A US Multi-center, Prospective, Non-interventional, Long-term, Effectiveness and Safety Study of Patients Treated with SKYTROFA (lonapegsomatropin-tcgd) (SkybriGHt)
A US Multi-center, Prospective, Non-interventional, Long-term, Effectiveness and Safety Study of Patients Treated with SKYTROFA (lonapegsomatropin-tcgd) (SkybriGHt)
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Clinical Trial Information
Trial Contact: Tilme, Linda; Casillas, Bridey L
Trial Phone: 321.843.5278 ; 321.841.9772
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IRB No: 23.093.05
Protocol Abbrev: ASND0037
Principal Investigator: Joshua H Yang, MD
Age Group: Pediatric
Secondary Protocol No: ASND0037
ClinicalTrials.gov ID: NCT05820672
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Objective
The goal of this study is to generate evidence on long-term effectiveness and safety of SKYTROFA (lonapegsomatropin) in patients with growth hormone deficiency under routine clinical care
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Key Eligibility
Inclusion Criteria:
Patients who are on treatment with SKYTROFA (lonapegsomatropin)
Patients being clinically managed in USA
Patients with an appropriate written informed consent/assent as applicable for the age of the patient
