Purpose

This is a long-term, multi-center, observational study in children 2.5 to <17 years with achondroplasia (ACH). The objective is to evaluate growth, ACH-related medical complications, assessments of health-related quality of life, body pain, functional abilities, cognitive functions, and treatments of study participants. No study medication will be administered.

Condition

Eligibility

Eligible Ages
Between 30 Months and 17 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Signed informed consent by study participant or parent(s) or legally authorized representative (LAR) and signed informed assent by the study participant (when applicable) - Aged 2.5 to <17 years at study entry - Diagnosis of ACH - Study participants and parent(s) or LAR(s) are willing and able to comply with study visits and study procedures

Exclusion Criteria

  • Have hypochondroplasia or short stature condition other than ACH (e.g. trisomy 21, pseudoachondroplasia, psychosocial short stature) - In females, having had their menarche - Height < -2 or > +2 standard deviations for age and sex based on reference tables on growth in children with ACH - Annualized height growth velocity ≤1.5 cm/year over a period ≥6 months prior to screening - Have a concurrent disease or condition that in the view of the Investigator and/or Sponsor, may impact growth or where the treatment is known to impact growth. - Significant abnormality in screening laboratory results. - Have been treated with growth hormone, insulin-like growth factor 1 (IGF 1), or anabolic steroids in the previous 6 months or long-term treatment (>3 months) at any time - Have had regular long-term treatment (>1 month) with oral corticosteroids (low-dose ongoing inhaled steroid for asthma is acceptable) - Have had previous guided growth surgery or limb-lengthening surgery within 12 months prior to screening.

Study Design

Phase
Study Type
Observational
Observational Model
Case-Only
Time Perspective
Prospective

Recruiting Locations

Vanderbilt University Medical Center
Nashville, Tennessee 37232
Contact:
LeeAnna Melton
615-343-6761
leeanna.melton@vumc.org

More Details

Status
Recruiting
Sponsor
QED Therapeutics, Inc.

Study Contact

QED Therapeutics, Inc.
1-877-280-5655
PROPELstudyinfo@QEDTX.com

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.