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CompletedNCT01516229

Special Survey for Long Term Application

Specific Survey of Norditropin® in Achondroplasia: Survey for Long-term Application

Status
Completed
Phase
Study type
Observational
Enrollment
395 (actual)
Sponsor
Novo Nordisk A/S · Industry
Sex
All
Age
1 Year – 15 Years
Healthy volunteers
Not accepted

Summary

This study is conducted in Japan. The aim of this study is to assess the incidence rate of adverse drug reactions (ADRs) when using somatropin (Norditropin®) for treatment of for achondroplasia without epiphyseal line closure under normal clinical practice conditions.

Conditions

Interventions

TypeNameDescription
DRUGsomatropinPrescription of somatropin at the discretion of the physician

Timeline

Start date
1997-05-01
Primary completion
2007-03-31
Completion
2007-03-31
First posted
2012-01-24
Last updated
2017-02-27

Locations

2 sites across 1 country: Japan

Source: ClinicalTrials.gov record NCT01516229. Inclusion in this directory is not an endorsement.

Special Survey for Long Term Application (NCT01516229) · Clinical Trials Directory