RecruitingNCT06410976
Rare condition
Hypochondroplasia
5
studies recruiting now
as of 7 Sept 2026
13
studies registered in total
as of 7 Sept 2026
15
countries with a recruiting site
as of 7 Sept 2026
5 Feb 2026
most recent study posted
among recruiting studies
Recruiting trials
RecruitingPhase 2NCT07126262
A Study of Vosoritide Versus Placebo in Children With Hypochondroplasia Aged 0 to < 36 Months
RecruitingNCT07388966
Prospective Longitudinal Monocentric Study to Measure Limb Movement in Patients With FGFR3-related Skeletal Dysplasia
RecruitingNCT06212947
A Multicenter Multinational Observational Study of Children With Hypochondroplasia
RecruitingNCT05328050
Registry for Patients With Achondroplasia / Hypochondroplasia (OMPR-Ach/Hy)
Showing the 5 most recently updated recruiting studies, as recorded 7 Sept 2026. Live status on each study page.
Search all Hypochondroplasia studiesWhere recruiting studies are running
Countries with at least one recruiting site among the studies above, 7 Sept 2026. Tap a country to search trials there.
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Patient organisations
We do not yet list a dedicated organisation for this condition. The directories below are the best route.
About Hypochondroplasia
RareTrial does not yet hold a plain-language description of this condition. The most reliable starting point is Orphanet’s expert page, which lists specialist centres, registries and patient organisations, and the gene involved (FGFR3).
Treatments being studied
2 in clinical development, from Open Targets (CC BY 4.0). Not medical advice.
Phase 3Vosoritide (Voxzogo)
Phase 2Somatropin (Genotropin)
Information, not medical advice. Trial listings are shown as recorded on ClinicalTrials.gov; whether any study is right for you is a decision for you and your clinicians, and eligibility is decided by each research team. Disease information from Orphanet (CC BY 4.0).