A Study to Compare PK Characteristics and Safety Profiles Between AD-228B and AD-2284
Phase 1
Recruiting
- Conditions
- Primary Hypercholesterolaemia
- Interventions
- Drug: AD-228BDrug: AD-2284
- Registration Number
- NCT06884098
- Lead Sponsor
- Addpharma Inc.
- Brief Summary
Primary endpoint of this study is to evaluate the pharmacokinetic characteristics of AD-228B in healthy subjects.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
- Body weight equal to or greater than 50kg (Female 45kg) and Body mass index (BMI) between 18.0 kg/m2 and 30.0 kg/m2 at the time of screening visit
- The Age equal to or greater than 19 in healthy volunteers at the time of screening visit
Exclusion Criteria
- Participation in other clinical study with an investigational drug within the 6 months from scheduled first administration
- Other exclusions applied
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Sequence A (RT) AD-228B Period 1: Reference Drug (AD-2284), Period 2: Test Drug (AD-228B) Sequence A (RT) AD-2284 Period 1: Reference Drug (AD-2284), Period 2: Test Drug (AD-228B) Sequence B (TR) AD-228B Period 1: Test Drug (AD-228B), Period 2: Reference Drug (AD-2284) Sequence B (TR) AD-2284 Period 1: Test Drug (AD-228B), Period 2: Reference Drug (AD-2284)
- Primary Outcome Measures
Name Time Method Maximum concentration of drug in plasma (Cmax) pre-dose (0hour) to 72hours Cmax of AD-228B
Area under the plasma concentration-time curve during dosing interval (AUCt) pre-dose (0hour) to 72hours AUCt of AD-228B
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
NCT06884098 AD-228B AD-2284 pharmacokinetic comparison molecular targets hypercholesterolemia
AD-228B vs standard-of-care lipid-lowering agents efficacy safety primary hypercholesterolemia
Biomarkers LDL-C APOE PCSK9 response prediction AD-228B AD-2284 hypercholesterolemia
NCT06884098 Addpharma phase 1 adverse events management strategies healthy volunteers
Competitor drugs AD-228B AD-2284 bioequivalence lipid-lowering agents clinical trials
Trial Locations
- Locations (1)
H Plus Yangji Hospital
🇰🇷Seoul, Korea, Republic of