Clinical Trials Directory

Trials / Completed

CompletedNCT00570011

Low and Conventional Dose of Somatropin in Growth Hormone Deficient Adult Patients

Efficacy of Two Different Dose Regimens of Somatropin in Growth Hormone Deficient Adult Patients

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
112 (actual)
Sponsor
Eli Lilly and Company · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

An international study in which patients with GHD were randomized to receive somatropin at a dose of either 3 microg/kg/day or 6 microg/kg/day for the first three months. The dose was then doubled (6 microg/kg/day, LD or 12 microg/kg/day, CD) for the next three-months.

Conditions

Interventions

TypeNameDescription
DRUGSomatropin3 microg/kg/day for the first three months.The dose was then doubled (6 microg/kg/day) for the next three-months.
DRUGSomatropin6 microg/kg/day for the first three months. The dose was then doubled (12 microg/kg/day) for the next three-months.

Timeline

Start date
1997-06-01
Completion
1998-12-01
First posted
2007-12-10
Last updated
2007-12-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00570011. Inclusion in this directory is not an endorsement.