Clinical Trials Directory

Trials / Completed

CompletedNCT04946903

A Study to Evaluate the Pharmacokinetics and Safety Between HCP1902 and Co-administration of RLD2007, RLD2008

A Randomized, Open Label, Single Dose, 2-way Crossover Clinical Trial to Evaluate the Pharmacokinetic Characteristics and Safety Between HCP1902 and RLD2007/RLD2008 in Healthy Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
33 (actual)
Sponsor
Hanmi Pharmaceutical Company Limited · Industry
Sex
All
Age
19 Years – 54 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to evaluate the pharmacokinetic characteristics and safety between HCP1902 and co-administration of RLD2007/RLD2008 in healthy volunteers

Conditions

Interventions

TypeNameDescription
DRUGRLD2007Take it once per period.
DRUGRLD2008Take it once per period.
DRUGHCP1902Take it once per period.

Timeline

Start date
2021-06-10
Primary completion
2021-08-10
Completion
2021-08-10
First posted
2021-07-01
Last updated
2022-08-02

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT04946903. Inclusion in this directory is not an endorsement.

A Study to Evaluate the Pharmacokinetics and Safety Between HCP1902 and Co-administration of RLD2007, RLD2008 (NCT04946903) · Clinical Trials Directory