A US Non-interventional, Effectiveness and Safety Study of Patients Treated With SKYTROFA

NCT05820672 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 900

Last updated 2026-04-21

No results posted yet for this study

Summary

The goal of this study is to genrate evidence on long-term effectiveness and safety of SKYTROFA (lonapegsomatropin) in patients with growth hormone deficiency under routine clinical care

Conditions

  • Growth Hormone Deficiency

Interventions

OTHER

No intervention

No intervention

Sponsors & Collaborators

  • Ascendis Pharma Endocrinology Division A/S

    lead INDUSTRY

Principal Investigators

  • Medical Director, MD · Ascendis Pharma A/S

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-03-20
Primary Completion
2033-03-31
Completion
2033-03-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05820672 on ClinicalTrials.gov