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)

  • Clinical Trial Information

    Trial Contact: Tilme, Linda; Beltran, Yajira

    Trial Phone: 321.843.5278 ; 321.841.7619

  • IRB No: 23.093.05

    Protocol Abbrev: ASND0037

    Principal Investigator: Joshua H Yang, MD

    Phase: Drug: Phase III

    Age Group: Pediatric

    ClinicalTrials.gov ID: NCT05820672

  • 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

  • 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