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RECRUITING
NCT07706764
PHASE3

A Study to Test the Effects and Safety of Palopegteriparatide in Adolescents With Long-term Hypoparathyroidism

Sponsor: Ascendis Pharma A/S

View on ClinicalTrials.gov

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

Interventions

COMBINATION_PRODUCT

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