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Study identifier: NCT06668805 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Noonan Syndrome  ·  Sponsor: BioMarin Pharmaceutical

PhasePhase 2
Planned participants30
Who can joinAll sexes, 3 Years to 11 Years
Healthy volunteersNo

About this study

The purpose of this study in children with Noonan syndrome is to evaluate the effect of 3 doses of vosoritide on growth as measured by AGV after 6 months of treatment. The long-term efficacy and safety of vosoritide at the therapeutic dose will be evaluated up to FAH.

This description comes directly from the study's public registry record.

Talk to the study team

Trial Specialist  ·  1-800-983-4587  ·  medinfo@bmrn.com

Study Manager  ·  1-800-983-4587  ·  Medinfo@bmrn.com

Always discuss trial participation with your own doctor first.

Locations (36)

Childrens Hospital Los AngelesLos Angeles, California, United StatesRecruiting
Children's Hospital of Orange County Main Campus - OrangeOrange, California, United StatesRecruiting
Children's Hospital ColoradoAurora, Colorado, United StatesRecruiting
Nemours Children's Hospital, Delaware (Alfred I. Dupont Hospital for Children)Wilmington, Delaware, United StatesRecruiting
Children's National Medical CenterWashington D.C., District of Columbia, United StatesRecruiting
Nicklaus Children's HospitalMiami, Florida, United StatesNot Yet Recruiting
Emory University School of MedicineAtlanta, Georgia, United StatesRecruiting
St. Luke's Children's Endocrinology and DiabetesBoise, Idaho, United StatesRecruiting
Ann & Robert H. Lurie Children's Hospital of ChicagoChicago, Illinois, United StatesRecruiting
Riley Hospital for Children at Indiana University HealthIndianapolis, Indiana, United StatesRecruiting
University of IowaIowa City, Iowa, United StatesRecruiting
Kentucky Children's HospitalLexington, Kentucky, United StatesRecruiting

+ 24 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06668805