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Completed Phase 3 Interventional Results available

A Trial to Investigate Long Term Efficacy and Safety of Lonapegsomatropin in Adults With Growth Hormone Deficiency

ClinicalTrials.gov ID: NCT05171855

Public ClinicalTrials.gov record NCT05171855. 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, 11:30 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 Multicenter, Open-Label, Extension Trial to Investigate Long Term Efficacy and Safety of Lonapegsomatropin in Adults With Growth Hormone Deficiency

Brief summary

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

This was a phase 3 open-label multicenter extension study designed to evaluate the long-term safety and efficacy of Lonapegsomatropin administered once-weekly. The study participants were adults (males and females) with confirmed growth hormone deficiency (GHD) having completed the treatment period in study TCH-306 (foresiGHt; NCT04615273).

Study identification

NCT ID
NCT05171855
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
220 participants

Conditions and interventions

Eligibility (public fields only)

Age range
23 Years to 81 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 16, 2021 (Actual)
Primary completion
Dec 23, 2024 (Actual)
Completion
Dec 23, 2024 (Actual)
Last update posted
Jul 7, 2026

2021 – 2024

United States locations

U.S. sites
15
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
Ascendis Pharma Investigational Site Phoenix Arizona 85048 —
Ascendis Pharma Investigational Site Torrance California 90509 —
Ascendis Pharma Investigational Site Chicago Illinois 60611 —
Ascendis Pharma Investigational Site Indianapolis Indiana 46202 —
Ascendis Pharma Investigational Site Boston Massachusetts 02114 —
Ascendis Pharma Investigational Site Dearborn Michigan 48126 —
Ascendis Pharma Investigational Site Rochester Minnesota 55905 —
Ascendis Pharma Investigational Site St Louis Missouri 63110 —
Ascendis Pharma Investigational Site Las Vegas Nevada 89148 —
Ascendis Pharma Investigational Site Reno Nevada 89511 —
Ascendis Pharma Investigational Site New York New York 10017 —
Ascendis Pharma Investigational Site Portland Oregon 97239 —
Ascendis Pharma Investigational Site Dallas Texas 75390 —
Ascendis Pharma Investigational Site San Antonio Texas 78232 —
Ascendis Pharma Investigational Site Seattle Washington 98108 —

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 70 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05171855, 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 NCT05171855 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →