 18, 2024
Est. primary completion date February 19, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria: 1. Healthy adult volunteers aged = 19 years. 2. Body weight =55kg with calculated body mass index (BMI) of 18 to 30 kg/m2 3. Those who meet the blood pressure criteria during screening tests: - Systolic Blood Pressure: 90 to 139 mmHg - Diastolic Blood Pressure: 60 to 89 mmHg 4. Those who have no congenital diseases or chronic diseases and have no abnormal symptoms or findings. 5. Those who are eligible for clinical trials based on laboratory (hematology, blood chemistry, serology, urology) and ECG results at screening. 6. Those who agree to contraception during the participation of clinical trial. 7. Those who voluntarily decide to participate and agree to comply with the cautions after fully understand the detailed description of this clinical trial. Exclusion Criteria: 1. Those who received investigational products or participated in bioequivalence tests within 6 months before the first administration of clinical trial drugs. 2. Those who take barbiturate and any related drugs which may cause induction or inhibition of drug metabolism within 1 month and those who take drug could affect to clinical trial within 10 days before the first administration of investigational products. 3. Those who donated whole blood or apheresis within 8 weeks or 4 weeks respectfully, or received blood transfusion within a month. 4. Those who have a history of gastrointestinal surgery except simple appendectomy and hernia surgery. 5. Those who exceed an alcohol and cigarette consumption criteria write below within 1 month before the first administration of investigational products. - Alcohol: Man - 21 glasses/week, Woman - 14 glasses/week (1glass: Soju 50mL, Wine 30mL, or beer 250mL) - Smoking: 20 cigarettes/day 6. Those who have any history of diabetic mellitus, nephropathy, biliary obstruction, shock, angioedema, cardiac insufficiency, dihydropyridine sensitivity, unstable angina, hypothyroidism and hypersensitive to Sunset yellow FCF. 7. Those who have genetic problems such as galactose intolerance, Lapp lactose deficiency or glucose-galactose malabsorption. 8. Those who are deemed insufficient to participate in this clinical trial by investigators. 9. Woman who are pregnant or breastfeeding.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
CKD-348(6)
QD, PO
CKD-828, D097, D337
QD, PO

Locations

Country Name City State
Korea, Republic of H plus Yangji hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Chong Kun Dang Pharmaceutical

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary AUCt of CKD-348(6) AUCt: Area under the concentration-time curve from time zero to time Pre-dose (0 hour), 0.25, 0.5, 0.75, 1, 1.25, 1.5, 2, 3, 4, 5, 6, 7, 8, 10, 12, 24, 48, 72 hours
Primary Cmax of CKD-348(6) Cmax: Maximum plasma concentration of the drug Pre-dose (0 hour), 0.25, 0.5, 0.75, 1, 1.25, 1.5, 2, 3, 4, 5, 6, 7, 8, 10, 12, 24, 48, 72 hours
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