Exploratory Trial to Evaluate the Pharmacokinetic Properties and Safety of CKD-341 in Healthy Subjects

NCT05571813 | Completed Phase 1

• 1 other identifier: A126_01BE2205P
• Study Type: interventional
• Target: 30
• Locations: 1 country
• Sites: 1

Brief Summary

Exploratory Trial to Evaluate the Pharmacokinetic Properties and Safety of CKD-341 in Healthy Subjects

Conditions

Hypertension

Outcome Measures

Primary Outcomes (2)

• AUCt of CKD-341, D958

  Area under the CKD-341, D958 concentration in blood-time curve from zero to final

  Pre-dose(0 hour), post-dose 0.25, 0.5, 0.67, 0.83, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 4, 5, 6, 7, 8, 12, 24, 48, 72 hours

• Cmax of CKD-341, D958

  The maximum CKD-341, D958 concentration in blood sampling time

  Pre-dose(0 hour), post-dose 0.25, 0.5, 0.67, 0.83, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 4, 5, 6, 7, 8, 12, 24, 48, 72 hours

Study Arms (6)

Sequence 1

EXPERIMENTAL

Period1: D958 Period2: CKD-341 Formulation I Period3: CKD-341 Formulation II

Drug: CKD-341

Sequence 2

EXPERIMENTAL

Period1: CKD-341 Formulation II Period2: D958 Period3: CKD-341 Formulation I

Drug: CKD-341

Sequence 3

EXPERIMENTAL

Period1: CKD-341 Formulation I Period2: CKD-341 Formulation II Period3: D958

Drug: CKD-341

Sequence 4

EXPERIMENTAL

Period1: CKD-341 Formulation II Period2: CKD-341 Formulation I Period3: D958

Drug: CKD-341

Sequence 5

EXPERIMENTAL

Period1: CKD-341 Formulation I Period2: D958 Period3: CKD-341 Formulation II

Drug: CKD-341

Sequence 6

EXPERIMENTAL

Period1: D958 Period2: CKD-341 Formulation II Period3: CKD-341 Formulation I

Drug: CKD-341

Interventions

CKD-341 DRUG

A single dose of 1tablets under fasting condition

Also known as: D958

Sequence 1; Sequence 2; Sequence 3; Sequence 4; Sequence 5; Sequence 6

Eligibility Criteria

• Age: 19 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Healthy male volunteers, aged ≥ 19 years old at the time of screening
• Those with a body mass index (BMI) of 17.5 kg/m2 or more and less than 30.5 kg/m2
• Those who do not have congenital or chronic diseases and have no pathological symptoms or findings as a result of medical examination
• Clinical laboratory tests (hematology tests, blood chemistry tests, urinalysis, serological tests, etc.) conducted by the principal investigator(or the investigator who has been delegated) according to the characteristics of the drug and screening tests such as vital signs and electrocardiogram tests Result Those who are judged to be suitable as test subjects
• Before participating in the trial, the purpose and contents of the trial were fully explained, and the participants agreed to participate in this study voluntarily who signed
• After the first administration of the clinical trial drug, for up to 14 days after the last administration of the investigational drug, you, your spouse, or your partner must agree to maintain the use of an appropriate medically acceptable method of contraception\* except for hormonal contraceptives and not donate sperm or eggs ruler
• Those who have the ability and willingness to participate during the entire examination period

You may not qualify if:

• A history of clinically significant blood, renal, endocrine, respiratory, gastrointestinal, urinary, cardiovascular, liver, psychiatric, neurological, or immune disease (except for simple dental history of calculus, impacted teeth, wisdom teeth, etc.) or evidence one who has 1-1. Patients with hypersensitivity or a history of hypersensitivity to this drug or ingredients contained in this drug, dihydropyridine derivatives, thiazide diuretics, or sulfonamide drugs 1-2. Pregnant (2nd and 3rd trimester) or women who may be pregnant 1-3. Lactating women 1-4. Patients with biliary atresia 1-5. Patient with Severely liver dysfunction 1-6. Patient with Severely aortic valvular stenosis 1-7. Shock patient 1-8. Patients with genetic problems such as intolerance to this drug's additives 1-9. Patients with diabetes or moderate to severe renal impairment (glomerular filtration rate \<60mL/min/1.73m2) who used aliskiren-containing agents in combination 1-10. Patients with anuria 1-11. Patients with severe renal failure (creatinine clearance \<30 mL/min) 1-12. Patients with refractory hypokalemia 1-13. Patients with hyponatremia and hypercalcemia 1-14. Patients with symptomatic hyperuricemia (history of gout or urolithiasis) 1-15. Untreated Addison's syndrome patients 1-16. Patients receiving lithium therapy 1-17. Patients taking terfenadine or astemizole
• Those with a history of gastrointestinal diseases (esophageal diseases such as achalasia or esophageal stricture, Crohn's disease) or surgery(except simple appendicectomy, hernia surgery, and tooth extraction surgery) that may affect drug absorption ruler
• A person who shows the following values as a result of conducting a clinical laboratory test
• \- ALT or AST \> 2 times the upper limit of the normal range
• Smokers who smoked more than 20 cigarettes a day within 6 months of screening
• Those who have taken other clinical investigational drugs or bioequivalence investigational drugs within 6 months before the first administration of the clinical investigational drug
• Those who meet the following as a result of measuring vital signs at screening
• Those who have a systolic blood pressure of less than 90 mmHg or more than 140 mmHg or a diastolic blood pressure of less than 60 mmHg or more than 90 mmHg in the sitting position
• Severe bradycardia (less than 50 beats/min)
• Those with a history of regular alcohol intake within 1 month of screening
• More than 14 drinks/Week for women
• More than 21 drinks/Week for men
• A person who has taken a drug known to significantly induce or inhibit drug metabolizing enzymes within 30 days before the first administration of the clinical trial drug
• Those who have taken prescription or non-prescription drugs within 10days prior to the first administration of clinical trial drugs
• Those who have donated whole blood within 2 months before the first administration of the clinical trial drug, donated component blood within 1 month, received blood transfusion within 1 month, or have plans for the trial during the clinical trial period

Sponsors & Collaborators

• Chong Kun Dang Pharmaceutical: lead

Study Sites (1)

Central Hospital

Gyeonggi-do, South Korea

Location

MeSH Terms

Conditions

Hypertension

Condition Hierarchy (Ancestors)

Vascular Diseases; Cardiovascular Diseases

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: CROSSOVER
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 6, 2022
• First Posted: October 7, 2022
• Study Start: November 2, 2022
• Primary Completion: December 4, 2022
• Study Completion: December 23, 2022
• Last Updated: March 22, 2023

Record last verified: 2022-10

Locations

KR (1)