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Clinical Trial to Compare Pharmacokinetics After Administration of ATB-101 or Co-administration of ATB-1011 and ATB-1012

Healthy Adult Volunteers Clinical Trial

Official title:
A Phase I Clinical Trial to Compare and Evaluate Safety and Pharmacokinetic Characteristics After Administration of ATB-101 or Co-administration of ATB-1011 and ATB-1012 in Healthy Adult Volunteers

Clinical Trial 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 Volunteers

Clinical Trial Description

Pharmacokinetic endpoints 1. Primary endpoint : AUCt, Cmax of Dapagliflozin, Olmesartan 2. Secondary endpoint : AUC∞, Tmax, t1/2, CL/F, Vd/F of Dapagliflozin, Olmesartan Safety evaluation 1. Adverse reactions (but only in case of TEAE) 2. Concomitant drugs 3. Vital signs 4. Laboratory test ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05017987
Study type Interventional
Source Autotelicbio
Contact
Status Completed
Phase Phase 1
Start date June 19, 2021
Completion date July 12, 2021
View Details
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