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Completed Phase 3 Interventional Results available

A Long-Term Trial Investigating Safety and Efficacy of TransCon hGH in Children With Growth Hormone Deficiency Who Have Completed a Prior TransCon hGH Clinical Trial

ClinicalTrials.gov ID: NCT03344458

Public ClinicalTrials.gov record NCT03344458. 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 Oct 27, 2026, 11:28 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

enliGHten: A Multicenter, Phase 3, Long-Term, Open-Label Trial Investigating Safety and Efficacy of TransCon hGH Administered Once-Weekly in Children With Growth Hormone Deficiency (GHD) Who Have Completed a Prior TransCon hGH Clinical Trial

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A multicenter, phase 3, long-term extension trial of TransCon hGH administered once-weekly in children with growth hormone deficiency (GHD) who previously participated in a phase 3 TransCon hGH trial. Approximately 300 children (males and females) with GHD will be included. All study participants will receive TransCon hGH. This is a global trial that will be conducted in, but not limited to, the United States, Poland, Bulgaria, Ukraine, Armenia, Russia and Australia.

Study identification

NCT ID
NCT03344458
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ascendis Pharma A/S
Industry
Enrollment
298 participants

Conditions and interventions

Eligibility (public fields only)

Age range
1 Year to 18 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
Dec 19, 2017 (Actual)
Primary completion
Feb 21, 2023 (Actual)
Completion
Feb 21, 2023 (Actual)
Last update posted
Jul 7, 2026

2017 – 2023

United States locations

U.S. sites
22
U.S. states
14
U.S. cities
21
Facility City State ZIP Site status
Ascendis Pharma Investigational Site Birmingham Alabama 35233 —
Ascendis Pharma Investigational Site Los Angeles California 90048 —
Ascendis Pharma Investigational Site Orange California 92868 —
Ascendis Pharma Investigational Site Sacramento California 95821 —
Ascendis Pharma Investigational Site Centennial Colorado 80112 —
Ascendis Pharma Investigational Site Jacksonville Florida 32207 —
Ascendis Pharma Investigational Site Orlando Florida 32806 —
Ascendis Pharma Investigational Site Tallahassee Florida 32308 —
Ascendis Pharma Investigational Site Saint Paul Minnesota 55102 —
Ascendis Pharma Investigational Site Jackson Mississippi 39216 —
Ascendis Pharma Investigational Site Lebanon New Hampshire 03756 —
Ascendis Pharma Investigational Site Mineola New York 11501 —
Ascendis Pharma Investigational Site New York New York 10029 —
Ascendis Pharma Investigational Site Cleveland Ohio 44195 —
Ascendis Pharma Investigational Site Oklahoma City Oklahoma 73104 —
Ascendis Pharma Investigational Site Portland Oregon 97227 —
Ascendis Pharma Investigational Site Portland Oregon 97239 —
Ascendis Pharma Investigational Site Dallas Texas 75390 —
Ascendis Pharma Investigational Site Fort Worth Texas 76104 —
Ascendis Pharma Investigational Site Charlottesville Virginia 22908 —
Ascendis Pharma Investigational Site Norfolk Virginia 23507 —
Ascendis Pharma Investigational Site Tacoma Washington 98405 —

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 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03344458, 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 Jul 7, 2026 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03344458 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →