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Completed No phase listed Observational

A Multi-center, Longitudinal, Observational Study of Children With Achondroplasia

ClinicalTrials.gov ID: NCT03875534

Public ClinicalTrials.gov record NCT03875534. 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 28, 2026, 11:02 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

ACHieve: A Multi-center, Longitudinal, Observational Study of Children With Achondroplasia

Brief summary

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

This is a long-term, multi-center, longitudinal, observational study in children with achondroplasia (ACH). The aim is to study height velocity and comorbidities in children with ACH. This is a natural history study and no study medication will be administered.

Study identification

NCT ID
NCT03875534
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Ascendis Pharma A/S
Industry
Enrollment
260 participants

Conditions and interventions

Conditions

Interventions

Not listed

Eligibility (public fields only)

Age range
0 Years to 8 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
Jun 19, 2019 (Actual)
Primary completion
Jan 12, 2024 (Actual)
Completion
Jan 12, 2024 (Actual)
Last update posted
Mar 19, 2024

2019 – 2024

United States locations

U.S. sites
10
U.S. states
10
U.S. cities
10
Facility City State ZIP Site status
Ascendis Pharma Investigational Site Little Rock Arkansas 72211 —
Ascendis Pharma Investigational Site Oakland California 94609 —
Ascendis Pharma Investigational Site Aurora Colorado 80045 —
Ascendis Pharma Investigational Site Wilmington Delaware 19803 —
Ascendis Pharma Investigational Site Saint Paul Minnesota 55102 —
Ascendis Pharma Investigational Site Columbia Missouri 65212 —
Ascendis Pharma Investigational Site Buffalo New York 14203 —
Ascendis Pharma Investigational Site Houston Texas 77030 —
Ascendis Pharma Investigational Site Seattle Washington 98105 —
Ascendis Pharma Investigational Site Madison Wisconsin 53705 —

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 25 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03875534, 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 Mar 19, 2024 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03875534 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →