Clin2
NCT07126262Possibly a fitRecruiting

Vosoritide for growth in infants with hypochondroplasia

Hypochondroplasia

Treatments studied

Part of Bones, joints & muscles, Genetic & congenital clinical trials.

This study tests a daily injection called vosoritide to see if it helps children with hypochondroplasia grow taller. It is for babies and toddlers up to 35 months old who are shorter than average for their age.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
60 people
Ages
birth to 3 years
Study type
Interventional

Who can take part

  • Your child must be between birth and 35 months old when starting the study.
  • A genetic test must confirm a diagnosis of hypochondroplasia (a change in the FGFR3 gene).
  • Your child's height must be significantly shorter than average for their age and sex.
  • Your child's weight must be at least 6.6 pounds (3 kg) on the first day of treatment.
  • Your child cannot have any other condition that causes short stature, like achondroplasia or Down syndrome.
  • Your child cannot have taken growth hormone or certain other medicines in the past 6 months.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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