A Study to Evaluate the Pharmacokinetics and the Safety After Administration of "BR1017-1" and Co-administration of "BR1017-1A" and "BR1017-1B"
Phase 1
Completed
- Conditions
- Essential HypertensionPrimary Hypercholesterolemia
- Interventions
- Registration Number
- NCT06184269
- Lead Sponsor
- Boryung Pharmaceutical Co., Ltd
- Brief Summary
The objective of this clinical study is to evaluate the pharmacokinetics and the safety after administration of "BR1017-1" and co-administration of "BR1017-1A" and "BR1017-1B" in healthy volunteers
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 58
Inclusion Criteria
- Those who weigh 50 kg or more and have body mass index (BMI) within the range of 18.0 to 30.0kg/m² at screening visit.
- Those who sign written consent spontaneously after listening to and understanding sufficient explanation of the purpose and contents of this clinical trial, characteristics of the Investigational products, expected adverse events, etc.
Exclusion Criteria
- Those who have taken drugs that induce and inhibit metabolizing enzymes such as barbiturate within 30 days prior to the first day of administration or have taken drugs concerned about affecting this clinical trial within 10 days prior to the first day of administration. (however, participation is possible considering pharmacokinetics and pharmacodynamics such as Interaction of investigational products, half-life of concomitant drugs, etc.)
- Those who have participated in other clinical trials(including bioequivalence tests) and administered their investigational products within 6 months prior to the first administration date.(However, the termination for participation in other clinical trials are based on the last administration date of their investigational products)
- Those who have a medical history of gastrointestinal surgery or gastrointestinal diseases that may affect the absorption of drugs. (Except for simple appendectomy, hernia surgery)
- Those who can't discontinue a diet (ex. raw grapefruit, grapefruit juice or its products) that may affect the absorption, distribution, metabolism, and excretion of the drug within 48 hours prior to the first day of administration.
- In the case of a female subject, those suspected pregnancy, pregnant woman, lactating woman.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description BR1017-1A+BR1017-1B BR1017-1A - BR1017-1A+BR1017-1B BR1017-1B - BR1017-1 BR1017-1 -
- Primary Outcome Measures
Name Time Method AUCτ 0-72 hours after administration Area under the concentration-time curve from time zero to time τ
Cmax 0-72 hours after administration Maximum concentration of drug in plasma
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Clinical Research Center, H PLUS Yangji Hospital
🇰🇷Seoul, Gwanakgu, Korea, Republic of