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A Study to Test the Effects and Safety of Palopegteriparatide in Adolescents With Long-term Hypoparathyroidism
Sponsor: Ascendis Pharma A/S
Summary
This trial will enroll adolescents between ages of ≥12 and \<18 years with clinically diagnosed hypoparathyroidism . The purpose of the study is to see how well treatment with once-daily palopegteriparatide works and how safe it is. At least 12 participants will receive palopegteriparatide for 234 weeks. This trial will be conducted in Europe.
Official title: A Phase 3, Multicenter, Open-Label Single-Arm Clinical Trial to Assess the Safety, Tolerability, Pharmacokinetics, and Efficacy of Palopegteriparatide Administered Subcutaneously Daily in the Adolescent Population (12 Years to Less Than 18 Years of Age) With Chronic Hypoparathyroidism
Key Details
Gender
All
Age Range
12 Years - 18 Years
Study Type
INTERVENTIONAL
Enrollment
12
Start Date
2026-04-22
Completion Date
2031-08
Last Updated
2026-07-28
Healthy Volunteers
No
Conditions
Interventions
Palopegteriparatide
Subcutaneous injection for 234 weeks
Locations (3)
Ascendis Pharma Investigational Site
Bron, France
Ascendis Pharma Investigational Site
Le Kremlin-Bicêtre, France
Ascendis Pharma Investigational Site
Lodz, Poland