Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of DWP16001 After Oral Administration in Healthy Male Volunteers
Completed
Daewoong Pharmaceutical Co. LTD.
Phase 1
This is a dose block-randomized, double-blind, placebo- and active-controlled, single and
multiple dosing, dose-escalation clinical phase 1 trial to investigate the safety,
tolerability, pharmacokinetics and pharmacodynamics of DWP16001 after oral administration in
healthy male volunteers.
The purpose of the study is to evaluate the effect of kidney function on pharmacokinetics and
pharmacodynamics of DWP16001 following single and multiple oral doses in type 2 diabetes
patients with normal kidney function and renal impairment.
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