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Completed Phase 3 Interventional Results available

A Trial to Compare the Efficacy and Safety of Once-weekly Lonapegsomatropin With Placebo and a Daily Somatropin Product in Adults With Growth Hormone Deficiency

ClinicalTrials.gov ID: NCT04615273

Public ClinicalTrials.gov record NCT04615273. 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 20, 2026, 1:53 PM EDT

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

Official title

foresiGHt: A Multicenter, Randomized, Parallel-arm, Placebo-controlled (Double- Blind) and Active-controlled (Open-label) Trial to Compare the Efficacy and Safety of Once-weekly Lonapegsomatropin With Placebo and a Daily Somatropin Product in Adults With Growth Hormone Deficiency

Brief summary

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

A 38-week dosing trial of lonapegsomatropin, a long-acting growth hormone product, administered once-a-week versus placebo-control. A daily somatropin product arm is also included to assist clinical judgement on the trial results. A total of 264 adults (males and females) with growth hormone deficiency were included. Randomization occurred in a 1:1:1 ratio (lonapegsomatropin: placebo: daily somatropin product). This is a global trial conducted in, but not limited to, the United States, Europe, and Asia.

Study identification

NCT ID
NCT04615273
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
264 participants

Conditions and interventions

Eligibility (public fields only)

Age range
23 Years to 80 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 3, 2020 (Actual)
Primary completion
Nov 2, 2023 (Actual)
Completion
Dec 1, 2023 (Actual)
Last update posted
Jul 7, 2026

2020 – 2023

United States locations

U.S. sites
23
U.S. states
16
U.S. cities
21
Facility City State ZIP Site status
Ascendis Pharma Investigational Site Birmingham Alabama 35205 —
Ascendis Pharma Investigational Site Phoenix Arizona 85048 —
Ascendis Pharma Investigational Site Fresno California 93720 —
Ascendis Pharma Investigational Site Los Angeles California 90048 —
Ascendis Pharma Investigational Site Los Angeles California 90095 —
Ascendis Pharma Investigational Site Palo Alto California 94304 —
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 New York New York 10021 —
Ascendis Pharma Investigational Site Morehead City North Carolina 28557 —
Ascendis Pharma Investigational Site Portland Oregon 97239 —
Ascendis Pharma Investigational Site Pittsburgh Pennsylvania 15212 —
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 90 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04615273, 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 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04615273 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →