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NCT05775523 · ClinicalTrials.gov registry record

A Post-Authorisation Safety Study (PASS) of Patients Treated With Lonapegsomatropin

A clinical trial of Growth Hormone Deficiency, sponsored by Ascendis Pharma Endocrinology Division A/S.

Recruiting
Registry status
500
Enrollment target
20
Study locations

NCT05775523 is a study of Growth Hormone Deficiency that is actively recruiting participants, run by Ascendis Pharma Endocrinology Division A/S. The registered enrollment target is 500 participants, above the 356-participant average among 16 other Growth Hormone Deficiency trials with a reported enrollment target (40% higher). The trial reports 20 study locations across 15 states.

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The verdict

NCT05775523, a study of Growth Hormone Deficiency, is actively recruiting participants, sponsored by Ascendis Pharma Endocrinology Division A/S.

RECRUITING
Registry status
500 participants
Enrollment target
20
Study locations

Study Summary

The goal of this study is to further characterise the potential long-term safety risks of lonapegsomatropin in patients treated with lonapegsomatropin under real-world conditions in the post-marketing setting.

Conditions Studied

Interventions

  • DRUG No intervention

Study Locations (20)

California

  • Ascendis Investigational Site - Orange
  • Ascendis Investigational Site - Sacramento
  • Ascendis Investigational Site - San Francisco

Florida

  • Ascendis Investigational Site - Orlando
  • Ascendis Investigational Site - Orlando
  • Ascendis Investigational Site - Tampa

New Hampshire

  • Ascendis Investigational Site - Lebanon
  • Ascendis Investigational Site - Manchester

Arizona

  • Ascendis Investigational Site - Phoenix

Colorado

  • Ascendis Pharma Investigational Site - Centennial

District of Columbia

  • Ascendis Investigational Site - Washington D.C.

Georgia

  • Ascendis Investigational Site - Sandy Springs

Idaho

  • Ascendis Investigational Site - Boise

Trial Details

FieldValue
Enrollment Target 500 participants
Start Date 2023-03-20
Est. Completion 2033-03

What the Registry Record Tells You About NCT05775523

The ClinicalTrials.gov registry entry for NCT05775523 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 500 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 356-participant average among 16 other Growth Hormone Deficiency trials with a reported enrollment target (40% higher). The listed sponsor is Ascendis Pharma Endocrinology Division A/S, which has 7 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Growth Hormone Deficiency appearing as the primary indexed condition, and to 1 intervention - of which No intervention is the first listed.

NCT05775523 reports 20 study locations spanning 15 distinct geographic areas - top geographies include California, Florida, New Hampshire.

Frequently Asked Questions

What is clinical trial NCT05775523 about?

NCT05775523 is a clinical study titled "A Post-Authorisation Safety Study (PASS) of Patients Treated With Lonapegsomatropin". The goal of this study is to further characterise the potential long-term safety risks of lonapegsomatropin in patients treated with lonapegsomatropin under real-world conditions in the post-marketing setting.

What is the current status of trial NCT05775523?

This trial is currently recruiting. The enrollment target is 500 participants. The study started on 2023-03-20. Estimated completion is 2033-03.

What conditions does trial NCT05775523 study?

This clinical trial studies the following conditions: Growth Hormone Deficiency.

What interventions are being tested in trial NCT05775523?

The interventions under investigation include: No intervention (DRUG).

Who is sponsoring clinical trial NCT05775523?

This trial is sponsored by Ascendis Pharma Endocrinology Division A/S, which has 7 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05775523 being conducted?

This trial has 20 study locations across Arizona, California, Colorado, District of Columbia, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.