A Study to Compare PK Characteristics and Safety Profiles Between AD-228B and AD-2284
ConditionPrimary Hypercholesterolaemia
Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age19+
SponsorAddpharma Inc.
Primary endpoint of this study is to evaluate the pharmacokinetic characteristics of AD-228B in healthy subjects.
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
Participation in other clinical study with an investigational drug within the 6 months from scheduled first administration
Other exclusions applied