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
| Type | Name | Description |
|---|---|---|
| DRUG | Somatropin | 3 microg/kg/day for the first three months.The dose was then doubled (6 microg/kg/day) for the next three-months. |
| DRUG | Somatropin | 6 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.