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Hypochondroplasia Clinical Trials

Hypochondroplasia is a rare genetic condition generally characterized by short stature, stocky build, disproportionately short arms and legs, broad, short hands and feet, mild joint laxity, scoliosis, and macrocephaly.

Learn more about our hypochondroplasia clinical trials below.

Vosoritide

Studies

Study 111-902 Recruiting

A Multicenter Multinational Observational Study of Children With Hypochondroplasia

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Indication

A Multicenter Multinational Observational Study of Children With Hypochondroplasia

Goal

This study will assess growth over time and the clinical course of HCH in children by collecting growth measurements and other variables of interest.

Investigational therapeutic

N/A

Status

This study is currently recruiting participants

Study Type

Observational

Study Website

https://hypochondroplasiastudy.biomarin.com/