Amendment (g) Unblinded Extension Phase of Somatropin in Patients With Idiopathic Short Stature

This study has been completed.
Sponsor:
Information provided by:
Eli Lilly and Company
ClinicalTrials.gov Identifier:
NCT00191074
First received: September 12, 2005
Last updated: March 7, 2007
Last verified: March 2007

September 12, 2005
March 7, 2007
February 2001
Not Provided
  • Every 6 months: physical exam, pubertal staging, height, weight, and adverse event collection.
  • Every year: arm span measurements, head circumference measurements, x-ray for bone age, and
  • laboratory blood draws.
Same as current
Complete list of historical versions of study NCT00191074 on ClinicalTrials.gov Archive Site
Not applicable for Amendment (g).
Same as current
Not Provided
Not Provided
 
Amendment (g) Unblinded Extension Phase of Somatropin in Patients With Idiopathic Short Stature
Phase III Study of Humatrope in Non-Growth Hormone Deficient Children With Short Stature

After approval of amendment (g), patients who were still receiving study drug at the time were scheduled for a study visit. In addition, patients who had discontinued early from the core, blinded phase of the study were contacted.

All of these patients were offered the opportunity to enter the unblinded extension phase (if they met eligibility criteria) and continue somatropin treatment (regardless of initial treatment randomization) until they reached final height.

Not Provided
Interventional
Phase 3
Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Growth Disorder
Drug: somatropin, rDNA origin, for injection
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
11
January 2006
Not Provided

Inclusion Criteria:

Participation in core, blinded phase and ability to be contacted by investigators.

For patients who were on treatment at the time of amendment (g), growth velocity greater than or equal to 1.5 cm/year measured over the prior 12-month period. For patients who had chosen to discontinue treatment in the core, blinded phase, bone age less than or equal to 16 years for boys and less than or equal to 14 years for girls.

Exclusion Criteria:

Diabetes mellitus.

History, evidence or signs of active malignancy within 5 years prior to the start of the extension phase.

Any condition or medication that, in the opinion of the investigators, might significantly increase the risk or decrease the efficacy of growth hormone therapy.

Both
9 Years to 16 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00191074
843, B9R-MC-GDCH
Not Provided
Not Provided
Eli Lilly and Company
Not Provided
Study Director: Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon-Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST) Eli Lilly and Company
Eli Lilly and Company
March 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP