ClinicalTrials.gov record
Completed Phase 3 Interventional

Safety and Efficacy of Somatropin in Children With Growth Hormone Deficiency

ClinicalTrials.gov ID: NCT01502124

Public ClinicalTrials.gov record NCT01502124. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 14, 2026, 7:21 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Norditropin® and Norditropin® Cartridges: An Open-Label, Randomized, Comparative Safety and Efficacy Trial in Children With Growth Hormone Deficiency

Study identification

NCT ID
NCT01502124
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
78 participants

Conditions and interventions

Interventions

  • somatropin Drug

Drug

Eligibility (public fields only)

Age range
3 Years to 17 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 7, 2001
Primary completion
Mar 4, 2003
Completion
Mar 4, 2003
Last update posted
Feb 27, 2017

2001 – 2003

United States locations

U.S. sites
21
U.S. states
13
U.S. cities
18
Facility City State ZIP Site status
Novo Nordisk Investigational Site Los Angeles California 90027
Novo Nordisk Investigational Site Los Angeles California 90048-1869
Novo Nordisk Investigational Site Wilmington Delaware 19899
Novo Nordisk Investigational Site Washington D.C. District of Columbia 20010
Novo Nordisk Investigational Site Gainesville Florida 32608
Novo Nordisk Investigational Site Miami Florida 33155
Novo Nordisk Investigational Site Orlando Florida 32806-1101
Novo Nordisk Investigational Site Tampa Florida 33607
Novo Nordisk Investigational Site Atlanta Georgia 30342
Novo Nordisk Investigational Site Chicago Illinois 60612
Novo Nordisk Investigational Site Chicago Illinois 60614
Novo Nordisk Investigational Site Wichita Kansas 67226
Novo Nordisk Investigational Site Lexington Kentucky 40536-0284
Novo Nordisk Investigational Site Louisville Kentucky 40202
Novo Nordisk Investigational Site Worcester Massachusetts 01655
Novo Nordisk Investigational Site Manhasset New York 11030
Novo Nordisk Investigational Site Akron Ohio 44308-1062
Novo Nordisk Investigational Site Hershey Pennsylvania 17033
Novo Nordisk Investigational Site Pittsburgh Pennsylvania 15212
Novo Nordisk Investigational Site Pittsburgh Pennsylvania 15224
Novo Nordisk Investigational Site Seattle Washington 98105

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01502124, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 27, 2017 · Synced May 14, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01502124 live on ClinicalTrials.gov.

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