The purpose of this study is to support selection of an appropriate safe and efficacious dose for study in further development.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
65
TV-1106 0.554mg, TV-1106 0.924 mg, TV-1106 1.20 mg
Dose may be adjusted as required
Height velocity (HV)
Time frame: Month 6
Height velocity standard deviation score (HV-SDS)
Time frame: Months 6 and 12
Height standard deviation score (H-SDS)
Time frame: Months 6 and 12
Number of participants with adverse events
Time frame: up to 24 months
Height velocity (HV)
Time frame: Month 12
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Teva Investigational Site 68016
Minsk, Belarus
Teva Investigational Site 59060
Varna, Bulgaria
Teva Investigational Site 81022
Tbilisi, Georgia
Teva Investigational Site 81023
Tbilisi, Georgia
Teva Investigational Site 81025
Tbilisi, Georgia
Teva Investigational Site 63046
Athens, Greece
Teva Investigational Site 51159
Budapest, Hungary
Teva Investigational Site 51160
Budapest, Hungary
Teva Investigational Site 51181
Szombathely, Hungary
Teva Investigational Site 80052
Afula, Israel
...and 24 more locations