Main ContentfliGHt
Study title
Multi-center, phase 3, open label, 26-week trial investigating the safety, tolerability, and efficacy of Transcon hGH administered once weekly in children with growth hormone deficiency
- Principal Investigator: Dr. Naznin Dixit
Purpose
This study will assess safety and tolerability of an experimental drug in children with growth hormone deficiency (GHD).
Who can participate
Those eligible to participate in this study include:
- ChildrenĀ ages 3-17 diagnosed with growth hormone deficiency (GHD)
For more information
- Deepali Bhatt
University of Mississippi Medical Center
2500 N. State St.
Jackson MS 39216
(601) 815-9481 - IRB Number: 2017-0267