Overview
Clinical Trial to Compare Pharmacokinetics After Administration of ATB-101 or Co-administration of ATB-1011 and ATB-1012
Status:
Completed
Completed
Trial end date:
2021-07-12
2021-07-12
Target enrollment:
0
0
Participant gender:
All
All
Summary
To compare and evaluate safety and pharmacokinetic Characteristics after administration of ATB-101 or co-administration of ATB-1011 and ATB-1012 in fasted Healthy Adult VolunteersPhase:
Phase 1Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
AutotelicbioTreatments:
Olmesartan Medoxomil
Criteria
Inclusion Criteria:- Those who are over 19 years old at the screening visit
- Those who do not have clinically significant congenital or chronic diseases and have
no pathological symptoms or findings upon medical examination at the screening visit
- Those who determined as suitable study subjects by the principal investigator
- A person who signs the consent form at will, after hearing and understanding a
sufficient explanation of the purpose, contents, characteristics of the
investigational product, and expected adverse reactions of this clinical trial
Exclusion Criteria:
- Those who have a clinically significant disease or have a history of such disease
- Those who have a history of gastrointestinal surgery
- Those who have taken drugs that induce and inhibit metabolism enzymes such as barbital
drugs
- Those who participated in other clinical trials or bioequivalence studies and
administered the investigational products within 6 months of the first administration
date.
- Those who donated whole blood within 2 months or donated components within 2 weeks, or
received a blood transfusion within 1 month of the first administration date