A Clinical Trial to Investigate the Pharmacokinetics and Safety/Tolerability of CKD-386 in Healthy Adult Volunteers

Type2 Diabetes Mellitus Clinical Trial

Official title:

Phase I Clinical Trial to Compare the Pharmacokinetics and Tolerability of CKD-386 With Co-administration of D012, D326, and D337 in Healthy Adult Volunteers

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT04223895
• Other study ID #: A83_04BE1917P
• Status: Not yet recruiting
• Phase: Phase 1
• Start date: February 1, 2020
• Est. completion date: June 15, 2020

Study information

• Verified date: January 2020
• Source: Chong Kun Dang Pharmaceutical
• Contact: Yook-Hwan Noh
• Phone: 82-70-4665-9174
• Email: yook.noh[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the pharmacokinetics and Safety/Tolerability of CKD-386

Description:

Phase I clinical trial to compare the pharmacokinetics and tolerability of CKD-386 with co-administration of D012, D326, and D337 in healthy adult volunteers

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 30
• Est. completion date: June 15, 2020
• Est. primary completion date: March 4, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 19 Years and older

Eligibility

Inclusion Criteria:

1. Those who are over 19 years old at the screening visit

2. Those who weigh more than 50kg (45kg or more for women) at the screening visit and have a body mass index (BMI) within the range of 18-30kg/m^2

3. Those who meet the following conditions of blood pressure measured in a sitting position after sufficient rest at the screening visit

• Systolic blood pressure: 90mmHg or more and 139mmHg or less

• Diastolic blood pressure: 60mmHg or more and 89mmHg or less

4. Those who no congenital or chronic disease based on screening and no pathological symptoms or findings in medical examination results (e.g. EEG, ECG, chest and gastroscopy or gastrointestinal radiographs, if necessary)

5. The person in charge of the examination (or authorized test physician) who has determined that the test subject is suitable for the diagnostic test and electrocardiogram test such as hematology test, blood chemistry test, serology test and urine test performed according to the characteristics of the investigational drug product

6. Persons agreeing to exclude the possibility of pregnancy using appropriate contraceptive methods and not providing sperm or eggs from the date of first administration of the investigational drug to the 14th day after the last administration of the investigational drug

Exclusion Criteria:

1. Those who participated in other clinical trials (including bioequivalence studies) within 6 months before the first dose and received the investigational drug

2. Those who used drugs that induce and inhibit metabolic enzymes, such as barbital drugs, within one month before the first dose, or who used drugs that may interfere with this test within 10 days before the first dose

3. Those who have donated whole blood within 2 months before the first dose or component donation within 1 month, or have transfused within 1 month

4. Those who have had a history of gastrointestinal resection that may affect the absorption of the investigational drug (except appendectomy and hernia surgery)

5. A person who meets the following conditions within one month before the first administration date

• Excess alcohol: 21 cups / week for men and 14 cups / week for women.

[1 glass = 50 mL of shochu or 30 mL of liquor or 250 mL of beer]

• Smokers exceeding 20 cigarettes per day

6. Patients with the following diseases

• Patients with hypersensitivity to the main constituents or components of the investigational drug

• Severe hepatic impairment, biliary atresia or cholestasis

• Patients with hereditary angioedema or with a history of angioedema in the treatment of ACE inhibitors or angiotensin II receptor antagonists

• Diabetes mellitus

• Patients with moderate to severe renal impairment [glomerular filtration rate (eGFR) <60 mL / min / 1.73m^2]

• Renal vascular hypertension patients

• Patients with active liver disease, including unexplained persistent serum transaminase elevations or elevated serum transaminase elevations greater than three times the normal upper limit

• Patients with myopathy or have a history of family or genetic history of myopathy

• Hypothyroidism

• If you have a history of muscle toxicity for other HMG-CoA converting enzymes or fibrate class drugs

7. Genetic problems such as galactose intolerance, Lapp lactose deficiency, or glucose-galactose malabsorption

8. person who is considered to be unsuitable for participation in this clinical trial for reasons other than the above selection / exclusion criteria.

9. In the case of female volunteers, the suspected or lactating woman

Related Conditions & MeSH terms

• Diabetes Mellitus, Type 2
• Type2 Diabetes Mellitus

Intervention

Drug:
• CKD-386 Formulation 1
A single oral dose of 1 tablet under fasting conditions for each period
• CKD-386 Formulation 2
A single oral dose of 1 tablet under fasting conditions for each period
• D012, D326 and D337
A single oral dose of 3 tablets(D012, D326 and D337) under fasting conditions for each period

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Chong Kun Dang Pharmaceutical

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	AUCt of each main component or metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337	AUCt: Area under the concentration-time curve	0(predose)~72 hours
Primary	Cmax of each main component or metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337	Cmax: Maximum plasma concentration of the drug	0(predose)~72 hours
Secondary	AUCinf each main component or the metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337	AUCinf: Area under the concentration-time curve from zero up to 8	0(predose)~72 hours
Secondary	tmax each main component or the metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337	tmax: Time to maximum plasma concentration	0(predose)~72 hours
Secondary	AUCt/AUCinf each main component or the metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337	AUCt/AUCinf: AUCt/AUCinf Ratio	0(predose)~72 hours
Secondary	t1/2 each main component or the metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337	t1/2: Terminal elimination half-life	0(predose)~72 hours
Secondary	AUCt of each main component or metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D326, D337	AUCt: Area under the concentration-time curve	0(predose)~72 hours
Secondary	Cmax of each main component or metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D326, D337	Cmax: Maximum plasma concentration of the drug	0(predose)~72 hours