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A Bioequivalence Study of CT-L01 Compared to Co-administration (ALO 12.5 mg and MET XR 500 mg) in Healthy Volunteers

NCT05363592 PHASE1 COMPLETED

This is a randomized, open, single-dose, crossover-design, phase 1, single-center study to evaluate bioequivalence after co-administration of ALO and MET XR or administration of CT-L01 in healthy volunteers.

Details

Lead sponsorCelltrion
PhasePHASE1
StatusCOMPLETED
Enrolment48
Start dateSat Jun 25 2022 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionMon Jul 25 2022 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

South Korea