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Enrolling by invitation Phase 2Phase 3 Interventional

A Clinical Trial to Investigate Long-term Safety, Tolerability, and Efficacy of Weekly Subcutaneous Doses With TransCon CNP in Children and Adolescents With Achondroplasia

ClinicalTrials.gov ID: NCT05929807

Public ClinicalTrials.gov record NCT05929807. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 3:10 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Multicenter, Long-Term, Open Label Extension Trial Evaluating Safety, Tolerability, and Efficacy of Subcutaneous Doses of TransCon CNP Administered Once Weekly in Children and Adolescents With Achondroplasia

Study identification

NCT ID
NCT05929807
Recruitment status
Enrolling by invitation
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Ascendis Pharma Growth Disorders A/S
Industry
Enrollment
140 participants

Conditions and interventions

Conditions

Interventions

  • TransCon CNP Drug

Drug

Eligibility (public fields only)

Age range
3 Years to 15 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 20, 2023
Primary completion
Dec 31, 2038
Completion
Feb 28, 2039
Last update posted
Oct 26, 2025

2023 – 2039

United States locations

U.S. sites
8
U.S. states
8
U.S. cities
8
Facility City State ZIP Site status
Ascendis Pharma Investigational Site Little Rock Arkansas 72202
Ascendis Investigational Site Aurora Colorado 80045
Ascendis Investigational Site Wilmington Delaware 19803
Ascendis Investigational Site Saint Paul Minnesota 55102
Ascendis Pharma Investigational Site Columbia Falls Montana 65212
Ascendis Pharma Investigational Site Buffalo New York 14203
Ascendis Investigational Site Houston Texas 77030
Ascendis Pharma Investigational Site Madison Wisconsin 53705

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 9 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05929807, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 26, 2025 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05929807 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →