Vosoritide
(111-210 [Canopy ISS-2])
Trial Status Recruiting
Condition
Idiopathic Short Stature
Technology
- Peptide
Title
A Phase 2 Study of Vosoritide in Children With Idiopathic Short Stature
Study Description
This study will evaluate the effect of multiple doses of vosoritide and the effect of vosoritide compared to human growth hormone (hGH), in children with Idiopathic Short Stature.
Primary Outcome Measures*
- Change in annualized growth velocity (AGV), height, and height Z-score
Secondary Outcome Measures*
- Incidence of adverse events
- Change in pharmacodynamic parameters (urine cyclic guanine monophosphate, serum collagen X marker)
- Pharmacokinetics of vosoritide
Select Inclusion Criteria*
- Patients ≥3 and <10 (female) or < 11 (males) years of age
- Height Z-score ≤-2.25 standard deviations compared to age and sex matched population norms
- If ≥ 5 years at Screening, must be Tanner Stage I
Select Exclusion Criteria*
- Known chromosomal imbalance or genetic variant causing short stature syndrome, including but not limited to: Laron syndrome, Prader-Willi syndrome, Russell-Silver Syndrome, Turner syndrome, disproportionate skeletal dysplasias, abnormal SHOX gene analysis, or Rasopathy (including Noonan syndrome), ACAN deficiency
- History of treatment with a growth promoting agent
* Additional measures/criteria may apply.
For reference and comprehensive trial information, visit ClinicalTrials.gov NCT06382155