Clinical Trials Directory

Trials / Unknown

UnknownNCT03154840

Relative Bioavailability Among Different Eutropin Formulations

A Randomized, Open Label, Single Subcutaneous Dose 6x3 Crossover Study to Investigate the Relative Bioavailability Among Different Eutropin Formulations in Healthy Male Volunteers

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
24 (actual)
Sponsor
LG Chem · Industry
Sex
Male
Age
19 Years – 40 Years
Healthy volunteers
Accepted

Summary

1. Compares and evaluates the relative bioavailability of single-dose subcutaneous administration of each of the Eutropin formulations to healthy male volunteers. 2. Ensure safety and tolerability of single, subcutaneous administration of Eutropin formulations to healthy male volunteers.

Conditions

Interventions

TypeNameDescription
DRUGEutropin 4IU, Eutropin AQ 12IU, Eutropin Pen 36IUInvestigate the Relative Bioavailability among Different Eutropin Formulations

Timeline

Start date
2017-05-31
Primary completion
2017-07-10
Completion
2017-11-30
First posted
2017-05-16
Last updated
2017-07-21

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03154840. Inclusion in this directory is not an endorsement.