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A Study to Compare PK Characteristics and Safety Profiles Between AD-228B and AD-2284

Phase 1
Recruiting
Conditions
Primary Hypercholesterolaemia
Interventions
Drug: AD-228B
Drug: 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
GroupInterventionDescription
Sequence A (RT)AD-228BPeriod 1: Reference Drug (AD-2284), Period 2: Test Drug (AD-228B)
Sequence A (RT)AD-2284Period 1: Reference Drug (AD-2284), Period 2: Test Drug (AD-228B)
Sequence B (TR)AD-228BPeriod 1: Test Drug (AD-228B), Period 2: Reference Drug (AD-2284)
Sequence B (TR)AD-2284Period 1: Test Drug (AD-228B), Period 2: Reference Drug (AD-2284)
Primary Outcome Measures
NameTimeMethod
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
NameTimeMethod

Trial Locations

Locations (1)

H Plus Yangji Hospital

🇰🇷

Seoul, Korea, Republic of

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