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Drug-Drug Interaction of DWP16001 in Combination With DWC202204 and DWC202205 in Healthy Male Adults

Healthy Clinical Trial

Official title:
A Phase I Clinical Trial to Evaluate the Safety and Drug Interactions Between DWP16001 and in Combination With DWC202204 and DWC202205 in Healthy Adult Volunteers

Clinical Trial Summary

The purpose of this study is to evaluate drug-drug interaction by comparing the pharmacokinetics (PK)/pharmacodynamics (PD), safety, and tolerability of single/multiple doses of DWP16001 , DWC202204 and DWC202205 alone or in combination in healthy male adults.

Clinical Trial Description

* Open label, multiple dose, 2 part, two period, single sequence design. This study is conducted on open label because it evaluates PK/PD parameters that are not affected by the blind. Volunteers who are suitable for the inclusion criteria are granted the final target number before the first dosage, receiving a fixed IP, and conducting a planned clinical trial schedule. After having a rest period (7 days) in which the drug received is sufficiently metabolized and lost, the IP of the next period is administered. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05500898
Study type Interventional
Source Daewoong Pharmaceutical Co. LTD.
Contact
Status Not yet recruiting
Phase Phase 1
Start date August 26, 2022
Completion date February 28, 2023
View Details
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