Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06616883

Pharmacokinetics and Safety Profiles After Administration of DA-5221_01 and Co-administration of 5221_01-R1 and DA-5221_01-R2 in Healthy Adult Volunteers

An Open-label, Randomized, Single-dose, 2-sequence, 2-period, Cross-over Study to Compare and Evaluate the Safety and Pharmacokinetic Characteristics After Single Administration of DA-5221_01 and Concomitant Administration of DA-5221_01-R1 and DA-5221_01-R2 Under Fasting Conditions in Healthy Adult Volunteers

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
44 (estimated)
Sponsor
Dong-A ST Co., Ltd. · Industry
Sex
All
Age
19 Years
Healthy volunteers
Accepted

Summary

Pharmacokinetics and Safety Profiles After Administration of DA-5221\_01 and Co-administration of 5221\_01-R1 and DA-5221\_01-R2 in Healthy Adult Volunteers

Conditions

Interventions

TypeNameDescription
DRUGDA-5221_01single dose administration (DA-5221\_01 one tablet once a day)
DRUGDA-5221_01-R1 + DA-5221_01-R2single dose administration (DA-5221\_01-R1 one tablet once a day + DA-5221\_01-R2 one tablet once a day)

Timeline

Start date
2024-09-30
Primary completion
2024-11-14
Completion
2024-11-18
First posted
2024-09-27
Last updated
2024-09-27

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT06616883. Inclusion in this directory is not an endorsement.