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RECRUITING

A US Non-interventional, Effectiveness and Safety Study of Patients Treated With SKYTROFA

NCT05820672 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this study is to genrate evidence on long-term effectiveness and safety of SKYTROFA (lonapegsomatropin) in patients with growth hormone deficiency under routine clinical care

Conditions Studied

Interventions

  • OTHER 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 900 participants
Start Date 2023-03-20
Est. Completion 2033-03

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05820672

The ClinicalTrials.gov registry entry for NCT05820672 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 900 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ascendis Pharma Endocrinology Division A/S, which has 35 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05820672 reports 20 study locations spanning 15 distinct geographic areas — top geographies include California, Florida, New Hampshire. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05820672 about?

NCT05820672 is a clinical study titled "A US Non-interventional, Effectiveness and Safety Study of Patients Treated With SKYTROFA". The goal of this study is to genrate evidence on long-term effectiveness and safety of SKYTROFA (lonapegsomatropin) in patients with growth hormone deficiency under routine clinical care

What is the current status of trial NCT05820672?

This trial is currently recruiting. The enrollment target is 900 participants. The study started on 2023-03-20. Estimated completion is 2033-03.

What conditions does trial NCT05820672 study?

This clinical trial studies the following conditions: Growth Hormone Deficiency. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05820672?

The interventions under investigation include: No intervention (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05820672?

This trial is sponsored by Ascendis Pharma Endocrinology Division A/S, which has 35 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05820672 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.

Related

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