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A Study to Evaluate Long-Term Safety, Tolerability, & Efficacy of BMN 111 in Children With Achondroplasia (ACH)

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NCT02724228 · readout ≤ 498 d

Sponsored by BioMarin Pharmaceutical (industry) · BMRN — their whole pipeline →.

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
30actual
Sites
9
Countries
Australia, France, United Kingdom +1

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2016-01-26actualWhen the study began enrolling
Primary completionDec 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionFeb 2028estimatedThe whole study's end, after follow-up
First posted2016-03-31estimatedWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-03-13actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Achondroplasia

Intervention

  • Drug: BMN 111 — also filed as Modified recombinant human C-type natriuretic peptide, Vosoritide

Primary outcome

what the primary-completion date above is the date OF
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]
measured Until near final adult height is reached, and up to at least 16 years of age for females and 18 years of age for males, whichever occurs later

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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