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A Study of Vosoritide in Children With Noonan Syndrome With Inadequate Growth During or After Human Growth Hormone Treatment

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NCT06668805 · readout ≤ 224 d

Sponsored by BioMarin Pharmaceutical (industry) · BMRN — their whole pipeline →.

Phase
Phase 2
Status
Recruiting
Study type
Interventional
Design
Randomized · Triple · Treatment
Enrollment
30estimated
Sites
36
Countries
Australia, Canada, France +4

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-11-22actualWhen the study began enrolling
Primary completionMar 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionSep 2041estimatedThe whole study's end, after follow-up
First posted2024-10-31actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-11actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Noonan Syndrome

Intervention

  • Drug: Vosoritide Injection

Primary outcome

what the primary-completion date above is the date OF
Change from baseline in Annualized Growth Velocity (AGV)
measured At 6 months

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